The Manstein Clinical Research Lab at the Cutaneous Biology Research Center is hiring a Full-Time Clinical Research Coordinator I who will be responsible for coordinating one or more human clinical studies. The Manstein Lab focuses primarily on the development of medical devices for applications in human skin and other organs. The CRCI will support a team of clinicians, clinical fellows, and biomedical engineers in conducting clinical trials of new and/or improved medical devices. The CRCI will assist the CRC II in the submission of clinical protocols to the IRB, coordinating responses to IRB feedback, coordinating conduct of the clinical study, management and storage of study data, supporting annual review submissions to the IRB, and supporting the team in developing study reports. The CRC I will conduct regular assessments of participants and will help coordinate an online registry to monitor patient progress. The CRC will take part in other study activities in the unit such as assisting with participant outreach, quality control, grant applications, literature reviews, and manuscript preparation.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

Excellent attention to detail.
Must enjoy working with people and be proactive to help engage hard to reach participants.
Ability to quickly synthesize and manage data accurately from multiple sources.
Self-starter with excellent communication, organizational, and analytical skills.
Ability to work well as a member of a team and individually, and to interface with individuals across a wide range of disciplines and experience.
Ability to work well with technology and willingness to work with new technology.

Qualifications
SKILLS & COMPETENCIES REQUIRED:

• Collects and organizes patient data.
• Maintains records and databases.
• Assists with recruiting patients for clinical trials.
• Have excellent management and communication skills
• Obtains patient study data from medical records, physicians et.
• Performs administrative support duties as required
• Verifies accuracy of study forms
• Prepares data for analysis and data entry
• Documents patient visits and procedures
• Assists with interviewing study subjects
• Assist with study regulator submissions
• Writes consent forms
• Verifies subject inclusion/exclusion criteria

Education:

Bachelor's degree required.

EXPERIENCE:

New graduates with some relevant course/project work or those without any prior research experience will be considered for the Clinical Research Coordinator I position outlined above.

SUPERVISORY RESPONSIBILITY (authority to hire, promote, or terminate):

Not applicable.

FISCAL RESPONSIBILITY:

Not Applicable

WORKING CONDITIONS:

Laboratory and clinical environment.

EEO Statement
Massachusetts General Hospital is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. Applications from protected veterans and individuals with disabilities are strongly encouraged.Partner's Healthcare is acting as an Employment Agency in relation to this vacancy.