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Regulatory Analyst – COI in Research and Foreign Engagements
Company: University of Miami Health System
Location: Coral Gables, FL
Employment Type: Full Time
Date Posted: 10/18/2021
Expire Date: 12/18/2021
Job Categories: Other
Job Description
Regulatory Analyst – COI in Research and Foreign Engagements
The Office of the Vice Provost for Research & Scholarship, Disclosures & Relationship Management (DRM) has an exciting opportunity for a Regulatory Analyst – COI in Research and Foreign Engagements to work in the Coral Gables Campus.

CORE JOB SUMMARY

The DRM Regulatory Analyst assists the DRM Director with the development, oversight, and monitoring of compliance programs within the designated area. This position provides strategic advice and recommendations as to the adjudication and mitigation of Conflicts of Interest (COI), facilitates adherence to policies, rules, and regulations, and that policies and procedures are continuously monitored and evaluated.

CORE JOB FUNCTIONS
Conducts reviews of protocol and other submissions and communicates with researchers as it relates to and University polices
Provides QA or QC functions
Assists with Project Management
Creates and adheres to metrics-driven timelines
Keeps abreast of current federal regulations and guidance documents, State laws, University of Miami policies and procedures as well as departmental SOPs and informs OVPRS leadership of changes
Promotes quality improvement and best practice solutions
Communicates with the research community, all OVPRS groups and external customers as applicable and provides consistent excellent customer service
Communicates with the research community, all OVPRS groups and external customers as applicable and provides consistent excellent customer service
Department Specific Functions
Assists the Director in supporting the COI Committee including review of scientific protocols, setting meeting agendas, composing COI management plans, minutes, reports, and any additional necessary communications.
Facilitates adherence to applicable Federal, state, and local regulations and University policies and procedures as requested by the Vice Provost for Research & Scholarship.
Monitors new legislation or changes in regulations that might affect the University’s compliance in conducting scholarly activities (including research), recommending changes to administrative policies and procedures, as appropriate.
Drafts appropriate individual and institutional COI management plans for COI Committee’s review, prepares, distributes, and tracks adherence to such plans.
Coordinates responses to regulatory agencies and advises appropriate institutional officials of deficiencies and recommends necessary corrective actions, with follow up to ensure that needed actions have been implemented.
Interacts with appropriate persons/agencies (e.g., Human Subjects Research Office, Animal Care and Use Committee, Office of Technology Transfer, and General Counsel’s Office, etc.) to resolve compliance problems related to scholarly activities conducted at UM.
Develops and presents educational programs for groups and individuals conducting scholarly activities at UM.
Prepares DRM’s scholarly activities compliance standard operating protocols related to federal regulations and university policies.
Assists Director in the preparation of annual reports of DRM and University related activities, summarizing efforts taken and changes to be implemented at both University and departmental levels.
Assists Director in the creation and maintains web-based policy and procedures manuals intended to assist University community in maintaining compliance with scholarly activities standards and guidelines; updates as regulations change.
Serves as the designee of the Director as needed.
Maintains DRM related databases and audit files.
This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.

CORE QUALIFICATIONS

Education:

Bachelor’s Degree in a formal, natural, or social scientific discipline required

Experience:

Minimum 2 years of relevant experience. Previous regulatory analysis experience is preferred. Any appropriate combination of relevant education, experience and/or certifications may be considered.

Knowledge, Skills and Attitudes:
Ability to deal with high volumes and rigid deadlines.
Familiarity with research ethics and methodologies and ability to conduct independent literature research (including Internet-based research) are required.
Ability to communicate effectively in both oral and written form.
Ability to maintain effective interpersonal relationships.
Commitment to the University’s core values.
Ability to work independently and/or in a collaborative environment.
Proficiency in computer software (i.e. Microsoft Office).
Ability to accurately prepare and maintain records, files, reports, and correspondence.
Contact Information
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