Explore senior medical writer opportunities for experienced professionals who translate complex medical and scientific information into clear, accurate content. Ladders features vetted professional jobs paying $100,000 or more, including roles across medical communications, clinical research, pharmaceutical development, and healthcare.
Senior medical writers develop and review materials for scientific, clinical, regulatory, and healthcare audiences. Depending on the role, they may write clinical study reports, protocols, regulatory submissions, manuscripts, medical education content, or materials for healthcare professionals. They collaborate with researchers, clinicians, statisticians, regulatory experts, and clients to ensure content is accurate, consistent, and aligned with applicable standards.
Employers often seek strong scientific writing, editing, and project-management skills, along with the ability to interpret clinical data and explain technical concepts clearly. Many roles require a bachelor’s, master’s, or doctoral degree in a life-sciences or related field and several years of medical writing experience. Familiarity with clinical research, regulatory guidance, publication practices, and document review workflows may also be valuable.
Senior medical writers work at pharmaceutical and biotechnology companies, medical communications agencies, contract research organizations, healthcare organizations, and consulting firms. Career paths may lead to principal or lead writer positions, medical writing management, regulatory strategy, publications leadership, or broader scientific communications roles.
Browse senior medical writer openings and discover opportunities designed for experienced professionals. Ladders focuses on vetted jobs paying $100,000 or more, helping you explore positions that match your expertise, industry interests, and career goals. Review each listing for its responsibilities, qualifications, location, and compensation details.
Sponsor Dedicated - Senior Regulatory Submissions writer
$70K - $145K *
Shape the future of regulatory writing by leading medical documentation efforts, ensuring clarity and compliance across diverse projects while mentoring junior writers and collaborating with cross-fun...
Today
Senior Engineer, Process Data Science and Statistics
$101K - $152K *
Lead the development of analytical workflows for process monitoring and predictive modeling, enhancing decision support across manufacturing stages. Collaborate on AI-enabled tools and statistical ana...
5 days ago
Senior Product Development Engineer
$94K - $118K *
Lead product development initiatives, ensuring technical integrity from concept to commercialization. Collaborate with cross-functional teams, mentor engineers, and drive regulatory submissions for me...
Today
$95K - $115K *
Drive the creation and maintenance of technical documentation for cybersecurity and software development, collaborating with engineers and stakeholders to ensure clarity and accuracy in materials for...
Reposted today
$95K - $115K *
Drive the creation and maintenance of technical documentation for cybersecurity and software development, collaborating with engineers and stakeholders to ensure clarity and accuracy for diverse audie...
Reposted today
$110K - $130K *
Champion the creation of clear, concise technical documentation for cybersecurity and software development. Collaborate with engineers and stakeholders to transform complex information into user-frien...
1 week ago
Senior Specialist, Proposals & Client Service- (US)
$65K - $129K *
Lead the charge in developing competitive proposals and client services, enhancing operational excellence across clinical research programs. Collaborate with global teams to ensure high-quality submis...
Reposted 2 weeks ago
Consultant, MedTech IVD Solutions
$71K - $178K *
Shape the future of Medtech IVD solutions by driving client projects, mentoring junior consultants, and ensuring quality standards are met. Leverage your analytical skills to deliver insights and fost...
1 week ago
Senior Medical Director - Oncology
$254K - $382K *
Transform clinical research by leading strategic medical initiatives, ensuring operational excellence, and fostering collaboration across teams. Drive innovation and mentor future leaders while delive...
Reposted 1 week ago
Senior Proposal Writer/ Proposal Specialist
$80K - $100K *
Drive the development of compelling proposals for public-sector clients, enhancing relationships with local agencies while collaborating with service line leaders to ensure compliance and quality in s...
2 weeks ago
Senior Proposal Writer/ Proposal Specialist
$80K - $95K *
Transform your career by leading proposal development for public-sector clients. Collaborate with diverse teams to enhance relationships and deliver tailored solutions, ensuring compliance and quality...
