Jobs · New Jersey

Director, Global Scientific Content - Ophthalmology

Merck · Rahway, NJ · 3 days ago
$191k–$300k/yrFull-time

About the role

The Director, Global Scientific and Value Content-Health-care Professional (Dir GSVC) for Ophthalmology position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs, as well as Outcomes Research.

Responsibilities

  • Actively engaging with key stakeholders in the creation and adaptation of the V&I Planning and Scientific Platform, which provides the framework for GSVC Annual Product and Disease State Plans for Ophthalmology
  • Developing and adapting annual GSVC plans for one or more products and disease states aligned with the annual V&I Plans
  • Engaging key stakeholders and incorporating medical insights into GSVC Annual Product Plan(s) for Ophthalmology
  • Leading the development, review, approval, and communication of individual GSVC content within V&I for external scientific exchange

Requirements

  • Minimum Education and Experience Level: MD/PharmD/PhD, plus minimum of five years of relevant Medical Affairs experience; OR MSN, BS degree in Pharmacy, MS degree in Life Sciences, plus minimum 10 years of relevant Medical Affairs experience; OR BS degree in Nursing, Life Sciences, plus minimum 15 years of relevant Medical Affairs experience.
  • Relevant working experience in Medical Communications in the pharmaceutical industry
  • Excellent scientific writing/verbal communication skills
  • Ability to develop or deliver scientific content for purpose of scientific exchange with external customers
  • Proven ability to network, prioritize, negotiate and cross-functionally collaborate
  • Organizational, problem-solving and prioritization skills
  • Strong analytical skills and ability to translate strategy into action plans
  • Demonstrated leadership through initiatives, mentoring, and process improvements

Qualifications

  • Advanced degree (PharmD, PhD)
  • Knowledge of ophthalmology
  • Experience leading the development of Global or Regional Medical/Scientific Affairs Plans
  • Experience with promotional review or medical/legal review activities
  • Prior experience working across geographies with different regulation/compliance requirements
  • Strong track record of mentoring or managing people

Skills

  • Content Development
  • Cross-Functional Teamwork
  • Global Project Management
  • Healthcare Education
  • Medical Affairs
  • Medical Communications
  • Medical Knowledge
  • Multidisciplinary Collaboration
  • Project Management
  • Results-Oriented
  • Scientific Reviews
  • Stakeholder Engagement
  • Strategic Planning
  • Strategic Thinking
  • Vendor Management

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