Study Start‑Up Project Manager – Client Dedicated
Fortrea(9 days ago)
About this role
A Study Start-Up PM role focused on leading country-level submissions, approvals, and site readiness within a regulatory framework. The position involves managing compliance, facilitating interactions with authorities, and collaborating with global teams to support clinical study start-ups.
Required Skills
- regulatory Submissions
- Clinical Research
- Regulatory Compliance
- Stakeholder Management
- Documentation
- Project Management
- Regulatory Affairs
- Quality Standards
- Country Regulations
- Process Improvement
About Fortrea
fortrea.comFortrea, a leading CRO, advancing clinical trials through patient-focused clinical solutions that accelerate clinical development, drive trial success, and bring innovative therapies to those who need them most.
View more jobs at Fortrea →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Fortrea
Similar Jobs
Study Start Up Associate II
Clinical Careers Page(11 days ago)
Site & Study Start Up Specialist
Clinical Careers Page(23 days ago)
Study Start Up Associate
Clinical Careers Page(8 days ago)
Study Start Up Specialist
Roche(1 month ago)
Study Start-Up CRA
IQVIA(1 month ago)
Study Start Up Associate II
Clinical Careers Page(1 month ago)