Clinical Trial Operations Lead (Temp-to-Perm)

BioSpace; New York (NY); On-site; USD 94,000 - 107,000; Full time

Job summary

Protara Therapeutics is hiring a Clinical Project Manager, Temp to Perm, to support the Clinical Operations team across ongoing programs. You will act as a secondary operations contact, ensure CRO deliverables meet timelines, and oversee site activation and budgets.

The role requires 5+ years of trial management experience, knowledge of ICH/GCP/CFR guidelines, and the ability to travel to sites. The position offers an hourly rate with strong growth opportunities.

Qualifications

• Bachelor’s degree in clinical research, life science or a related field is required.
• 5+ years of relevant clinical trial management experience in pharma/biotech.
• Knowledge of ICH, GCP, and CFR guidelines.
• Experience with different EDC platforms is preferred.
• Proficient in MS Office Suite and data handling.

Responsibilities

• Serve as secondary clinical operations contact for one or more trials.
• Coordinate regulatory submissions and safety reporting.
• Oversee CRO oversight and budgets, site initiation, and enrollment tracking.
• Monitor eTMFs and ensure inspection readiness.
• Communicate with CROs, sites, investigators and internal teams.
• Travel to clinical sites as needed (approx. 30%).

Skills

Project management

Communication

Problem-solving

ICH/GCP/CFR knowledge

Education

Bachelor’s degree in clinical research or life science

Tools

Smartsheets

MS Office Suite

EDC platforms

Job description

Protara Therapeutics is hiring a Clinical Project Manager, Temp to Perm, to support the Clinical Operations team across ongoing programs. You will act as a secondary operations contact, ensure CRO deliverables meet timelines, and oversee site activation and budgets.

The role requires 5+ years of trial management experience, knowledge of ICH/GCP/CFR guidelines, and the ability to travel to sites. The position offers an hourly rate with strong growth opportunities.