Pharma Materials Review & MRP Lead

Scorpion Therapeutics; Florham Park (NJ); On-site; USD 130,000 - 180,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k) (eligible employees)

Long-term incentive programs

Job summary

Scorpion Therapeutics is seeking a senior project management lead to drive the U.S. Material Review Process (MRP) for advertising, promotional and labeling materials.

You will coordinate cross-functional reviews with Medical, Regulatory, Commercial, Legal, and Compliance teams and oversee timelines, status, and approvals. This role requires strong leadership, Veeva expertise, and experience with print/digital materials.

Qualifications

• 8+ years project management (or equivalent) experience.
• SME in material review process/policies/systems.
• Strong Veeva expertise.
• Experience in print and digital formats.
• Bachelor’s degree in Business Management, Science, Education, or related.
• Pharmaceutical industry experience preferred.
• Marketing/communication or agency experience; product launch experience.
• Adobe Acrobat; MS Word/Excel/PowerPoint; Veeva PromoMats.

Responsibilities

• Facilitate cross-functional review/approval of advertising, materials, training, and labeling.
• Lead communication of material status; provide timeline oversight through U.S. MRP.
• Serve as MRP lead consultant/trainer for teams uploading/approving materials.
• Provide leadership: mentor/coaching; develop contingency plans; improve processes.

Skills

Advanced project management

Data-driven decision-making

Collaboration & interpersonal skills

Policy & guidelines adherence

Leadership in lessons learned

Education

Bachelor’s degree (Business Management, Science, Education, Communications or related)

Tools

Adobe Acrobat

MS Word

MS Excel

MS PowerPoint

Veeva PromoMats

Job description

Scorpion Therapeutics is seeking a senior project management lead to drive the U.S. Material Review Process (MRP) for advertising, promotional and labeling materials.

You will coordinate cross-functional reviews with Medical, Regulatory, Commercial, Legal, and Compliance teams and oversee timelines, status, and approvals. This role requires strong leadership, Veeva expertise, and experience with print/digital materials.