Source Job

US

  • Plays an essential role supporting Global Medical Information / Medical Content Development Team on content development-related engagements.
  • Writes and creates medical and scientific content related to Medical Affairs, Medical Information and Medical Communications.
  • Drives the client document development process from gathering materials and developing scientifically rigorous content to facilitating document review.

Medical Writing Project Management Client Management Analytical Thinking Communication Skills

15 jobs similar to Medical Content Development Manager / Project Lead Contract

Jobs ranked by similarity.

US

  • Review, annotate, and amend publication manuscript drafts to tight deadlines.
  • Work on rapid turnaround deliverables following guidance set by Sci Comms Solutions Lead.
  • Liaise with Authors to take manuscripts to submission.

Sorcero's medical AI platform transforms life sciences decision-making, accelerating patient access to life-saving treatments. Sorcero is a Certified B Corp headquartered in Washington, DC, recognized by over a dozen awards, including Fast Company's Most Innovative companies of 2024.

US

  • Responsible for planning, development, and oversight of scientific content.
  • Provide clients with strategic medical communication recommendations.
  • Independently lead execution of content development activities.

Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to identify effective, holistic, science-based strategies through medical communications. Over a third of their staff hold advanced scientific or medical degrees, and most work from where they live.

US

  • Planning, development, and oversight of scientific content for assigned accounts.
  • Leading client interactions and brand strategy, as well as the scientific portion of brand planning and business development.
  • Managing resource allocation, partnering with client services to develop SOWs and timelines and identifying areas for new and organic growth.

Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to identify effective, holistic, science-based strategies to address their objectives through medical communications. Our flexible structure provides better work-life balance; they attract the best talent and are more responsive to their clients.

$80,000–$100,000/yr
US

  • Draft and copyedit submissions for abstracts, posters and peer-reviewed manuscripts.
  • Work collaboratively with other team members and actively participate in pub planning activities.
  • Perform fact/data check on writing documents (manuscripts, white papers, dossiers, etc.).

Natera is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. The Natera team consists of highly dedicated professionals from world-class institutions, who care deeply for our work and each other.

$85,000–$100,000/yr
US

  • Manage content curation across a variety of medical specialties and clinical interests.
  • Monitor medical news, journal articles, clinical research, and healthcare trends to identify timely, relevant content for clinician audiences.
  • Evaluate scientific journal articles and distill meaningful takeaways for clinicians without losing nuance.

Doximity is transforming the healthcare industry by connecting doctors and enabling collaboration. They're the leading digital platform for U.S. medical professionals, with over 80% of physicians as members, and they foster an inclusive and diverse work environment.

US

  • Author, review, and manage clinical, regulatory, technical, and medical documents including protocols, study reports, and regulatory submissions.
  • Ensure strategic alignment and consistency of scientific messaging across documents while maintaining compliance with global regulatory requirements.
  • Drive the end-to-end writing process, manage timelines, and lead cross-functional reviews to deliver high-quality, on-time deliverables.

Kiniksa Pharmaceuticals is a commercial-stage biopharmaceutical company developing and commercializing novel therapies for diseases with unmet need, focusing on cardiovascular indications. The company fosters a highly collaborative, patient-first culture led by accomplished life sciences leaders, empowering talented individuals to make a real impact.

Europe

  • Lead project workstreams from end-to-end, ensuring the high-quality design and delivery of customer solutions.
  • Solve complex problems for Life Sciences leaders, leveraging Veeva’s unique data and software insights.
  • Mentor and manage Associate Consultants, overseeing their work and professional development within your workstream

Veeva is building the industry cloud for Life Sciences through software, data, AI, and Business Consulting working together. Veeva Business Consulting was launched in 2019 and has grown quickly and organically to a global organization of over 400 people.

$110,000–$120,000/yr
US Unlimited PTO

  • Define and refine content strategy by identifying what resonates across different physician specialties.
  • Own day-to-day content planning, creation, and publishing across social channels.
  • Write and edit compelling copy for email campaigns, newsletters, website articles, and in-product communications.

Impiricus is an AI-powered HCP Engagement Engine transforming how life sciences companies support physicians. Named the #1 fastest growing company in North America by Deloitte in 2025, they ethically connect HCPs to pharma resources, reducing costs and accelerating patient access.

$84,000–$112,000/yr
US Canada

  • Review and edit promotional content/materials for grammar and consistency.
  • Fact check/Cross-check and proofread existing content.
  • Retain medical, legal, and regulatory guidance to ensure consistency and accuracy.

P10 was born of the idea that if something isn’t working—or could work better—change it. P10 brings together a team of diverse, remote-only seasoned professionals to deliver exceptional value for clients.

Global Unlimited PTO

  • Write promotional content such as ad copy, headlines, questionnaires, emails, and landing page text to improve click-through rates and signups for clinical trial recruitment campaigns.
  • Translate complex medical information from trial protocols into clear, engaging, and patient-friendly messaging while maintaining accuracy.
  • Revise copy based on feedback and campaign data, conduct QA scoring, and contribute to improving templates and workflows for better performance.

Trialfacts recruits participants for clinical trials, connecting academic researchers and commercial sponsors with the right people for their studies. It is a 19-year-old company with 35 team members across 7 countries, operating with a mission-driven culture focused on accelerating health research.

US Canada

  • Develop client-ready deliverables including protocols, statistical analysis plans, and technical reports.
  • Manage the delivery of project components by collaborating with other staff members.
  • Contribute to development of proposals and presentations under guidance of senior team members.

Precision Medicine Group is a portfolio organization that helps its clients with sophisticated evidence synthesis projects. The company has a start-up culture with vision in its field.

US

  • Write copy for organic social content across Instagram, TikTok, and YouTube.
  • Write first-draft creative briefs for the creative team, translating campaign strategy.
  • Apply healthcare knowledge to write copy that is accurate, accessible, and on-brand.

Solace is cutting through the red tape of healthcare by pairing patients with expert advocates and giving them the tools to make better decisions—and get better outcomes. The U.S. based team is lean, mission-driven, and growing quickly.

US

  • Develop, execute, monitor, and adapt strategic MSL stakeholder engagement plans.
  • Lead high-quality scientific exchange through both proactive and reactive interactions.
  • Identify and communicate insights, trends, and activities of other Medical Affairs organizations.

They focus on engaging key opinion leaders (KOLs) and healthcare providers in high-quality scientific exchange. They drive insight generation and contribute to the development and execution of medical strategy.

Europe

  • Preparation of Initial Investigational New Drug (IND) applications and amendments.
  • Provide guidance and support to other in‑house units in the preparation or review of manuals, training guidelines, and similar documentation.
  • Serve as a resource for new medical writers, offering direction, feedback, and support as needed.

Theradex Oncology is a full-service CRO, conducting early and late-phase oncology trials in the U.S, Europe and Asia. Their focus is cancer, understanding the science behind each potential cancer therapy and the challenges of moving therapies from mice to man.

Canada US

  • Develop client-ready deliverables such as study protocols, statistical analysis plans, and technical reports for health technology assessment submissions.
  • Manage project components by collaborating with team members to ensure timely delivery, financial performance, and high-quality outputs, while handling day-to-day client communications.
  • Provide mentorship and direction to junior researchers, contribute to business development proposals, and apply technical expertise in systematic reviews and indirect treatment comparisons like NMA and MAIC.

Precision Medicine Group is a global portfolio organization specializing in evidence synthesis for health technology assessments in the pharmaceutical industry. The company has a culture similar to a start-up, is well-funded, and prides itself on being a visionary leader in its field.