Regulatory Affairs Coordinator - Cancer Center Protocol Office

Job Description - Regulatory Affairs Coordinator - Cancer Center Protocol Office (3302443)

Regulatory Affairs Coordinator - Cancer Center Protocol Office - ( 3302443 )

General Summary:

The Regulatory Affairs Coordinator (RAC) will work with investigators, sponsors, Institutional Review Boards (IRB) and research support staff to ensure that regulatory requirements are met for clinical trials. This role reports to the Regulatory Affairs Project/Program Manager and works closely with research teams across the Cancer Center and MGB hospitals to ensure regulatory compliance for multiple trials. 

Detailed Responsibilities include managing the following for multiple studies:

- Preparation and submission of clinical trials to the local and central IRB(s). 

- Creation and extensive revisions of informed consent documents

- Tracking and facilitating the progress of new trials through the review process

- Correspondence with the IRB of record, investigators, and sponsors throughout the review process 

- Collection, completion, and submission of regulatory documents to various regulatory entities. 

- Creation and maintenance of electronic regulatory binders and other relevant files during the approval process

- Additionally, this role will support high priority Phase I oncology trials utilizing an expedited review pathway 

Please note that this is a remote role and there will be no work at the physical office/location. Applicants may work in all states with the following exceptions: WY, ND, Puerto Rico, and the U.S. Virgin Islands. 

Qualifications

- BA/BS required 

- Detail-orientation with the ability to manage multiple projects simultaneously

- Strong organizational skills

- Excellent oral and written communication skills

- Prior regulatory or clinical research experience with an academic medical center or industry a plus

Candidates with no relevant experience will be hired as RAC I

Qualifications

- BA/BS required 

- Detail-orientation with the ability to manage multiple projects simultaneously

- Strong organizational skills

- Excellent oral and written communication skills

- Prior regulatory or clinical research experience with an academic medical center or industry a plus

Candidates with no relevant experience will be hired as RAC I

Massachusetts General Hospital is an Affirmative Action Employer. By embracing diverse skills, perspectives, and ideas, we choose to lead. 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.

Primary Location

Work Locations

MGH Main Campus

Job

Job

Research

Organization

Organization

Massachusetts General Hospital(MGH)

Schedule

Schedule

Full-time

Standard Hours 40

Shift

Shift

Day Job

Employee Status

Employee Status

Regular

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