Research Physician - Investigator

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Join us as a Research Physician II – Lead advanced clinical research projects, ensure the integrity and accuracy of medical investigations, and contribute to the advancement of medical science through your expertise and leadership.

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 - enabling 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. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

• What You’ll Do:
• •Once trained, acting as principal investigator (PI) or co-investigator ensuring ICH/GCP and local regulations are met
• •Conducting clinical trials in line with the protocol and to ensure the recruitment of eligible participants onto the studies
• •Review screening, pre-screening, and screening success rates for clinical trials
• •Providing information and support to consenting participants for a clinical study
• •Responsible for checking patient inclusion/exclusion to studies
• •Liaising with and developing positive relations with sponsors, clients and clients’ contractors as required, projecting a helpful and courteous company image
• •Carrying out clinical evaluation and clinical investigation of participants
• •Constantly seeking and suggesting quality improvements
• •Taking responsibility for ensuring serious adverse events / adverse events are reported appropriately
• •Having responsibility for the medical wellbeing of participants during the clinical trial and referral to specialists or GP as required

• Required Knowledge, Skills, Abilities:
• •Good knowledge of internal medicine, 2 years post qualification clinical experience
• •Ideally some previous experience within clinical research
• •Have working knowledge of GCP (ICH/GCP and local regulations compliance)
• •Demonstrate the inclination to provide practical help and guidance to colleagues, providing practical solutions for any problems and supporting their development
• •Show meticulous attention to detail in recording patient information and data ensuring any queries are acted upon in a timely and efficient manner
• •Be a team player, capable of building and sustaining positive relationships with colleagues as well as patients

• Why Join Us?
• When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.