ICF MEDICAL WRITING PROJECT MANAGER
Descripción de la oferta de empleo
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.
Discover Impactful Work As an ICF Medical Writing Project Manager, you'll lead ambitious projects that strictly adhere to timelines and quality standards.
Collaborate with world-class teams to make a significant impact on patient care.
A day in the Life.
• Develops project timelines, standards, budgets, and forecasts.
• Collaborates with cross-functional teams to meet project deliverables.
• Ensures timely achievement of final deliverables.
• Advances or resolves risks to project quality, budget, or timeline.
• Ensures compliance with quality processes and requirements.
Keys to Success.
• BS/BA (preferably in a scientific field) with a minimum of 2 years of relevant experience or an advanced degree with at least 1 year of relevant experience.
Experience • Experience managing medical writing or clinical projects.
• Experience in the pharmaceutical/CRO industry preferred.
• Proven experience in medical writing (eg, Regulatory and/or plain language).
Knowledge, Skills, Abilities • Proficient project management skills, including budgeting and forecasting.
• Solid planning and organizational abilities.
• Excellent interpersonal and communication skills; self-motivated.
• Good knowledge of global regulatory and document development guidelines.
• Effective decision-making and problem-solving skills.
Physical Requirements / Work Environment Primarily office-based with flexibility for remote work.
Occasional travel may be required for client meetings or team collaboration.
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 + 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.
with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today! 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.
Detalles de la oferta
- Sin especificar
- 18/11/2024
- 16/02/2025
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