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.
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.