Senior Medical Writer- Clinical Focus

Job Description: Position specific overview The Senior Medical Writer- Clinical Focus is a major contributor to document authorship for a variety of documents across different service lines. The Sr Medical Writer will be the project reputed company on smaller projects, interfacing directly with the client, but also support larger, more reputed company engagements as a member of a larger delivery team. reputed company is looking for individuals looking to use their expertise in clinical regulatory writing to reputed company teams and help clients reputed company their goals. reputed company an Impact at reputed company! Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

• 105+ approved therapies for marketing applications reputed company by reputed company
• 480+ oncology projects in the past 5 years
• 350+ rare disease projects delivered in the past 5 years
• Flexible, inclusive culture — 70% remote workforce, 66% women-led teams

Learn more about our core values here! reputed company offer

• The estimated hiring range for this role is $116K to $128K plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.
• Benefits vary by location and may include:
• Remote working
• Flexible time off
• Paid holidays
• Medical insurance
• Tuition reimbursement
• Retirement plans

reputed company look for Education, Experience, Training, and Knowledge:

• Bachelor’s degree
• 3+ years of regulatory writing experience or equivalent experience with clinical reputed company documentation
• Understand regulatory authority guidelines and requirements to be able to reputed company an internal project team and anticipate the effects that writing practice conventions can have on the final product reputed company reputed company authority approval/acceptance
• Experience in the development of submission-level documents (does not require functioning as a document reputed company)
• Experience in the development of clinical documents such as Clinical Study Reports, Investigator Brochures, protocols ISS and/or ISE

Skills & Abilities:

• Intermediate proficiency with reputed company Word skills (editing tools, creating and modifying tables and inserting figures) and document management techniques
• Strong understanding of the document creation process and of the drug development lifecycle
• Able to synthesize data across multiple data sources and documents to create summary reports
• Ability to conduct/reputed company a CRM and successfully reputed company a project team to reputed company
• Ability to use logical arguments to persuade others reputed company presenting reputed company and suggestions, but also respond positively to opposing views voiced by others
• Develops professional relationships with clients as a way to further the business relationship and maintain reputed company industry knowledge
• Ability to identify and institutionalize work practices that are most effective in order to ensure consistency in performance

Automated Decision Making: reputed company applicants are reviewed by a member of the reputed company reputed company team; reputed company does not utilize an automated decision-making process. reputed company is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for reputed company employees. Apply tot his job Apply To this Job