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Technical Writer

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Plan, write, edit, review and coordinate the approval of lab operating procedures and scientific validations to support pharma sponsors or internal use.
• Facilitate trial development and product registration.
• Ensure and coordinate quality checks for accuracy, collates reviewer’s comments, adjusts content of document as required based on internal/external input, and prepares final version.
• Exhibit flexibility in moving across development and preparation of multiple document types.
• Work with internal and external pharma sponsors to develop and prepare documents.
• Work with teams to ensure smooth and timely development of documents.
• Influence or negotiate change of timelines and content with other team members.
• Effectively collect and evaluate information from multiple sources


Job Requirements
Basic Qualifications:

• Bachelor’s Degree.
• At least 3-5 years experience in drug development or clinical laboratory experience
• Demonstrated mastery of written English with experience in medical, scientific or technical writing fields (at least 1 year); professional verbal skills in English.
• Cognitive abilities including; verbal reasoning, attention to detail, critical thinking, and analytical ability.
• Demonstrated excellent project management and time management skills.
• Strong interpersonal skills and the ability to be flexible in varying environments and with multiple customer groups.
• Demonstrated high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentation and templates).
• Ability to work well across cultures and time zones .
• Qualified candidates must be legally authorized to be employed in the United States.


Additional Skills/Preferences:

• Graduate degree with formal research component or in life sciences.
• Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience, particularly in Oncology.
• Experience in clinical laboratory, clinical trial process or regulatory activities.
• Experience writing clinical laboratory procedures, regulatory or clinical trial documents.
• Ability to work well independently and as part of a team.

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