Research Regulatory Coordinator

Brown Medicine•Providence, RI

3d•$58,490 - $96,491•Onsite

About The Position

The Regulatory Coordinator performs multiple tasks in order to meet compliance requirements in research. This position will be overseeing clinical research regulatory requirements for the department. The Regulatory Coordinator will provide support in managing clinical trials for the department. The Regulatory Coordinator is to be responsible for clinical studies through the regulatory portion of the trial submission process to maintaining the regulatory integrity of assigned clinical trials from approval to closure. The Regulatory Coordinator instructs and advises other staff in regulatory/compliance issues and collaborates with investigators to resolve all regulatory inquiries. Brown University Health employees are expected to successfully role model the organization's values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another. In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include: Instill Trust and Value Differences Patient and Community Focus and Collaborate

Requirements

BASIC KNOWLEDGE: Bachelor’s degree in health-related or scientific field, is required.
Sound knowledge of all federal, local and state guidelines pertaining to Clinical Research.
Must be an independent person, who is capable of making sound judgment pertaining to regulatory issues and have the ability to work independently within the scope of the job requirements.
Strong-self-starter, interpersonal skills, and influence are necessary
Team-oriented with excellent oral and written communication skills
Strong problem-solving skills
Excellent self- management and organizational skills
Detail-oriented
Computer skills in Microsoft office
Comprehensive knowledge of FDA guidelines
Must be proficient in various database applications
Ability to foster smooth communications and teamwork among clinical research faculty, fellows and staff as well as external organizations necessary
SoCRA (Society of Clinical Research Associates) certified or eligible within 18 months of hire
EXPERIENCE: 3-5 years in direct clinical trial administration experience or relevant clinical development and regulatory experience
Understanding of compliance requirements with federal, state or local programmatic regulations are necessary
This position is a sedentary position. One must be able to transport paperwork to another building (sometimes up to 10 lbs.) at one time. Bending and stooping may also be requirements for filing of paperwork. Standing to copy may also be required.
This position requires a quick-thinker, who can independently make basic and sometimes complex decisions pertaining to the completion and transmission of required regulatory documentation to internal departments as well as external agencies, including, but not limited to study sponsors, local and federal agencies.
The candidate should be able to answer protocol regulatory inquiries from researchers and physicians, as well as from the local Institutional Review Board.
This person should also be able to work with outside monitors and work independently. He/she should be able answer inquiries related to regulatory issues, and if not known, communicate with the correct person to determine the answer.

Responsibilities

Consults with and/or provides advice regarding regulatory documents and/or processes related to clinical trials conduct.
Serves as the regulatory subject matter expert through all phases of a clinical study.
Serves as a lead and mentor to other clinical research staff, to include the execution of new initiatives and process improvement.
Develops and/or revises regulatory policies and procedures.
Initiates and leads special projects, to include process improvement and regulatory training.
Ensures proper regulatory compliance in accordance with sponsoring agency requirements.
Liaises with sponsors, investigators and team members, providing trial information and updates as required in written, oral and meeting format, adhering to appropriate timelines.
Develops protocols with the Principle Investigator and provides recommendations on research plan.
Coordinates and facilitates the submission of Investigational New Drug (IND) and/or Investigational Device Exemption (IDE) applications.
In collaboration with the Principle Investigator, interprets protocols and creates consent documents needed for clinical research study.
Prepares regulatory approval applications, respond to stipulations, and shepherd applications and correspondence through the processes until approvals are obtained.
Participates in Study Initiation Visits and Interim Monitoring Visits.
Maintains study specific regulatory binder.
Performs other duties as assigned.