29 Emplois pour Senior/Clinical Research Associate - Belgique
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
Senior Clinical Research Associate (Site Manager)
Beerse, Antwerpen
J&J Family of Companies
Publié il y a 27 jours
Emploi consulté
Description De L'emploi
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
R&D Operations
**Job Sub** **Function:**
Clinical Trial Support
**Job Category:**
Professional
**All Job Posting Locations:**
Beerse, Antwerp, Belgium
**Job Description:**
We are looking for a driven Senior Site Manager (Clinical Research Associate) to serve as the primary contact point between the Sponsor and the Investigational Site for trials in Late Development (phase 1b-2-3). As Senior Site Manager, you will be assigned to trial sites to ensure compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), as well as applicable regulations and guidelines. You will do so from study start-up until site closure. Our new colleague should be flexible and able to work independently. We are seeking to hire a strong communicator and team player, with quick learning and problem-solving abilities. The Senior Site Manager will collaborate with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA), and Clinical Trial Manager (CTM) to ensure overall site management while performing trial-related activities for assigned protocols. You will be part of a hardworking, enthusiastic, and committed team of +100 people eager to deliver and helping to improve the lives of millions of patients!
**Principal Responsibilities:**
+ Responsible for executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study-specific systems and other reports/dashboards), and site/study close-out according to SOPs, Work Instructions (WIs), and policies.
+ Responsible for the implementation of an analytical risk-based monitoring model at the site level and to work with the site to ensure timely resolution of issues found during monitoring visits.
+ Participating in site-level recruitment strategy and contingency planning and implementation in partnership with other functional areas.
+ Attends regularly scheduled team meetings and training.
+ May participate to process improvement and training.
+ May be assigned as a coach or mentor to less experienced colleagues.
+ Leads and/or participates in special initiatives as assigned.
+ May assume additional responsibilities or special initiatives such as 'Champion' or ''Subject Matter Expert'.
**Education and Experience Requirements:**
+ BA/BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience)
+ A minimum of 3 years of clinical trial monitoring experience is preferred, however, other relevant working experiences and skills may be considered by the hiring manager
+ Strong proven understanding of GCP, local laws, and regulations
+ Strong IT skills in appropriate software and company systems
+ Willingness to travel with occasional overnight stay away from home
+ Drivers license B required
+ Fluent in Dutch and English (for candidates based in the Netherlands)
+ Fluent in Dutch, English, and French (for candidates based in Belgium)
R&D Operations
**Job Sub** **Function:**
Clinical Trial Support
**Job Category:**
Professional
**All Job Posting Locations:**
Beerse, Antwerp, Belgium
**Job Description:**
We are looking for a driven Senior Site Manager (Clinical Research Associate) to serve as the primary contact point between the Sponsor and the Investigational Site for trials in Late Development (phase 1b-2-3). As Senior Site Manager, you will be assigned to trial sites to ensure compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), as well as applicable regulations and guidelines. You will do so from study start-up until site closure. Our new colleague should be flexible and able to work independently. We are seeking to hire a strong communicator and team player, with quick learning and problem-solving abilities. The Senior Site Manager will collaborate with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA), and Clinical Trial Manager (CTM) to ensure overall site management while performing trial-related activities for assigned protocols. You will be part of a hardworking, enthusiastic, and committed team of +100 people eager to deliver and helping to improve the lives of millions of patients!
**Principal Responsibilities:**
+ Responsible for executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study-specific systems and other reports/dashboards), and site/study close-out according to SOPs, Work Instructions (WIs), and policies.
+ Responsible for the implementation of an analytical risk-based monitoring model at the site level and to work with the site to ensure timely resolution of issues found during monitoring visits.
+ Participating in site-level recruitment strategy and contingency planning and implementation in partnership with other functional areas.
+ Attends regularly scheduled team meetings and training.
+ May participate to process improvement and training.
+ May be assigned as a coach or mentor to less experienced colleagues.
+ Leads and/or participates in special initiatives as assigned.
+ May assume additional responsibilities or special initiatives such as 'Champion' or ''Subject Matter Expert'.
**Education and Experience Requirements:**
+ BA/BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience)
+ A minimum of 3 years of clinical trial monitoring experience is preferred, however, other relevant working experiences and skills may be considered by the hiring manager
+ Strong proven understanding of GCP, local laws, and regulations
+ Strong IT skills in appropriate software and company systems
+ Willingness to travel with occasional overnight stay away from home
+ Drivers license B required
+ Fluent in Dutch and English (for candidates based in the Netherlands)
+ Fluent in Dutch, English, and French (for candidates based in Belgium)
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1
Clinical Research Associate
Advanced Resource Managers
Aujourd'hui
Emploi consulté
Description De L'emploi
Title: Clinical Research Associate (FSP)
Location: Belgium (remote)
Salary: Up to €62,000 plus car allowance/company car and benefits
My client is a top global CRO specialising in the completion of complex clinical trials and is a global leader in delivering comprehensive, integrated drug development services to the pharmaceutical, biotechnology, and medical device industries.
