We are seeking a Study Coordinator to perform a variety of administrative tasks for a global CRO after they have secured a major global contract with a blue chip pharmaceutical company for a COVID-19 trial.
The role is the support of clinical trials and assistance in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrolment in clinical studies.
Provide clinical research support to investigators and site staff including:
- Verify and/or correct research study information on source documents. Research queries and variances, and provide feedback to the site data collector;
- Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness;
- Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits;
- Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget;
You Need;
- Equivalent education and experience - High School Diploma and 3 years' relevant work experience in a clinical environment or medical setting, e.g. medical assistant, laboratory technician
- Basic knowledge of clinical trials;
- In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules;
Details of contract:
- Start 3rd of August
- 5 urgent vacancies
- 10 - 52 week contract
- W2 workers preferred
- 40 hours a week
- Local hospital site
- PPE equipment provided
