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Key Responsibilities-
(i) Review and guide on R&D efforts, clinical trials, and develop medical communication plans
• Evaluate ongoing clinical trials to ensure scientific rigor, regulatory compliance, and relevance to the target patient population.
• Review medical communication strategies, including scientific publications, key messaging, and stakeholder engagement, to enhance effectiveness and credibility.
• Provide actionable recommendations to improve communication consistency, clarity, and impact.
• Assess current R&D efforts for alignment with medical and market needs.
(ii) Product pack review and recommendations
• Examine product packaging, labelling, and promotional content for medical accuracy, regulatory compliance, and market appeal.
• Identify opportunities for clarity, accessibility, and alignment with target audiences, ensuring
adherence to healthcare regulations and branding guidelines.
• Suggest improvements to enhance patient education, HCP communication, and product
differentiation.
(iii) Review of Medical Operations and Process Enhancement
• Conduct a systematic review of current medical operations, stakeholder interactions, and
compliance mechanisms.
• Identify gaps in processes and recommend optimization strategies to improve operational
effectiveness.
• Develop insights into cross-functional collaboration, ensuring alignment between medical
affairs, marketing, and regulatory teams.
• Ensure regular check-ins, stakeholder briefings, and milestone-based reporting
You understand that this Scope of Engagement depends on the achievement of key milestones which includes the following performance metrics and success evaluation:
• Improved/alignment of R&D and medical communication with industry best practices.
• Enhanced product pack clarity, compliance, and market relevance.
• Strategic roadmap/suggestions for measurable improvements in medical operations efficiency
and cross-functional collaboration.
Qualifications:
Advanced degree in Medicine, Pharmacy, Life Sciences, or related field (MD, PhD, PharmD).
Proven experience in medical affairs, clinical trials, and regulatory compliance.
Strong understanding of medical communications, scientific publications, and clinical research methodologies.
Expertise in product packaging, labeling, and promotional content review.
Demonstrated ability to collaborate effectively across cross-functional teams, including R&D, marketing, and regulatory affairs.
Excellent communication and presentation skills, with the ability to translate complex medical information into clear, actionable insights.
A leading fmcg organisation
Pharmaceuticals, FMCG
1
Pharmaceuticals
7 months
-
Remote
FMCG
7 months
20+ years
Remote
Automobiles & Auto Ancilliaries
7 months
20+ years
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