
ICF Medical Writing Project Manager
Are you a skilled medical writer with a passion for project management? Look no further! Thermo Fisher Scientific is seeking an ICF Medical Writing Project Manager to join our dynamic team. In this role, you will use your expertise in medical writing and project management to lead cross-functional teams in the development of Investigator's Brochures, Clinical Study Reports, and other essential documents for clinical trials. We are looking for a highly organized and detail-oriented individual who can effectively communicate with both internal and external stakeholders. If you are ready to take on a challenging and rewarding role, we encourage you to apply.
- Lead cross-functional teams in the development of essential documents for clinical trials, such as Investigator's Brochures and Clinical Study Reports.
- Utilize expertise in medical writing to ensure accuracy, clarity, and compliance with relevant regulations and guidelines.
- Manage project timelines, resources, and budgets to ensure timely and high-quality delivery of documents.
- Communicate effectively with internal team members and external stakeholders to gather input, provide updates, and address any issues or concerns.
- Collaborate with other departments, such as regulatory affairs and clinical operations, to ensure alignment and consistency in project deliverables.
- Conduct thorough reviews and edits of documents to ensure they meet company standards and client expectations.
- Stay up-to-date with industry best practices and regulations related to medical writing and project management.
- Identify and address potential risks or challenges that may impact project timelines or deliverables.
- Foster a positive and collaborative team environment, promoting open communication and ideas sharing.
- Provide mentorship and guidance to junior medical writers and project team members.
- Represent the company and its values in a professional manner at all times.
- Continuously strive for process improvement and efficiency in project management and medical writing.
- Demonstrate a high level of attention to detail and accuracy in all project deliverables.
- Adhere to company policies and procedures, as well as ethical and legal standards.
- Participate in training and professional development opportunities to enhance skills and knowledge.
Bachelor's Or Master's Degree In A Relevant Scientific Field, Such As Biology, Chemistry, Or Pharmacology.
At Least 5 Years Of Experience In Medical Writing, Preferably In The Pharmaceutical Or Biotechnology Industry.
Strong Project Management Skills, Including The Ability To Manage Multiple Projects Simultaneously, Meet Deadlines, And Effectively Communicate With Cross-Functional Teams.
Familiarity With Ich Guidelines, Fda Regulations, And Other Relevant Industry Standards For Medical Writing.
Excellent Writing And Editing Skills, With A Keen Attention To Detail And The Ability To Translate Complex Scientific Data Into Clear And Concise Language For Various Audiences.
Project Management
Data Analysis
Time Management
Editing
Budget management
Quality Control
Scientific research
Team Leadership
Regulatory compliance
Scientific Communication
Cross-Functional Collaboration
Medical Writing
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Attention to detail
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a ICF Medical Writing Project Manager is $90,000 to $120,000 per year. However, this can vary depending on factors such as location, experience, and specific job responsibilities. Some companies may offer higher salaries for this role, while others may offer lower salaries. It is important to research the specific company and job listing to get a more accurate salary range.
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Thermo Fisher Scientific is a U.S.-based provisioner of scientific instrumentation, reagents and consumables, and software and services to healthcare, life science, and other laboratories in academia, government, and industry.

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