Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At 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. \n\nWe have a vacancy for an ICF Medical Writing Program Manager based in a number of global locations.\n\nDiscover Impactful Work:\nLead patient-centric medical writing programs with a focus on Informed Consent Forms (ICFs). Manage complex projects, engage with clients, and ensure flawless delivery and quality of documents, contributing to world-class research outcomes.\n\nA day in the Life:\n•\tDevelop and adapt project plans and timelines.\n•\tEngage and manage client relationships.\n•\tCollaborate with cross-functional teams.\n•\tMonitor project progress and provide status updates.\n•\tMentor junior staff and ensure compliance with quality processes.\n\nKeys to Success:\n•\tAdvanced project management skills.\n•\tOutstanding planning and organizational abilities.\n•\tExcellent communication, negotiation, and decision-making skills.\n•\tIn-depth knowledge of regulatory and document development guidelines.\n•\tProven ability to lead and mentor junior staff.\nEducation\n•\tBS/BA (preferably in a scientific field) with a minimum of 8 years of relevant experience, or an advanced degree with a minimum of 6 years of relevant experience.\nExperience\n•\tExperience managing medical writing or clinical projects.\n•\tExperience working in the pharmaceutical/CRO industry.\n•\tPreferably, experience in medical writing (Regulatory and/or plain language).\nKnowledge, Skills, Abilities\n•\tAdvanced skills in budgeting, forecasting, and resource management.\n•\tExpert planning and organizational skills.\n•\tExcellent interpersonal and communication skills.\n\nPhysical Requirements / Work Environment\nThis role is office-based, with the flexibility for remote work as needed. Candidates must be able to work under strict deadlines and manage multiple projects simultaneously.\nBenefits\nWe 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!\nOur 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 with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. \n\nApply today! http://jobs.thermofisher.com\nThermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.