Principal Medical Writer

Syneos Health, Inc.; New York (NY); Remote; USD 110,000 - 150,000; Full time

Job summary

Cadent is seeking an autonomous Principal Medical Writer to lead development of peer-reviewed publications and other medical communications. You will ensure strategic alignment, accuracy, and quality across manuscripts, reviews, abstracts, posters, and slides with direction from authors.

Responsibilities include mentoring junior writers, coordinating with clients and teams, and preparing reference packs with rigorous data verification.

Qualifications

• PhD/MD/PharmD/MBBS/MS in health sciences or equivalent required.
• 4–6 years of professional medical communications experience.
• Familiarity with publication guidelines; CMPP a plus.
• Proficiency with MS Office, PubMed/EMBASE, and visualization tools.

Responsibilities

• Independently develop narratives for client medical communications across manuscripts, abstracts, posters, and slides.
• Interpret complex scientific data for diverse audiences including regulatory documentation and data presentations.
• Synthesize and visualize data for medical communication assets.
• Review drafts from junior writers with high attention to detail and accuracy.
• Collaborate with clients and internal teams to outline projects and ensure timely delivery.
• Prepare materials for legal and regulatory review as needed.

Skills

Interpersonal skills

English fluency

Audience communication

Attention to detail

Education

PhD/MD/PharmD/MBBS/MS in health sciences

ISMPP CMPP certification (optional)

Tools

Microsoft Office

PubMed/EMBASE

Reference management software

Scientific visualization software

Job description

Updated: Today
Location: Remote, India
Job ID:17977

You are looking to be a communications change maker.

In this role, you will take a leading role in development of high-quality and strategic peer-reviewed publications that deliver on our clients’ science and business strategy. The Principal Medical Writer will ensure the strategic alignment, accuracy, credibility, and quality of the manuscripts, literature reviews, abstracts, posters, slide decks, and other written pieces you develop with author direction.

Responsibilities

A highly autonomous writer who delivers high-quality medical communications while contributing to quality leadership, mentorship, and streamlined project delivery across assigned accounts.

• Independently develop innovative and creative narratives for client medical communication needs, customized for their product, situational landscape, and audience(s) of interest, including slides, manuscripts, abstracts, posters, or other digital and print content forms
• Interpret complex scientific and medical data for different audiences, including trial protocols, data presentations, regulatory documentation, and statistical analysis methods
• Synthesize, prioritize, and visualize data effectively when developing medical communication assets
• Apply critical analysis with strong attention to detail and good proofreading skills, including review of drafts created by junior medical writers
• Work with clients, other team members, and external stakeholders to kick off and determine outline for projects
• Collaborate with creative studio, production, editorial, and account management teams for project delivery
• Ensure that all author and stakeholder feedback is accurately and appropriately incorporated
• Ensure accuracy and rigor, including provision of a full reference pack and annotations for fact checking
• Prepare materials for legal and regulatory review as necessary
• Understand and champion scientific and communication strategies for 1 or more clients
• Serve as subject matter expert in 2 to 4 disease states
• Actively participate in internal and external meetings representing our work to clients, authors, and other external stakeholders
• Ensure adherence to internal or client-directed specifications and templates for deliverables
• Train new joiners and fellow colleagues as and when required
• Work in a fast-paced, deadline-driven, team-oriented environment, managing multiple projects in support of 1 or more clients at any given time
• Proactively manage timelines to ensure on-time project completion
• Raise issues appropriately and propose solutions
• Perform additional tasks as assigned, including participation in advisory boards, development of slides for the meeting and/or summaries, or travel to scientific meetings

Qualifications

• PhD, MD, PharmD, M. Pharm, MBBS, M. Science or other advanced professional degree in the health sciences
• 4 to 6 years of professional medical communications experience
• Knowledge of good publication practice guidelines; ISMPP CMPP certification a plus but not required
• Proficiency with Microsoft Office Software (Word, Excel, and PowerPoint), medical literature databases (PubMed and/or EMBASE), referencing and scientific visualization software
• Excellent interpersonal skills with the ability to interact with account teams, other writers, editors, physicians, and clients
• Ability to communicate medical/technical information to a wide variety of audiences and formats
• Efficiently prioritize multiple tasks and provide effective direction to others; quickly evaluate the resources necessary to accomplish a goal and put those into action
• Strong written and verbal fluency in English

At Cadent, we are dedicated to building a diverse, inclusive and authentic workplace. If your past experience doesn’t align perfectly, we encourage you to apply anyway. At times, we will consider transferable skills from previous roles. We also encourage you to join our Talent Network to stay connected to additional career opportunities.

Cadent is a US Medical Communications company with employees located across the US. The home office is in New York City. Cadent specializes in high science, high touch peer to peer medical communications. The company excels in translating complex science into compelling messages that deliver value and action. Cadent builds relationships and collaboration between the biopharmaceutical industry and healthcare professionals.

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Disclaimer: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Discover what our more than 29,000 employees already know: work here matters everywhere. We work hard,and smart, all in the name of getting much-needed therapies to thosewho need them most. A career with Syneos Health means your everyday work improvespatients’ lives around the world. Selecting us as an employer secures a career inwhich you’re guaranteed to:

Syneos Health ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients.