4 Emplois pour Ucb Pharma - Belgique
Description De L'emploi
We are looking for a **Junior Consultant** to join our team.
**Main Areas of Responsibility**
As a junior consultant at IN2Pharma, you will be trained to support more senior colleagues in ensuring the client's products meet the required standards of quality and safety and in ensuring regulatory compliance for a defined range of products of the client's portfolio. This gives you the opportunity to acquire experience within one or several of the following domains:
Medical & Regulatory Affairs
+ Medical writing: expert reports, clinical evaluations, literature study
+ Medical education of sales representatives: product training on medicinal or healthcare products
+ Review and approve promotional material for medicinal and healthcare products
+ Adapt SPC, PIL and packaging materials in line with the registration file and legislation
Pharmacovigilance (PV)
+ Local Literature Review for adverse events on the MAH's medicinal products
+ Assist in the PV quality system set-up or maintenance: PV SOPs, gap analysis, compliance check with applicable regulations
+ Training of MAH's employees in PV awareness
Quality Assurance (QA)
+ Support the QP/RP in all aspects related to quality and compliance ensuring local requirements are met
+ Support the QP/RP in the administrative release to the market in compliance with procedures. This includes: QA check, CoA request, Artwork request, Contact with warehouse/supply,.
+ Investigate customer complaints and non-conformance issues
**Technical Skill Requirements**
+ Master degree in life sciences
+ Good knowledge of national and European regulations and legislations for medicinal products
+ Good communication skills in Dutch, French and English (both verbal and written)
+ Strong initiative, problem solver and good organizational skills
+ Accurate & efficient: concern for quality, compliance and consistency
+ Good communicator & team player
**Our offer**
+ A permanent full-time position with a competitive package and supplementary benefits
+ Challenging and alternating job as consultant within a dynamic team
+ Development opportunities by working on various projects for different pharmaceutical companies
IN2Pharma is a consulting company passionate about offering solutions in Medical, Regulatory Affairs and Quality Assurance projects for pharmaceutical and healthcare industry in Benelux. Our offices are located in Kampenhout at the business center "Hof ter Loonst" and in Gentbrugge.
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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
**Main Areas of Responsibility**
As a junior consultant at IN2Pharma, you will be trained to support more senior colleagues in ensuring the client's products meet the required standards of quality and safety and in ensuring regulatory compliance for a defined range of products of the client's portfolio. This gives you the opportunity to acquire experience within one or several of the following domains:
Medical & Regulatory Affairs
+ Medical writing: expert reports, clinical evaluations, literature study
+ Medical education of sales representatives: product training on medicinal or healthcare products
+ Review and approve promotional material for medicinal and healthcare products
+ Adapt SPC, PIL and packaging materials in line with the registration file and legislation
Pharmacovigilance (PV)
+ Local Literature Review for adverse events on the MAH's medicinal products
+ Assist in the PV quality system set-up or maintenance: PV SOPs, gap analysis, compliance check with applicable regulations
+ Training of MAH's employees in PV awareness
Quality Assurance (QA)
+ Support the QP/RP in all aspects related to quality and compliance ensuring local requirements are met
+ Support the QP/RP in the administrative release to the market in compliance with procedures. This includes: QA check, CoA request, Artwork request, Contact with warehouse/supply,.
+ Investigate customer complaints and non-conformance issues
**Technical Skill Requirements**
+ Master degree in life sciences
+ Good knowledge of national and European regulations and legislations for medicinal products
+ Good communication skills in Dutch, French and English (both verbal and written)
+ Strong initiative, problem solver and good organizational skills
+ Accurate & efficient: concern for quality, compliance and consistency
+ Good communicator & team player
**Our offer**
+ A permanent full-time position with a competitive package and supplementary benefits
+ Challenging and alternating job as consultant within a dynamic team
+ Development opportunities by working on various projects for different pharmaceutical companies
IN2Pharma is a consulting company passionate about offering solutions in Medical, Regulatory Affairs and Quality Assurance projects for pharmaceutical and healthcare industry in Benelux. Our offices are located in Kampenhout at the business center "Hof ter Loonst" and in Gentbrugge.