2 weeks ago
Medical Writer - Perlmutter Cancer Center Clinical Trials Office
$84K - $88K *
Unlock potential by providing expert writing support for Investigator Initiated Trials in Molecular Oncology. Collaborate with diverse teams to enhance clinical research and foster new investigator in...
3 weeks ago
$80K - $95K *
Empower your career by crafting clear, impactful technical documentation. Collaborate with engineers and developers to produce user manuals, guides, and reports that enhance understanding and usabilit...
1 week ago
$95K - $100K *
Join a dynamic team as a Senior Medical Editor, ensuring accuracy and clarity in health brand communications. Collaborate with cross-functional teams during critical projects, leveraging your expertis...
Reposted 1 week ago
$69K - $93K *
Elevate the quality of medical content by leading editorial efforts across multiple brands. Collaborate with cross-functional teams to ensure accuracy and clarity while mentoring junior editors and ma...
Reposted 2 weeks ago
Associate Director, Medical Writing
$189K - $223K *
Drive the creation of high-quality medical writing deliverables to support clinical development programs, ensuring compliance with regulatory standards. Collaborate across functions to deliver timely...
Reposted yesterday
$96K - $144K *
Join a team that's shaping the future of life sciences consulting. Collaborate on diverse projects, enhance your analytical and leadership skills, and gain valuable insights into the pharmaceutical in...
3 weeks ago
$79K - $157K *
Drive impactful clinical data management across global projects, ensuring high-quality data delivery from start to finish. Collaborate with cross-functional teams and lead process improvements while m...
1 week ago
$100K - $150K *
Lead the medical planning and design of complex healthcare environments, collaborating with clients and teams to deliver innovative solutions. Provide expertise across programming, design, and project...
Today
$100K - $150K *
Champion innovative healthcare design by leading medical planning efforts, collaborating with clients and teams to create high-performing environments that meet operational needs and enhance patient c...
Today
$110K - $130K *
Advance your career by leading biostatistics projects, developing protocols, and collaborating across teams, ensuring quality deliverables and effective communication in the clinical research domain...
Reposted 5 days ago
$88K - $105K *
Lead the charge in enhancing revenue compliance initiatives by collaborating with cross-functional teams to ensure adherence to billing regulations and coding guidelines while mitigating organizationa...
1 week ago
$85K - $105K *
Unlock creativity by leading impactful copywriting projects for diverse health brands. Collaborate with teams to translate complex information into compelling messages, driving brand strategies and en...
3 weeks ago
GMP Compliance and Quality Assurance Auditor and SOP Technical Writer.
$95K - $115K *
Elevate compliance and quality assurance standards by managing GxP projects, providing expert consultation, and driving continuous improvement in regulatory practices. Collaborate with clients to ensu...
3 weeks ago
$78K - $156K *
Join a team that's advancing heart disease treatment through innovative EP technologies. Provide expert clinical support, training, and mentorship while driving sales growth and enhancing customer rel...
5 days ago
What does a senior medical writer do?
A senior medical writer creates, edits, and reviews scientific, clinical, regulatory, or healthcare content. Typical deliverables can include clinical study documents, regulatory submissions, manuscripts, and medical education materials.
What qualifications are typically required for senior medical writer jobs?
Requirements vary by employer, but many roles call for a degree in a life-sciences or related discipline, substantial medical writing experience, excellent writing and editing skills, and the ability to interpret scientific or clinical data.
Where do senior medical writers work?
Senior medical writers may work for pharmaceutical or biotechnology companies, contract research organizations, medical communications agencies, healthcare organizations, and consulting firms.
How much do senior medical writer jobs pay?
Compensation depends on factors such as experience, location, employer, and specialization. Ladders focuses on vetted professional opportunities paying $100,000 or more; check individual listings for compensation details.
What career opportunities can follow a senior medical writer role?
Experienced writers may advance to lead or principal medical writer positions, manage writing teams, or move into regulatory strategy, publications leadership, or broader scientific communications.