19 Emplois pour Senior/clinical research associate - Brussels
Senior/Clinical Research Associate
Brussels
ThermoFisher Scientific
Publié il y a 12 jours
Emploi consulté
Description De L'emploi
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
We currently have an opportunity for a CRA to join our Clinical Operations department in Belgium as a CRA at all levels, depending on experience. This opportunity can be based from our office in Brussels or home based anywhere in Belgium. The position is available on full- time and part- time basis.
Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants.
**As a Sr/Clinical Research Associate, you will:**
+ Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, challenging projects.
+ Have excellent communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work.
+ Perform and coordinate all aspects of the clinical monitoring process.
+ You shall also be qualified to conduct monitoring activities independently.
+ Benefit from award winning training programmes that will assist your technical and professional skills and knowledge
**Keys to Success:**
+ University degree in a life-sciences field
+ Minimum 1+ year of independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation
+ Demonstrated understanding of ICH-GCP, EU and FDA requirements
+ Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
+ Exceptional communication, collaboration, organisational and time management skills
+ Fluency in English, French and Dutch languages is essential
**What we offer:**
At PPD clinical research services we hire the best, develop ourselves and each other, and recognise the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development programme, ensuring you reach your potential.
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
We currently have an opportunity for a CRA to join our Clinical Operations department in Belgium as a CRA at all levels, depending on experience. This opportunity can be based from our office in Brussels or home based anywhere in Belgium. The position is available on full- time and part- time basis.
Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants.
**As a Sr/Clinical Research Associate, you will:**
+ Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, challenging projects.
+ Have excellent communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work.
+ Perform and coordinate all aspects of the clinical monitoring process.
+ You shall also be qualified to conduct monitoring activities independently.
+ Benefit from award winning training programmes that will assist your technical and professional skills and knowledge
**Keys to Success:**
+ University degree in a life-sciences field
+ Minimum 1+ year of independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation
+ Demonstrated understanding of ICH-GCP, EU and FDA requirements
+ Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
+ Exceptional communication, collaboration, organisational and time management skills
+ Fluency in English, French and Dutch languages is essential
**What we offer:**
At PPD clinical research services we hire the best, develop ourselves and each other, and recognise the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development programme, ensuring you reach your potential.
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Désolé, cet emploi n'est pas disponible dans votre région
0
Clinical Research Associate
Brussels
Panda International
Aujourd'hui
Emploi consulté
Description De L'emploi
Job Role: Clinical Research Associate II – MedTech
About the Role:
A leading MedTech organization is seeking a detail-oriented and proactive Clinical Research Associate II (CRA II) to join the MedTech Clinical Operations team. In this role, you will manage clinical activities at multiple study sites, ensuring patient safety, protocol compliance, and high-quality data collection, while fostering strong relationships with site staff and internal stakeholders.
Key Responsibilities:
- Manage clinical study activities across multiple sites for assigned projects.
- Ensure study site compliance with protocols, SOPs, GCP, and regulatory requirements.
- Conduct site visits, monitor performance, and provide timely support to resolve site issues.
- Verify Investigator Site Files and support documentation maintenance.
- Support patient recruitment, retention, and training initiatives.
- Facilitate internal communication of key study data and events.
- Participate in implementation of new clinical systems and processes.
- Interface and collaborate with investigators, IRBs/ECs, vendors, and internal stakeholders.
- Maintain accurate study site status knowledge and provide updates to project teams.
- Support internal continuous improvement and operational excellence initiatives.
Requirements:
- Bachelor’s degree in Life Science, Physical Science, Nursing, or Biological Science (Master’s/PhD/MD/PharmD preferred).
- Minimum 2 years of relevant clinical research experience; 1 year with advanced degree.
- Previous medical device monitoring experience or equivalent.
- Knowledge of regulations and standards in clinical research for medical devices/combination products.
- Relevant industry certifications preferred (e.g., CCRA, RAC, CDE).
- Strong written and verbal communication, leadership, and organizational skills.
- Proficiency in Microsoft Office (Excel, Word, PowerPoint).
- Clinical/medical background is a plus.
- Ability to travel up to 80% of the time.
