Fsp Principal Medical Writer (apac) (India)

Fsp Principal Medical Writer (apac) (India)

Work Schedule Other Environmental Conditions Office 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 taking science a step beyond through research development and delivery of life-changing therapies With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio our work spans laboratory digital and decentralized clinical trial services Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future Summarized Purpose We are excited to expand our India Medical Writing FSP Team We are looking for a Principal Medical Writer to be dedicated to a client in the FSP space experience in Neurology would be valuable but not essential As a Principal Medical Writer you will provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients As the lead writer you will review documents for the team and provide training and guidance to junior team members As a subject matter expert you will provide advice on document development strategy regulations and industry best practices You will collaborate with internal and external clients supporting and enabling effective and efficient communication that results in operational excellence Essential Functions Researches writes and edits clinical study reports and study protocols and summarizes data from clinical studies May serve as primary author who writes and provides input on complex clinical and scientific and program level documents including IBs INDs and MAAs Provides senior level review of routine and complex documents Provides training and mentorship for other writers and program managers on document preparation the use of software for document development document types regulatory requirements and therapeutic area knowledge Ensures compliance with quality processes and requirements for assigned documents As the subject matter expert develops and reviews best practices methods and techniques for achieving optimal results including various client- specific processes and leads process improvement initiatives May also develop review and manage performance metrics for assigned projects Represents the department at project launch meetings review meetings and project team meetings Education and Experience Bachelor s degree in a scientific discipline or equivalent and relevant formal academic vocational qualification Advanced degree preferred Previous experience that provides the knowledge skills and abilities to perform the job comparable to 8 years Experience in managing and directing complex medical writing projects required Experience working in the pharmaceutical CRO industry preferred Submissions document experience advantageous Additional qualifications in medical writing AMWA EMWA RAC advantageous Knowledge Skills and Abilities Significant knowledge of global regional national and other document development guidelines In-depth knowledge in one or more specialty areas such as preclinical therapeutic regulatory submissions communications etc Excellent data interpretation and medical writing skills including grammatical editorial and proofreading skills Excellent project management skills Advanced interpersonal oral and written communication and presentation skills Excellent negotiation skills Excellent judgment high degree of independence in decision making and problem solving Ability to mentor and lead junior level staff What We Offer At PPD clinical research services we hire the best develop ourselves and each other and recognize the power of being one team We understand that you will want to grow both professionally and personally throughout your career and therefore at PPD clinical research services you will benefit from an ensuring you reach your potential As well as being rewarded a competitive salary we have an extensive perks package based around the health and well-being of our employees We have a where PPD clinical research services truly value a work-life balance We have grown sustainably year on year but continue to offer a collaborative environment with teams of colleagues eager to share expertise and have fun together We are a global organization but with a local feel Our Mission is to enable our customers to make the world healthier cleaner and safer As one team of 100 000 colleagues we share a common set of values - Integrity Intensity Innovation and Involvement - working together to accelerate research solve complex scientific challenges drive technological innovation and support patients in need StartYourStory with PPD part of Thermo Fisher Scientific where diverse experiences backgrounds and perspectives are valued

📌 Fsp Principal Medical Writer (apac)
🏢 Thermo Fisher Scientific
📍 India

The original job offer can be found in Kit Job:
kitjob.in/job/178911985