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Clinical Development Programme Lead in Paris, France (f/m/d)
The Medical Lead, Clinical Development is responsible for leading and driving inputs into clinical development strategy for the key programs and studies.
This role will act as medical lead on these programs as well as sponsor's safety physician.
This position offers an exciting opportunity in a growing organization with multiple development programs to provide an impact from the start and then grow as the company builds out its clinical development enterprise.
The requirements:
* Medical Doctor (MD) required, with experience in Neurology or Psychiatry preferred (Board Eligible (BE)/Board Certified (BC) Neurologist is a plus).
* 3-5+ years of experience in a CRO/pharma/biotech organization with experience in GCP; pharmaceutical experience is most preferred.
* Experience working in a medical monitor/ safety physician role with demonstrated knowledge of review of safety cases and drafting of clinical narratives.
* Strong verbal and written communication/presentation skills
* High ethical & quality standards demonstrated through actions and communication.
* Demonstrated experience working within a fast-paced, matrix environment.
* Fluent English, French would be a plus
If this sound interesting to you or someone in your network has the relevant skills please apply now or contact me with your CV:
Clinical Development Programme Lead
- Location France
- Salary Negotiable
- Discipline Clinical Development
- Reference PR/396276_1668174843
The Medical Lead, Clinical Development is responsible for leading and driving inputs into clinical development strategy for the key programs and studies.
This role will act as medical lead on these programs as well as sponsor's safety physician.
This position offers an exciting opportunity in a growing organization with multiple development programs to provide an impact from the start and then grow as the company builds out its clinical development enterprise.
The requirements:
* Medical Doctor (MD) required, with experience in Neurology or Psychiatry preferred (Board Eligible (BE)/Board Certified (BC) Neurologist is a plus).
* 3-5+ years of experience in a CRO/pharma/biotech organization with experience in GCP; pharmaceutical experience is most preferred.
* Experience working in a medical monitor/ safety physician role with demonstrated knowledge of review of safety cases and drafting of clinical narratives.
* Strong verbal and written communication/presentation skills
* High ethical & quality standards demonstrated through actions and communication.
* Demonstrated experience working within a fast-paced, matrix environment.
* Fluent English, French would be a plus
If this sound interesting to you or someone in your network has the relevant skills please apply now or contact me with your CV: