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Clinical Research Physician

LocationUK, South London (Accellacare)
Work modehybrid
Typefull-time
Company size10,000+ people
First seen1w ago
Last seen2d ago
Clinical Research Physician
About the company
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
About the role
Clinical Research Physician – Accellacare South London (ONSITE), based in Orpington , London, UK - permanent full time contract ( part time is possible for candidates in the UK GMC Specialist register)
Are you looking for an outstanding opportunity to develop your career with a fast-growing leading edge Clinical research company and to be involved in the future of medicine across the globe? Accellacare concentrates on phase 2, 3 and 4 clinical trials providing excellent standards of data quality, safety and patient care and ultimately delivering excellent patient experience. We work in close partnership with most big pharmaceutical companies and these are the qualities they look for in a leading Dedicated Clinical Research Trials Organisation.
We are growing our international footprint across the globe and invite you to join us and become part of our success story.
This role is with Accellacare, part of ICON’s clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.
Main duties and responsibilities
Working as a Principal Investigator or a Sub Investigator on Accellacare clinical trials at our site in Orpington, London, UK
Occasionally support the other Accellacare UK research sites
Comply with ICH/GCP standards and UK clinical trials regulation.
Interview, screen, enrol and monitor the clinical trial participants.
Provide medical care for the clinical trial participants.
Perform study specific tasks (clinical examination and evaluations, review of blood test results, X rays results, etc.)
Ensure that the clinical trials participants safety and wellbeing are protected at all times.
Ensure excellent standards of patient safety and quality of the service.
Record Adverse events/Serious Adverse events.
Ensure that Good Documentation Practice is followed at all time.
Develop positive relations with sponsors, clients and monitors as required.
Participate in GMC appraisals/Revalidation scheme.
Skills/qualifications and experience
Fully qualified, GMC registered Physician with a licence to practice
Right to work in the UK
At least 5 years experience as a doctor post graduation
At least 2 year experience in the UK since GMC registration
Previous experience as a Consultant or Specialist Registrar will be an advantage , specifically in Dermatology, Cardiology, Endocrinology or Respiratory Medicine
Previous research experience will be an advantage
Previous clinical trials experience in a commercial company as an Investigator will be an advantage
#LI-CL1
#LI-ACCELLACARE
Legal
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
•
Competitive base salary and performance related incentives
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Health and wellbeing programmes including medical, dental, and vision coverage where applicable
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Retirement and pension plans
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Life assurance and disability coverage
•
Employee assistance programmes and wellbeing resources
•
Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
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