Location: UK (Scotland Midlands South East & South West preferred)
Contract: 12-month fixed-term (with potential extension based on business needs)
Model: Client-dedicated role (FSP)
Looking to advance your career in clinical research Fortrea is seeking Clinical Research Associates II to join our FSP team on a 12-month fixed-term contract with the possibility of extension based on business needs.
What youll do:
- Conduct and oversee site monitoring visits in line with protocols and regulatory requirements
- Manage site activities from initiation through to closeout
- Ensure patient safety data integrity and GCP compliance
- Support feasibility site selection and vendor coordination
- Contribute to team development and quality improvement efforts
What were looking for:
- Degree in life sciences or a related field
- Minimum 2 years experience in clinical research (e.g. CRA Site Management)
- Knowledge of regulatory guidelines and clinical trial processes
- Strong communication and organizational skills
- Willingness to travel and a valid drivers license
Join a global innovative organization and gain exposure to diverse clinical trials while growing your career in a supportive environment.
Learn more about our EEO & Accommodations request here.
Location: UK (Scotland Midlands South East & South West preferred) Contract: 12-month fixed-term (with potential extension based on business needs) Model: Client-dedicated role (FSP)Looking to advance your career in clinical research Fortrea is seeking Clinical Research Associates II to join our FS...
Location: UK (Scotland Midlands South East & South West preferred)
Contract: 12-month fixed-term (with potential extension based on business needs)
Model: Client-dedicated role (FSP)
Looking to advance your career in clinical research Fortrea is seeking Clinical Research Associates II to join our FSP team on a 12-month fixed-term contract with the possibility of extension based on business needs.
What youll do:
- Conduct and oversee site monitoring visits in line with protocols and regulatory requirements
- Manage site activities from initiation through to closeout
- Ensure patient safety data integrity and GCP compliance
- Support feasibility site selection and vendor coordination
- Contribute to team development and quality improvement efforts
What were looking for:
- Degree in life sciences or a related field
- Minimum 2 years experience in clinical research (e.g. CRA Site Management)
- Knowledge of regulatory guidelines and clinical trial processes
- Strong communication and organizational skills
- Willingness to travel and a valid drivers license
Join a global innovative organization and gain exposure to diverse clinical trials while growing your career in a supportive environment.
Learn more about our EEO & Accommodations request here.
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