Pharmaceutical & Biotechnology

Clinical Program Director

  • Contract
  • London City, London, UK
  • 42079555

Desired Skills: clinical trial,Phase I-IV

PE Global is currently recruiting for a Protocol & Clinical Program Excellence Director for a leading multi-national Pharma client based in London.

This is an initial 12-18 months contract position working Hybrid from London office.

Up to £570/day via Umbrella company.

Duties of the role/Responsibilities

  • Provides scientific and operational support to the Central Integrated Scientific Review
  • Committee (C-ISRC), supporting, as requested, the Head Protocol & Clinical Program Excellence with the review of Clinical Development Plans (CDPs) and Key clinical documents (Study protocols, DMC charters, etc), to maintain high levels of quality and consistency across the therapeutic areas.
  • Develops harmonized processes, tools and resources to enable a seamless C-ISRC process
  • Supports and acts as delegate to the Head Protocol & Clinical Program Excellence in activities like interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, data monitoring committees, advisory boards etc.) and internal stakeholders as needed.
  • Supports enhancement and simplification of the company’s clinical development approach (CDP, clinical trial designs, protocol and its review) to improve speed and outcome success of clinical programs.
  • Supports the Head Protocol & Clinical Program Excellence to build cross-function
  • collaborations and initiatives leading to a step-wised transition to the futuristic digital clinical trial era.

Education/Experience

  • MD or advanced degree in life sciences/healthcare (or clinically relevant degree) is required. PharmD, or PhD strongly preferred
  • More than 5 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV.
  • More than 3 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry
  • Excellent interpersonal, negotiation, conflict resolution verbal and written communication skills

Interested candidates should submit an updated CV.

Please click the link below to apply, alternatively send an up to date CV to anett@peglobal.co.uk

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***