Clinical Research Physician

TN United Kingdom; Metropolitan Borough of Solihull; On-site; GBP 60,000 - 100,000; Full time

Job summary

An innovative global leader in clinical research is seeking a Clinical Research Physician to oversee clinical trials and ensure participant safety. This role involves designing and implementing trials, ensuring regulatory compliance, and collaborating with researchers for data analysis. The ideal candidate will be a registered GMC with expertise in neurology and experience with paediatric patients. Join a dynamic team and contribute to groundbreaking research in a supportive environment that values diversity and equal opportunity.

Qualifications

• Registered GMC with experience in neurology studies.
• PALS/EPALS certified and experienced with paediatric patients.

Responsibilities

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

Skills

GMC Registration

Neurology Experience

PALS Certification

EPALS Certification

Experience with Paediatric Patients

Job description

Job Opportunity: Clinical Research Physician

We are partnered with a global leading Clinical Research Organisation seeking a Clinical Research Physician to join their dynamic team. In this role, you will oversee clinical trials, ensure participant safety, and perform remote patient visits. The ideal candidate will be a registered GMC, experienced in neurology studies across multiple phases, and possess PALS/EPALS certification.

Requirements:

• Previous experience working with paediatric patients
• GMC Registration Number
• Experience in neurology
• PALS/EPALS certification

Responsibilities:

1. Study Oversight: Design, plan, and implement clinical trials evaluating investigational treatments.
2. Participant Safety: Act as a medical monitor to ensure safety and address medical concerns.
3. Data Analysis: Collaborate with biostatisticians and researchers to interpret results and provide insights.
4. Regulatory Compliance: Ensure trials meet ethical, regulatory, and GCP guidelines.
5. Protocol Development: Develop and review trial protocols, informed consent forms, and investigator brochures.

About Planet Pharma:

Planet Pharma is an American-headquartered employment agency providing global staffing services. With offices in Chicago and Central London, we operate in over 30 countries, supporting a network of over 2,500 contractors worldwide. Recognized by FORBES as the 17th best professional staffing firm, we offer expertise in Regulatory Affairs, Pharmacovigilance, QA, QC, Clinical Development, and more.

We are an equal opportunities employer and welcome applications from all qualified candidates regardless of race, sex, disability, religion, sexual orientation, or age.

Learn more at www.planet-pharma.com.

To apply or for more information, please click ‘apply’ or contact Jenson Green (Recruiter I) at Planet Pharma.