Senior Clinical Research Coordinator

3 months ago

Oxford, United Kingdom GenesisCare Full time

At GenesisCare we want to hear from people who are as passionate as we are about innovation and working together to drive better life outcomes for patients around the world.

Are you ready to embark on an exciting journey as a Senior Clinical Research Coordinator at our state-of-the-art cancer care centres located in Oxford and Milton Keynes? Join our dedicated team at GenesisCare UK and be part of something extraordinary.

The Role:
As a Senior Clinical Research Coordinator with us, you'll play a pivotal role in being responsible for the conduct of all clinical trial activities being undertaken in the Oxford and Milton Keynes centres. You will work closely with the National Research Manager to improve processes and systems that increase recruitment and optimise efficiency.

At all times you will ensure that all research is conducted in accordance with Good Clinical Practice (GCP) Guidelines, and all applicable laws, regulations and guidelines, Standard Operating Procedures (SOPs) and research specific protocols.

This is your opportunity to make a meaningful impact in cancer research and develop your career.

What You'll Do:
Your key responsibilities:
Clinical Trial Conduct:

- Have a thorough understanding of all trials being conducted in the Oxford/Milton Keynes centre and as applicable all centres conducting research, particularly the protocol, investigator brochure, participant information and consent forms, budget, timelines, and safety reporting requirements.
- Work with the National Research Manager to ensure the research governance framework and processes are fully implemented in responsible areas, including, not limited to, research approval, activation and ongoing safety reporting.
- Assist the National Research Manager with feasibilities and the Start Up team with study start up activities including vendor selection and completion of regulatory documentation.
- Proactively manage all aspects of the trial process including trial timelines, budgets, resources and vendor relationships
- Assist with protocol development, PIL/IC development and other research documents to support a clinical trial.
- Identify quality risks and issues, respond to issues raised by project team and plan/implement appropriate corrective and preventative action plans
- Manage Study budgets ensuring invoices are timely and accurate, communicate out of scope budget items
- Undertake Clinical Research Coordinator roles and responsibilities for allocated trials (as per Clinical Research Coordinator Position Description)
- Liaise with and facilitate collaboration between relevant departments and third parties to ensure the provision of quality clinical services
- Maintain open and regular communication with key stakeholders, in particular sponsor representatives.

Maintain Quality and Compliance:

- Contribute to and ensure all internal policies and systems are followed
- Maintain up-to-date knowledge in regulatory, administrative and clinical frameworks and current clinical issues and practice as they pertain to research
- Ensure all research is performed in accordance with GCP guidelines, and all applicable laws, regulations and guidelines, Standard Operating Procedures (SOPs) and research specific protocols.

What You'll Have:
Experience and skills:

- An undergraduate degree deemed equivalent in Science, Nursing, Pharmacy or related disciplines.
- Demonstratable experience as a clinical trial co-ordination, or as a Clinical Research Associate, with extensive site management experience.
- A background in nursing, oncology or research is essential.
- Excellent communication and interpersonal skills with the ability to work both independently and as part of a team in an effective, proactive and co-operative manner.
- High level of initiative and flexibility and the ability to meet deadlines while balancing multiple priorities.

Qualifications and Knowledge:

- Strong computer literacy with knowledge of clinical trials software and MS Office suite.
- Knowledge of Good Clinical Practice Good Clinical Practice (GCP) Guidelines and all applicable Laws, regulations and regulations relating to the conduct of clinical research in the UK.

Other requirements for this role:

- Flexibility in working times and locations.
- Ability to travel if required.

Why Choose GenesisCare:
Discover what's in store for you when you join the GenesisCare UK team:

- Shape your work-life balance with 25 days of annual leave, plus bank holidays, and the option to buy more or sell back annual leave.
- Prioritise your well-being with complimentary private medical and dental coverage, access to Employee Assistance Program, and Income Protection.
- Access our world-class radiotherapy - free to you and your immediate family, if required.
- Secure your future with a competitive Company Contributory Pension Scheme.
- Nurture your mental health and well-being through our well-being community, with access to Babylon Health and Headspace Wellbeing.
- Enjoy hassle

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