Source Job

UK

  • Author clinical study reports, protocols, informed consent forms, narratives, and investigator brochures across therapeutic areas.
  • Represent Medical Writing at meetings, drive document development, and articulate strategy and timelines.
  • Mentor junior staff, manage multiple priorities, and foster collaboration to resolve conflict.

Medical Writing Clinical Research Biostatistics MS Word

10 jobs similar to Senior Medical Writer

Jobs ranked by similarity.

US

  • Leads writing and preparing clinical and regulatory documents for drug and device development.
  • Coordinates review, approval, and quality control across functions to ensure compliance and timelines.
  • Develops knowledge of US and international regulations and participates in process improvements.

AbbVie discovers and delivers innovative medicines and solutions addressing serious health issues in immunology, oncology, neuroscience, and aesthetics. They are a large global biopharmaceutical company committed to having a remarkable impact on people's lives.

Europe 5w PTO

  • Produce high-quality content for diverse medical communications projects, demonstrating excellent scientific understanding.
  • Develop content with minimal supervision, within budget and on time, using client approval systems.
  • Attend conferences, present work to clients, and manage day-to-day client communication and relationships.

Lumanity is dedicated to improving health outcomes by accelerating and optimizing access to life-changing medicines. As a global strategic partner, they bring together strategy, evidence, engagement, and technology to engineer breakthrough value.

UK

  • Write clear and concise medical copy for HCPs and patients, adhering to ABPI guidelines and quality processes.
  • Collaborate with strategy, creative, and account teams to develop effective campaigns.
  • Manage projects from concept to completion, ensuring timelines and quality standards.

Real Chemistry is a global healthcare communications and marketing agency that partners with top pharmaceutical and biotech companies. The company fosters a culture of innovation and collaboration, with over 5 years of growth, and has been certified as a Great Place to Work.

UK Spain South Africa Greece Portugal Hungary

  • Lead authoring and development of high-complexity Phase II-IV clinical regulatory documents for a top pharma partner.
  • Own the end-to-end medical writing process from planning through final delivery, ensuring alignment with strategy and timelines.
  • Coordinate cross-functional teams across geographies and facilitate comment resolution to drive document development.

Fortrea delivers solutions that bring life-changing treatments to patients faster. They are a global organization that empowers employees to shape their own career path with comprehensive training and management support.

US

  • Develop scientific copy for various deliverables on assigned brands and products.
  • Work independently and collaboratively with medical writers and directors to develop scientifically accurate copy.
  • Manage workflow for assigned projects and meet associated deadlines.

Real Chemistry is a global agency providing a full suite of services across healthcare communications and marketing to top pharmaceutical and biotech clients. They foster a culture rooted in being best together with a commitment to excellence, offering a comprehensive benefits program and perks.

UK

  • Develop medical affairs and publications content across multiple workstreams, ensuring high scientific quality and credibility.
  • Create materials tailored for different medical audiences with minimal internal review, demonstrating excellent quality control.
  • Collaborate with clients to ensure projects meet strategic marketing and medical needs, maintaining a client-centric attitude.

ApotheCom is a leader in medical communications, part of Inizio, a global healthcare consulting and communications group. With over 12,000 employees globally, Inizio creates compelling content and engages communities to achieve outcomes that matter.

US

  • Drive growth of Regulatory Science and Medical Writing services across pharmaceutical, biotechnology, and life sciences clients.
  • Lead strategic sales efforts, identify client needs, and partner cross-functionally to deliver tailored solutions supporting regulatory approvals.
  • Serve as the primary liaison between client and company for all sales-related activities, enhancing visibility and market presence.

Veristat accelerates life-changing therapies to patients worldwide with more than 30 years of expertise. They have a flexible, inclusive culture with 70% remote workforce and 66% women-led teams, having prepared over 105 approved therapies and delivered over 350 rare disease projects.

  • Drafts and maintains medical information content for the Medical Information Call Center (MIC).
  • Provides guidance to Medical Information Managers on drafting standard medical responses and FAQs.
  • Reviews MIC case records to ensure accuracy of response and compliance with regulations.

Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for serious diseases. The company is consistently recognized as one of the industry's top places to work, with a diverse and inclusive culture.

US

  • Partner with medical and cross-functional teams to provide statistical leadership for real-world evidence and publication strategies.
  • Perform advanced statistical analyses including meta-analyses, causal inference, and external control studies.
  • Write statistical analysis plans, review medical literature, and ensure quality of statistical programming.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. The company offers the security and career opportunities of a global organization while allowing direct work with a single sponsor.

Global

  • Provide subject matter expertise to teams for global disclosure strategies of clinical documents under regulatory requirements.
  • Manage planning, preparation, and quality control for disclosures, including oversight of vendor deliverables.
  • Lead development of standard processes and technological solutions to ensure compliance with disclosure regulations.

Pfizer is a global biopharmaceutical company dedicated to discovering and developing innovative therapies. As a large multinational employer with a culture of individual ownership, it employs tens of thousands of people and fosters a collaborative and inclusive environment.