Practical’s:
- Location: Diegem, Belgium
- Duration: 12-month contract
- Start Date: ASAP
- Work Model: Full-time, travel required up to 80%
Interested or know someone who might be?
Send your CV or inquiries to to apply or learn more.
Désolé, cet emploi n'est pas disponible dans votre région
1
Clinical Research Associate
Machelen, Vlaams Brabant
Panda International
Aujourd'hui
Emploi consulté
Description De L'emploi
About the Role
We are looking for an experienced CRA III (or Senior CRA, depending on experience) to support a high-profile pre-approval neurovascular medical device trial across 11 hospitals/research sites in Belgium, France, and Ireland. This role involves frequent site monitoring, ensuring patient safety, regulatory compliance, and high-quality data collection.
Key Responsibilities
- Conduct site initiation, monitoring, and close-out visits.
- Oversee site compliance with study protocols, GCP, and regulations.
- Maintain Investigator Site Files and ensure accurate documentation.
- Support recruitment, retention, and site performance.
- Troubleshoot site issues and implement corrective actions.
- Collaborate with investigators, IRBs/ECs, vendors, and internal teams.
- Provide regular updates on site and trial progress.
What We’re Looking For
- Bachelor’s degree in Life Sciences (or equivalent).
- 4–6 years of on-site monitoring experience (medical device preferred).
- Background in neurovascular or cardiovascular trials is a plus.
- Proficiency in English, Dutch, and French (working level – full fluency not required).
- Strong organizational and communication skills.
- Proficiency with Microsoft Office tools.
- Willingness to travel extensively across BE/FR/IE (monitoring visits every 1–2 months).
Désolé, cet emploi n'est pas disponible dans votre région
2
Director/Senior Director, Decentralized Clinical Trials (DCT), Business Development & Strategy, E...
Brussels
IQVIA
Publié il y a 6 jours
Emploi consulté
Description De L'emploi
**Join us on our exciting journey!**
IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.
**Director/Senior Director, Decentralized Clinical Trials (DCT), Business Development & Strategy, EMEA.**
**1 year contract.**
IQVIA's Decentralized Clinical Trials (DCT) enables remote and hybrid clinical studies by connecting patients through digital tools, wearable devices, and virtual visits. It improves accessibility, speeds up recruitment, and ensures compliance across diverse global regulations.
**Responsibilities**
**Client engagement and understanding of client business.**
+ Captures market share by aligning offerings with client needs and regional trends.
+ Maintains and further establishes strong professional relationships across the client organization; with a particular focus on Decentralized Clinical Trials, proactively but appropriately engages with client teams.
+ Responsible for developing and maintaining deep client knowledge; understanding of their business priorities, organizational culture, product portfolio and pipeline, spend/budget priorities.
+ Manages a systematic client-feedback approach, soliciting information from client teams about experience of working with IQVIA.
**Operations management : Leads on the operational management and oversight of IQVIA's DCT activities for local and international markets**
+ Manage assigned strategic and key account relationships individually or in coordination with Global and Regional Sales Teams
+ Identify and respond to customer needs to define potential opportunities for DCT and propose appropriate tailored solutions in line with client needs.
+ Collaborates with IQVIA's Internal RFX, Pricing & Contracts team to support the sales cycle from RFX to sales.
+ Coordinating across clinical operations, technology, and commercial teams to ensure cohesive delivery of DCT solutions.
**Shaping client's perception of IQVIA**
+ Ensures regulatory and operational alignment by tailoring approaches to accommodate Europe's diverse and complex regulatory landscape
+ Identifies opportunities to engage with Client teams to bring relevant marketing and Thought Leadership materials.
+ Manages the annual Strategic Management Review conference.
+ Identifies, or creates opportunities to introduce relevant IQVIANs or teams who are working in areas of high interest for the client, as part of 'peer to peer' engagement (i.e., beyond IQVIA capability presentations, or specific pitches / RFPs)
**Bringing innovation to Client**
+ The Director will champion innovation, integrating emerging technologies and methodologies to differentiate IQVIA services
+ Building on their knowledge of client priorities and in close partnership with the Clinical, Technology Business Partners, and Global Account Director identifies strategic discussions and major opportunities for IQVIA.