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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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Corporate Travel Counselor T4M Pharma
Télécommande
American Express Global Business Travel
Aujourd'hui
Emploi consulté
Description De L'emploi
Amex GBT is a place where colleagues find inspiration in travel as a force for good and - through their work - can make an impact on our industry. We're here to help our colleagues achieve success and offer an inclusive and collaborative culture where your voice is valued.
As an American Express T4M Corporate Travel Counselor, this person will provide a specialized servicing to Pharma client travelers that will require high touch service.
The Travel Counselor should be prepared to offer a unique level of service, outstanding GDS skills, as well as vast destination knowledge.
This Travel Counselor will be accountable for both individual goals, as well as shared team goals, and will be responsible for providing customer service and accurate completion of both international, domestic travel arrangements, and special requests.
Hours of operation are Monday through Friday 9am - 5.30pm CET.
As a Travel Consultant, you'll join our highly skilled team, providing outstanding service to our corporate business clients. We're most proud of our warm and inclusive culture, innovation in the travel tech space, internal promotions, and career advancement opportunities. Most of our Traveler Care leadership started in this role, and you can find us in almost every other department at Amex GBT.
**What You'll Do**
+ Advise and arrange travel for corporate business customers (both individuals and groups)
+ Conduct analysis and research on travel options, and pro-actively anticipate traveler needs to sell additional services
+ Arrange and book domestic and international business travel, in a variety of complexity, for air, road, rail, and accommodations
+ Use various Global Distribution Systems (GDSs), including Sabre, Apollo, Galileo and Amadeus. Training may be provided
+ Ensure compliance to customers' agreed travel policy, service provider policies, and regulatory requirements
+ Use positive telephone service techniques and act on special customer requests
+ Collaborate within your team to coach, mentor, and provide constructive feedback to improve service levels
We look forward to sharing more detailed job functions and key performance indicators during the interview process.
**What We're Looking For**
+ Passion for excellence in client service, including proactive anticipation of needs
+ Native GDS expertise (Sabre, Apollo, Amadeus and/or Galileo)
+ Professional communication Fench (written and verbal)
+ Attention to detail
+ Act with integrity, and look after personal traveler information
+ Possess a strong understanding of the travel industry (background in business travel, leisure travel, or airline reservation)
+ Resolving customer issues quickly and independently / with supplier
+ Teamwork and openness to feedback
**Location**
Belgium
**The #TeamGBT Experience**
Work and life: Find your happy medium at Amex GBT.
+ **Flexible benefits** are tailored to each country and start the day you do. These include health and welfare insurance plans, retirement programs, parental leave, adoption assistance, and wellbeing resources to support you and your immediate family.
+ **Travel perks:** get a choice of deals each week from major travel providers on everything from flights to hotels to cruises and car rentals.
+ **Develop the skills you want** when the time is right for you, with access to over 20,000 courses on our learning platform, leadership courses, and new job openings available to internal candidates first.
+ **We strive to champion Inclusion** in every aspect of our business at Amex GBT. You can connect with colleagues through our global INclusion Groups, centered around common identities or initiatives, to discuss challenges, obstacles, achievements, and drive company awareness and action.
+ And much more!
All applicants will receive equal consideration for employment without regard to age, sex, gender (and characteristics related to sex and gender), pregnancy (and related medical conditions), race, color, citizenship, religion, disability, or any other class or characteristic protected by law.
Click Here ( for Additional Disclosures in Accordance with the LA County Fair Chance Ordinance.
Furthermore, we are committed to providing reasonable accommodation to qualified individuals with disabilities. Please let your recruiter know if you need an accommodation at any point during the hiring process. For details regarding how we protect your data, please consult the Amex GBT Recruitment Privacy Statement ( .
**What if I don't meet every requirement?** If you're passionate about our mission and believe you'd be a phenomenal addition to our team, don't worry about "checking every box;" please apply anyway. You may be exactly the person we're looking for!
Click Here to Learn More (
As an American Express T4M Corporate Travel Counselor, this person will provide a specialized servicing to Pharma client travelers that will require high touch service.
The Travel Counselor should be prepared to offer a unique level of service, outstanding GDS skills, as well as vast destination knowledge.
This Travel Counselor will be accountable for both individual goals, as well as shared team goals, and will be responsible for providing customer service and accurate completion of both international, domestic travel arrangements, and special requests.
