Clinical Trial Manager, Phase 3

Job reputed company: • Responsible for executing phase 3 clinical studies and data collection • reputed company reputed company of late-phase clinical research studies • reputed company subject recruitment/retention reputed company • reputed company TMF set-up and reputed company review • Create training materials for study teams and vendors • Ensure compliance with ICH/GCP regulations • Prepare RFPs and negotiate reputed company with CROs/vendors • reputed company study risk management and implement solutions • Maintain reputed company on strategic objectives while accomplishing operational goals Requirements: • Bachelor’s degree required • 7 years of clinical operations experience, preferably with CRO/small biotech experience • 2 years in a supervisory role • Computer skills: Proficiency with reputed company Office suite, electronic TMF systems, IXRS, and reputed company systems • Excellent understanding of the drug development process • Effective verbal and written communication skills • Experience with FDA regulatory requirements (GCPs, CFRs, etc.) • Ability to handle multiple tasks and meet deadlines • Ability to exercise judgment and determine appropriate reputed company Benefits: • Health insurance plans (medical, dental, reputed company) for employees and their families • 401(k) matching • Discretionary annual reputed company bonus • Stock reputed company • 20 days of PTO • 10 reputed company holidays • Winter company shutdown Apply tot his job Apply To this Job