Remote Regional Medical Scientific Director

MSD; Rahway (NJ); Remote; GBP 157.000 - 247.000; Vollzeit

Benefits dieser Stelle

Medical, Dental, Vision benefits

401(k) retirement plan

Flexible work arrangements

Zusammenfassung

Merck & Co., Inc. is seeking a Regional Medical Scientific Director to exchange scientific information with national and regional Scientific Leaders.

The role guides research strategy, supports company-sponsored and investigator‑initiated studies, and promotes scientific insights across therapeutic areas. The position emphasizes collaboration, adherence to GCP, SOPs, and regulatory guidelines, with a focus on pharmaceutical medical affairs and cross‑functional networking.

Qualifikationen

• PhD, PharmD, DNP, DO, or MD.
• Proven ability to engage with senior external stakeholders.
• Minimum 3 years of relevant therapeutic area experience beyond degree program.
• Strong knowledge of FDA, OIG, HIPAA, and industry guidelines.

Aufgaben

• Develops professional relationships with national and regional scientific leaders to provide approved medical information.
• Conducts peer‑to‑peer scientific discussions and maintains a reliable medical contact within the company.
• Addresses questions outside the regional scope and directs inquiries to appropriate resources.
• Leads protocol discussions and site identification for investigator‑initiated studies when requested.
• Engages in scientific congresses and medical meetings to exchange data and insights.

Kenntnisse

Med. communications

Medical affairs

Stakeholder engagement

Scientific networking

Oncology

Hematology

Scientific exchange

Research collaboration

Ausbildung

PhD/PharmD/DNP/DO/MD

Jobbeschreibung

Merck & Co., Inc. is seeking a Regional Medical Scientific Director to exchange scientific information with national and regional Scientific Leaders.

The role guides research strategy, supports company-sponsored and investigator‑initiated studies, and promotes scientific insights across therapeutic areas. The position emphasizes collaboration, adherence to GCP, SOPs, and regulatory guidelines, with a focus on pharmaceutical medical affairs and cross‑functional networking.