Medical Writing Program Manager QC and Publishing Lead (FSP)
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Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Job Title: FSP Medical Writing Program Manager (QC and Publishing Lead)
At Thermo Fisher Scientific you will 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.
Summarized Purpose:
We are excited to expand our Medical Writing FSP Team and appoint a Program Manager (FSP Document Review Lead) to provide oversight to a client-dedicated document review and publishing team. This role involves acting as the primary point of contact addressing client needs and concerns and ensuring a high-level of client satisfaction. Additionally the role will include managing and allocating resources effectively including staffing and technology to meet project requirements and deadlines. Key skills for this position include strong organizational and planning abilities excellent communication and client management skills and experience in resource management and team leadership. The ideal candidate will have relevant experience in document review or medical writing a proven track record in managing complex projects and teams and the ability to work under pressure and meet tight deadlines.
Essential Functions:
- Supports development monitoring and adapting project plans timelines and forecasts for complex review activities.
- Serves as the client point of contact for risk escalation evaluating and resolving or escalating risks related to project quality budget or timeline.
- Ensures compliance with quality processes and requirements for assigned programs maintaining consistency within and between project documents.
- Develops reviews and manages performance metrics for assigned projects.
- Provides senior-level review of document review materials.
- Trains new reviewers on processes and technical aspects of document review.
- May serve as primary reviewer for regulatory documents.
Education and Experience:
- Bachelors degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred.
- Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 8 years).
- Experience in document review or medical writing required for CSR Protocol ICF IB and other Regulatory Submission Documents
- Experience in allocating resources preferred.
- Experience working in the pharmaceutical/CRO industry preferred.
- Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous.
Knowledge Skills and Abilities:
- Solid project management skills to include resource management and timeline development
- Excellent data interpretation and medical writing skills including grammatical editorial and proofreading skills
- Extensive knowledge of global regional national and other document development guidelines
- Excellent oral and written communication skills with strong presentation skills
- Excellent negotiation skills
- Self-motivated and adaptable
- Excellent judgment; high degree of independence in decision making and problem solving
- Ability to mentor and lead entry-level staff
What We Offer:
At PPD clinical research services we hire the best develop ourselves and each other and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career and therefore at PPD clinical research services you will benefit from anaward-winning learning and development programme ensuring you reach your potential.
As well as being rewarded a competitive salary we have an extensive benefits package based around the health and well-being of our employees. We have aflexible working culture where PPD clinical research services truly value a work-life balance. We have grown sustainably year on year but continue to offer a collaborative environment with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel.
Our Mission is to enable our customers to make the world healthier cleaner and safer. As one team of 100000 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.
Required Experience:
Manager
Key Skills
- Project Management Methodology
- Project / Program Management
- Program Management
- Management Experience
- Microsoft Powerpoint
- Project Management
- Microsoft Project
- Budgeting
- DoD Experience
- Leadership Experience
- Supervising Experience
- Contracts
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
