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Are you a Research Physician/Doctor who wants to improve patient’s lives for the better?
Are you looking to advance your career into the clinical trials space?
Do you want to work for a leading multinational organisation, renowned throughout the industry for its meteoric rise to success and dependability to deliver on global contracts across multiple therapeutic areas and phases?
If the answer is yes to these questions you need to read on because we are currently looking to recruit a Research Physician 3 for our dedicated research site in the Midlands.
This site is conveniently located opposite Queen Elizabeth Hospital and has access to a wide and diverse population of patients with complex health requirements.
There is an every evolving portfolio of studies across numerous therapeutic areas and, with a focus on teamwork and collaboration, the site team pride themselves on ensuring a positive patient experience at all times.
As a Research Physician 3, you will be responsible for ensuring the commercial success of your site through the safe performance of your local clinical studies. You will also act as the principal investigator (PI) or sub-investigator for some or all of the studies at your site where you accept responsibility for all sponsor research studies while also ensuring ICH/GCP and local regulations are met. This role will also see you demonstrating leadership capability through your guidance and training of colleagues while you work on multiple studies.
Key roles and responsibilities of the Research Physician 3 role are:
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
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
To be considered for this exciting opportunity you will need the following skills and experience -
Be a GMC registered doctor with previous experience within clinical research
Possess demonstrable experience of being a principle/sub investigator within 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
Interested? Great, please apply ASAP.
Synexus is an Affirmative Action and Equal Opportunity Employer.
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