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Precision for Medicine is seeking a (Senior) Regulatory and Start Up Specialist to join their team in France. This role is crucial for ensuring the timely and quality delivery of site activation readiness. The specialist will work closely with various teams, including Feasibility, Clinical Operations, Project Management, Regulatory to mitigate any risks. This position can be fully remote.Responsibilities:
- Delivery of site activation readiness.
- Maintaining project plans and trackers.
- Act as SME for collection and maintenance of site level critical path to Site Activation data points, including site contracts and budget negotiation requirements.
- Participate/support the negotiation of study budgets and the execution of investigator contracts .
- Bachelor’s degree in life sciences or related field.
- At least 1 year of experience as a Regulatory/ SU specialist in a CRO or pharmaceutical/ biotech industry.
- Experience drafting, reviewing and negotiating agreements related to clinical research.
- Experience developing and negotiating the budget.
- Fluency in French and English.
- Opportunity to work with a growing CRO, Precision for Medicine.
- Be fully home based.
- Impact positive change for the company.
Precision for Medicine
Precision for Medicine is dedicated to enhancing clinical research and development. They achieve this by providing specialized services that integrate scientific understanding with advanced analytical platforms. They help optimize clinical trials, accelerate drug development, and enable a deeper understanding of disease mechanisms, ultimately aiming to improve patient outcomes through precision medicine approaches and tailored therapeutics.