+ Actively engages in the Sales and Account Management community, bringing in relevant ideas and success stories from other major accounts.
**Requirements**
+ Extensive knowledge of Decentralized Clinical Trials
+ 10+ years of experience of working in a Sales, Sales engineer, Business development or similar position within the pharmaceutical, CRO, Tech, health, life science or other related regulated industry
+ Proven track record of managing mid-level and high-level contacts
+ Strong organizational, planning, project management skills
+ A developing record of customer contacts at the outsourcing, procurement and mid - management level
+ Excellent Business/Industry awareness and a thorough understanding of industry trends and impact on the business
+ Excellent analytical skills in assessing and interpreting customer business data
+ Ability to maintain demanding timelines
+ Ability to influence others internally and externally
+ Adaptability and flexibility to changing priorities
+ Demonstrated ability to work creatively in a fast-paced environment
+ Exceptional attention to detail and ability to work simultaneously on multiple priorities
+ Ability to work independently and as a team player
+ Excellent skills using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel
+ Excellent oral and written communication skills
+ Ability to establish and maintain effective working relationships with co-workers, managers, and clients
**Why Join?**
Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. In Technology, you will have access to the most cutting-edge technology, the largest data sets, the best analytics tools and, in our opinion, some of the finest minds in the Healthcare industry.
You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries.
We know that meaningful results require not only the right approach but also **the right people** . Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.
It's an exciting time to join and reimagine what's possible in healthcare.
**Moving healthcare forward. Together.**
_IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential._
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.
**Director/Senior Director, Decentralized Clinical Trials (DCT), Business Development & Strategy, EMEA.**
**1 year contract.**
IQVIA's Decentralized Clinical Trials (DCT) enables remote and hybrid clinical studies by connecting patients through digital tools, wearable devices, and virtual visits. It improves accessibility, speeds up recruitment, and ensures compliance across diverse global regulations.
**Responsibilities**
**Client engagement and understanding of client business.**
+ Captures market share by aligning offerings with client needs and regional trends.
+ Maintains and further establishes strong professional relationships across the client organization; with a particular focus on Decentralized Clinical Trials, proactively but appropriately engages with client teams.
+ Responsible for developing and maintaining deep client knowledge; understanding of their business priorities, organizational culture, product portfolio and pipeline, spend/budget priorities.
+ Manages a systematic client-feedback approach, soliciting information from client teams about experience of working with IQVIA.
**Operations management : Leads on the operational management and oversight of IQVIA's DCT activities for local and international markets**
+ Manage assigned strategic and key account relationships individually or in coordination with Global and Regional Sales Teams
+ Identify and respond to customer needs to define potential opportunities for DCT and propose appropriate tailored solutions in line with client needs.
+ Collaborates with IQVIA's Internal RFX, Pricing & Contracts team to support the sales cycle from RFX to sales.
+ Coordinating across clinical operations, technology, and commercial teams to ensure cohesive delivery of DCT solutions.
**Shaping client's perception of IQVIA**
+ Ensures regulatory and operational alignment by tailoring approaches to accommodate Europe's diverse and complex regulatory landscape
+ Identifies opportunities to engage with Client teams to bring relevant marketing and Thought Leadership materials.
+ Manages the annual Strategic Management Review conference.
+ Identifies, or creates opportunities to introduce relevant IQVIANs or teams who are working in areas of high interest for the client, as part of 'peer to peer' engagement (i.e., beyond IQVIA capability presentations, or specific pitches / RFPs)
**Bringing innovation to Client**
+ The Director will champion innovation, integrating emerging technologies and methodologies to differentiate IQVIA services
+ Building on their knowledge of client priorities and in close partnership with the Clinical, Technology Business Partners, and Global Account Director identifies strategic discussions and major opportunities for IQVIA.
+ Actively engages in the Sales and Account Management community, bringing in relevant ideas and success stories from other major accounts.
