FDA ยท 2 days ago
Supervisory Epidemiologist
Silver Spring, MD
Full-time
Remote
Senior Level
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Responsibilities
Oversees the consistent application of policy, regulatory guidance, analysis, interpretation, and programmatic support within the Division to other parts of OCEA, OPEQ, and CDRH.
Develops and implement policies and plans that are sound and feasible in relation to OCEA, OPEQ, and Center goals.
Assists in the oversight of DCEA2 regulatory and scientific work, including developing policy and program support regarding clinical evidence.
Serves as a technical expert and resource for team(s) to provide expertise, direction, and feedback to staff on policies and program support within one or more regulatory program areas.
Oversees team members and subject matter experts that provide consultative support on real-world data to other CDRH offices involved in the total product life cycle of medical device review.
Leads multistakeholder collaboration and engagement with the Offices of Health Technology, academia, professional societies, patient groups, industry, federal partners, and real-world evidence data coordinating centers with the goal of novel evidence generation.
Provides signatory authority on novel or complex issues and provides supervisory review for work products addressing regulatory policies, processes, and tools.
Plans work to be accomplished by subordinates, sets and adjusts short-term priorities, and prepares schedules for completion of work.
Assigns work to subordinates based on priorities, using selective consideration of the difficulty and requirements of assignments and the capabilities of employees.
Qualification
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Required
Oversees the consistent application of policy, regulatory guidance, analysis, interpretation, and programmatic support within the Division to other parts of OCEA, OPEQ, and CDRH.
Develops and implement policies and plans that are sound and feasible in relation to OCEA, OPEQ, and Center goals.
Assists in the oversight of DCEA2 regulatory and scientific work, including developing policy and program support regarding clinical evidence.
Serves as a technical expert and resource for team(s) to provide expertise, direction, and feedback to staff on policies and program support within one or more regulatory program areas.
Oversees team members and subject matter experts that provide consultative support on real-world data to other CDRH offices involved in the total product life cycle of medical device review.
Leads multistakeholder collaboration and engagement with the Offices of Health Technology, academia, professional societies, patient groups, industry, federal partners, and real-world evidence data coordinating centers with the goal of novel evidence generation.
Provides signatory authority on novel or complex issues and provides supervisory review for work products addressing regulatory policies, processes, and tools.
Plans work to be accomplished by subordinates, sets and adjusts short-term priorities, and prepares schedules for completion of work.
Assigns work to subordinates based on priorities, using selective consideration of the difficulty and requirements of assignments and the capabilities of employees.
Company
FDA
The Food and Drug Administration is an agency within the Department of Health and Human Services.
Founded in 1906
10001+ employees
H1B Sponsorship
FDA has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2023 (49)
2022 (58)
2021 (51)
2020 (73)
Funding
Current Stage
Late StageLeadership Team
Bakul Patel
Director, Digital Health Center of Excellence - US FDA
D
Daniel Walter
Consumer Safety Officer
Recent News
BioSpace
2024-12-11
2024-12-07
Company data provided by crunchbase
