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Clinical Program Director

Posted 13 days ago

  • Nottingham, Nottinghamshire
  • Any
  • External
  • Expired - 3 months ago
Clinical Program Director
Permanent / Full time
Global Biotech
Planet Pharma has collaborated with a Global Pioneering Biotech headquartered in Europe. Our clients are currently seeking an experienced Director/Program Lead to support and lead their clinical operations development activities. The role will include responsibilities such as:
Providing strategic input and taking accountability for all clinical aspects within the assigned therapeutic indication/program.
Ensuring adherence to timelines, budget, and quality standards outlined in the applicable Standard Operating Procedures (SOPs) and Work Instructions (WIs).
Collaborating with various stakeholders to create the Clinical Development Plan (CDP), which includes effective and innovative trial designs aligned with the Target Product Profile (TPP).
Strong Vendor/CRO management experience
Your experience:
10+ years of line management experience
Current/Ex heads of clin ops for small-size biotech companies
10+ years working with MDs and Scientific teams to design the global strategy
Designed strategy and led programs across USA, EMEA, LATAM, and JAPAC
Clear examples of promotion at previous employers and long tenure
Interested? Apply now for immediate consideration or contact Trae Cook-Appiah on #####
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its headquarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really make us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry-accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation, or age.