Clinical Research Coordinator II

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

About The Position

The Clinical Research Coordinator II supports clinical research studies by following established policies, procedures, and study protocols. The role includes recruiting, evaluating, and consenting patients; collecting and organizing patient data; scheduling study visits; conducting clinical tests such as phlebotomy and EKGs; and maintaining study data. The coordinator also contributes to assessing subject suitability and recruitment strategies, performs data analysis and quality checks, and helps prepare reports and presentations. The role is with the Diabetes Research Center at Massachusetts General Hospital, working with a team of diabetes doctors, nurses, and educators under the general supervision of the Nurse Director, Program Manager, and Principal Investigator. It offers direct work with research participants and clinical staff in a large academic center. The center conducts clinical research to improve the diagnosis, prevention, and treatment of diabetes and its complications.

Requirements

  • Bachelor’s degree in a science field, or qualifying experience in lieu of a degree.
  • One to two years of related post-bachelor’s degree research experience.
  • Ability to work more independently and as a team member.
  • Computer literacy and analytical skills, including the 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 potentially contribute to protocol recommendations.
  • Administer and score study questionnaires and evaluate their results.
  • Maintain research data, patient files, regulatory binders, and study databases.
  • Perform data analysis and quality assurance/quality control checks; organize and interpret data.
  • Assist with annual review preparation and help the Principal Investigator complete study reports and presentations.
  • May assist with training and orientation of new staff members.
  • Recruit, evaluate, and consent patients; collect and organize patient data; schedule study visits; and perform clinical tests such as phlebotomy and EKGs.

Benefits

  • Competitive base pay
  • Comprehensive benefits
  • Career advancement opportunities
  • Differentials and premiums, as applicable
  • Bonuses, as applicable
  • Recognition programs
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