**Requirements**
+ Extensive knowledge of Decentralized Clinical Trials
+ 10+ years of experience of working in a Sales, Sales engineer, Business development or similar position within the pharmaceutical, CRO, Tech, health, life science or other related regulated industry
+ Proven track record of managing mid-level and high-level contacts
+ Strong organizational, planning, project management skills
+ A developing record of customer contacts at the outsourcing, procurement and mid - management level
+ Excellent Business/Industry awareness and a thorough understanding of industry trends and impact on the business
+ Excellent analytical skills in assessing and interpreting customer business data
+ Ability to maintain demanding timelines
+ Ability to influence others internally and externally
+ Adaptability and flexibility to changing priorities
+ Demonstrated ability to work creatively in a fast-paced environment
+ Exceptional attention to detail and ability to work simultaneously on multiple priorities
+ Ability to work independently and as a team player
+ Excellent skills using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel
+ Excellent oral and written communication skills
+ Ability to establish and maintain effective working relationships with co-workers, managers, and clients
**Why Join?**
Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. In Technology, you will have access to the most cutting-edge technology, the largest data sets, the best analytics tools and, in our opinion, some of the finest minds in the Healthcare industry.
You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries.
We know that meaningful results require not only the right approach but also **the right people** . Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.
It's an exciting time to join and reimagine what's possible in healthcare.
**Moving healthcare forward. Together.**
_IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential._
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Désolé, cet emploi n'est pas disponible dans votre région
3
Clinical Research Associate (CRA)
1830 Machelen, Vlaams Brabant
Jefferson Wells
Publié il y a 13 jours
Emploi consulté
Description De L'emploi
Contracting – Antwerpen
Originele vacature is te vinden op StepStone.be – Maak nu een Jobagent aan op StepStone en vind je droombaan! Vind gelijkaardige jobs, informatie over werkgevers en carrièretips op StepStone.be! Original job ad is published on StepStone.be - Set up a Jobagent at StepStone now and find your dream job! For similar jobs, information on employers and career tips visit StepStone.be! La version originale de cette offre d'emploi est disponible sur stepstone.be – Créez maintenant votre Job Agent sur StepStone et trouvez le job de vos rêves ! Trouvez des jobs similaires, des informations sur les employeurs qui recrutent et des conseils de carrière sur stepstone.be!
Désolé, cet emploi n'est pas disponible dans votre région
4
Clinical Research Associate (CRA)
Machelen, Vlaams Brabant
Jefferson Wells
Aujourd'hui
Emploi consulté
Description De L'emploi
Contracting – Antwerpen
- Ensure the safety and well-being of study subjects at assigned clinical sites.
- Support the operational execution of clinical trials and ensure high-quality data collection.
- Perform trial activities in compliance with SOPs, GCP, and applicable regulatory requirements.
- Be accountable for site performance and delivery of high-quality data within project timelines.
- Assist Clinical Operations staff and site personnel to resolve issues and implement CAPAs when needed.
- Verify that Investigator Site Files are maintained according to regulations and company procedures.
- Support patient recruitment and retention activities.
- Conduct site visits to ensure compliance with protocol and regulations.
- Contribute to the internal communication of important clinical data and events.
- Support the organization of Investigator meetings and study trainings.
- Serve as a reliable resource for up-to-date site status knowledge for stakeholders.
- Assist in the implementation of new clinical systems and processes.
- Collaborate with Investigators, IRBs/ECs, vendors, and internal staff.
- Comply with all applicable laws, regulations, and company compliance policies.
- Bachelor's Master's , PhD in Life Sciences, Physical Sciences, Nursing, or Biological Sciences required.
- Fluency in English, French and Dutch.
- Previous clinical research experience required.
- Experience in medical device monitoring (or equivalent) required.
- Solid understanding of regulations and standards in clinical research and medical devices/combination products.
- Relevant industry certifications (e.g., CCRA, RAC, CDE) are an asset.
- Clinical/medical background is a plus.
