Clinical Research Coordinator II Pulmonary Research

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

About The Position

The Division of Pulmonary and Critical Care Medicine at Massachusetts General Hospital conducts clinical and translational research across pulmonary diseases including COPD, asthma, interstitial lung disease, pulmonary hypertension, bronchiectasis, lung transplantation, pleural diseases, and acute lung injury. The Clinical Research Coordinator II supports the management and execution of clinical research studies from start-up through closeout under the guidance of the Senior Clinical Program Manager for Clinical Research and other senior research leaders. The role helps ensure compliance with institutional, sponsor, and regulatory requirements, including those of MGH, Mass General Brigham, the NIH, and the FDA. Following established policies, procedures, and study protocols, the coordinator assists with recruiting, evaluating, and consenting patients; collecting and organizing patient data; scheduling study visits; performing clinical tests; and maintaining study data. The position also contributes to assessment of subject suitability and recruitment strategy, conducts data analysis and quality checks, and assists with reports and presentations. The position is onsite at 90 Blossom Street and is scheduled for 40 hours per week on the day shift.

Requirements

  • Bachelor's degree in science required; experience may be accepted in lieu of a degree.
  • One to two years of related post-bachelor's degree research experience required.
  • Ability to work more independently and as a team member.
  • Computer literacy, analytical skills, and ability to resolve technical problems.
  • Ability to interpret the acceptability of data results.
  • Working knowledge of data management programs.

Responsibilities

  • Assist in determining study subject suitability and serve as a resource for patients and families.
  • Provide input into recruitment strategies and may contribute to protocol recommendations.
  • Recruit, evaluate, and consent patients for studies.
  • Collect and organize patient data, schedule study visits, and maintain and update study-generated data.
  • Perform clinical tests such as phlebotomy and EKGs, as applicable.
  • Administer and score study questionnaires.
  • Maintain research data, patient files, regulatory binders, and study databases.
  • Perform data analysis and QA/QC checks, and organize and interpret data.
  • Assist with annual review preparation and help the PI complete study reports and presentations.
  • May assist with training and orienting new staff members.

Benefits

  • Comprehensive benefits
  • Career advancement opportunities
  • Differentials, premiums, and bonuses as applicable
  • Recognition programs
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