Clinical Research Program Lead

1200 The General Hospital Corporation; Boston (MA); Hybrid; USD 63,000 - 103,000; Full time

Job summary

Mass General Brigham is seeking a Program Manager to oversee the day-to-day operational management of the Center's clinical research portfolio and supervise Clinical Research Coordinators. You will ensure adherence to protocols, timelines, and data quality while coordinating grant activities and stakeholder communications.

The role requires a Bachelor's degree in a relevant field and 3–5 years of clinical research experience, including IRB coordination and staff supervision.

Qualifications

• Bachelor's degree in psychology, public health, health sciences, biological sciences, or related field.
• 3–5 years of progressively responsible experience in clinical research, research administration, or program management.
• Experience coordinating human subjects research and working with IRBs.
• Experience supervising or mentoring research staff.
• Experience managing multiple concurrent projects and competing priorities.
• Experience using REDCap and Microsoft Office applications, including Excel.

Responsibilities

• Direct the day-to-day implementation of the Center's active clinical research studies, ensuring adherence to study protocols, timelines, recruitment goals, and operational milestones.
• Directly supervise Clinical Research Coordinators, including onboarding, training, coaching, and performance management.
• Coordinate administrative activities supporting grant proposal development and submission.
• Coordinate data quality assurance activities and ensure completeness of research datasets.

Skills

Program management

GCP knowledge

Staff supervision

Communication skills

Data management

Regulatory compliance

Education

Bachelor's degree in psychology/public health/health sciences/biological sciences

Master's degree in related field

Tools

REDCap

Microsoft Office

Job description

Mass General Brigham is seeking a Program Manager to oversee the day-to-day operational management of the Center's clinical research portfolio and supervise Clinical Research Coordinators. You will ensure adherence to protocols, timelines, and data quality while coordinating grant activities and stakeholder communications.

The role requires a Bachelor's degree in a relevant field and 3–5 years of clinical research experience, including IRB coordination and staff supervision.