Medical Science Liaison Specialist in Endocrinology

3 weeks ago

Sydney, New South Wales, Australia Merck Group Full time
Our diverse team at Merck Group is passionate about innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. We dream big and are dedicated to caring for our rich mix of people, customers, patients, and planet. We are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients
Our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life.

Your Role
As a Medical Science Liaison, Endocrinology you will be responsible for driving scientific engagement and providing high-level medical and scientific expertise across diverse therapeutic areas. This role involves close collaboration with healthcare professionals (HCPs), internal cross-functional teams, and external stakeholders to advance medical research, support product portfolios, and manage patient support programs (PSPs).

Main responsibilities
  • Engage with HCPs, and key opinion leaders (KOLs) to build strong relationships and disseminate key clinical and scientific data.
  • Lead and participate in advisory boards, speaker tours, and medical education initiatives to communicate recent developments and real-world evidence.
  • Collaborate with the medical and commercial teams on product launches, lifecycle management, and strategy development for new indications and emerging therapies.
  • Support and/or develop PSPs and digital ecosystems aimed at improving patient outcomes and adherence across various therapeutic areas.
  • Work on diverse portfolios, handling both mature and newly introduced products, ensuring the alignment of medical strategies with business goals.
  • Provide scientific input into medical information, regulatory submissions, and marketing materials.
  • Stay current on relevant clinical trials, emerging data, and treatment guidelines to inform internal teams and external stakeholders.
  • Participate in regional and global medical congresses, keeping up to date with the latest research and innovations.


Who You Are
  • Graduate or Post-Graduate degree in life sciences.
  • Strong understanding of clinical trial design, regulatory processes, and real-world evidence in the therapeutic areas mentioned above.
  • Experience with or strong interest in Patient Support Programs and improving patient outcomes.
  • Willing to learn and grow in their career in medical affairs
  • Ability to work on diverse portfolios and handle multiple therapeutic areas and projects with flexibility.
  • Excellent communication, presentation, and interpersonal skills for engaging with HCPs, KOLs, and cross-functional teams.
  • Proven ability to interpret complex scientific data and translate it into actionable insights for internal and external stakeholders.
  • Willingness to travel for conferences, HCP engagements, and internal meetings.


Desirable Attributes
  • Experience working in cross-functional teams and a proven ability to adapt to changing priorities and projects.
  • Experience with digital health initiatives or patient-centred digital tools is a plus.

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