Clinical Scientist- CDI- M/F
Clinical Scientist- CDI- M/F
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Job Description
Who we are
Pierre Fabre is the 2nd largest dermocosmetics laboratory in the world the 2nd largest private French pharmaceutical group and the market leader in France for products sold over the counter in pharmacies.
Its portfolio includes several medical franchises and international brands including Pierre Fabre Oncologie Pierre Fabre Dermatologie Eau Thermale Avne Klorane Ducray Ren Furterer ADerma Naturactive Pierre Fabre Oral Care.
Established in the Occitanie region since its creation and manufacturing over 95% of its products in France the Group employs some 10000 people worldwide. Its products are distributed in about 130 countries.86% of the Pierre Fabre Group is held by the Pierre Fabre Foundation a governmentrecognized publicinterest foundation while a smaller share is owned by its employees via an employee stock ownership plan.
In 2019 Ecocert Environment assessed the Groups corporate social and environmental responsibility approach in accordance with the ISO 26000 sustainable development standard and awarded it the Excellence level.
Pierre Fabre is recognized as one of the Worlds Best Employers 2021 by Forbes. Our group is ranked in the Top 3 in the cosmetics industry and in the Top 10 in the pharmaceutical industry worldwide.
Your mission
The Pierre Fabre R&D Medical Care is hiring a Clinical Scientist to join the Clinical Development Department.
The location of the position will be Toulouse (preferentially) or Boulogne with flexibility in terms of commuting from France/Europe and home office.
You have many roles to play:
- Strategic Contributions:
- Collaborate with the Clinical Development Director (CDD) to synthesize literature preclinical data regulatory guidance and clinical insights to build program rationale.
- Support the Clinical Development Director in proposals at advisory boards investigator meetings and site initiations.
- Stay up to date with the clinical landscape by attending scientific and clinical conferences.
- Clinical Study Support:
- Contribute to study design and develop clinical documents (e.g. protocols investigator brochures informed consent forms study manuals clinical study reports).
- Work closely with CDDs and Clinical Operations to address protocol questions from health authorities and ethics committees.
- Conduct regular clinical/medical data review under the supervision of CDDs.
- Participate in clinical site and vendor selection.
- Operational Excellence:
- Assist in organizing clinical meetings (e.g. advisory boards data safety monitoring boards and steering committees).
- Engage with Clinical Operations for site startup engagement and recruitment.
- Support medical monitoring activities and data quality reviews.
- CrossFunctional Collaboration:
- Act as a task force leader for best practices or special initiatives.
- Represent the core team at governance reviews and present on special topics.
We offer an attractive remuneration/benefits package: Incentives profitsharing Pierre Fabre shareholding with matching contribution health and provident insurance 16 days of holidays (RTT) in addition to 25 days of personal holidays public transport participation very attractive CE...
Who you are
Profile:
Doctor in Medicine scientific PhD with a specialty in clinical development or reserach nurse or pharmacist.
You have indepth knowledge of oncology precision medicine and of course experience in clinical protocol development study conduct and data quality oversight.
Knowledge of Good Clinical Practices (GCP) and regulatory requirements for Oncology clinical trials.
We are convinced that diversity is a source of fulfillment social balance and complementarity for our employees which is why our offers are open to all without restriction.
Employment Type
Full-Time