Responsibilities
- Independently conduct on-site and remote monitoring visits, ensuring protocol, regulatory, and ICH‐GCP compliance, including source data verification (SDV), case report form (CRF) review, and investigational product accountability
- Apply risk-based monitoring approaches, conduct root‐cause analyses, and implement corrective/preventive actions to address site performance issues
- Maintain regular contact with investigative sites between visits to track issue resolution and protocol adherence
- Provide trial status updates to Clinical Team Manager (CTM) and ensure CTMS data is current
Experience
- Up to 2 years of independent clinical monitoring experience (comparable to CRA I + CRA II), ideally within CRO/pharma.
- Valid driver’s license and right to work in Belgium
- Strong knowledge of ICH‐GCP, EU/FDA regulations and local Belgian requirements
Benefits
- Competitive salary with company car or car allowance
- Private healthcare
- Financial assistance with home office setup
- Ability to purchase an extra holiday in addition to the 30-day holiday
Please apply via LinkedIn or contact me at
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2
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.
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3
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).
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4
Clinical Research Associate
AL Solutions
Aujourd'hui
Emploi consulté
Description De L'emploi
Clinical Research Associate – Belgium
Chloe O’Shea is excited to partner with a leading global CRO known for delivering innovative, high-quality solutions in clinical development. We are seeking a Clinical Research Associate (CRA) to join a dedicated single-sponsor team in Belgium. This is a fantastic opportunity to gain hands-on experience in clinical trials, with exposure to cutting-edge therapy areas such as CAR-T and gene therapy. While prior experience in these fields is a plus, full training and support will be provided.
The Role
As a CRA, you will support the successful delivery of clinical trials across Belgium. You will assist in site management activities, act as a point of contact for investigative sites, and ensure compliance with protocols, ICH-GCP, and Belgian regulatory requirements. This role is ideal for ambitious CRAs with 6 months to 2 years of experience who are eager to develop their skills in innovative therapy areas.
Key Responsibilities
- Support site qualification, initiation, monitoring, and close-out activities under supervision.
- Ensure compliance with ICH-GCP, Belgian regulatory requirements, and sponsor SOPs.
- Assist with source data verification, investigational product accountability, and accurate site documentation.
- Build strong relationships with site personnel, providing guidance and support as needed.
- Identify and escalate site-level challenges proactively to your line manager.
- Maintain trial documentation in CTMS, eTMF, and EDC systems.
- Contribute to team knowledge sharing and learn best practices from senior CRAs.
Requirements
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related discipline.
- 6 months to 2 years of clinical trial experience or CRA exposure.
- Knowledge of ICH-GCP and Belgian clinical trial regulations is preferred.
- Strong communication, organisational, and relationship-building skills.
- Eagerness to learn and develop in innovative therapy areas such as CAR-T and gene therapy.
What’s in It for You?
This role offers a competitive salary and benefits package, opportunities for flexible working, and structured career progression within a global CRO. You will gain valuable exposure to advanced therapies, working in a collaborative culture that supports professional growth, work-life balance, and wellbeing.
If you are a motivated CRA looking to advance your career and contribute to innovative clinical research, we’d love to hear from you. Apply today to join a global team making a real difference for patients.
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5
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
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À propos du dernier Senior/clinical research associate Emplois dans Belgique !
6
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!
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7
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
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Freelance Clinical Research Associate
EPM Scientific
Aujourd'hui
Emploi consulté
Description De L'emploi
EPM Scientific are currently partnered Sponsor who are seeking a freelance Clinical Research Associate (CRA) to support an exciting project. See a short summary below:
Contract Conditions:
- Start Date: ASAP
- Contract: 1 FTE, 12-month contract (opportunity to extend)
- Medical Device Project - Neurovascular
- Location: Belgium (Remote)
- Languages: Dutch, French & English required
- Project: Medical Device, Neurovascular
Key Responsibilities:
- Monitor clinical trial sites, ensuring compliance with GCP, protocol, and regulatory requirements
- Act as the primary point of contact for site staff, supporting site initiation, monitoring, and close-out activities
- Ensure timely and accurate documentation, data collection, and reporting in line with project timelines
- Collaborate with cross-functional teams including Clinical Project Managers, Medical Monitors, and Regulatory Affairs
- Contribute to risk-based monitoring strategies and support audit readiness
Requirements:
- Strong experience as a CRA (5+ years preferred)
- Solid understanding of ICH-GCP and relevant regulatory environments.
- Proven ability to work independently and manage multiple sites
- Excellent communication and organizational skills
- Must Speak Dutch, French, and English
If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.
Désolé, cet emploi n'est pas disponible dans votre région
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