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Clinical Research Physician

Planet Pharma Staffing Limited

Metropolitan Borough of Solihull

On-site

GBP 60,000 - 100,000

Full time

30+ days ago

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An established industry player in clinical research is seeking a Clinical Research Physician to lead innovative medical trials. This role involves designing and implementing clinical studies, ensuring participant safety, and collaborating with researchers for data analysis. The ideal candidate will have GMC registration, experience in neurology, and hold PALS/EPALS certification. Join a dynamic team committed to advancing medical knowledge and improving patient outcomes. This opportunity offers a chance to make a significant impact in the field of clinical research while working in a supportive and inclusive environment.

Registered GMC with experience in neurology studies.
PALS/EPALS certification is essential for the role.

Design and oversee clinical trials ensuring participant safety.
Collaborate with biostatisticians to interpret study results.
Ensure regulatory compliance and develop trial protocols.

GMC Registration

Experience with Neurology

PALS/EPALS certification

Experience with Paediatric patients

We are currently partnered with a global leading Clinical Research Organisation who are seeking a Clinical Research Physician to join their dynamic team. In this role you will be driving medical innovation by overseeing clinical trials, ensuring their safety, and performing remote visits to patients. The right person will be a registered GMC, have experience working within neurology studies in multiple phases, and hold the PALS/EPALS certification.

Requirements:

Previous experience working with Paediatric patients
GMC Registration Number
Experience with Neurology
PALS/EPALS certification

Responsibilities:

Study Oversight: Design, plan, and implement clinical trials to evaluate the efficacy and safety of investigational treatments.
Participant Safety: Act as a medical monitor for trials, ensuring participant safety and addressing any medical concerns.
Data Analysis: Collaborate with biostatisticians and researchers to interpret study results and provide medical insights.
Regulatory Compliance: Ensure all trials meet ethical, regulatory, and Good Clinical Practice (GCP) guidelines.
Protocol Development: Develop and review clinical trial protocols, informed consent forms, and investigator brochures.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

Please click ‘apply’ or contact Jenson Green (Recruiter I) at Planet Pharma for more information:

E: JGreen@planet-pharma.co.uk

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