Clinical Research Physician

Planet Pharma; Silsden; On-site; GBP 40,000 - 80,000; Part time

Job summary

An established industry player is seeking a Clinical Research Physician to lead medical innovation through clinical trials. This role emphasizes participant safety and involves designing, planning, and implementing trials, ensuring compliance with ethical and regulatory standards. The ideal candidate will be a registered GMC with expertise in neurology studies and a certification in PALS/EPALS. Join a dynamic team dedicated to advancing healthcare and making a significant impact in the field. If you are passionate about clinical research and patient care, this opportunity is perfect for you.

Qualifications

• Registered GMC with experience in neurology studies.
• PALS/EPALS certification required for the role.

Responsibilities

• Design and implement clinical trials for investigational treatments.
• Ensure participant safety and address medical concerns during trials.
• Collaborate on data analysis with biostatisticians.

Skills

GMC Registration

Experience with Neurology

PALS/EPALS certification

Experience with Paediatric patients

Job description

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 have 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.

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its headquarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

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: [e-mail]

Seniority level

Mid-Senior level

Employment type

Part-time

Job function

Health Care Provider, Research, and Public Relations

Industries

Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing