Clinical Development Director
other jobs Cpl Life Sciences
Added before 6 Days
- England,London,City of London
- Full Time, Contract
- Salary negotiable
Job Description:
Full job descriptionClinical Development Director (Medical Director) – 6 Month Contract | UK (Hybrid, London)
We are currently supporting a global pharmaceutical organisation seeking an experienced Clinical Development Director (CDD) to provide clinical and scientific leadership across a global clinical development programme.
This is a 6-month contract role (Inside IR35) offering the opportunity to contribute to late-stage development activities across a defined global programme, working closely with cross-functional clinical and scientific teams.
Key Responsibilities
*Lead and/or support delivery of clinical development deliverables across assigned programme(s)
*Contribute to clinical development strategy and integrated development plans (IDP/CDP)
*Develop and review clinical sections of protocols, Investigator’s Brochures, safety updates, and regulatory submission documents
*Support clinical data review and interpretation in collaboration with Statistics, Data Management, and Medical teams
*Contribute to Clinical Study Reports (CSRs), publications, abstracts, and presentations
*Provide input into regulatory interactions and health authority submissions
*Support safety monitoring activities including DSURs/PSURs and safety signal review
*Participate in inspection readiness activities and QA collaboration
*Engage with internal and external stakeholders including KOLs, regulatory agencies, advisory boards, and internal governance forums
*May lead clinical trials and/or act as Clinical Scientific Lead depending on assignment
We are currently supporting a global pharmaceutical organisation seeking an experienced Clinical Development Director (CDD) to provide clinical and scientific leadership across a global clinical development programme.
This is a 6-month contract role (Inside IR35) offering the opportunity to contribute to late-stage development activities across a defined global programme, working closely with cross-functional clinical and scientific teams.
Key Responsibilities
*Lead and/or support delivery of clinical development deliverables across assigned programme(s)
*Contribute to clinical development strategy and integrated development plans (IDP/CDP)
*Develop and review clinical sections of protocols, Investigator’s Brochures, safety updates, and regulatory submission documents
*Support clinical data review and interpretation in collaboration with Statistics, Data Management, and Medical teams
*Contribute to Clinical Study Reports (CSRs), publications, abstracts, and presentations
*Provide input into regulatory interactions and health authority submissions
*Support safety monitoring activities including DSURs/PSURs and safety signal review
*Participate in inspection readiness activities and QA collaboration
*Engage with internal and external stakeholders including KOLs, regulatory agencies, advisory boards, and internal governance forums
*May lead clinical trials and/or act as Clinical Scientific Lead depending on assignment
Job number 3919415
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Company Details:
Cpl Life Sciences
Company size: 50–99 employees
Industry: Scientific
CPL UK is a group of Specialist Talent businesses which service the Professional Services, Science, Technology, Engineering, Mathematics and Health se...