Medical Content Expert Writer

Join EVERSANA as a Medical Content Expert Writer and play a pivotal role in developing high-quality scientific and medical content for leading life sciences and pharmaceutical clients. You will collaborate with cross-functional teams to create engaging, accurate, and compliant materials that support commercialization, medical affairs, and patient education initiatives. This remote opportunity offers a dynamic environment focused on innovation, diversity, and making a positive impact on patient lives worldwide.

Job Overview

As part of the Medical Content Development team, you will craft a variety of medical communications, support regulatory compliance, and contribute to the advancement of novel therapies across multiple therapeutic areas. You will engage with clients, manage document workflows, and ensure the highest standards of scientific rigor and ethical integrity in all deliverables.

Key Responsibilities

• Create and edit medical and scientific content including Scientific Response Documents, FAQs, slide sets, abstracts, posters, and training materials.
• Lead the document development process from material gathering to facilitating reviews with medical, legal, and regulatory teams.
• Manage content on document management platforms (e.g., Veeva PromoMats/MedComms), ensuring proper reference anchoring and annotations.
• Conduct literature searches, data fact-checking, and ensure compliance with industry guidelines.
• Mentor team members, contribute to SOPs, templates, and support onboarding and training as needed.

Required Skills & Qualifications

• Advanced degree (PharmD, MPharm, MS Pharm, PhD, or MD) with at least 4 years of medical writing experience in the life sciences or pharmaceutical industry.
• Proficiency in medical content development, scientific communications, and document management systems.
• Exceptional written, oral, and interpersonal communication skills; ability to summarize complex scientific data.
• Familiarity with AMA Style, GPP, ICMJE, and other medical publishing and regulatory guidelines.
• Experience with literature search tools (PubMed, Ovid, Embase) and reference management software (EndNote, Mendeley, etc.).
• Strong project management skills and the ability to work both independently and collaboratively in a matrix environment.
• Demonstrated integrity, professionalism, and commitment to diversity and inclusion.