Job Description

What can we offer you?

Apart from job satisfaction, we can offer you:

YOURSELF

25 days' holiday (with the option to buy more)*

HEALTH

Private Healthcare*
Optional dental insurance, health assessments and health cash plans*
Cycle to Work scheme*

WEALTH

Company Pension Scheme, matching contributions up to 5% of salary*
Life assurance*
Annual staff bonus scheme*
Season ticket loans*

Job Purpose

As

Clinical Research Physician

, you'll play a critical role as part of the medical team at our state-of-the-art clinical trial imaging clinic adjacent to Hammersmith Hospital in West London.


Working on a part-time basis, you'll share responsibility for providing rostered onsite medical cover for patients. Ensuring participant safety during imaging procedures, you'll be called upon to administer radiotracers and manage contrast agents, assuming responsibility for all medical decisions relating to imaging protocols for those within your care.


Working in close collaboration with other specialist colleagues within our study teams, you'll also be responsible for the medical oversight of participants in our PET and MRI clinical trials. This involves monitoring for imaging-related adverse events, ensuring compliance with radiation safety and regulatory requirements, maintaining ICH-GCP documentation standards and performing other trial-related duties contributing to the scientific validity of clinical trials.


Playing a vital role in upholding the highest ethical and scientific standards, this position places you at the heart of our commitment to responsible innovation. You'll work alongside leading experts in PET and MRI imaging, contributing directly to studies that genuinely extend the boundaries of medical science.

Key Responsibilities

Providing medical expertise and leadership throughout all phases of clinical trials Serving as the medical point of contact for clinical studies, ensuring the medical integrity of all trial-related activities. Ensuring all study-specific documentation is reviewed prior to initiation. Supervising and developing training of temporary non-Perceptive clinical staff including those on training programmes and development fellowships.

Specific activities

Performing appropriate procedures, including but not limited to the insertion of venous cannulas, administration of study-specific medication including IMP, PET radioligands and MRI contrast agents. Ensuring all studies are performed in compliance with the protocol, GCP, GMP, SOPs IRB/ethics committee and regulatory authorisations. Reviewing all study-specific documentation prior to providing clinical services. Contributing to the implementation and maintenance of relevant Standard Operating Procedures (SOPs)

Functional Competencies & Behavioural Skills

Competence in inserting radial arterial cannulas advantageous Possesses a thorough understanding of the scientific principles underpinning study design, pharmacokinetics, human toxicology, of statistics and pharmacodynamic assessments Excellent interpersonal and communication skills, energetic in approach and comfortable operating in a complex organisational environment Demonstrates effective communication with different audiences Able to appreciate the wider context in which the company operates and form collaborative relationships with colleagues, clients, client prospects and academic partners Self-motivated and used to working independently whilst also capable of collaborating closely with others in multi-disciplinary teams Development orientated and committed to own CPD

Experience, Education and Certifications

Medical degree (MBBS, B. Med or equivalent) with full GMC registration. Trained in Advanced Life Support (ALS) - or willing to undergo training to become certified Experience in the set-up, conduct, analysis and interpretation of early phase clinical drug development preferred, with expertise in the set-up and running of PET/MRI trials an advantage Experience in conducting human trials according to ICH GCP preferred, as well as a thorough appreciation of the pertaining ethical guidelines * English: fluent