Clinical Research Assistant

Massachusetts General Hospital

Waltham, MAFull-time

40K–60K a year

Behavioral Health Market Context

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Job Description

passionate about making a difference in the field of medicine and possess strong organizational and communication skills, we encourage you to apply. Join us in our mission to drive innovative and impactful research at one of the top hospitals in the world.

Assist in the coordination and execution of clinical research studies, including recruitment of study participants, scheduling appointments, and maintaining study records.

Collaborate with researchers and healthcare professionals to collect, organize, and analyze data for ongoing studies.

Ensure compliance with all ethical guidelines, institutional policies, and regulatory requirements related to clinical research.

Communicate effectively with study participants, providing them with clear instructions and addressing any questions or concerns they may have.

Maintain accurate and organized study files, including consent forms, medical records, and other relevant documents.

Monitor and report adverse events or deviations from the study protocol to the appropriate authorities.

Assist with the preparation and submission of research proposals, protocols, and reports.

Attend and actively participate in research team meetings, providing updates on study progress and contributing ideas for improvement.

Keep up-to-date with current research practices and regulations, participating in training and educational opportunities as needed.

Perform other administrative and clerical tasks as needed to support the smooth operation of the research team.

Massachusetts General Hospital is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Qualifications

    Benefits

      Responsibilities

      • In this role, you will have the opportunity to work alongside renowned researchers and healthcare professionals, contributing to groundbreaking medical advancements and improving patient care
      • Assist in the coordination and execution of clinical research studies, including recruitment of study participants, scheduling appointments, and maintaining study records
      • Collaborate with researchers and healthcare professionals to collect, organize, and analyze data for ongoing studies
      • Ensure compliance with all ethical guidelines, institutional policies, and regulatory requirements related to clinical research
      • Communicate effectively with study participants, providing them with clear instructions and addressing any questions or concerns they may have
      • Maintain accurate and organized study files, including consent forms, medical records, and other relevant documents
      • Monitor and report adverse events or deviations from the study protocol to the appropriate authorities
      • Assist with the preparation and submission of research proposals, protocols, and reports
      • Attend and actively participate in research team meetings, providing updates on study progress and contributing ideas for improvement
      • Keep up-to-date with current research practices and regulations, participating in training and educational opportunities as needed
      • Perform other administrative and clerical tasks as needed to support the smooth operation of the research team


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