Williams Syndrome Research Coordinator I

Massachusetts General Hospital

Lexington (MA)

On-site

USD 44,000 - 60,000

Full time

14 days+

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Job summary

Massachusetts General Hospital's Lurie Center for Autism in Lexington is seeking a Research Coordinator I to support Williams syndrome trials. You will assist with initiation, monitoring, and reporting of studies under the PI, following SOP and GCP guidelines.

The role emphasizes recruiting participants, data collection, scheduling, and regulatory support. A Bachelor's degree and strong organizational skills are essential, with up to 1 year of related experience preferred.

Qualifications

  • Bachelor's Degree in a related field required.
  • Can this role accept experience in lieu of a degree? Yes (as stated in the posting)

Responsibilities

  • Review proposals for sponsor and organizational guidelines compliance.
  • Recruiting patients for clinical research studies and conducting phone interviews.
  • Monitor participant enrollment, study progress, and protocol compliance.
  • Verify accuracy of study forms and update per protocol.
  • Prepare data for analysis and data entry.
  • Maintain study databases and electronic data capture systems.
  • Document patient visits and procedures.
  • Assist with regulatory binders and QA/QC procedures.
  • Coordinate communication among investigators, study staff, sponsors, and collaborators.
  • Assist with abstracts, presentations, manuscripts, and progress reports.

Skills

Attention to detail
Organizational skills
Follow directions
Interpersonal skills
Communication skills
Computer literacy
Clinical research protocols
Subject rights respect

Education

Bachelor's degree related field

Tools

Data capture systems

Job description

Massachusetts General Hospital's Lurie Center for Autism in Lexington is seeking a Research Coordinator I to support Williams syndrome trials. You will assist with initiation, monitoring, and reporting of studies under the PI, following SOP and GCP guidelines.

The role emphasizes recruiting participants, data collection, scheduling, and regulatory support. A Bachelor's degree and strong organizational skills are essential, with up to 1 year of related experience preferred.

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