Medical Writer - Medical Information

Thermo Fisher Scientific

1d • Onsite

About The Position

The Medical Writer will provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. Collaborates with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.

Requirements

• PharmD
• Experience with Medical Information (equivalent to 2+ years)
• Previous experience that provides the knowledge, skills and abilities to perform the job (comparable to 2+ years)
• Solid medical writing skills, including grammatical, editorial and proofreading skills
• Ability to interpret and present complex data accurately and concisely
• Effective administrative, organizational and planning skills; attention to detail and quality
• Ability to work on own initiative and effectively within a team
• Effective oral and written communication skills
• Great judgment and decision-making skills
• Good computer skills and skilled with client templates; good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)
• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
• Able to work upright and stationary for typical working hours.
• Ability to use and learn standard office equipment and technology with proficiency.
• Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Nice To Haves

• Experience working in the pharmaceutical/CRO industry preferred

Responsibilities

• Develops and updates standard medical response documents, custom response documents, frequently asked questions, and Academy of Managed Care Pharmacy formulary dossiers, specific to the peri- and post-approval phases of the product lifecycle.
• Researches and responds to escalated medical information inquiries from healthcare providers.
• Conducts literature searches for standard response documents utilizing secondary databases.
• Utilizing professional judgment, integrates pertinent clinical data into standard response documents with clear, concise, accurate and balanced medical writing following organizational, client, and regulatory guidelines.
• Participates as required in project launch meetings, review meetings, and project team meetings, serving as a liaison for communication with the client.
• Collaborates and effectively communicates with internal and external client contacts to provide high quality medical information writing deliverables in a timely manner and within budget.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees