Clinical Research Physician (Part-time 0.6 FTE)

Clinical Research Physician (Part-time 0.6 FTE) page is loaded## Clinical Research Physician (Part-time 0.6 FTE)locations: GBR – London (Hammersmith Hospital)time type: Part timeposted on: Posted Todayjob requisition id: JR104196*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: fluentAt Perceptive, we enable the world’s pharmaceutical, biotech, and clinical research organizations to rapidly discover and advance life-changing treatments.Together, our global team delivers unmatched scientific and technological expertise, global operational experience, and end-to-end solutions to help the global research community realize tomorrow’s new therapies. To do this, we need people like you.Join our talent community and receive the latest Perceptive news, and content, and be first in line for new job opportunities.Join our #J-18808-Ljbffr