Our client, a global CRO, is seeking a Senior Clinical Research Physician to join their team.
In this role, you will lead early-stage clinical trials, oversee study protocols, and ensure ethical conduct and compliance throughout each study. You will work closely with experienced sponsor teams and contribute to innovative projects aimed at advancing healthcare and improving patient outcomes.
You will play a pivotal role in maintaining patient safety, enhancing quality systems, and ensuring that the clinical data generated meets the highest standards. This position offers significant opportunities for leadership and career development, including the chance to build and mentor a clinical research team and influence sponsor interactions. A strong focus on patient recruitment is critical, balancing trial integrity and safety while consistently achieving enrollment targets, including patient diversity goals.
Key Responsibilities
* Provide strategic medical oversight for clinical trials, ensuring protocols are followed and participant safety is prioritized.
* Critically evaluate and interpret trial data to uphold accuracy, quality, and scientific integrity.
* Support study design and feasibility assessments, offering guidance to clinical operations and investigative teams.
* Ensure all trials meet regulatory standards and Good Clinical Practice (GCP), maintaining meticulous documentation and confidentiality.
Requirements
* Qualified medical doctor (MD) with full GMC registration and active licence to practise.
* Broad experience in designing, managing, and delivering clinical trials, including work with CROs.
* Established track record as a Principal Investigator or in senior clinical leadership roles.
* Thorough knowledge of UK regulatory requirements and adherence to Good Clinical Practice (GCP).
* Highly organized and analytical, with strong communication skills and proven ability to oversee complex, multi-site studies.