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Clinical Trials Sub Investigator (Research Physician)

TN United Kingdom

Winchester

On-site

GBP 65,000 - 68,000

Full time

Yesterday
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Job summary

An established industry player is seeking a Clinical Trials Sub Investigator for its Winchester site. This full-time role offers a unique opportunity to support innovative mental health trials while undertaking specialized training in pharmaceutical medicine. The ideal candidate will be a dedicated medical doctor with clinical research experience, committed to participant safety and trial integrity. Join a pioneering organization that values growth and excellence in cognitive health, and contribute to impactful research that transforms lives. This role promises a rewarding career path in a supportive environment focused on advancing medical knowledge.

Benefits

25 days annual leave plus bank holidays
Employee Assistance Program
Mortgage Advisor Scheme
Electric Vehicle Scheme

Qualifications

  • Medical doctor with at least 2 years of clinical experience.
  • GMC registered with a license to practice.

Responsibilities

  • Assist Principal Investigator in conducting trials according to ICH GCP.
  • Perform medical screenings to confirm participant eligibility.

Skills

Clinical Research
Patient Safety Management
Medical Emergencies
Informed Consent
Medical Screenings

Education

Medical Doctor
Postgraduate Membership (MRCP or equivalent)

Tools

GMC Registration
ALS Certificate

Job description

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Clinical Trials Sub Investigator (Research Physician), Winchester

Client: Re:Cognition Health

Location: Winchester, United Kingdom

Job Category: Other

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EU work permit required: Yes

Job Reference: d851fd1b80e5

Job Views: 6

Posted: 26.04.2025

Expiry Date: 10.06.2025

Job Description:

Re:Cognition Health (London based) is a pioneering brain and mind clinic that specializes in the treatment and care of people showing symptoms of cognitive impairment. Utilizing the latest progressive medical research and evidence-based treatments, we are passionate about transforming and optimizing cognitive performance through education, clinical excellence, and access to emerging treatments. This is an exciting time for Re:Cognition Health, especially with its expansion into the US via its subsidiary.

We value dedicated, hardworking individuals eager to contribute to our growth. Our vision is to become the worldwide leader in diagnosing, treating, and managing cognitive impairment. Join our team where everyone is valued and impactful work is done!

Re:Cognition Health operates clinics in London, Winchester, Surrey, Birmingham, Guildford, Plymouth, Bristol, and Washington DC. These centers are also major sites for international trials of disease-modifying and symptomatic drugs for Alzheimer’s and other neurological conditions in adults and children. Our multidisciplinary team provides comprehensive, patient-centered care using the latest research and treatments.

We seek individuals passionate about research, dedicated to their expertise, hardworking, and interested in growth and success.

We are looking for a Clinical Trials Sub Investigator at our Winchester site to support trials investigating innovative treatments for mental health disorders.

The ideal candidate is a dedicated, experienced medical doctor in cognitive disease and clinical research. This full-time role offers the opportunity to undertake a 4-year Pharmaceutical Medicine Specialty Training (PMST) to achieve a CCT in pharmaceutical medicine from the Faculty of Pharmaceutical Medicine. Re:Cognition Health is a recognized PMST training center.

The organization is a GMC Designated Body; candidates undertaking PMST will transfer to the Deanery for revalidation.

Role:

The primary responsibility is ensuring the safety, well-being, and interests of trial participants, under the supervision of the Principal Investigator who oversees the trial conduct and delegates duties to the Sub-Investigator.

Key Responsibilities:
  • Assist the Principal Investigator in conducting trials according to ICH GCP (R2).
  • Understand and explain trial protocols to potential participants and obtain informed consent.
  • Perform medical screenings (ECGs, vitals, venipuncture, lumbar puncture) to confirm eligibility.
  • Assess participant eligibility based on inclusion/exclusion criteria before randomization.
  • Conduct follow-up assessments (clinical exams, ECGs, blood tests) and dosing procedures.
  • Review and evaluate vital signs, lab results, and other data, reporting abnormalities.
  • Represent the site during sponsor meetings and monitoring visits, providing medical input.
  • Lead emergency response training and resuscitation equipment checks.
  • Support recruitment efforts as a research physician.
Ideal Candidate:
  • Medical doctor with at least 2 years of post-registration clinical experience.
  • Completed foundation and core medical competencies.
  • GMC registered with license to practice and compliant with revalidation.
  • Member of a medical defense organization (e.g., MDU, MPS).
  • Experience in participant safety management and medical emergencies.
  • Postgraduate membership (e.g., MRCP or equivalent).
  • Valid ALS certificate from Resuscitation Council (UK).
  • Previous clinical trial experience.
  • Aspiring to become a Principal Investigator.

Benefits include 25 days annual leave plus bank holidays, Employee Assistance Program, Mortgage Advisor Scheme, and Electric Vehicle Scheme.

Salary: £65,000–£67,500 per annum, depending on experience.

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