Site Identification & Partnerships Lead

Worldwide Clinical Trials; United Kingdom; On-site; GBP 60,000 - 80,000; Full time

Job summary

Worldwide Clinical Trials in the United Kingdom is seeking a Site Identification and Relationship Manager to support post-award site identification activities, feasibility management, and CDA coordination. You will oversee training of resources and coordinate site activation support, while collaborating with global teams to ensure study feasibility and enrollment quality.

The role requires strong communication, problem-solving, and travel readiness, with experience in clinical drug development

Qualifications

• 5+ years of transferable experience in industry, health care, or data-driven feasibility.
• Background in medicine, science, or other relevant discipline across a broad range of therapeutic areas, preferably with substantial international experience in clinical drug development.
• Knowledge of the principles of Good Clinical Practice.
• Minimum Bachelor’s degree or equivalent years experience.
• Must have competent computer skills in MS Word, Excel, and PowerPoint

Responsibilities

• Develop site identification strategies and feasibility questionnaire management.
• Coordinate CDA outreach and site recommendation activities.
• Provide training to assigned resources and oversee Site Activation Specialist support.
• Support post-award site identification activities across global teams.

Skills

Effective communicator

Lead client discussions

Creative problem solving

Remote teamwork

Excellent organizational skills

Travel readiness

Education

Bachelor’s degree

Tools

MS Word

MS Excel

PowerPoint

Job description

Worldwide Clinical Trials in the United Kingdom is seeking a Site Identification and Relationship Manager to support post-award site identification activities, feasibility management, and CDA coordination. You will oversee training of resources and coordinate site activation support, while collaborating with global teams to ensure study feasibility and enrollment quality.

The role requires strong communication, problem-solving, and travel readiness, with experience in clinical drug development