Clinical Research Associate

Clinical Research Associate
Full Time
Off-Site (Regional Home-based)


RESPONSIBILITIES include:
- Monitoring clinical practices for multi-site trials.
- Assisting in selection of Investigator.
- Compiling, editing and distributing study documents.
- Undertaking study initiation and closeout activities.
- The submission of Ethic Committee applications.
- Negotiating document changes according to study specific guidelines.
- Maintaining clinical (SOPs.
- Building and maintaining productive working relationships with clinical and Investigator site staff.
- Conducting clinical site evaluation visits.
- Training site personnel according to SOP requirements and device usage for study.
- Arranging site and investigator meetings.
- Conducting site monitoring visits and following-up to identify significant problems and issues, ensuring compliance with local regulations, guidelines and policies and ICH GCP.

QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
- BSc in Life Science degree or equivalent (will also accept Registered Nurce)
- Clinical trial site monitoring experience related to the duties and responsibilities specified in the clinical research associate role.
- Knowledge of ICH GCP
www.espoirbridge.com

Agency/Employer: Clinqua Clinical Trails
Town or City: several regional positions available
Location: Edinburgh and Lothians
Sector: Health
Related Job Titles: Clinical Research Associate
Permanent/Contract: Permanent, Full time
Experience: 1 years
Date: 17-09-2008
Salary: 37000 British Pound / Year

Apply to this job

Tell a friend about this job opportunity