Are you passionate about clinical research and eager to be part of projects that directly impact people's health?
You will join a strategic project within a leading pharmaceutical company, working closely with medical teams and investigators, and actively participating in all phases of clinical studies, from study start-up to close-out.
What do we offer?
Permanent contract through Manpower to provide services on a project within a top-tier pharmaceutical company.
A high-impact project focused on clinical research and the development of innovative medicines.
A collaborative environment with continuous training and close interaction with multidisciplinary teams.
What will your day-to-day look like?
You will be responsible for monitoring and following up on clinical studies at assigned investigator sites, ensuring compliance with the protocol, Good Clinical Practices (GCP), and regulatory requirements.
Your main responsibilities will include:
Conducting study initiation, monitoring (on-site and remote), and close-out visits.
Verifying the quality and accuracy of clinical data and the correct management of informed consent.
Overseeing adverse event reporting and ensuring ethical and regulatory compliance.
Keeping study documentation up to date and preparing visit reports.
Providing ongoing support to investigators to ensure proper patient recruitment and follow-up.
What are we looking for?
University degree in health sciences, biology, pharmacy, medicine, or related fields.
Previous experience as a Clinical Research Associate or in clinical research (experience in observational or clinical studies is highly valued).
Good knowledge of Good Clinical Practices (GCP) and applicable regulations.
Strong analytical skills, attention to detail, and a focus on data quality.
Good communication skills, autonomy, and the ability to manage multiple sites and tasks.
High level of confidentiality, professional ethics, and scientific rigor.
Apply now and take the next step in your career in clinical research!