Senior Regulatory Operations Specialist
- Location
- New York, NY
- Listed
- 3 days ago
About the role
- Agency: Olixir
- Job Function: Production
- Job Subfunction: Production Operations
About the role
As a Senior Regulatory Operations Specialist, you'll oversee regulatory submissions for diverse brand portfolios, ensuring compliance with industry standards, agency protocols, and client requirements. You'll leverage exceptional planning, problem-solving, and communication skills to efficiently manage submissions and deadlines, utilizing expertise in FDA/OPDP regulations.
- Manage multiple client brands across various business lines, prioritizing workload to meet deadlines and ensuring compliance with agency processes.
- Serve as subject matter expert on standard operating procedures for assigned brands, mentoring junior team members and contributing to internal best practices.
- Coordinate with cross-functional teams, communicating submission status, requirements and challenges, and maintaining accurate trackers and process documents.
- Oversee regulatory submissions, including uploading documents, annotating pieces, tracking status and addressing missing metadata or MLR comments.
- Ensure seamless execution of resubmissions, final submissions and validation, adhering to client-specific regulatory processes and agency administrative protocols.
- Associate's or Bachelor's degree, with 3+ years of experience in pharmaceutical advertising or a regulated industry, and Veeva PromoMats Certification (a plus).
- Advanced knowledge of MLR processes, annotation/referencing, submission structures and client portals (Veeva Vault, Aprimo).
- Strong organizational, problem-solving and communication skills.
- Proficiency in Microsoft Office and Teams.
- Ability to manage multiple brands, prioritize tasks and meet deadlines in a fast-paced environment.
- Leadership skills, with proactive communication, critical thinking and collaboration.
- $65,000-$80,000
- To the extent permissible by local law, Omnicom's policy requires employees to work in the office for a minimum of three days a week, unless additional in-office days are directed by their agency or manager.
Omnicom is committed to hiring and developing exceptional talent. We agree that talent is uniquely distributed, and we're focused on developing inclusive teams that can bring the best solutions to everything we do. We strongly believe that celebrating what makes us different makes us better together. Join us-we look forward to getting to know you. We will process your personal data in accordance with our Recruitment Privacy Notice.
Equal opportunity and legal notices
For US Job Seekers
It is the policy of Omnicom and any of its affiliates to provide equal employment opportunities to all employees and applicants for employment without regard to race, religion, color, ethnic origin, gender, gender identity, age, marital status, veteran status, sexual orientation, disability, or any other basis prohibited by applicable federal, state, or local law. EOE/AA/M/D/V/F.
From Interpublic's careers page, first listed on Rolev.ai on November 6, 2026. Rolev.ai is not the employer.
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Common questions
Where is the Senior Regulatory Operations Specialist job at Interpublic located?
This Senior Regulatory Operations Specialist position at Interpublic is located in New York, NY. Always check Interpublic's application page for specific state eligibility or relocation policies.
How do I apply for the Senior Regulatory Operations Specialist position at Interpublic?
This listing links directly to Interpublic's Workday application page. You can apply directly on Interpublic's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.