Descripción de la oferta
This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Environmental Conditions
Office
At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. 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.
We are excited to expand our Medical Writing FSP Team in Europe This would be a remote role. We are looking for a Principal Medical Writer to be dedicated to a client in the FSP space; 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. Researches, writes, and edits clinical study reports and study protocols, and summarizes data from clinical studies.
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. May also develop, review, and manage performance metrics for assigned projects.
Represents the department at project launch meetings, review meetings, and project team meetings.
Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Experience in managing and directing complex medical writing projects required
Experience in Neurosciences advantageous
Additional qualifications in medical writing (AMWA; Significant knowledge of global, regional, national, and other document development guidelines
Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills
Excellent project management skills
Ability to mentor and lead junior level staff.
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 award-winning learning and development programme, ensuring you reach your potential.
We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We are a global organization but with a local feel.
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. #