- Proficiency in Microsoft Office (Excel, Word, PowerPoint)
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You're interested in this job? We kindly invite you to apply or send me your CV,
PowerPoint, ECS, Medical Devices, Company Procedures, CRA, Delivery, Wellbeing Support, Problem Management, Clinical Research, Life Science, Asset, Law, Regulation, Site Visits, Training, Monitoring, Policy, Nursing, Project Timelines, Company Compliance, Natural science, VOS, Health & Safety, System Process, Life Science, Clinical Research, Patient Support, MS Excel, Clinical Operations, MS Office Suite, Medical Devices, Data acquisition, CAPA, Implementation, Vendors
Désolé, cet emploi n'est pas disponible dans votre région
5
Research Associate
1420 Eigenbrakel, Waals Brabant
Jefferson Wells
Aujourd'hui
Emploi consulté
Description De L'emploi
Contracting – Brabant Wallon
Originele vacature is te vinden op StepStone.be – Maak nu een Jobagent aan op StepStone en vind je droombaan! Vind gelijkaardige jobs, informatie over werkgevers en carrièretips op StepStone.be! Original job ad is published on StepStone.be - Set up a Jobagent at StepStone now and find your dream job! For similar jobs, information on employers and career tips visit StepStone.be! La version originale de cette offre d'emploi est disponible sur stepstone.be – Créez maintenant votre Job Agent sur StepStone et trouvez le job de vos rêves ! Trouvez des jobs similaires, des informations sur les employeurs qui recrutent et des conseils de carrière sur stepstone.be!
Originele vacature is te vinden op StepStone.be – Maak nu een Jobagent aan op StepStone en vind je droombaan! Vind gelijkaardige jobs, informatie over werkgevers en carrièretips op StepStone.be! Original job ad is published on StepStone.be - Set up a Jobagent at StepStone now and find your dream job! For similar jobs, information on employers and career tips visit StepStone.be! La version originale de cette offre d'emploi est disponible sur stepstone.be – Créez maintenant votre Job Agent sur StepStone et trouvez le job de vos rêves ! Trouvez des jobs similaires, des informations sur les employeurs qui recrutent et des conseils de carrière sur stepstone.be!
Désolé, cet emploi n'est pas disponible dans votre région
Soyez le premier informé
À propos du dernier Senior/clinical research associate Emplois dans Brussels !
6
Experienced Clinical Research Associate, FSP Belgium
Zaventem, Vlaams Brabant
IQVIA
Publié il y a 13 jours
Emploi consulté
Description De L'emploi
**_Clinical Research Associate_**
IQVIA Belgium is looking for talented and motivated team member to join our Sponsor dedicated team CRA (Junior - Senior) . At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.
**Your responsibilities will include:**
+ Performing site selection, initiation, monitoring and close-out visits
+ Supporting the development of a subject recruitment plan
+ Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
+ Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
+ Collaborating with experts at study sites and with client representatives
**Your Profile**
+ University degree in scientific discipline or health care
+ Experience in Pharma Industry, and/or Clinical Trials environment
+ Very good computer skills including MS Office
+ Excellent command of Dutch, French and English language. Belgium based.
+ Organizational, time management and problem-solving skills
+ Ability to establish and maintain effective working relationships with coworkers, managers, and clients
+ Flexibility to travel
+ Driver's license class B
**What you can expect:**
+ Resources that promote your career growth
+ Leaders that support flexible work schedules
+ Programs to help you build your therapeutic knowledge
+ Excellent working environment in a stabile, international, reputable company
+ Company car, mobile phone and attractive benefits packaging
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
IQVIA Belgium is looking for talented and motivated team member to join our Sponsor dedicated team CRA (Junior - Senior) . At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.
**Your responsibilities will include:**
+ Performing site selection, initiation, monitoring and close-out visits
+ Supporting the development of a subject recruitment plan
+ Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
+ Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
+ Collaborating with experts at study sites and with client representatives
**Your Profile**
+ University degree in scientific discipline or health care
+ Experience in Pharma Industry, and/or Clinical Trials environment
+ Very good computer skills including MS Office
+ Excellent command of Dutch, French and English language. Belgium based.
+ Organizational, time management and problem-solving skills
+ Ability to establish and maintain effective working relationships with coworkers, managers, and clients
+ Flexibility to travel
+ Driver's license class B
**What you can expect:**
+ Resources that promote your career growth
+ Leaders that support flexible work schedules
+ Programs to help you build your therapeutic knowledge
+ Excellent working environment in a stabile, international, reputable company
+ Company car, mobile phone and attractive benefits packaging
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Désolé, cet emploi n'est pas disponible dans votre région
7
Experienced Clinical Research Associate, Multi-Sponsor, Belgium
Brussels
IQVIA
Publié il y a 13 jours
Emploi consulté
Description De L'emploi
**_Clinical Research Associate_**
IQVIA Belgium is looking for talented and motivated experienced CRA to join our Site Management team. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
**Your responsibilities will include:**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.- Collaborate and liaise with study team members for project execution support as appropriate.
