Clinical Research Coordinator I – Preventive Medicine

Mass General Brigham

. Assist with clinical research studies following established policies, procedures, and study protocols .

Posted 10/23/2026full-timeSomerville • Massachusetts • United StatesMid-LevelSenior💰 $21 - $29 per hourWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical research methodologies, including patient recruitment, data management, and compliance with regulatory standards. Proficient in performing clinical tests such as phlebotomy and EKGs while maintaining a high level of professionalism and attention to detail.

Highest-signal resume keywords

Clinical Research ProtocolsPhlebotomyEKGsData ManagementPatient Recruitment

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchData EntryPatient SchedulingRegulatory SubmissionsQA/QC Procedures

Soft Skills

Attention to DetailOrganizational SkillsInterpersonal SkillsCommunication SkillsAbility to Follow Directions

Tools & Technologies

Computer Literacy

Industry Keywords

Clinical TrialsPatient ConsentStudy ProtocolsComplianceResearch Project Work

About the role

Key responsibilities & impact

Assist with clinical research studies following established policies, procedures, and study protocols
Recruit, evaluate, and consent patients for studies
Conduct phone interviews and interview study subjects
Collect, organize, prepare, and enter patient and study data
Schedule patients for study visits
Perform clinical tests such as phlebotomy and EKGs
Maintain and update study-generated data
Review proposals for compliance with sponsor and organizational guidelines
Verify sponsor requirements are met
Verify study forms and update them per protocol
Document patient visits and procedures
Assist with regulatory binders and QA/QC procedures
Assist with study regulatory submissions

Requirements

What you’ll need

Bachelor's Degree in a related field of study required
Experience may be accepted in lieu of a degree
Some relevant research project work; 0–1 year preferred
Careful attention to detail and good organizational skills
Ability to follow directions
Good interpersonal and communication skills
Computer literacy
Working knowledge of clinical research protocols
Ability to demonstrate respect and professionalism for subjects' rights and individual needs
Ability to provide degree equivalency verification within the stated grace period if completing a bachelor's degree
Ability to perform or assist with clinical tests such as phlebotomy and EKGs

Benefits

Comp & perks

Comprehensive benefits
Career advancement opportunities
Differentials
Premiums
Bonuses as applicable
Recognition programs
Reasonable accommodation for individuals with disabilities
40 scheduled hours per week
Hybrid work arrangement