Clinical Operations Leader for Pipeline Development

6 days ago


Leatherhead, Surrey, United Kingdom Incyte Full time
Job Overview

The Associate Director Clinical Operations is responsible for leading the planning, execution, and oversight of development operations activities in the UK and Ireland. This role involves working closely with Development Operations teams to ensure alignment on country strategy, execution, follow-up, and support for outsourced and internal clinical trials.

About the Role

We are seeking an experienced Clinical Operations professional to join our team as an Associate Director. The successful candidate will have a minimum of 5-7 years' experience working in clinical operations within the biopharmaceutical industry or Clinical Research Organization (CRO).

Key Responsibilities
  • Lead the planning, execution, and oversight of development operations activities in the UK and Ireland.
  • Work closely with Development Operations teams to ensure alignment on country strategy, execution, follow-up, and support for outsourced and internal clinical trials.
  • Collaborate with key stakeholders, including Medical Affairs, Market Access, and General Manager, to ensure continuous alignment on country strategy and execution.
  • Develop and maintain effective relationships with key investigators and research institutions.
  • Manage local clinical operations resources based on UK and Ireland activities and engagement.
  • Hire local clinical operations team members with support from functional management as needed.
  • Conduct performance reviews of direct reports and oversee proper handover and training documentation for internal monitoring activities.

Requirements
  • Minimum Bachelor of Science degree or equivalent degree.
  • Minimum of 5-7 years' experience working in clinical operations within the biopharmaceutical industry or CRO, including at least 3 years in a role of primary responsibility for clinical trial execution and management.
  • Operational and direct managerial experience in the planning, executing, and reporting of clinical trials.
  • Good knowledge of GCP, clinical trial design, statistics, regulatory processes, inspection readiness, and drug development process.
  • Excellent organisational, problem-solving, and written/verbal communication skills.
  • Goal-oriented, self-starter with proven ability to work independently in accordance with stated timelines and quality.
  • Must be able to travel up to 10% domestically and internationally.

Salary Range: $140,000 - $180,000 per annum

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