Clinical Research Coordinator II

Mass General Brigham•Boston, MA

1d•Onsite

About The Position

We are seeking a full-time Clinical Research Coordinator II at the Corrigan Minehan Heart Center Clinical Research Program in Boston, Massachusetts, USA. The Heart Center has a dynamic and growing program in clinical and translational research, dedicated to advancing our understanding of a wide range of cardiovascular diseases and innovative interventions. The individual hired for this position will work as an integral member of a diverse team of researchers to ensure the successful execution of groundbreaking cardiovascular clinical trials. The Natarajan Lab spans Massachusetts General Hospital and the Broad Institute of MIT. Our key focus is precision cardiovascular medicine through observational genomics-based studies and prevention-focused clinical trials.

Requirements

Bachelor’s degree required.
Minimum of 1 year of Clinical Research experience is required.
Strong interpersonal and communication skills, including the ability to interact with patients and study subjects.
Excellent attention to detail.
Capability to work well independently and within a multi-disciplinary team.
Ability to balance and prioritize multiple dynamic projects and commitments.
Bachelor's Degree 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.
Some familiarity with medical terminology is needed.

Nice To Haves

Willingness to commit to at least two years in the position is preferred.
Past experience in laboratory skills, and patient facing experience is strongly encouraged.
Can this role accept experience in lieu of a degree? Yes

Responsibilities

Manages trials under the supervision of the PI, working towards independent execution of clinical trials
Maintains a good understanding of the study protocols and study start-up/closeout process
Orients and trains junior team members on the study protocols as appropriate
Subject recruitment and enrollment.
Maintenance of trial IRB and regulatory documentation.
Study finance management.
Acting as liaison with internal and external collaborators and sponsors to move trials forward.
Managing research data, biological samples, and supporting other research project operations as needed.
Conduct blood draws, and collect saliva and other samples as required by the protocol
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.