Manager Clinical III

Montefiore Einstein; New York (NY); On-site; USD 73,000 - 98,000; Full time

Job summary

Montefiore Einstein is seeking a Phase 1 Clinical Trial Manager to support the CCTO Phase 1 Program Director and Medical Director in expanding operations for solid tumor trials in the Bronx.

The CTM will coordinate daily trial operations, liaise with investigators, research staff, sponsors, and cross-functional teams, manage billing tasks, and monitor portfolio performance using data metrics; a proactive, organized leader is essential.

Qualifications

• Bachelor's degree required; Master’s preferred.
• 3–5 years experience in clinical research.
• SOCRA/CCRC certification preferred.
• Knowledge of ICH-GCP, FDA, and NCI regulations.
• Excellent communication and relationship-building skills.
• Strong organizational and problem-solving abilities.

Responsibilities

• Oversee and coordinate daily Phase 1 trial operations.
• Serve as primary liaison between investigators, staff, and sponsors.
• Manage research billing tasks and ensure compliance.
• Review data metrics to monitor portfolio performance.
• Support expansion of solid tumor studies.

Skills

Communication skills

Organization

Cross-functional collaboration

Clinical research knowledge

Billing/compliance knowledge

Education

Bachelor's degree

Master's degree preferred

Tools

MS Office

Databases

Internet

Job description

City/State:Bronx, New YorkGrant Funded:YesDepartment:Cancer Clinical Trials Office - Operations-Early PhaseWork Shift:DayWork Days:MON-FRIScheduled Hours:9 AM-5:30 PMScheduled Daily Hours:7.5 HOURSPay 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.RequirementsBachelor's degree required, Master's degree preferred3-5 years experience in clinical researchCCRP (SOCRA) or CCRC certification preferredKnowledge of ICH-GCP and NCI and FDA regulations regarding clinical trialsProficiency 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 patientsProactive approach to anticipating, resolving, and escalating operational issuesWell organized and detail orientedMontefiore Medical Center is an equal employment opportunity employer. Montefiore Medical Center will recruit, hire, train, transfer, promote, layoff and discharge associates in all job classifications without regard to their race, color, religion, creed, national origin, alienage or citizenship status, age, gender, actual or presumed disability, history of disability, sexual orientation, gender identity, gender expression, genetic predisposition or carrier status, pregnancy, military status, marital status, or partnership status, or any other characteristic protected by law.