Senior/ICF Medical Writing Project Manager

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific, you’ll 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.We have a vacancy for an ICF Medical Writing Project Manager based in a number of global locations.Our Medical Writing team is growing and we are looking for a Senior/ICF Medical Writing Project Manager in multiple locations in EMEA region.Discover Impactful WorkLead ambitious initiatives that craft the future of clinical research. Your expertise will enable us to deliver flawless Informed Consent Forms (ICFs) and other critical documents, ensuring outstanding quality and compliance.A Day In The LifeDevelop project timelines, standards, budgets, and forecasts.Collaborate with cross-functional teams to meet deliverables.Monitor timelines and provide status updates.Identify and resolve client management issues.Ensure compliance with quality processes.Keys To SuccessProven project management skills.Strong planning and organizational abilities.Excellent interpersonal and communication skills.Ability to work independently and under pressure.EducationPrefer BS/BA in a scientific field with 5 years experience, or an advanced degree with 3 years experience.ExperienceExperience managing medical writing or clinical projects.Pharmaceutical/CRO industry experience preferred.Advantageous to have experience in regulatory and/or plain language medical writing.Knowledge, Skills, AbilitiesSolid project management, budgeting, and forecasting skills.Effective problem-solving and decision-making abilities.Proficient in global and regional regulatory guidelines.BenefitsWe offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!What We OfferAs well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We’ve 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 organisation but with a local feel.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. 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 at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.