Lead Clinical Research Physician

3 weeks ago

Chorley, Lancashire, United Kingdom Thermo Fisher Scientific Full time

At Thermo Fisher Scientific, you will engage in impactful work that contributes positively on a global scale. Our mission is to empower our clients to enhance global health, safety, and cleanliness. We equip our teams with the necessary resources to reach personal career aspirations while advancing scientific research through the development and delivery of transformative therapies.

Our clinical research efforts, particularly through our PPD clinical research portfolio, focus on optimizing the patient journey in clinical trials. This includes enhancing site selection and patient recruitment, thereby facilitating greater participation in clinical research. Your commitment to prioritizing patient welfare will lead to improved health outcomes for individuals and communities now and in the future.

Are you a GMC registered physician interested in a dynamic role within the clinical research sector?

Do you have a passion for enhancing patient lives?

We are seeking to fill the position of Clinical Research Physician at our Synexus Clinical Research site.

This role involves a standard workweek of Monday to Friday, totaling 37 hours, with a primary focus on ensuring patient safety. As the principal investigator (PI) or co-investigator for various studies, you will be responsible for overseeing all sponsor research studies while ensuring compliance with ICH/GCP and local regulations.

Key Responsibilities:

  • Conduct clinical evaluations and assessments of participants to ensure eligibility and monitor safety and compliance.
  • Participate in Site Initiation Visits (SIV), Pre-Selection Visits (PSV), and Investigator meetings as necessary.
  • Engage in recruitment strategies to meet enrollment targets, ensuring studies are conducted within planned timelines.
  • Review enrollment progress, pre-screening and screening success rates, and participant retention.
  • Interpret study protocols and Investigator's Brochures (IB).
  • Manage and review Interactive Voice Response Systems (IVRS) and Case Report Forms (CRF)/Electronic Data Capture (EDC), if applicable.
  • Oversee the management of investigational medical products (IMP).
  • Supervise multiple studies or those with larger participant numbers.
  • Complete documentation for PI handover.
  • Ensure the safety of participants through ethical practices, prioritizing this at all times during the study.
  • Fulfill all medical responsibilities, ensuring clinical trials adhere to acceptable medical, scientific, and ethical standards, in compliance with protocols, SOPs, ICH, and local GCP guidelines.

Qualifications:

  • Must be a GMC registered doctor with no practice limitations.
  • Previous experience in clinical research is preferred.
  • Working knowledge of GCP (ICH/GCP and local regulations) is essential.
  • Ability to provide practical assistance and guidance to colleagues, fostering their development.
  • Demonstrate meticulous attention to detail in recording patient information and data, ensuring timely resolution of any queries.
  • Exhibit teamwork skills, building and maintaining positive relationships with colleagues and patients.

Our mission is to empower our clients to create a healthier, cleaner, and safer world. As part of Thermo Fisher Scientific, we value diverse experiences, backgrounds, and perspectives. We are committed to accelerating research, solving complex scientific challenges, driving technological innovation, and supporting patients in need.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.

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