PPD’s medical writing team offers agile, expert support to help clients communicate clinical trial information to patients, sites and regulatory authorities. With more than 25 years’ experience partnering with pharmaceutical, biotech, government and medical device clients, PPD medical writers translate complex scientific information into high-quality, regulatory compliant outputs across a comprehensive range of documents.
Our team applies innovative technology, therapeutic expertise and a commitment to quality to ensure that documents are clear, scientifically accurate and fully compliant with all International Council on Harmonisation (ICH) and regulatory requirements.
We offer medical writer roles (for professionals with no to little experience) up through principal level (with years of writing experience). Whether you're early in your career or have years of experience, we offer the training and growth opportunities that a writer of any level can leverage.
Our global medical writing department includes a dedicated team of medical writers who prepare clinical and non-clinical regulatory submission documents in accordance with legislation, guidelines and client requirements. Medical writers are responsible for managing the document development process, facilitating team interactions and authoring the documents. Other tasks include presentation of clinical messages in clinical study reports, summarization of preclinical and clinical studies for preparation of investigator's brochures and referencing current research and regulatory guidelines for preparation of protocols. Their work documenting clinical study trials covers a wide range of therapeutic indications.
START A CAREER IN MEDICAL WRITING
Do you have an advanced degree in biological sciences? Do you have experience summarizing complex scientific concepts? Our associate medical writer role might be right for you. By joining our team, you will receive excellent resources for onboarding and training and continuous mentorship to help you be effective.
The program manager, medical writing, leads client programs with high visibility among internal and client teams, often requiring a high degree of client engagement and management. You will manage client relationships and identify and resolve client management issues, in addition to ensuring the timely delivery and the quality of multiple program documents. This position will develop, monitor and adapt project plans, client and program-specific processes, timelines and budgets/forecasting for programs. This role will serve as a subject matter expert for assigned programs.
The role of program manager, medical writing, is suitable for professionals inside and outside the organization with experience in managing and directing complex projects, preferably within the pharmaceutical industry or a CRO.
The global medical writing department includes a dedicated and trained team of document review specialists with extensive experience reviewing regulatory documents for accuracy, consistency and readability. Our document review specialists have advanced degrees and/or certification from the Board of Editors in the Life Sciences (BELS).