Oral & Maxillofacial Clinical Research Coordinator II – Hybrid

Mass General Brigham; Boston (MA); Hybrid; USD 33,000 - 54,000; Full time

Job summary

Mass General Brigham is seeking a Clinical Research Coordinator II for the Oral and Maxillofacial Surgery team in Boston, hybrid work arrangement, full-time position. The role supports study protocols by recruiting and consenting participants, collecting data, and coordinating visit schedules.

You will perform clinical tests, assist with data analysis and QA/QC, and help prepare reports for annual reviews. Qualifications include a Bachelor's degree and 1-2 years of related research experience.

Qualifications

• Bachelor's Degree in Science required.
• Related post-bachelor's degree 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

• Assists with determining the suitability of study subjects and acts as a resource for patients and families.
• Has input into recruitment strategies and may contribute to protocol recommendations.
• Administers scores and evaluates study questionnaires.
• Maintains research data, patient files, regulatory binders, and study databases.
• Performs data analysis and QA/QC checks and organizes and interprets data.
• Assists with preparation for annual review and assists PI in completing study reports and presentations.
• May assist with training and orientation of new staff members.

Skills

Independent work

Team collaboration

Data management

Analytical skills

Computer literacy

Problem solving

Data interpretation

Education

Bachelor's Degree in Science

Job description

Mass General Brigham is seeking a Clinical Research Coordinator II for the Oral and Maxillofacial Surgery team in Boston, hybrid work arrangement, full-time position. The role supports study protocols by recruiting and consenting participants, collecting data, and coordinating visit schedules.

You will perform clinical tests, assist with data analysis and QA/QC, and help prepare reports for annual reviews. Qualifications include a Bachelor's degree and 1-2 years of related research experience.