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Clinical Research Associate

Oxford, Oxfordshire
£48,000 to £78,000
Job Type
20 Sep 2022
ROLE: Clinical Research Associate START: ASAP CONTRACT: 12 Months PAY: £43,000 - £78,000 Per Annum (DOE) LOCATION: Witney (Office Based) We are looking for an organised, flexible Clinical Research Associate to oversee IVD clinical trials. The Clinical Research Associate will establish trial sites, train site staff, and manage Investigational devices and trial materials. The Clinical Research Associate will conduct regular site visits, prepare final reports, and liaise with interested parties regarding all trial aspects. You will play a leading role in generating and overseeing documentation and records. To be successful in this role, you should be able to recognize logistical problems and initiate appropriate solutions. Ideal candidates will be detail-oriented, have the ability to multitask, and be able to collaborate with various role players. The primary functions of the CRA role are: Day-to-day management of the conduct of clinical investigations at study sites as a representative of the ADC Clinical Affairs team. Monitoring to ensure studies are conducted according to protocols, applicable ADC procedures, GCP and all applicable regulations, and to ensure that subject safety and data integrity are maintained. Clinical Research Associate Responsibilities: Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial. Training site staff on protocol requirements, proper source documentation, and case report form completion. Tracking and managing IVDs and trial materials. Conducting regular monitoring visits and close out visits and writing visit reports. Implementing action plans for sites not meeting expectations. Ensuring compliance with SOPs and local regulations, and ICH and GCP guidelines. Other tasks and responsibilities as needed. Clinical Research Associate Requirements: Degree in Life Sciences field. Experience with IVD and /or Medical Device studies is desirable 1-2 years of experience in a clinical research role or as a Clinical Research Associate is desirable. Experience of Electronic Data Capture (EDC) and electronic Trial Master File (TMF) is desirable Knowledge of the Medical device industry, terminology, and practices. Knowledge of relevant regulations and their practical implementation. Strong verbal and written communication skills. Ability to manage and prioritise workload effectively. Available to travel in the UK and abroad, and ability to manage travel schedules, such as flight schedules. Overnight nights may be required.Randstad Business Support is acting as an Employment Business in relation to this vacancy
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  • Job Reference: 717194857-2
  • Date Posted: 20 September 2022
  • Recruiter: Randstad Business Support
    Randstad Business Support
  • Location: Oxford, Oxfordshire
  • Salary: £48,000 to £78,000
  • Bonus/Benefits: Expenses
  • Sector: Healthcare & Medical
  • Job Type: Contract