Emplois actuels liés à Clinical Research Associate France - Paris, Île-de-France - Pharmiweb
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Senior Clinical Research Associate
il y a 1 mois
Paris, Île-de-France Parexel Temps pleinAbout the RoleParexel is seeking a Senior Clinical Research Associate to join our team in France. As a key member of our clinical research team, you will be responsible for managing and monitoring clinical trials across assigned oncology studies.Key ResponsibilitiesManage site relationships and ensure compliance with regulatory requirementsConduct on-site...
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Senior Clinical Research Associate
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Senior Clinical Research Associate
il y a 4 semaines
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Senior Clinical Research Associate
il y a 4 semaines
Paris, Île-de-France Parexel Temps pleinAbout this roleParexel is seeking a Senior Clinical Research Associate to join our team in France. As a Senior Clinical Research Associate, you will be responsible for all site management and monitoring activities across assigned oncology studies.Key responsibilitiesManage and monitor clinical trials across assigned oncology studiesWork with industry leaders...
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Clinical Research Associate
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Senior Clinical Research Associate – Global Clinical Trials
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Clinical Research Associate II Role
il y a 3 semaines
Paris, Île-de-France Parexel Temps pleinUnlock Your Potential in Clinical ResearchParexel is seeking a dedicated Clinical Research Associate II to join our team in France. As a home-based professional, you will be fully committed to a single sponsor, working on vital clinical studies for leading global biotechs and Pharma top 50.We offer tremendous long-term job security and career prospects. Our...
Clinical Research Associate France
il y a 4 semaines
At ICON, we're committed to advancing and improving patients' lives through clinical development. As a Clinical Research Associate, you'll play a critical role in identifying, selecting, initiating, and closing out investigational sites for clinical studies in phases II-IV. You'll work closely with a close-knit team of highly qualified CRAs to ensure adherence to applicable regulations and principles of ICH-GCP.
The Role- Coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation.
- Submit protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested.
- Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required.
- Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness.
- Dependent on level of experience, assist in training and mentoring less expert CRA's and/or lead CRA's working on international projects.
- 18 months+ of monitoring experience in phase I-III trials as a CRA.
- Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data.
- Excellent written and verbal communication in English.
- Ability to produce accurate work to tight deadlines within a pressurized environment.
- Valid driving license and willingness to travel at least 60% of the time (international and domestic).
We offer a competitive salary package, annual bonuses, and a range of health-related benefits to employees and their families. 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.
At ICON, we're 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.
