Job Description:

Location: Paramus, NJ

Salary: TBD

Description: Our client is currently seeking a Senior Medical Writing Manager


Responsible for authoring and overseeing the completion of a broad range of clinical development documents in support of company products and projects.

This individual will work with a cross functional global study team to author and edit documents.



Responsibilities:


(Include but not limited to the following. Other duties may be assigned)

• Write and edit clinical development documents companywide for sense, clarity, accuracy.


• Manage clinical development documents, create and maintain document timelines, as well as ensuring that documents comply with SOPs as well as external regulatory requirements.


• Provide writing support for a wide range of documents, including investigator's brochures, clinical study protocols and reports, integrated summaries, informed consent documents, and SOPs.

Qualifications:

• Exceptional English language skills and ability to write and edit complex material to ensure accuracy, clarity, and effectiveness.


• Clear understanding of authoring for clinical development documents


• A solid understanding of the clinical development process, including the documents that are required at each stage.

Contact: bchauhan@judge.com


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