Strategic Feasibility Lead

Job description

Strategic Feasibility Lead

Contract - start date from 1st May 2026 - June 2027

Strategic Feasibility plays a pivotal role in the successful delivery of clinical trials. We are partnering with a global pharmaceutical company seeking an experienced Strategic Feasibility Lead to join their Program Delivery team within Global Clinical Sciences & Operations.

This is a fantastic opportunity to influence clinical development programmes spanning Phase I through to Phase IV, working at both study and programme level in a truly global setting.

The Role

You will lead and oversee feasibility activities in collaboration with CRO partners and internal stakeholders, ensuring clinical programmes are set up for efficient and timely delivery.

Key responsibilities include:

• Synthesising internal and external data to develop robust, insight-driven feasibility strategies supporting clinical programmes and individual studies
• Supporting clinical planning at programme and study level, including accurate recruitment forecasting
• Leading feasibility execution from early engagement through to country and site selection, in partnership with CRO feasibility teams
• Coordinating cross-functional input and building alignment around programme and study plans
• Responding to ad hoc stakeholder queries with clear, data-backed recommendations
• Contributing to the development of improved country and site selection strategies and supporting the evolution of in-house feasibility tools
• Ensuring all deliverables meet industry best practice standards and comply with relevant guidelines and regulations
• Identifying opportunities to enhance programme delivery, site engagement, and participant recruitment capabilities

About You

• Minimum 4 years’ experience within Pharmaceutical, Biotechnology and/or CRO environments of designing and developing feasibility studies
• Strong data analysis/mining skills with knowledge of associated software inc. Citeline
• Proven experience working across global, cross-functional teams
• Solid working knowledge of GCP guidelines across multiple regions
• Previous leadership of projects, teams or strategic initiatives is advantageous

This role would suit someone who enjoys combining data, strategy and collaboration to drive

better trial outcomes. It offers real visibility, influence and the opportunity to add measurable value across a global development portfolio.

Hybrid working is available with the expectation of min. 2 days/week onsite work in Slough.

Keywords: feasibility, citeline, clinical trial, pharmaceutical, drug, good clinical practice, GCP, data analysis, data mining, citeline, VRS9367SE, Slough, London, Reading, Oxford

Extra information

Status

Open

Education Level

Secondary School

Location

Slough

Type of Contract

Full-time jobs

Published at

05-03-2026

Full UK/EU driving license preferred

No

Car Preferred

No

Must be eligible to work in the EU

No

Cover Letter Required

No

Languages

English