GForce Life Sciences
Content Operations Specialist
Skills
6 days ago
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Important information
Contract type:
Part time
Location:
Waltham, MA, USA
Work mode:
Onsite
Published on:
22 October 2026
What they need
Content Operations Specialist
6 month contract
Hybrid in Waltham, MA
PART TIME: Tuesday - Thursday, 3 DAYS per week
Mostly remote, occasional on-site meetings
Must be able to work on a W2
Summary
Our client, a healthcare organization, has engaged GForce Life Sciences to provide a Content Operations Specialist. This role will support the end-to-end management of promotional digital content, with a primary focus on Medical, Legal, and Regulatory (MLR) / Copy Clearance Committee (CCC) coordination, content readiness, and operational excellence. The position involves acting as a liaison between Brand Marketing, agency partners, CCC, and Digital Operations teams to ensure efficient review, approval, and deployment of promotional materials.
Duties / Expectations of Role
- Coordinate end-to-end MLR/CCC submission activities for promotional and digital assets, including two website migrations to a new platform.
- Ensure promotional materials meet submission requirements, including annotations, references, screenshots, metadata, and supporting documentation.
- Manage submission timelines, review cycles, certification, and stakeholder communications; facilitate incorporation of CCC feedback through approval and implementation.
- Identify and resolve content readiness gaps prior to submission to minimize review delays.
- Guide promotional assets through development, review, approval, and publishing workflows; maintain asset status and documentation within approved systems.
- Support website migration initiatives by organizing content, reviewing manuscripts, validating metadata, and ensuring content is submission-ready.
- Partner with development, content, and brand teams to ensure content accuracy and regulatory compliance during migration.
- Serve as a primary contact between Brand Marketing, agency partners, Operations teams, and CCC reviewers, facilitating communication, timelines, and dependencies.
- Support process improvements by suggesting operational enhancements, developing SOPs, templates, and reusable content strategies to improve efficiency and scalability.
Mandatory Requirements
- Bachelor's degree or equivalent professional experience.
- 3+ years supporting content operations, promotional review, marketing operations, or project management within the pharmaceutical, biotechnology, or healthcare industry.
- Experience coordinating MLR, MRC, or CCC review processes for promotional materials.
- Strong understanding of pharmaceutical promotional content lifecycle and regulatory approval processes.
- Exceptional organizational skills and attention to detail.
- Proven ability to manage multiple projects and priorities.
- Strong written and verbal communication skills.
- Experience working with cross-functional teams and external agency partners.
- Familiarity with content management, digital asset management, and workflow platforms such as Veeva PromoMats, Adobe Workfront, or Adobe Experience Manager.
Preferred Qualifications
- Experience supporting digital content, website, or omnichannel marketing programs.
- Knowledge of modular content strategies and content reuse frameworks.
- Support for website migration or digital modernization projects.
- Understanding of pharmaceutical compliance and promotional submission requirements.
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