Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
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Target PR Range: 95-105/hr
*Depending on experience
Duties:
The Senior Medical Writer (SMW) will work independently and with team members to write and review the content of within-scope documents. These may include CSRs, protocols, protocol amendments, ICFs, narratives, IBs and IB updates in a variety of therapeutic areas. The SMW is responsible for document development (eg driving meetings, strategy discussions, timing) and is expected to resolve issues and escalate problems as necessary. Â The SMW is also responsible for tracking projects and for adhering to regulatory guidelines and document standards.
Job Duties:
•   Works independently and with team members to create and review the content of within-scope documents. These may include CSRs, Protocols, protocol amendments, ICFs, narratives, IBs and IB updates in a variety of therapeutic areas. The Medical Writer is expected to drive document development, track deliverables and ensure timely document completion.
•   Writes or contributes to other Regulatory documents such as Clinical Summaries and Briefing Documents.
•   Represents Medical Writing at project meetings
   ? Drives document development;
   ? Articulates document strategy and timelines;
   ? Understands decision-makers and works to keep discussions focused.
   ? Synthesizes key messages and presents clear, accurate text for discussion.
• Solves problems, fosters collaboration, resolves conflict
Skills:
Experience Needed:
•   12+ Years of experience of industry experience
•   Ability to work independently
•   Strong knowledge of the clinical research process and regulations/guidelines required. Scientific and technical reading, writing and editing skills required.
•   Well-developed organizational, interpersonal and communication skills, and the ability to develop and present varied and unique ideas.
 • Good working knowledge of MS WORD, Adobe Acrobat, Project, Powerpoint and use of one or more electronic document management systems
Education:
BA or BS Advance Degree
*CO/NYC candidates might not be considered
Senior Medical Writer
Posted: 09/24/2024
2024-09-24
2024-11-08
Employment Type:
Contract
Job Category: Regulatory Sciences and Medical Writing
Job Number: 614070
Is job remote?: Yes
Country: United States
Job Description
Target PR Range: 95-105/hr
*Depending on experience
Duties:
The Senior Medical Writer (SMW) will work independently and with team members to write and review the content of within-scope documents. These may include CSRs, protocols, protocol amendments, ICFs, narratives, IBs and IB updates in a variety of therapeutic areas. The SMW is responsible for document development (eg driving meetings, strategy discussions, timing) and is expected to resolve issues and escalate problems as necessary. Â The SMW is also responsible for tracking projects and for adhering to regulatory guidelines and document standards.
Job Duties:
•   Works independently and with team members to create and review the content of within-scope documents. These may include CSRs, Protocols, protocol amendments, ICFs, narratives, IBs and IB updates in a variety of therapeutic areas. The Medical Writer is expected to drive document development, track deliverables and ensure timely document completion.
•   Writes or contributes to other Regulatory documents such as Clinical Summaries and Briefing Documents.
•   Represents Medical Writing at project meetings
   ? Drives document development;
   ? Articulates document strategy and timelines;
   ? Understands decision-makers and works to keep discussions focused.
   ? Synthesizes key messages and presents clear, accurate text for discussion.
• Solves problems, fosters collaboration, resolves conflict
Skills:
Experience Needed:
•   12+ Years of experience of industry experience
•   Ability to work independently
•   Strong knowledge of the clinical research process and regulations/guidelines required. Scientific and technical reading, writing and editing skills required.
•   Well-developed organizational, interpersonal and communication skills, and the ability to develop and present varied and unique ideas.
 • Good working knowledge of MS WORD, Adobe Acrobat, Project, Powerpoint and use of one or more electronic document management systems
Education:
BA or BS Advance Degree
*CO/NYC candidates might not be considered
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