Clinical Trials Senior Monitor (Clinical Research)

Location: Brookline, Massachusetts, United States; remote work with occasional onsite monitoring visits and travel required

Salary: $98,900–$108,400 per year

Company

hirify.global conducts cancer research, provides patient care, educates physician-researchers, and collaborates with Harvard Medical School-affiliated hospitals.

What you will do

• Oversee and approve monitoring activities, including interim monitoring reports, follow-up letters, and closeout reports.
• Provide daily supervision, workload coordination, mentoring, and guidance for clinical trials monitoring personnel.
• Coordinate monitoring contracts, assignments, timelines, budgets, and variance reporting.
• Support development of monitoring training curricula and onboarding for new monitors.
• Develop and use metrics systems to assess monitoring effectiveness and report results to leadership.
• Identify protocol performance issues, implement corrective strategies, and lead or co-lead monitoring team meetings.

Requirements

• Bachelor’s degree in a field relevant to research compliance; a master’s degree is preferred.
• 5+ years of clinical trial monitoring experience, including mentoring other monitors.
• Expertise in research ethics, responsible conduct of research, and applicable federal, state, and local regulations.
• Ability to interpret regulations and translate them into operational policies and procedures.
• Strong communication, prioritization, teamwork, leadership, and motivation skills.
• Ability to travel and attend onsite monitoring visits as required by project needs.

Nice to have

• Prior experience as a lead monitor or supervisor of a monitoring team.
• Experience working in an academic research setting with administrators, faculty, and research staff.
• Knowledge of emerging regulatory trends, institutional best practices, conflict of interest, and related research compliance areas.

Culture & Benefits

• Work within an inclusive, diverse, and equitable research and patient-care environment.
• Collaborate with clinical research teams and Harvard-affiliated institutions.
• Combine remote data review with onsite monitoring activities.
• Support the institute’s mission to advance cancer research and patient care.