Senior Clinical Research Program Lead — TB & HIV Trials

Lifespan; Providence (RI); On-site; USD 64,000 - 106,000; Full time

Job summary

Brown University Health seeks an experienced Sr. Clinical Research Program Coordinator to lead a research program and manage study activities for TB, HIV, and NTM studies across local, national, and international sites.

The role focuses on protocol implementation, data capture, and site coordination. The position requires coordinating with international partners, overseeing regulatory filings and study start-up, and ensuring timely achievement of project goals in a fast-paced environment.

Qualifications

• Bachelor's degree in a related discipline is required.
• Master's degree or equivalent experience preferred.
• Nursing degree or equivalent clinical background preferred.
• Minimum three years experience in study coordination, including the conduct of clinical trials.

Responsibilities

• Possesses knowledge and understanding of policies, procedures, and regulations governing human subject research.
• Prepares and processes new research proposals, amendments, continuing review applications, adverse events, budgets, and accounts.
• Digests complex clinical information to determine if documentation is accurate and complete; ensures safeguards.
• Independently leads implementation of multiple research studies: local and national/international.
• For local studies: leads protocol completion, assists recruitment, provides education and training, reports adverse events.
• For national/international studies: assists with grant preparation, participates in study design and data collection, coordinates meetings, contributes to protocol development and data tool development.

Skills

Study coordination

IRB compliance

Microsoft Office

STATA

Education

Bachelor's Degree

Master's degree or equivalent

Nursing degree or equivalent

Tools

Research databases

Job description

Brown University Health seeks an experienced Sr. Clinical Research Program Coordinator to lead a research program and manage study activities for TB, HIV, and NTM studies across local, national, and international sites.

The role focuses on protocol implementation, data capture, and site coordination. The position requires coordinating with international partners, overseeing regulatory filings and study start-up, and ensuring timely achievement of project goals in a fast-paced environment.