CRC II - Diabetes & Metabolism Trials

Mass General Brigham

Boston (MA)

On-site

USD 33,000 - 54,000

Full time

2 days ago
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Job summary

Mass General Brigham seeks a clinical research support professional to assist with patient recruitment, data collection, and study coordination at our Boston-area site.

You will contribute to data management, perform basic analyses, and help prepare reports and presentations under the supervision of the PI. The role emphasizes collaboration within a multi-disciplinary team and adherence to study protocols and regulatory requirements.

Qualifications

  • Education: Bachelor's Degree in Science required.
  • Experience: Post-bachelor's research experience 1-2 years 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 suitability of study subjects and act as a resource for patients and families.
  • Contribute to recruitment strategies and protocol recommendations.
  • Administer scores and evaluate study questionnaires.
  • Maintain research data, patient files, regulatory binders, and study databases.
  • Perform data analysis and QA/QC checks and interpret data.
  • Assist with preparation for annual review and with study reports and presentations.
  • Assist with training and orientation of new staff members.

Skills

Data analysis
Teamwork
Computer literacy
Analytical skills
Problem solving
Data management

Education

Bachelor's degree in Science

Tools

Data management software

Job description

Mass General Brigham seeks a clinical research support professional to assist with patient recruitment, data collection, and study coordination at our Boston-area site.

You will contribute to data management, perform basic analyses, and help prepare reports and presentations under the supervision of the PI. The role emphasizes collaboration within a multi-disciplinary team and adherence to study protocols and regulatory requirements.

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