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Associate - Medical Affairs Uk Tmr

3+ years
Not Disclosed
10 March 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Title: Associate - Medical Affairs UK TMR
Location: Bangalore, Karnataka, India
Category: Medical
Job Type: Full Time, Regular
Job Id: R-81323

Company Overview:
Lilly, a global healthcare leader headquartered in Indianapolis, Indiana, strives to make life better by discovering and delivering life-changing medicines. Our employees worldwide contribute to improving disease management and enhancing the lives of patients.

Role Summary:
The UK Technical Medical Reviewer (TMR) is responsible for ensuring the accuracy and compliance of promotional materials in line with regulatory documents, SOPs, PMAP requirements, and external codes such as the UK ABPI and Irish IPHA Codes. The TMR works closely with UK brand teams and reports to a manager within LCCI, with a dotted line to the Senior Director of Operations in the Northern European Hub.

Key Objectives/Deliverables:

Review and Approval of Promotional Materials:

  • Ensure medical accuracy and consistency of promotional materials in Veeva Vault PromoMats (VVPM).

  • Validate that all statements and claims align with regulatory documents and credible sources.

  • Check that visual representations accurately reflect data, ensuring consistency across sections, charts, and footnotes.

  • Confirm adherence to PMAP Guidance and legal requirements such as trademarks, GDPR, and referencing guidelines.

  • Review materials for correct language, grammar, and adherence to style guides.

Process Execution and Improvement:

  • Deliver training and onboarding for new hires in marketing and medical teams.

  • Provide coaching and support for continuous learning and compliance.

  • Produce detailed metrics and insights for UK leadership, identifying process inefficiencies.

  • Enhance quality systems by identifying compliance gaps and proposing proactive solutions.

Data Analysis and Process Optimization:

  • Draft, update, and implement PMAP procedures and guidance documents.

  • Apply Lean and Six Sigma principles to eliminate process bottlenecks.

  • Analyze data sets to identify trends and provide data-driven recommendations.

  • Define and refine process metrics to improve workflow efficiency.

Cross-Functional Leadership and Collaboration:

  • Lead strategic initiatives for process improvement and transformation.

  • Collaborate with brand teams and medical certifiers to manage pre-launch risk.

  • Participate in Six Sigma workstreams and cross-functional process enhancements.

Minimum Experience/Skills Requirements:

  • Minimum 3 years of experience as an editor, copywriter, or proofreader.

  • Strong analytical skills and attention to detail.

  • Ability to work collaboratively with cross-functional teams.

  • Proven ability to prioritize and manage multiple tasks.

Preferred Skills:

  • Proficiency in Veeva Vault PromoMats.

  • Strong problem-solving and process improvement abilities.

  • Strong self-motivation and strategic thinking skills.

Educational Requirements:

  • Master's degree or equivalent experience in a scientific discipline.

Other Information:

  • Location: LCCI, Bangalore

  • Travel: Minimal (<10%)

Lilly is committed to providing equal opportunities and ensuring diversity in its workforce. If accommodation is required during the application process, please submit a request through the provided accommodation form.

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