At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. Alongside clinical research through our

PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on - now and in the future.

As a Manager Clinical Relations you will lead a team, in charge of delivering recruitment objectives, business growth and randomization targets through recruitment, engagement and retention of patients at sites. This role will cover United Kingdom, South Africa and Germany.

Key responsibilities are as follows:

• Leads, mentors and develops their team. Approves courses of action on salary administration, hiring, corrective action, and terminations. Reviews and approves time records, expense reports, requests for leave, and overtime. Assures department adherence to good ethical and regulatory standards.
• Creates and develops business strategies by understanding industry needs.
• Motivates and leads a team in a dynamic environment.
• Ensures success in accessing patients suitable for clinical studies at the sites through all forms of community outreach activities, focusing on GP and hospital networks and cultivating relationships with Key Opinion leaders in the community and managers/leaders in other institutions that may provide access to patients.
• Increases site delivery by contributing to overall randomization targets and working towards quarterly goals.
• Maintains knowledge of current enrolling studies, timelines for the studies and protocol requirements.
• Ensures increases to the database and actively contribute and/or develops to initiatives and strategies to enroll potential participants onto the database.