Parexel - Clinical Research Physician Opportunity

About Parexel

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

About the Role

We are seeking a dedicated and motivated Clinical Research Physician to join our Early Phase Clinical Unit (EPCU) in London. This is an exciting opportunity to play a pivotal role in early-phase clinical research, contributing to the development of innovative therapies while ensuring the highest standards of participant safety, regulatory compliance, and scientific integrity.

As a Clinical Research Physician, you will provide medical oversight for studies involving healthy volunteers and patients participating in early-phase clinical trials. You will work closely with multidisciplinary research teams, acting as a Clinical Investigator and helping to deliver high-quality clinical research in accordance with ICH-GCP standards.

Key Responsibilities

In this role you will:

• Serve as a Clinical Investigator during clinical trials, ensuring participant safety, data integrity, and compliance with ICH-GCP and study protocols.
• Provide medical oversight and support for clinical studies of investigational and marketed pharmaceutical products conducted within the EPCU.
• Conduct pre-study medical assessments, including medical histories and physical examinations, and determine volunteer suitability for study participation and panel enrolment.
• Ensure study participants provide fully informed written consent prior to participation.
• Review and interpret clinical data, including vital signs, ECGs, laboratory results, adverse events, and other safety parameters.
• Participate in an on-call rota, providing medical support outside standard business hours.
• Maintain proficiency in Advanced Life Support (ALS), and respond effectively to medical emergencies within the unit.
• Assist with or perform the administration of investigational medicinal products, as required.
• Monitor, assess, communicate, and manage adverse events and other clinical findings throughout study conduct.
• Prepare and present safety information at study and safety review meetings.
• Perform study-specific clinical procedures and assessments as required.