Remote Veeva Content QA & Submission Lead – Healthcare Marketing (contract)

Remote Full-time
Location: Fully Remote Contract Duration: 10 months, possible extension Company: Sanofi – FLEXT Direct Contingent Workforce Program Job Description Sanofi’s contingent workforce program, FLEXT Direct, is seeking a Content Quality & Submission Lead for a 10-month contract with the possibility to extend. We are seeking a detail-oriented Content Quality & Submission Lead (Veeva Specialist) to manage the end-to-end quality, compliance, and submission of digital promotional materials within the Veeva platform. This role ensures all content is accurately anchored, version-controlled, and submission-ready, serving as a critical bridge between marketing, regulatory, medical, legal, writers, and designers. This role involves translating RC and MLR feedback into clear, actionable guidance, conducting comprehensive end-to-end quality control (including claims, references, ISI, and formatting), and supporting the development and maintenance of core claims libraries. The Content Quality & Submission Lead also owns project tracking and workflow coordination to ensure timelines, quality standards, and compliance requirements are consistently met. Key Responsibilities • Manage submission of promotional assets into Veeva. • Perform end-to-end quality control of digital promotional materials. • Ensure accurate anchoring, version control, and submission readiness. • Translate RC and MLR feedback into actionable updates for content teams. • Review claims, references, ISI, formatting, and overall compliance. • Support development and maintenance of core claims libraries. • Coordinate workflows and track projects to ensure timelines and quality standards are met. • Act as a liaison between marketing, regulatory, medical, legal, writers, and designers. Qualifications • Minimum 3 years of relevant experience in content quality, submission, or compliance roles. • Required experience with Veeva (Vault PromoMats or similar). • Experience working in a regulated environment. • Strong attention to detail and organizational skills. • Ability to manage multiple projects and stakeholders simultaneously. • Excellent written and verbal communication skills. Apply tot his job
Apply Now →

Similar Jobs

Clinical Research Associate​/Senior - FSP - Remote

Remote Full-time

Clinical Trial Research Coord I- Vallejo

Remote Full-time

Remote Expert Sourcing & Research Coordinator

Remote Full-time

Clinical Program Manager (Remote)

Remote Full-time

Clinical Research Associate - Freelance

Remote Full-time

Clinical Research Regulatory Coordinator II

Remote Full-time

CLINICAL RESEARCH COORDINATOR, SR

Remote Full-time

Clinical Research Coordinator - Must be local to Overland Park, KS!

Remote Full-time

Clinical Research Leader - JJMT Electrophysiology

Remote Full-time

​​Senior Clinical Research Coordinator​​ 2

Remote Full-time

Flexible Live Chat Representative Roles – Entry-Level Remote Positions at $25–$35/Hour (No Experience Required)

Remote Full-time

Dispatch Call Center Agent- Overnight

Remote Full-time

Senior Business Travel Consultant - Night Shift - Remote

Remote Full-time

Oracle Financial Specialist

Remote Full-time

Proofreader/Copy Editor (Remote, Contract)

Remote Full-time

Upward Bound Coordinator & Student Advisor (2 Vacancies)

Remote Full-time

Experienced Customer Experience Project Manager – Transforming End-to-End Guest Experience through Strategic Program Management and Technology Enhancements

Remote Full-time

**Experienced Customer Service Representative – Flexible Remote Work Opportunities with arenaflex**

Remote Full-time

**Experienced Customer Service Representative - Airport Ticket/Gate Agent**

Remote Full-time

Virtual Client Success Manager - Personal Development

Remote Full-time
← Back to Home