Clinical Coordinator Jobs

3,359 jobs found — updated daily

Clinical Research Coordinator II Center for Neuroscience Clinical Trials

Mass General Brigham•Boston, MA
•$24 - $39•Onsite

About The Position

The Clinical Research Coordinator II provides assistance with clinical research studies at the Center for Neuroscience Clinical Trials, working under the supervision of the Administrative Director of the CNCT and the Principal Investigator. The role follows established policies, procedures, and study protocols and supports participant recruitment, screening, evaluation, consent, data collection, study visit scheduling, study records and databases, and communications with research collaborators. The coordinator serves as a point of contact and liaison for study participants, physicians, sponsors, clinical research associates, laboratories, and testing facilities. The role also supports study documentation and regulatory submissions, staff training, budgets and reimbursements, meeting coordination, equipment, supplies, and other research administration.

Requirements

  • Bachelor's degree in a science field.
  • At least 1 year of research experience after completing a bachelor's degree.

Responsibilities

  • Assist with clinical research studies according to study guidelines and protocols.
  • Screen potential study patients for eligibility, recruit and evaluate participants, and conduct telephone interviews or schedule in-person screening visits as required by study protocols.
  • Perform clinical tests such as questionnaires or cognitive assessments when certified and needed, and coordinate laboratory testing and shipping with research lab colleagues.
  • Collect data, maintain patient information databases and study subject records, and prepare data for analysis and entry.
  • Educate participants about studies, provide procedural instructions and follow-up, prepare study advertising materials, answer study-protocol inquiries, and refer participants to a supervisor or clinical staff when appropriate.
  • Serve as a liaison between patients and physicians, act as a first point of contact for study communications, advocate for participants, support a positive trial experience, and promote protocol compliance.
  • Communicate with sponsor companies, clinical research associates, central laboratories, and internal and external testing facilities.
  • Schedule research meetings with monitors or sponsors.
  • Create, distribute, file, and update study documents in accordance with protocols.
  • Prepare and manage study information and participant packets, including schedules, directions, and reimbursement information.
  • Train staff on study procedures.
  • Prepare and submit IRB applications, amendments, annual reviews, and serious adverse event documents.
  • Oversee study budgets and participant reimbursements.
  • Monitor and set up needed equipment, maintain inventory, and order supplies.
  • Maintain study regulatory documents and perform research administrative tasks.
  • Perform other duties as assigned and comply with all policies and standards.

Benefits

  • Comprehensive benefits
  • Career advancement opportunities
  • Differentials, premiums, and bonuses as applicable
  • Recognition programs
  • Reasonable accommodation during the application or interview process and in performing essential job functions

Build a Resume for Clinical Coordinator

The resume builder that gets results.

  • Get clear feedback so you look as qualified as you are
  • Align your resume with the job to get further in the process, faster
  • Take the guesswork out of resume writing

Explore Related Job Searches

© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service