Manager Clinical III

Montefiore New Rochelle; New York (NY); Hybrid; USD 76,000 - 95,000; Full time

Job summary

Montefiore New Rochelle is seeking a Phase 1 Clinical Trial Manager to support the CCTO Phase 1 program for solid tumor trials. You will oversee daily operations and serve as the primary liaison among investigators, research staff, ancillary departments, and sponsors.

The role requires 3-5 years in clinical research, a Bachelor's degree, and preferably CCRP/CCRC certification, with strong knowledge of ICH-GCP and FDA regulations. Proactive problem solving and strong communication are essential.

Qualifications

• Bachelor's degree required; Master's preferred.
• 3-5 years experience in clinical research.
• CCRP or CCRC certification preferred.
• Knowledge of ICH-GCP, NCI, and FDA clinical trials regulations.
• Strong communication and organizational skills.

Responsibilities

• Oversee daily operations of solid tumor Phase 1 trials.
• Coordinate investigators, staff, departments, and sponsors.
• Support research billing and ensure billing compliance.
• Monitor data metrics and portfolio performance.
• Escalate operational issues proactively.

Skills

MS Office Proficiency

Communication Skills

Cross-functional Collaboration

Education

Bachelor's degree

Master's degree preferred

Tools

EDC

CTMS

Job description

## Manager Clinical IIIApply: 1695 Eastchester Road: Full time: Posted Yesterday: JR234203**City/State:**Bronx, New York**Grant Funded:**Yes**Department:**Cancer Clinical Trials Office - Operations-Early Phase**Work Shift:**Day**Work Days:**MON-FRI**Scheduled Hours:**9 AM-5:30 PM**Scheduled Daily Hours:**7.5 HOURS**Pay Range:**$76,000.00-$95,000.00The Phase 1 Clinical Trial Manager (CTM) will assist the CCTO Phase 1 Program Director and the Medical Director of the Early Phase Therapeutics program in expanding research operations. The CTM will oversee and coordinate daily operations of the solid tumor focused Phase 1 trials and serve as the primary point of coordination between investigators, research staff, ancillary departments, and sponsors. The CTM will handle research billing tasks and is responsible for ensuring research billing compliance, and will review data metrics to monitor portfolio performance. The portfolio includes studies sponsored by pharmaceutical companies, federal grants, and investigator-initiated protocols. Other duties as assigned. **Requirements*** Bachelor's degree required, Master's degree preferred* 3-5 years experience in clinical research* CCRP (SOCRA) or CCRC certification preferred* Knowledge of ICH-GCP and NCI and FDA regulations regarding clinical trials* Proficiency with computers (e.g., MS Office, databases, Internet)* Excellent communication skills, with a demonstrated ability to build effective working relationships with investigators, cross-functional teams, and patients* Proactive approach to anticipating, resolving, and escalating operational issues* Well organized and detail oriented