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
**Your Profile**
+ University degree in scientific discipline or health care
+ 2+ years of experience as a CRA
+ Very good computer skills including MS Office
+ Excellent command of Dutch, French and English language. Belgium based.
+ Organizational, time management and problem-solving skills
+ Ability to establish and maintain effective working relationships with coworkers, managers, and clients
+ Flexibility to travel
+ Driver's license class B
**What you can expect:**
+ Resources that promote your career growth
+ Leaders that support flexible work schedules
+ Programs to help you build your therapeutic knowledge
+ Excellent working environment in a stabile, international, reputable company
+ Company car, mobile phone and attractive benefits packaging
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
IQVIA Belgium is looking for talented and motivated experienced CRA to join our Site Management team. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
**Your responsibilities will include:**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.- Collaborate and liaise with study team members for project execution support as appropriate.
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
**Your Profile**
+ University degree in scientific discipline or health care
+ 2+ years of experience as a CRA
+ Very good computer skills including MS Office
+ Excellent command of Dutch, French and English language. Belgium based.
+ Organizational, time management and problem-solving skills
+ Ability to establish and maintain effective working relationships with coworkers, managers, and clients
+ Flexibility to travel
+ Driver's license class B
**What you can expect:**
+ Resources that promote your career growth
+ Leaders that support flexible work schedules
+ Programs to help you build your therapeutic knowledge
+ Excellent working environment in a stabile, international, reputable company
+ Company car, mobile phone and attractive benefits packaging
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Désolé, cet emploi n'est pas disponible dans votre région
8
Executive Search – Research Associate
Brussels
TRANSEARCH
Aujourd'hui
Emploi consulté
Description De L'emploi
TRANSEARCH International is one of the leading executive search organisations in the world. Headquartered in Europe, we have representation in The Americas, Asia Pacific, Europe, Middle East and Africa. Our global presence allows us to service companies around the world - covering all the major industry sectors.
TRANSEARCH International Belgium is currently looking to hire an additional Research Associate to join our Brussels office.
You will be part of our Research team and work closely with our Consultants. You will be responsible for carrying out research as well as other appropriate tasks specifically around adding value to our Executive Search service.
Your tasks will include but not be limited to:
Briefing: You will join Consultants in client meetings to jointly take job briefs for active positions, asking accurate questions to be able to target the right candidates for the right opportunities.
You will then prepare market mappings and put together high-level information packs for candidates to better understand the client, role and job challenges.
Candidate Research: You will be responsible for researching and sourcing information on prospective candidates from a range of external and internal databases, deep web searching, social media and other means and ensuring that all information is managed appropriately.
You should be comfortable with carrying out lengthy and in-depth database searches, should be organised and be able to manage your own time well.
Candidate interaction: You will have qualitative conversations with candidates, mainly over the phone, to analyse skills, knowledge, personality and motivations.
Can we be bold for a moment?
Make no mistake, Executive Search is a very demanding environment. It’s no 9-to-5 job, but we offer tremendous autonomy so you can organize your time in order to have an excellent work-life balance.
We’re in people business and our service level defines our success. It can be very frustrating not having control over every aspect of the job. But it is incredibly rewarding as a job as well. You learn new stuff every day, you interact with high level profiles and you have a real impact on people’s life.
If you find your ideal job is as a Researcher, you can do it for as long as you want to !
And if you want to explore other responsibilities, TRANSEARCH is the right place for you too. You will be able to grow within the organization, take initiatives, interact at international level and make great personal and professional steps.
Profile:
- You have great communication skills.
- You ideally have a first experience or interest the search business or in an HR related environment.
- Self-starter, someone who can organize his/her time.
- Structured and very well organized.
- Value-driven individual.
- Work hard - play hard mentality.
- Language skills: English, Dutch, French.
Désolé, cet emploi n'est pas disponible dans votre région
9