[Hiring] Senior Clinical Research Coordinator @Mass General Brigham

Role Description

The Center for Precision Psychiatry (CPP) at Mass General Hospital is seeking applications for a full-time Sr. Clinical Research Coordinator (CRC) to coordinate and administer projects led by Dr. Rebecca Fortgang. This position is particularly well-suited for anyone interested in pursuing graduate study in the fields of psychology, public health, or medicine. Experience working with clinical research studies and strong interpersonal skills are strongly preferred.

• Works very independently under minimal supervision to enroll eligible patients in clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies.
• Will be the liaison between the clinical team, sponsor, and Institutional Review Board (IRB) to ensure appropriate communication and reporting.
• Will assist management in the areas of Quality Control, Training, & Development and may provide input into the assessment of departmental procedures.
• The position involves a combination of data abstraction and entry, regulatory management, and patient coordination.

Does this position require Patient Care? No

Essential Functions

• Assist the clinical team in screening potential patients for study participation.
• Maintain point of contact communication with enrolled patients and assist with front-line questions regarding study participation.
• Verify adequate documentation of consent, required screening tests and procedures, and eligibility criteria to ensure patients meet all criteria.
• Enroll patients as required by the study sponsor and internal enrollment monitor team.
• Obtain protocol clarifications from the study sponsor and communicate information to the research team.
• Organize and prepare for internal and external audits.
• Prepare and submit protocol amendments, continuing reviews, and safety reports to the IRB.
• Revise informed consent documents to include new risk information and/or updated protocol requirements through the course of the study.

Qualifications

• Bachelor's Degree Related Field of Study required
• Can this role accept experience in lieu of a degree? Yes

Requirements

• Prior experience within the Research Protocols 2-3 years preferred
• Previous Research Experience 3-5 years required

• Exceptional time management and organization skills.
• Excellent written and verbal communication skills.
• Knowledge of current and developing clinical research trends.
• Sound interpersonal skills and the ability to mentor others.
• Ability to work independently and display initiative.
• Ability to identify problems and develop solutions.
• Demonstrated ability to successfully manage multiple projects.
• Established rapport with investigators and sponsors with the ability to resolve operational matters within a disease group.

Benefits

• Competitive base pay.
• Comprehensive benefits.
• Career advancement opportunities.
• Differentials, premiums, and bonuses as applicable.
• Recognition programs designed to celebrate your contributions and support your professional growth.