Role at a glance
- Job function
-
Product, Strategy & Operations Program & Project Management
- Salary
- Not Disclosed
- Location
- Remote - Serbia
- Work arrangement
- Remote
- Employment
- Full-time
- Experience
- Senior Level Experience managing medical writing or clinical projects.
- Education
- Prefer BS/BA in a scientific field with 5 years' experience, or an advanced degree with 3 years' experience.
Spotted an issue?
We’ll check it against the original posting.
Role Summary
Senior project management role based in Europe, leading initiatives to deliver Informed Consent Forms (ICFs) and other critical clinical research documents with attention to quality and compliance.
What You'll Do
- 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.
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Senior project management professional with experience managing medical writing or clinical projects and strong regulatory and communication skills.
Required
- Experience managing medical writing or clinical projects.
- Proven project management skills.
- Solid project management, budgeting, and forecasting skills.
- Strong planning and organizational abilities.
- Excellent interpersonal and communication skills.
- Ability to work independently and under pressure.
- Effective problem-solving and decision-making abilities.
- Proficient in global and regional regulatory guidelines.
Preferred
- Prefer BS/BA in a scientific field with 5 years' experience, or an advanced degree with 3 years' experience.
- Pharmaceutical/CRO industry experience preferred.
- Advantageous to have experience in regulatory and/or plain language medical writing.
Original job description
Content provided by the employer
Original job description
Content provided by the employer
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Thermo Fisher Scientific offers impactful work globally, enabling customers to improve health and safety.
We have a vacancy for a Senior ICF Medical Writing Project Manager based in Europe (locations listed).
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
- Prefer BS/BA in a scientific field with 5 years' experience, or an advanced degree with 3 years' 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.
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.
About the company
Thermo Fisher Scientific
Large Enterprise
Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.