Research Physician II
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Job Location:
Manchester - UK
Monthly Salary:
Not Disclosed
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
At Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life To enable our customers to make the world healthier cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research development and delivery of life-changing therapies.
Alongside clinical research through our PPD clinical research portfolio our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials such as securing sites and recruiting patients allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on now and in the future.
Are you a GMC registered Doctor who is interested in working in the dynamic clinical research industry
Are you passionate about improving patients lives for the better
We are currentlylooking to recruita Clinical Research Physicianfor our Synexus Clinical Research site in Manchester United Kingdom open to travel to support our sites in England.
Working days Monday to Friday 37 hours a week the main priority will always be patient safety. Acting as the principal investigator (PI) or co-investigator for some or all of the studies at the site they have the responsibility for all sponsor research studies while also ensuring ICH/GCP and local regulations are met.
Key responsibilities for a Clinical Research Physicianare as follows:
- Carries out clinical evaluation and assessment of participants to ensure eligibleparticipants are recruited and monitored for safety and adherence.
- Principle Investigator (PI) or Co Investigator for some or all of the studies at the site ensuring ICH/GCP and local regulations are met.
- Attends Site Initiation Visits (SIV) Pre-Selections Visits (PSV) and Investigatormeetings as required.
- Participates in recruitment initiatives and strategy development to ensure targetsare achieved; ensuring recruiting studies enroll according to plan within timelinesand targets.
- Reviews enrolment progress pre-screening and screening success rates screenfailure rates safety and retention of participants.
- Interprets protocols and IB.
- Manages and reviews IVRS CRF/EDC if applicable.
- Oversees management of investigational medical product (IMP).
- Oversees multiple studies and/or studies with higher numbers.
- Completes documentation for PI handover.
- Cares for and protects the safety of participants through ethical conduct; this
should receive the highest priority at all times during all aspects of the study. - Fulfills and complies with all medical duties ensuring that clinical trials areperformed to acceptable medical scientific and ethical standards and meet therequirements as per protocol SOP/COP ICH and local GCP guidelines andregulations.
- Travels 3-5 days to other sites.
To be considered for this exciting opportunity you will require the following skills and experience:
- Be a GMC registered doctor with no limitations to practice
- Ideally some previous experience 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 a team player capable of building and sustaining positive relationships with colleagues as well as patients
Our Mission is to enable our customers to make the world healthier cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100000 colleagues we share a common set of values - Integrity Intensity Innovation and Involvement - working together to accelerate research solve complex scientific challenges drive technological innovation and support patients in need. #StartYourStory with PPD part of Thermo Fisher Scientific where diverse experiences backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.
Key Skills
- EMR Systems
- Post Residency Experience
- Occupational Health Experience
- Pain Management
- SOAP
- Primary Care Experience
- Medical Management
- Suturing
- Workers' Compensation Law
- Pharmacy Residency
- Botox Experience
- Epic
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
