Clinical Research Coordinator II - Oral and Maxillofacial Surgery

Mass General Brigham•Boston, MA

7h•Hybrid

About The Position

Following established policies, procedures, and study protocols, the Clinical Research Coordinator II assists with clinical research studies. The role supports patient recruitment, evaluation, and consent; collection and organization of patient data; scheduling study visits; and maintenance of study data. The position may also include performing clinical tests such as phlebotomy and EKGs, although the posting indicates that patient care is not required. The coordinator provides input on participant suitability and recruitment strategies, administers and evaluates study questionnaires, and maintains research data, patient files, regulatory binders, and study databases. The role also involves data analysis, interpretation, quality assurance and quality control, and assistance with annual reviews, reports, and presentations. The position is hybrid and based at 15 Parkman Street, with a 40-hour workweek on the day shift.

Requirements

Bachelor's degree in science, or relevant 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, with the ability to resolve technical problems.
Ability to interpret the acceptability of data results.
Working knowledge of data management programs.

Responsibilities

Assist in determining the suitability of study subjects and serve as a resource for patients and families.
Provide input into recruitment strategies and may contribute to protocol recommendations.
Administer and evaluate study questionnaires.
Maintain research data, patient files, regulatory binders, and study databases.
Perform data analysis and quality assurance and quality control checks; organize and interpret data.
Assist with preparation for annual reviews and help the Principal Investigator complete study reports and presentations.
May assist with training and orienting new staff members.
Support clinical research activities, including recruiting, evaluating, and consenting patients; collecting and organizing patient data; scheduling study visits; and maintaining study data.