Clinical Research Coordinator/Data Analyst

Mass General Brigham•Boston, MA

1d•$21 - $29•Onsite

About The Position

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; and maintaining and updating data generated by the study. Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification.

Requirements

Bachelor's Degree Related Field of Study required
Some relevant research project work 0-1 year preferred
Careful attention to detail and good organizational skills.
Ability to follow directions.
Good interpersonal and communication skills.
Computer literacy.
Working knowledge of clinical research protocols.
Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
Ability to work independently is a must.
Strong communication skills, a strong desire to contribute to the research team and a positive, proactive, attitude are required.

Nice To Haves

Competencies with Excel, VBA, and/or STATA are preferred
Experience in database design and management is preferred
Must demonstrate statistical/analytic and reasoning skills to perform high level of problem solving.
Experience with Excel, STATA, and VBA programming is heavily preferred.

Responsibilities

Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
Recruiting patients for clinical trials and conducting phone interviews.
Verifies the accuracy of study forms and updates them per protocol.
Prepares data for analysis and data entry.
Documents patient visits and procedures.
Assists with regulatory binders and QA/QC Procedures.
Assists with interviewing study subjects.
Assists with study regulatory submissions.
Obtaining and maintaining patient data and study records.
Screening and recruiting patients for clinical studies.
Conducting data analysis on exercise studies submitted to the MGH Exercise Core Laboratory.
Working on all aspects of clinical research project design, implementation, and communication of results.
Participates in research protocols spanning a large range of areas that primarily relate to applied human exercise physiology.
Records and analyzes data from cardiopulmonary exercise studies submitted to the MGH exercise core laboratory.
Actively participates in research database creation, upkeep, and analysis.
May assist with writing protocols and manuscripts for submission to research journals and national scientific meetings.