Experienced Clinical Research Associate, FSP Belgium

IQVIA Argentina; Zaventem; Hybride; EUR 42 000 - 65 000; Plein temps

Avantages offerts par ce poste

Company car

Mobile phone

Benefits package

Résumé du poste

IQVIA Belgium is seeking a Clinical Research Associate to join our Sponsor dedicated team (Junior - Senior). You will conduct site visits, support recruitment planning, and ensure regulatory compliance while coordinating with study sites and client teams to advance clinical trials.

The role requires a scientific degree, pharma/clinical trials experience, and fluent Dutch, French and English. Belgium-based travel is expected, with a company car and a strong, international work environment.

Qualifications

• 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.

Responsabilités

• 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.

Connaissances

Dutch

French

English

MS Office

Formation

University degree in scientific discipline or health care

Description du poste

Clinical Research Associate

For candidates able to start before December 2026, a discretionary sign-on bonus of up to 4,300 EUR may be offered, with the final amount confirmed at offer stage, subject to role level and relevant experience.

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 https://jobs.iqvia.com

IQVIA 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.