Clinical Research Physician, Part-time
- Employer
- RBW Consulting
- Location
- North East England (GB)
- Salary
- Competitive salary based on experience including bonus and benefits
- Start date
- 26 Jan 2021
- Closing date
- 25 Feb 2021
View more
- Discipline
- Medical Affairs, Clinical Research Physician
- Hours
- Part Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Clinical Research Physician (Part-time)
Location - North Tees
Salary - £Negotiable with bonus and benefits
Our client, a leading global organisation is recruiting a Clinical Research Physician to join their team. We are interested in speaking with experienced candidates who have worked acting as a principal investigator (PI) or co-investigator. This role will have the benefit of working on a wide range of research studies and is available on a permanent or part-time basis
Key responsibilities will be
- Acting as principal investigator (PI) or co-investigator 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?
- GMC registered doctor
- Possess some experience within commercial clinical research
- Have working knowledge of GCP (ICH/GCP and local regulations compliance)
- Show meticulous attention to detail and be a team player
For further information please contact Louise Clark +44 (0)1293 584300
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