Sr Icf Medical Writing Project Manager (Remote)

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. We have a vacancy for an ICF Medical Writing Senior Project Manager based in a number of global locations. Discover Impactful Work: Lead 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 Life:

• Develop 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 Success:
• Proven project management skills.
• Strong planning and organizational abilities.
• Excellent interpersonal and communication skills.
• Ability to work independently and under pressure. Education
• BS/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. Experience
• Experience 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, Abilities
• Solid project management, budgeting, and forecasting skills.
• Effective problem-solving and decision-making abilities.
• Proficient in global and regional regulatory guidelines. Physical Requirements / Work Environment
• Office-based role with exposure to electrical office equipment.
• Occasional travel to client sites; domestic and rare international travel.
• Frequent stationary periods, hand movements, and light lifting (15-20 lbs). Benefits We 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! 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 with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! http://jobs.thermofisher.com Thermo 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.