Senior Regulatory Operations Lead — MLR Submissions

Digitas Health; Philadelphia (Philadelphia County); On-site; USD 36,000 - 47,000; Full time

Job summary

Digitas Health is seeking a Senior Associate, Regulatory Operations to lead project-level submissions for pharmaceutical clients, ensuring MLR reviews comply with client and internal standards. You will track progress through review stages, advise on submission timelines, and coordinate with internal stakeholders.

The role requires a bachelor's degree plus 2–4 years of experience in complex submission deliverables, with strong proficiency in Adobe Acrobat and Microsoft Office.

Qualifications

• Minimum of a bachelor's degree and 2-4 years of experience in the preparation of complex submission deliverables under tight deadline constraints.
• Proficient with Adobe Acrobat and Microsoft Office Suite.
• Clear communication and attention to detail.
• Top-notch organizational skills.

Responsibilities

• Assemble submission packages with screenshots, annotations, and references.
• Ensure components conform to client and Digitas Health guidelines.
• Estimate time/effort to create submission components and coordinate timelines.
• Balance multiple projects simultaneously.
• Follow up with internal teams to communicate status and timing.
• Manage client expectations with clear, concise communication.

Skills

Clear communication

Attention to detail

Organizational skills

Technical writing

Education

Bachelor's degree

Tools

Adobe Acrobat

Microsoft Office Suite

Job description

Digitas Health is seeking a Senior Associate, Regulatory Operations to lead project-level submissions for pharmaceutical clients, ensuring MLR reviews comply with client and internal standards. You will track progress through review stages, advise on submission timelines, and coordinate with internal stakeholders.

The role requires a bachelor's degree plus 2–4 years of experience in complex submission deliverables, with strong proficiency in Adobe Acrobat and Microsoft Office.