Hours of operation are Monday through Friday 9am - 5.30pm CET.
As a Travel Consultant, you'll join our highly skilled team, providing outstanding service to our corporate business clients. We're most proud of our warm and inclusive culture, innovation in the travel tech space, internal promotions, and career advancement opportunities. Most of our Traveler Care leadership started in this role, and you can find us in almost every other department at Amex GBT.
**What You'll Do**
+ Advise and arrange travel for corporate business customers (both individuals and groups)
+ Conduct analysis and research on travel options, and pro-actively anticipate traveler needs to sell additional services
+ Arrange and book domestic and international business travel, in a variety of complexity, for air, road, rail, and accommodations
+ Use various Global Distribution Systems (GDSs), including Sabre, Apollo, Galileo and Amadeus. Training may be provided
+ Ensure compliance to customers' agreed travel policy, service provider policies, and regulatory requirements
+ Use positive telephone service techniques and act on special customer requests
+ Collaborate within your team to coach, mentor, and provide constructive feedback to improve service levels
We look forward to sharing more detailed job functions and key performance indicators during the interview process.
**What We're Looking For**
+ Passion for excellence in client service, including proactive anticipation of needs
+ Native GDS expertise (Sabre, Apollo, Amadeus and/or Galileo)
+ Professional communication Fench (written and verbal)
+ Attention to detail
+ Act with integrity, and look after personal traveler information
+ Possess a strong understanding of the travel industry (background in business travel, leisure travel, or airline reservation)
+ Resolving customer issues quickly and independently / with supplier
+ Teamwork and openness to feedback
**Location**
Belgium
**The #TeamGBT Experience**
Work and life: Find your happy medium at Amex GBT.
+ **Flexible benefits** are tailored to each country and start the day you do. These include health and welfare insurance plans, retirement programs, parental leave, adoption assistance, and wellbeing resources to support you and your immediate family.
+ **Travel perks:** get a choice of deals each week from major travel providers on everything from flights to hotels to cruises and car rentals.
+ **Develop the skills you want** when the time is right for you, with access to over 20,000 courses on our learning platform, leadership courses, and new job openings available to internal candidates first.
+ **We strive to champion Inclusion** in every aspect of our business at Amex GBT. You can connect with colleagues through our global INclusion Groups, centered around common identities or initiatives, to discuss challenges, obstacles, achievements, and drive company awareness and action.
+ And much more!
All applicants will receive equal consideration for employment without regard to age, sex, gender (and characteristics related to sex and gender), pregnancy (and related medical conditions), race, color, citizenship, religion, disability, or any other class or characteristic protected by law.
Click Here ( for Additional Disclosures in Accordance with the LA County Fair Chance Ordinance.
Furthermore, we are committed to providing reasonable accommodation to qualified individuals with disabilities. Please let your recruiter know if you need an accommodation at any point during the hiring process. For details regarding how we protect your data, please consult the Amex GBT Recruitment Privacy Statement ( .
**What if I don't meet every requirement?** If you're passionate about our mission and believe you'd be a phenomenal addition to our team, don't worry about "checking every box;" please apply anyway. You may be exactly the person we're looking for!
Click Here to Learn More (
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1
Candidature spontanée délégué médical (GP/SP/PHARMA) expérimenté (m/f/x)
Zaventem
IQVIA
Publié il y a 8 jours
Emploi consulté
Description De L'emploi
Vous êtes délégué(e) médical(e) ou pharmaceutique expérimenté(e) et vous n'avez pas trouvé la fonction adéquate sur notre site ? Nous vous invitons à laisser votre cv ici en vue de futures opportunités.
**Mission**
En tant que Délégué(e) Médical(e) et/ou pharmaceutique, vous êtes le lien entre le client et les médecins (généralistes et spécialistes) et/ou les pharmaciens de votre région.
- Vous rendez visite aux médecins, spécialistes et/ou pharmaciens et les informez à propos de votre portefeuille de produits
- Vous développez une relation de confiance durable avec votre réseau de médecins.
- Vous planifiez et analysez vos visites de manière stratégique afin d'atteindre vos objectifs.
