Phase 1 Oncology Clinical Trial Manager — Operations Lead

montefiore; New York (NY); On-site; USD 76,000 - 95,000; Full time

Job summary

Montefiore Medical Center in Bronx, NY seeks a Phase 1 Clinical Trial Manager to support the Cancer Clinical Trials Office operations. You will oversee daily solid tumor Phase 1 trials and coordinate investigators, staff, and sponsors to expand research operations.

The role requires 3-5 years in clinical research, a Bachelor's degree (Master's preferred), and familiarity with ICH-GCP and FDA regulations. Strong communication and organizational skills are essential.

Qualifications

• 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 FDA regulations regarding clinical trials.
• Proficiency with computers (e.g., MS Office, databases, Internet).
• Excellent communication skills, with ability to build effective working relationships.
• Proactive approach to anticipating, resolving, and escalating operational issues.
• Well organized and detail oriented.

Responsibilities

• Assist the CCTO Phase 1 Program Director and Medical Director in expanding research operations.
• Oversee and coordinate daily operations of solid tumor Phase 1 trials.
• Serve as the primary contact between investigators, research staff, ancillary departments, and sponsors.
• Handle research billing tasks and ensure billing compliance.
• Review data metrics to monitor portfolio performance.

Skills

Clinical research

Communication skills

Attention to detail

Proactive problem solving

MS Office

Education

Bachelor's degree

Master's degree preferred

Tools

MS Office

Job description

Montefiore Medical Center in Bronx, NY seeks a Phase 1 Clinical Trial Manager to support the Cancer Clinical Trials Office operations. You will oversee daily solid tumor Phase 1 trials and coordinate investigators, staff, and sponsors to expand research operations.

The role requires 3-5 years in clinical research, a Bachelor's degree (Master's preferred), and familiarity with ICH-GCP and FDA regulations. Strong communication and organizational skills are essential.