Clinical Research Associate II

massgeneralbrigham; Boston (MA); À distance; USD 33 000 - 54 000; Plein temps

Résumé du poste

Mass General Brigham Incorporated seeks a Multicenter Clinical Research Associate to support coordination and monitoring of investigator-initiated oncology trials across participating sites. The role emphasizes regulatory oversight, data quality, and communications with site personnel.

Responsibilities include tracking trial progress, preparing updates and safety reports, and ensuring consent and eligibility criteria. Remote work is supported with domestic travel for onsite monitoring as needed.

Qualifications

• Bachelor's Degree required.
• Related research experience 1-2 years required.
• Strong communication and computer literacy.
• Excellent attention to detail and organizational skills.
• Ability to work independently and in a team.
• Willingness to travel nationally.
• Familiarity with clinical research protocols is a plus.

Responsabilités

• Track multicenter trial progress across sites.
• Coordinate regulatory submissions and monitoring.
• Prepare updates, meeting minutes and safety reports.
• Verify consent, eligibility criteria and data accuracy.
• Conduct on-site and remote monitoring visits as needed.
• Maintain trial documentation and essential regulatory binders.

Connaissances

Independent work

Team collaboration

Computer literacy

Attention to detail

Time management

Problem solving

Communication skills

Travel availability

Formation

Bachelor's Degree

Description du poste

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.

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

At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to yo