Clinical Research Coordinator I, OCRCCI

Site: The Brigham and Womens Hospital Inc.

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.

Job Summary

Working under general supervision from a manager lead coordinator or Principal Investigator provides support to clinical research studies.
May be responsible for the following activities: screening and scheduling potential participants for clinical trials developing and implementing
patient recruitment strategies performing applicable clinical tests such as phlebotomy ECGs etc maintaining and updating data generated
by the study assisting in the team effort of making judgment of suitability of potential participants for clinical trials assorted administrative
work on patient documents folders and research projects.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
Coordinates the implementation both internally and externally of sponsored clinical research studies.
Initiates and maintains recruitment contact with study participants. Responsible for screening applicants ensuring they meet
appropriate criteria and makes independent judgement as to the suitability of their participation. May be required to perform
clinical tests such as phlebotomy ECGs etc.

Working in concert with Principal Investigator and/or Research Manager and experienced coordinators to develop and
implement patient recruitment strategies.

Working in conjunction with RCNet Manager and CCI Administrative Director on miscellaneous administrative duties integral
to CCI/RCNet programs.

Interacts with patients/subjects with regard to the study including patient education procedural instruction follow-up. Serves
as a liaison between patient and physician and as a resource for participants and their families.

Responsible for collection of data and maintaining patient information databases for the study. Develops organizes and/or
maintains the study forms. Responsible for data validation and quality control data entry into CRFs if applicable. May be
required to input data and do minimal analysis and run various reports.

In conjunction with Research Manager completed regulatory paperwork for institutional review board approval.
Responsible for mailing various study information or packets to study participants.
Answers phone calls and inquires regarding the study protocol. Refers participants when appropriate to principal and coinvestigators.

Communicates regularly with the PI(s) about all aspects of the research trial.
Responsible for collection data and maintaining patient information databases for the study. Develops organizes and/or
maintains the study forms. Responsible for data validation and quality control data entry into CRFs if applicable. May be
required to input data and do minimal analysis and run various reports.

In conjunction with Research Manager completed regulatory paperwork for institutional review board approval.
Responsible for mailing various study information or packets to study participants.
Answers phone calls and inquires regarding the study protocol. Refers participants when appropriate to principal and coinvestigators.
Communicates regularly with the PI(s) about all aspects of the research trial.

Education
Bachelors Degree Related Field of Study required

Can this role accept experience in lieu of a degree
Yes

Licenses and Credentials

Experience
Some relevant research project work 0-1 year preferred

Knowledge Skills and Abilities
- 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.

Additional Job Details (if applicable)

Hybrid

221 Longwood Avenue

40

Regular

Day (United States of America)

Pay Range

$21.00 - $29.01/Hourly

Grade

5

At Mass General Brigham we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive and any offer extended will take into account your skills relevant experience if applicable education certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however it does not encompass all elements contributing to your total compensation addition to competitive base pay we offer comprehensive benefits career advancement opportunities differentials premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.

2200 The Brigham and Womens Hospital Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religious creed national origin sex age gender identity disability sexual orientation military service genetic information and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process to perform essential job functions and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973 the Vietnam Veterans Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990 applicants who require accommodation in the job application process may contact Human Resources at .