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Review Committee Specialist
- Contract
- Medical Communications
- United States
Review Committee Specialist - Contract - Remote, US
Ensure integrity, compliance, and precision at every step of the promotional review journey.
À±½·ÊÓÆµ is seeking a Review Committee Specialist to support promotional review processes in the oncology and biotechnology space.
This is a fully remote role in the US.
Primary Responsibilities:
The successful candidate will coordinate review committee activities, maintain documentation systems, and assist with regulatory submissions. This role focuses on ensuring compliance, efficiency, and accuracy in the review and approval of promotional materials.
Skills & Requirements:
- Bachelor's degree or equivalent experience.
- Experience managing Medical Legal Regulatory (MLR) review committees.
- Strong customer service ethic and ability to interact with management, customers, vendors, and partners.
- Detail-oriented with problem-solving and conflict resolution skills.
- Ability to meet deadlines while managing multiple projects effectively.
- Excellent written and verbal communication skills.
- Proactive, self-motivated, and adaptable to dynamic environments.
- Familiarity with drug development and commercialization processes.
- Proficiency in Adobe Acrobat Professional, Veeva PromoMats, Veeva Vault, MS Excel, MS Word, and MS PowerPoint.
The Review Committee Specialist's responsibilities will be:
- Guide sponsors on review cycle timelines and assist with planning from submission to approval.
- Review promotional materials for accuracy, verify and route submissions appropriately, and provide proactive guidance.
- Facilitate assigned review committee meetings, ensuring adherence to policies and procedures and accurate recording of outcomes.
- Ensure timely incorporation of required revisions into impacted materials.
- Coordinate submissions of materials to the FDA Office of Prescription Drug Promotion (OPDP) as needed.
- Manage files and systems supporting the review process.
- Prepare for and participate in quality assurance checks and audits.
- Oversee associated processes, including vendor communications, system updates, and enhancements.
- Stay informed about marketplace changes and new regulatory guidance.
If you are having difficulty in applying or if you have any questions, please contact Anthony Rabinkov at a.rabinkovproclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
À±½·ÊÓÆµ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. À±½·ÊÓÆµ is acting as an Employment Agency in relation to this vacancy.
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