- Vous identifiez les 'Key Opinion Leaders' dans votre région.
- Vous recueillez et interprétez les feedbacks des médecins, spécialistes et/ou pharmaciens.
- Vous participez activement aux séminaires, réunions d'équipe et cycle meetings.
**Secteur**
- Différentes régions en Wallonie et/ou à Bruxelles. A déterminer en fonction des opportunités futures et de votre domicile.
**Votre profil**
Vous disposez d'une expérience en tant que Délégué Médical et/ou pharmaceutique ou dans une fonction similaire au sein du secteur des soins de santé.
- Vous êtes, de préférence, titulaire d'un diplôme de bachelier ou de master.
- Vous communiquez couramment en français et possédez un permis de conduire B.
- Vous aimez les challenges et êtes orienté(e) résultats.
**Notre offre**
- Un contrat à durée indéterminée.
- Un package salarial attractif avec des avantages extralégaux (voiture de société, carte carburant, assurance hospitalisation, assurance groupe, indemnités journalières,.) et 30 jours de congé.
- Une fonction stimulante avec beaucoup d'autonomie et des opportunités de développement professionnel.
- Une formation continue : actualisation scientifique sur les pathologies et les molécules, ainsi qu'une formation aux techniques de vente.
**Intéressé(e) ?**
Vous envisagez un nouveau défi dans votre carrière ? Vous souhaitez avoir un impact dans le domaine de la santé et continuer à évoluer ? Postulez dès aujourd'hui !
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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
**Mission**
En tant que Délégué(e) Médical(e) et/ou pharmaceutique, vous êtes le lien entre le client et les médecins (généralistes et spécialistes) et/ou les pharmaciens de votre région.
- Vous rendez visite aux médecins, spécialistes et/ou pharmaciens et les informez à propos de votre portefeuille de produits
- Vous développez une relation de confiance durable avec votre réseau de médecins.
- Vous planifiez et analysez vos visites de manière stratégique afin d'atteindre vos objectifs.
- Vous identifiez les 'Key Opinion Leaders' dans votre région.
- Vous recueillez et interprétez les feedbacks des médecins, spécialistes et/ou pharmaciens.
- Vous participez activement aux séminaires, réunions d'équipe et cycle meetings.
**Secteur**
- Différentes régions en Wallonie et/ou à Bruxelles. A déterminer en fonction des opportunités futures et de votre domicile.
**Votre profil**
Vous disposez d'une expérience en tant que Délégué Médical et/ou pharmaceutique ou dans une fonction similaire au sein du secteur des soins de santé.
- Vous êtes, de préférence, titulaire d'un diplôme de bachelier ou de master.
- Vous communiquez couramment en français et possédez un permis de conduire B.
- Vous aimez les challenges et êtes orienté(e) résultats.
**Notre offre**
- Un contrat à durée indéterminée.
- Un package salarial attractif avec des avantages extralégaux (voiture de société, carte carburant, assurance hospitalisation, assurance groupe, indemnités journalières,.) et 30 jours de congé.
- Une fonction stimulante avec beaucoup d'autonomie et des opportunités de développement professionnel.
- Une formation continue : actualisation scientifique sur les pathologies et les molécules, ainsi qu'une formation aux techniques de vente.
**Intéressé(e) ?**
Vous envisagez un nouveau défi dans votre carrière ? Vous souhaitez avoir un impact dans le domaine de la santé et continuer à évoluer ? Postulez dès aujourd'hui !
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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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2
Clinical Research Associate II / Senior Clinical Research Associate Large Pharma
Mechelen
ICON Clinical Research
Publié il y a 8 jours
Emploi consulté
Description De L'emploi
CRA II Senior CRA Belgium
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
**What You Will Be Doing:**
+ Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
+ Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
+ Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
+ Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
+ Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
**Your Profile:**
+ Advanced degree in a relevant field such as life sciences, nursing, or medicine.
+ Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
+ Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
+ Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
+ Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
+ Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license
\#LI-DK2
\#LI-Remote
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
**What You Will Be Doing:**
+ Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
+ Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
+ Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
+ Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
+ Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
**Your Profile:**
+ Advanced degree in a relevant field such as life sciences, nursing, or medicine.
+ Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
+ Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
+ Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
+ Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
+ Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license
\#LI-DK2
\#LI-Remote
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
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3