Product and Regulatory Approvals SpecialistPrimary Location: Hartford, CT
Additional Locations: AZ-Phoenix, CT-Hartford Apply
Candidate can be located in Hartford or other Aetna office locations.
67247Fundamental Components: Prepares routine regulatory filings/follow-ups. Drafts correspondence using existing procedures and precedence. Files standard forms and related materials that meet regulatory and legal requirements. Identifies issues that need resolution using existing rules/regulations/guidelines. Supports State Consultants with regulatory review activities including: objection response support, loading of forms in filing system, redlining, pdf, historical filing research/retrieval, etc. Provides day-to-day maintenance of compliance system and operations. Acts as a reference (resource) in specified areas of expertise. Maintains positive, productive relationship with customers and regulatory contacts. Produces a variety of correspondence, reports, and presentations using the appropriate software.Performs manipulation of text from various types of source information and processing documents of a varied nature to final form.May participate in special projects/assignments. Background Experience: SERFF or Tracker filing experience is desired. Bachelor's degree or equivalent work experience. Potential Telework Position: Yes Percent of Travel Required: 0 - 10% EEO Statement: Aetna is an Equal Opportunity, Affirmative Action Employer Benefit Eligibility: Benefit eligibility may vary by position. Candidate Privacy Information: Aetna takes our candidate's data privacy seriously. At no time will any Aetna recruiter or employee request any financial or personal information (Social Security Number, Credit card information for direct deposit, etc.) from you via e-mail. Any requests for information will be discussed prior and will be conducted through a secure website provided by the recruiter. Should you be asked for such information, please notify us immediately.
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