Senior Medical Writer: Regulatory Content Leader

MSD; Guaduas; Sur place; COP 370 934 000 - 583 983 000; Plein temps

Avantages offerts par ce poste

Medical, dental, vision insurance

401(k) plan

Paid holidays and vacation

Résumé du poste

Merck & Co., Inc. in Rahway, NJ, USA seeks an experienced Clinical and Regulatory Medical Writer to lead preparation of regulatory documents and public-facing materials, ensuring accuracy, regulatory compliance, and clear communication.

You will collaborate with cross-functional teams, apply health-literacy principles, and drive process improvements while mentoring others. Ideal candidates bring 3+ years in medical writing, strong project leadership, and excellent communication skills, with

Qualifications

• Experience leading multiple medical writing projects and cross-functional teams.
• Ability to interpret clinical data clearly per regulatory guidelines.
• Strong critical thinking and problem-solving skills.
• Experience with conflict resolution in cross-functional settings.
• Adaptable to changing project needs and workloads.
• Excellent written and oral communication and presentation skills.
• Proficiency with Office tools and willingness to learn new platforms.

Responsabilités

• Lead preparation and review of clinical regulatory and public-facing documents.
• Collaborate with cross-functional teams to ensure regulatory compliance.
• Apply health-literacy concepts and medical writing best practices.
• Escalate issues impacting timelines, quality, or compliance.
• Mentor junior writers and contribute to process improvements.
• Stay updated on regulatory requirements and disease areas.
• Participate in or lead department initiatives and knowledge sharing.

Connaissances

Project leadership

Clinical data interpretation

Critical thinking

Conflict resolution

Adaptability

Communication skills

Office tools & SharePoint

Formation

Bachelor’s degree in health/science

Outils

SharePoint

Microsoft Office

Description du poste

Merck & Co., Inc. in Rahway, NJ, USA seeks an experienced Clinical and Regulatory Medical Writer to lead preparation of regulatory documents and public-facing materials, ensuring accuracy, regulatory compliance, and clear communication.

You will collaborate with cross-functional teams, apply health-literacy principles, and drive process improvements while mentoring others. Ideal candidates bring 3+ years in medical writing, strong project leadership, and excellent communication skills, with