Fortrea is currently seeking an In House CRA to join our multi-sponsor team in the this home-based youll play a key part in supporting global clinical trials across all phases working closely with Clinical Trial Leaders and cross-functional teams to ensure smooth trial delivery.
Location: Remote
Type: Full-time permanent
What Youll Do:
Coordinate trial planning setup conduct and closeout activities in line with ICH-GCP standards.
Manage internal and external systems track trial progress and maintain documentation (including TMF).
Collaborate with internal teams CROs vendors and investigators to support trial execution.
Support trial submissions and the preparation of Clinical Trial Reports.
What Youll Need:
University degree or equivalent experience in clinical research.
Experience in trial administration within an international environment.
Solid knowledge of ICH-GCP and major regulatory frameworks (FDA EMA PMDA).
Excellent communication skills and proficiency with MS Office tools.
Why Apply:
Home-based flexibility with minimal travel
Stable long-term opportunity with a leading CRO
Attractive salary and benefits package
Interested in making a meaningful impact in clinical research Wed love to hear from you!
Learn more about our EEO & Accommodations request here.
Fortrea is currently seeking an In House CRA to join our multi-sponsor team in the this home-based youll play a key part in supporting global clinical trials across all phases working closely with Clinical Trial Leaders and cross-functional teams to ensure smooth trial delivery.Location: RemoteType...
Fortrea is currently seeking an In House CRA to join our multi-sponsor team in the this home-based youll play a key part in supporting global clinical trials across all phases working closely with Clinical Trial Leaders and cross-functional teams to ensure smooth trial delivery.
Location: Remote
Type: Full-time permanent
What Youll Do:
Coordinate trial planning setup conduct and closeout activities in line with ICH-GCP standards.
Manage internal and external systems track trial progress and maintain documentation (including TMF).
Collaborate with internal teams CROs vendors and investigators to support trial execution.
Support trial submissions and the preparation of Clinical Trial Reports.
What Youll Need:
University degree or equivalent experience in clinical research.
Experience in trial administration within an international environment.
Solid knowledge of ICH-GCP and major regulatory frameworks (FDA EMA PMDA).
Excellent communication skills and proficiency with MS Office tools.
Why Apply:
Home-based flexibility with minimal travel
Stable long-term opportunity with a leading CRO
Attractive salary and benefits package
Interested in making a meaningful impact in clinical research Wed love to hear from you!
Learn more about our EEO & Accommodations request here.
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