Senior Medical Writer

Thermo Fisher Scientific • Wilmington, NC

23h • Onsite

About The Position

The Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise. The Senior Medical Writer may assist program manager. The role involves collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence. When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference. Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

Requirements

• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic/vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years)
• Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills
• Ability to interpret and present complex data accurately and concisely
• Ability to work on own initiative and effectively within a team
• Excellent administration, attention to detail, organizational, planning, and problem-solving skills
• Strong project management skills
• Excellent oral and written communication skills with strong presentation skills
• Significant knowledge of global, regional, national and other document development guidelines
• Great judgment and decision-making skills; strong negotiation skills
• Excellent computer skills and skilled with client templates; good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)

Nice To Haves

• advanced degree preferred
• Experience working in the pharmaceutical/CRO industry preferred
• Additional qualifications in medical writing or medical information advantageous

Responsibilities

• Serve as a primary writer who creates and provides input on routine deliverables, such as medical information documents, publications and clinical study documents.
• Develop complex medical and scientific documents, including AMCP dossiers, infographics, slide presentations, manuscripts, study documents for complex programs.
• Review documents prepared by team members.
• May provide training and mentorship for medical writers and new hires.
• Ensure compliance with applicable SOPs, WI, quality processes, and requirements for documents.
• Provide input on and independently develop best practices for achieving optimal results, including various client-specific processes.
• May function as a project lead or assist with program management activities. Duties could include developing timelines, budgets, forecasts, and contract modifications; tracking deliverable metrics; and representing medical writing team in client meetings.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Number of Employees: 5,001-10,000 employees