About the Hiring Group
RTI Health Solutions (RTI-HS), a business unit of RTI International, is an independent and internationally recognized research organization. We provide healthcare consulting and research expertise to optimize decision-making for pharmaceutical, biotechnology, and medical device products across the development and marketing life cycle. Clients rely on our expertise, quality standards, and integrity to guide their product development and regulatory and market access strategies. Our service groupings include Value, Access, and HEOR; Patient-Centered and Outcomes Research; Epidemiology and Biostatistics; Medical Communications; Global Business Operations; and Strategic Consulting and Growth. RTI-HS has office locations in the US, UK, Spain, France, and Sweden.
Our team brings extensive experience in developing publications across a range of therapeutic areas, including pharmacoepidemiology, patient-centered outcomes research, and economic evaluations. We specialize in publishing SLRs, TLRs, and Delphi panels, working alongside expert researchers to ensure methodological rigor and clear data presentation. In this Senior Medical Writer role, you’ll guide these efforts in collaboration with internal teams and clients, delivering scientifically robust publications that meet the highest standards.
This role is preferably based in our Manchester office on a hybrid schedule, though we welcome applications from candidates based remotely within the UK.

PREFERRED QUALIFICATIONS:

• Familiarity with digital communications, including creating content for online platforms and managing digital communication strategies.
• Previous experience working on business development and proposal writing for publications.
  As a global employer of choice, RTI is committed to belonging in the workplace and the communities and markets where we serve our mission. We value a variety of thoughts, cultures, backgrounds and perspectives and welcome applicants without regard to race, color, religion, sex, age, marital status, sexual orientation, gender identity, national origin, creed, citizenship status, disability, protected veteran status, or any other classification protected by applicable discrimination laws or RTI policy. We are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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• Lead publication planning and development, collaborating with internal teams and external authors to deliver high-quality medical and scientific communications (e.g., manuscripts, abstracts, posters) for peer-reviewed journals and conferences.
• Interpret study results, literature, and supporting data to produce clear, impactful content for both scientific and non-scientific audiences.
• Manage publication workflows from concept to submission, including stakeholder coordination, compliance processes, strategic guidance, and quality control.
• Ensure all materials meet ethical and industry standards (e.g., ICMJE, GPP) and align with journal/conference requirements and client expectations.
• Oversee multiple concurrent timelines and priorities, delivering on time and within budget while fostering strong client relationships.
• Guide strategic discussions in meetings with internal and external teams, translating complex data into clear communication and actionable insight.
• Mentor and support junior writers, contributing to team development, consistent quality, and timely delivery.
• Identify challenges and generate innovative solutions, especially when facing ambiguous or unprecedented scenarios.
• Engage directly with clients through proposals, relationship building, and new publication opportunities.
• Help shape scientific communication strategies for new business, confidently presenting ideas during pitch meetings and across therapeutic areas.

What You’ll Need

• Bachelor’s, Master’s, or PhD degree in Science, English, Communications, or a related field.
• A minimum of 5 years’ professional experience in medical writing is required, ideally within a medical communications agency or the pharmaceutical/biotech industry. This should include at least 2 years in a senior or leadership role, preferably focused on outcomes research and real-world evidence generation
• Proven ability to mentor junior writers and guide them through complex writing and publishing tasks.
• Proven experience in managing multiple publication projects and collaborating with various stakeholders.
• Strong understanding of the publication process, including manuscript submission and industry guidelines.
• Exceptional writing and communication skills, with the ability to transform complex scientific data into clear, compelling narratives.
• Project management expertise, including the ability to prioritize and manage multiple tasks under tight deadlines.
• Proficiency in Microsoft Office Suite, reference management software (e.g., EndNote), and familiarity with publication management systems.
• In-depth knowledge of ICMJE, GPP3, and other publication standards.
• Ability to provide strategic insights to clients, helping them navigate complex publication landscapes.