What are the responsibilities and job description for the Promotional Reviewer position at Collabera?
We are seeking a highly skilled Medical Reviewer/Safety Reviewer III to join our team and provide expertise in medical and safety review for advertising and promotional materials. The ideal candidate will ensure compliance with medical accuracy, scientific validity, and relevant regulatory standards for assigned therapeutic areas, particularly Neuroscience and Parkinson's Disease.
This position is fully remote, and candidates with Medical Review experience and Veeva PromoMats familiarity are highly preferred.
Key Responsibilities:
- Medical Review:
- Evaluate promotional materials for medical accuracy, validity, and appropriateness in alignment with approved labeling, scientific data, and compliance standards.
- Determine the appropriateness of data and references used to support marketing claims.
- Collaboration & Communication:
- Partner with cross-functional teams, including Medical Affairs, Regulatory, and Legal (MLR), to address promotional material-related issues.
- Engage with commercial business partners early in the development of promotional materials to enhance efficiency.
- Represent Medical Affairs in MLR review processes to ensure compliance with industry regulations and guidelines.
- System & Process Management:
- Document reviews, comments, and approvals for promotional materials using Veeva PromoMats.
- Participate in collaborative meetings, training sessions, and project initiatives.
- Therapeutic Expertise:
- Stay updated with relevant medical literature and data within the assigned therapeutic area(s), particularly Neuroscience and Parkinson's Disease.
- Contribute to competitive reviews and publication analyses.
Required Qualifications:
Experience:
- 3 years of experience in ad/promo medical review, medical affairs, or regulatory ad/promo within the pharmaceutical industry.
- Prior Medical Review experience is highly preferred.
- Proficiency with Veeva PromoMats and Med-Com is essential.
Education:
- Advanced degree preferred (MS, PhD, PharmD, or equivalent).
Technical Skills:
- Strong understanding of MLR processes and regulatory compliance.
- Familiarity with scientific evidence interpretation and the patient treatment journey.
Soft Skills:
- Excellent oral and written communication skills.
- Strong project management, analytical, and problem-solving abilities.
- Ability to collaborate effectively with cross-functional teams.
- Adaptability to manage multiple priorities in a fast-paced environment.
Preferred Qualifications:
- Experience in Neuroscience and Parkinson's Disease therapeutic areas.
- Leadership skills and the ability to influence cross-functional teams effectively.
Salary : $30 - $50
