We are seeking a Lead Medical Writer to join our clients fast-paced, collaborative global medical communications team. This senior-level role is ideal for a seasoned writer who thrives on producing high-quality scientific content, mentoring junior writers, and playing a strategic role in client engagements across a wide range of therapeutic areas and communication channels.
Responsibilities:
Content Development & Scientific Excellence
- Lead the development of scientifically accurate, engaging, and high-impact content including manuscripts, abstracts, slide decks, posters, advisory board materials, MSL resources, and digital content.
- Ensure all deliverables align with client objectives, industry guidelines (e.g., GPP, ICMJE, FDA/EMA), and editorial best practices.
- Maintain a high standard of consistency, referencing, tone, and formatting across all projects.
Strategic Client Engagement
- Act as a trusted scientific advisor to clients, contributing to communication strategy, messaging development, and content planning.
- Represent the medical writing team in client meetings, scientific congresses, and internal strategic discussions.
- Lead scientific content discussions and ensure the successful delivery and impact of client-facing materials.
Team Leadership & Mentoring
- Provide editorial oversight, mentorship, and feedback to junior and mid-level writers to support their growth and ensure content quality.
- Assist in resource planning, onboarding, and performance reviews within the writing team.
- Foster a collaborative and supportive team culture, ensuring alignment with scientific standards and editorial excellence.
Project & Workflow Management
- Partner with project managers to deliver high-quality work on time and within budget.
- Support proposal development, timeline scoping, and budget forecasting as needed.
- Efficiently manage multiple projects and priorities across therapeutic areas and accounts.
Qualifications:
- An advanced degree in life sciences (PhD, PharmD, MD strongly preferred; MSc considered with relevant experience).
- 5–7+ years of experience in medical writing, preferably within a medical communications agency or pharmaceutical environment.
- Proven ability to work across diverse deliverables (medical affairs, publications, commercial) and therapeutic areas.
- Strong understanding of clinical trial data, regulatory environments, and scientific interpretation.
- A demonstrated ability to lead teams and client engagements, providing both strategic insight and scientific expertise.
- Outstanding written and verbal communication skills, with an eye for clarity, precision, and scientific impact.
- Proficiency with reference management tools (e.g., EndNote) and document formatting in PowerPoint, Word, and similar platforms.
Interested in learning more about this position? Please contact Kristyn Coldewey via email at kristyn.coldewey@meetlifesciences.com.