Richmond Pharmacology

About the Company

At Richmond, we're on a mission to transform healthcare by delivering faster answers and turning hope into tangible solutions. With over two decades of experience, we've perfected the art of precision, discipline, and innovation in clinical research.

Our commitment goes beyond our new name - it's a promise to drive progress, elevate patient care, and break down barriers that stand between patients and life-changing treatments. From innovative trial protocols to leveraging our London location and extensive patient database, we're dedicated to making a real impact.

Join us in embracing this exciting change. As Richmond, we're shaping a healthier, brighter future, one breakthrough at a time.
Stay connected and follow us for updates on our journey of innovation, healing, and hope.

#Richmond #FasterAnswers

Specialist services:

* Early phase adaptive studies including First-In-Human
* Cardiac Safety/Intensive ECG/Thorough QT studies
* Ethnic Bridging studies
* Early phase patient studies (therapeutic and non-therapeutic).

Full service:

* Consultancy and Expert Advice
* Protocol Writing & CRF Design
* Regulatory and Ethics Committee Applications
* Healthy Volunteer/Patient Recruitment for Phase I-IV
* Clinical Conduct, Pharmacy services
* Safety Laboratory and Bioanalytical services
* Data Management & Statistics and Report Writing

linktr.ee/richmondpharmacology

Listed Jobs

Company Name

Richmond Pharmacology

Job Title

Research Physician (Clinical Trials)

Job Description

Job Title: Research Physician (Clinical Trials) Role Summary: Conduct and manage early-phase clinical trials involving healthy and patient volunteers, contributing to protocol design, data analysis, and research publication under a senior medical leadership team. Expectations: Manage clinical trials from screening through data interpretation, collaborate in multidisciplinary teams, and participate in training, teaching, and process improvements. Key Responsibilities: - Oversee clinical trial execution, including subject screening, data collection, and safety monitoring. - Develop and refine trial protocols and analyze clinical data for research reporting. - Support research publication, quality assurance, and team training initiatives. Required Skills: - GMC registration and active medical practitioner status. - Experience in clinical trial management, data analysis, and protocol design. - Strong communication and collaborative skills for research team coordination. - Leadership potential for training, process improvement, and teaching activities. Required Education & Certifications: - Primary Medical Qualification (e.g., MBBS, MBChB). - Completed Foundation Programme or international equivalent. - Minimum three years of post-qualification clinical experience (e.g., FY3, JCF, CT1/ST1). - Valid GMC registration and eligibility to practice in the UK.

London, United kingdom

On site

Junior

09-11-2025