At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
Clinical Research Physician - Corby, Northamptonshire (ONSITE) - 12 months fixed term contract.
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.
Main duties and responsibilities
- Working as a Sub Investigator ( or Principal Investigator if you have already previous experience in this role ) on Accellacare clinical trials at our site in Corby .
- Being able to support our site in Coventry as well will be an advantage.
- 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
Previous research experience (preferred but not essential)
Previous clinical trials experience in a commercial company as Investigator will be an advantage.
Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
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