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Clinical Research Physician (sub)

Employer
RBW Consulting
Location
South West England (GB)
Salary
£Neg plus benefits
Start date
3 Oct 2022
Closing date
17 Oct 2022

View more

Discipline
Clinical Research, Investigator
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

ENTRY LEVEL OPPORTUNITY 

Clinical Research Physician (sub Investigator)

Location – Bristol, UK

Salary - £Negotiable and benefits

Our client, an established provider of clinical trials, is looking to recruit a co Investigator to join their team.  This is a great opportunity for a GMC registered doctor who is looking into alternatives to a career within the NHS, providing the opportunity to move into a career within clinical research working on a range of clinical studies.   No previous clinical research experience required. 

Key responsibilities will be

  • Acting as co investigator (PI) ensuring ICH/GCP and local regulations are met
  • Conducting clinical trials in line with the protocol and to ensure the recruitment of eligible participants onto the studies
  • Taking ownership of being prepared for all GMC appraisals to ensure a positive outcome
  • Review screening, pre-screening and screening success rates for clinical trials
  • Providing information and support to consenting participants for a clinical study
  • Responsible for checking patient inclusion/exclusion to studies
  • Liaising with and developing positive relations with sponsors, clients and clients’ contractors as required, projecting a helpful and courteous company image
  • Carrying out clinical evaluation and clinical investigation of participants
  • Taking responsibility for ensuring serious adverse events / adverse events are reported appropriately
  • Having responsibility for the medical wellbeing of participants during the clinical trial and referral to specialists or GP as required

What skills/ qualifications are required?

  • Be a GMC registered doctor
  • Possess experience within commercial clinical research beneficial
  • Knowledge of GCP (ICH/GCP and local regulations compliance)
  • Show meticulous attention to detail and be a team player
  • Flexible to travel when required

For more information in general on this role and other roles for Medics within clinical research please get in touch

Louise Clark +44 (0)1293 364114

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