Auto req ID 5153BR
Title Medical Writer-Contingent
Job Description
This job opportunity is a temporary assignment on-site at Novo Nordisk, fully managed by Kelly Services. This is not a regular, full-time employment directly with Novo Nordisk.
• With guidance, prepares manuscripts, abstracts, scientific posters, slide presentations and other documents necessary for publication support.
• With general direction, assists and/or prepares clinical trial reports, summary documents, package inserts, and other documents that support the regulatory needs of a project.
• With guidance assist, assist in preparing internal meeting slides and minutes
• With guidance assist Biostatistics group with preparation of Key Results Meeting (KRM) slides.
• Assists other medical writers, as per project timeline and workload demands.
• Remains current with the literature in therapeutic areas.
• Works within SSC to understand and implement document preparation procedures and Standard Operating Procedures (SOPs). Understands and follows regulatory, medical legal, and other relevant guidelines. Has knowledge of, and follows, Good Publication Practices.
• With general direction, interacts with NNI and HQ publication teams, journals, editors, authors, and others as necessary to ensure the successful completion of manuscripts and other publication and regulatory projects.
• Capable of managing multiple projects and tracking.
Minimum Requirements:
• A PhD in a life science or PharmD required
• A minimum of two years relevant experience required with an M.S.
• Demonstrated scientific writing (e.g., manuscripts, research grants, etc…) ability.
• General understanding of statistical methods, ability to learn and understand regulatory requirements and drug development processes and regulatory requirements.
• Generally proficient in the use and understanding of computer software.
Department CLINICAL MEDICAL REGULATORY
Position Location US - Princeton, NJ
City Princeton
State/Provinces US - NJ
Click Here to Apply
Title Medical Writer-Contingent
Job Description
This job opportunity is a temporary assignment on-site at Novo Nordisk, fully managed by Kelly Services. This is not a regular, full-time employment directly with Novo Nordisk.
• With guidance, prepares manuscripts, abstracts, scientific posters, slide presentations and other documents necessary for publication support.
• With general direction, assists and/or prepares clinical trial reports, summary documents, package inserts, and other documents that support the regulatory needs of a project.
• With guidance assist, assist in preparing internal meeting slides and minutes
• With guidance assist Biostatistics group with preparation of Key Results Meeting (KRM) slides.
• Assists other medical writers, as per project timeline and workload demands.
• Remains current with the literature in therapeutic areas.
• Works within SSC to understand and implement document preparation procedures and Standard Operating Procedures (SOPs). Understands and follows regulatory, medical legal, and other relevant guidelines. Has knowledge of, and follows, Good Publication Practices.
• With general direction, interacts with NNI and HQ publication teams, journals, editors, authors, and others as necessary to ensure the successful completion of manuscripts and other publication and regulatory projects.
• Capable of managing multiple projects and tracking.
Minimum Requirements:
• A PhD in a life science or PharmD required
• A minimum of two years relevant experience required with an M.S.
• Demonstrated scientific writing (e.g., manuscripts, research grants, etc…) ability.
• General understanding of statistical methods, ability to learn and understand regulatory requirements and drug development processes and regulatory requirements.
• Generally proficient in the use and understanding of computer software.
Department CLINICAL MEDICAL REGULATORY
Position Location US - Princeton, NJ
City Princeton
State/Provinces US - NJ
Click Here to Apply
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