Responsibilities. Leads the planning, development, and execution of scientific publications across therapeutic areas, ensuring alignment with publication strategy and scientific integrity. Writes and edits manuscripts, abstracts, posters, and slide decks for congress presentations in accordance with ICMJE and GPP guidelines. Collaborates with cross-functional teams including Medical Affairs, Clinical Development, Biostatistics, and Regulatory Aff...
Principal Medical Writer. Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work t...
Principal Medical Writer. Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work t...
Principal Medical Writer. ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Principal Medical Writer to join our diverse and dynamic team. As a Principal Medical Writer at ICON, you will be responsible for leading...
Description. Principal Medical Writer. Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streaml...
Work Schedule. Standard (Mon-Fri). Environmental Conditions. Office. FSP Senior. Regulatory. Medical Writer (. Remote. US. ). At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while...
The. Principal Medical Writer. represents medical writing on multi-disciplinary teams, collaborates on the development of clinical documents in accordance with all applicable regulations, Good Clinical Practices, and Standard Operating Procedures (SOPs), and oversees the work of contract writers on the clinical program as well as other writers who may work on the program. This is an individual contributor position, equivalent to the Associate Dir...
