Junior Clinical Research Associate, Sponsor Dedicated - Belgium

IQVIA Argentina; Zaventem; Sur place; EUR 32 000 - 52 000; Plein temps

Avantages offerts par ce poste

Company car

Mobile phone

Benefits package

Résumé du poste

IQVIA Belgium is seeking a Junior Clinical Research Associate to join our sponsor-dedicated team. You will gain experience across therapeutic areas, building a meaningful career within our global organization.

Responsibilities include site selection and monitoring visits, ensuring GCP/ICH compliance, and coordinating regulatory submissions, recruitment, and data queries while collaborating with study sites and client teams. Belgium-based role requiring travel.

Qualifications

• University degree in a scientific discipline or healthcare.
• Experience in pharma industry or clinical trials environment.
• Very good computer skills including MS Office.

Responsabilités

• Perform site selection, initiation, monitoring and close-out visits.
• Evaluate quality/integrity of site practices per GCP/ICH guidelines.
• Manage progress by tracking regulatory submissions, recruitment, CRF completion and data queries.
• Collaborate with study site experts and client representatives.

Connaissances

Pharma & Clinical Trials experience

MS Office

Dutch language skills

English language skills

French language skills

Organizational skills

Time management

Problem solving

Travel flexibility

Formation

University degree in scientific discipline or health care

Outils

MS Office

Description du poste

Junior Clinical Research Associate

IQVIA Belgium is looking for talented and motivated Junior CRA team member to join our Sponsor dedicated 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.

Your responsibilities will include:

• Performing site selection, initiation, monitoring and close-out visits

• 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

• Dutch, English and French language skills. 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.

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.