PPD

Senior Research Physician

Expiring today

Company
PPD
Location
United Kingdom
Salary
Competitive
Posted
26 Jan 2021
Closes
25 Feb 2021
Ref
1183207
Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Accelerated Enrollment Solutions (AES) is a business unit of PPD that offers both sponsors and contract research organizations best-in-class clinical trial research site and patient enrollment solutions, with tiered offerings combining the expertise, as needed, of industry leaders PPD, Synexus, Acurian and Optimal Research.

Our success is based on a simple, but crucial, principle. We place the patient at the heart of everything we do. Synexus is a world class Site Network Organisation with global expertise spanning patient recruitment, trial planning, management and patient retention.

We recruit and retain more engaged patients, at fewer sites, and in less time than traditional centres, enhancing the quality and efficiency of our customers' drug development programmes.

Are you a Doctor/Research Physician who wants to improve patient's lives for the better?

Are you looking to advance your career into the clinical trials industry as a Senior Research Physician?

We are currently looking to recruit a Senior Research Physician based at our clinical site in Waterloo, Merseyside.

Working Monday to Friday, 37 hours a week, the main priority will always be patient safety. Acting as the principal investigator (PI) for studies at the site they have the responsibility for all sponsor research studies while also ensuring ICH/GCP and local regulations are met.

Key roles and responsibilities of a Senior Research Physician are:
  • Acting as principal 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
  • Constantly seeking and suggesting quality improvements
  • 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


Qualifications:

To be considered for this exciting opportunity you will need the following skills and experience -
  • Be a GMC registered doctor
  • Acted as a PI within commercial clinical research
  • Have working knowledge of GCP (ICH/GCP and local regulations compliance)
  • Demonstrate the inclination to provide practical help and guidance to colleagues, providing practical solutions for any problems and supporting their development
  • Show meticulous attention to detail in recording patient information and data ensuring any queries are acted upon in a timely and efficient manner
  • Be team player, capable of building and sustaining positive relationships with colleagues as well as patients

Similar jobs

Similar jobs