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 Senior Project Manager based in a number of global locations.\n\nDiscover Impactful Work:\nLead 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.\n\nA day in the Life:\n•\tDevelop project timelines, standards, budgets, and forecasts.\n•\tCollaborate with cross-functional teams to meet deliverables.\n•\tMonitor timelines and provide status updates.\n•\tIdentify and resolve client management issues.\n•\tEnsure compliance with quality processes.\n\nKeys to Success:\n•\tProven project management skills.\n•\tStrong planning and organizational abilities.\n•\tExcellent interpersonal and communication skills.\n•\tAbility to work independently and under pressure.\n\nEducation\n•\tBS/BA (preferred field of study: scientific) with at least 5 years of relevant experience, or an advanced degree with at least 3 years of relevant experience.\nExperience\n•\tExperience managing medical writing or clinical projects.\n•\tPharmaceutical/CRO industry experience preferred.\n•\tAdvantageous to have experience in regulatory and/or plain language medical writing.\n\nKnowledge, Skills, Abilities\n•\tSolid project management, budgeting, and forecasting skills.\n•\tEffective problem-solving and decision-making abilities.\n•\tProficient in global and regional regulatory guidelines.\n\nPhysical Requirements / Work Environment\n•\tOffice-based role with exposure to electrical office equipment.\n•\tOccasional travel to client sites; domestic and rare international travel.\n•\tFrequent stationary periods, hand movements, and light lifting (15-20 lbs).\n\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. \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.