Clinical Research Associate II

Partner's Healthcare; Boston (MA); Remote; USD 33,000 - 54,000; Full time

Job summary

Mass General Brigham Incorporated’s Multicenter CRA role supports multicenter coordination for investigator-initiated oncology trials. It emphasizes regulatory files, data quality, and monitoring across sites outside the Harvard Cancer Consortium, with remote work and domestic travel.

You will handle documentation, communications, and trial status updates under supervision, ensuring compliance with regulations.

Qualifications

• Bachelor's Degree required.
• 1–2 years related research experience required.
• Ability to travel nationally.
• Strong organizational and time-management skills.
• Excellent written and oral communication abilities.

Responsibilities

• Track the progress of trials across all participating sites (accrual, biospecimen collection, regulatory submissions).
• Correspond with participating sites to support trial activities and answer questions about eligibility and procedures.
• Prepare and distribute informational updates, meeting minutes, and safety reports.
• Verify consent, screening tests, eligibility criteria, and regulatory documentation.
• Conduct onsite and remote monitoring visits and complete monitoring reports (domestic travel required).
• Perform source document verification and drug accountability and review site regulatory binders.

Skills

Independent work

Teamwork

Computer literacy

Attention to detail

Time management

Communication skills

Travel nationally

Education

Bachelor's Degree

Job description

Site: Mass General Brigham Incorporated

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.

Job Summary

The Multicenter Program within the MGB Cancer Institute Clinical Trials Office is seeking candidates experienced in clinical trial coordination and implementation to support multicenter coordination and monitoring of investigator-initiated oncology clinical trials. The Multicenter Program is an internal clinical trial operations team, specializing in the central coordination, monitoring and regulatory oversight of MGBCI investigator-initiated clinical trials that are expanded to participating sites outside of the Harvard Cancer Consortium. The multicenter CRA works under general supervision to support trial coordination, maintain regulatory files and monitor data and protocol compliance and data quality across participating study sites. The CRA will be trained in the institutional and federal regulations governing clinical research. The position involves a high volume of correspondence, regulatory document coordination and tracking, and clinical data review. This position does not include any direct patient contact.

The Multicenter CRA will perform the following duties under general supervision by the Clinical Research Manager:

• Track the progress of the trial across all participating sites (e.g., accrual, biospecimen collection and transfer, reportable events, regulatory submissions)
• Correspond with participating sites to support trial activities as needed
• Answer questions about eligibility, study procedures or data entry
• Prepare and distribute informational updates, including meeting minutes, missing data reports and safety reports
• Communicate essential trial information and documentation, including protocol amendments; request routine updates from sites to maintain current study status
• Facilitate database reviews and query resolution
• Present the Sponsor-Investigator study status reports related to trial progress and assigned tasks
• Verify adequate documentation of consent, required screening tests and procedures, and eligibility criteria to ensure patients meet all inclusion/exclusion criteria
• Conduct onsite and remote monitoring visits and complete corresponding monitoring reports (Domestic travel required for onsite monitoring)
• Perform source document verification and drug accountability
• Review study site regulatory binder and essential documents for completeness and accuracy
• Evaluate ongoing protocol and data compliance
• Issue, track and resolve queries
• Gather, track and organize essential regulatory documents from participating sites
• Facilitate and document Sponsor-Investigator review of safety reports, investigational drug brochure updates, study violations and adverse events
• Submit routine and expedited reports to the FDA, IRB, funding sponsor or other stakeholders

Qualifications

Education: Bachelor's Degree required

Experience: Related research experience 1-2 years required

Knowledge, Skills and Abilities

• Ability to work independently and as a team member.
• High degree of computer literacy.
• Ability to interpret the acceptability of data results.
• Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
• Careful attention to detail
• Superior organizational and time management skills and ability to prioritize multiple tasks
• Problem-solving skills, including the ability to gather information, identify resources, and develop alternatives
• Excellent written and oral communication skills
• Demonstrate initiative and accountability
• Ability and willingness to travel nationally.
• Working knowledge of clinical research protocols
• Analytical skills and ability to identify and resolve problems and develop alternatives
• Excellent judgment and ability to interpret information and protocol requirements

Additional Job Details (if applicable)

Remote Type: Remote

Work Location: 101 Merrimac Street

Scheduled Weekly Hours: 40

Employee Type: Regular

Work Shift: Day (United States of America)

Pay Range

$24.28 - $39.43/Hourly

Grade: 6

Benefits and Compensation

In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth.

EEO Statement

0100 Mass General Brigham Incorporated is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642.

Mass General Brigham Competency Framework

At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.