The Clinical Regulatory Content Writer (1099 Contractor) – Hospice has the primary responsibility to draft and update hospice regulatory policy content for incorporation into HealthCare ConsultLink on...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

Title: Sr Regulatory Writer R&D Location: Park Ridge, NJ area Schedule: M-F Full Time Type: Direct Hire Responsibilities: Our client is seeking Regulatory writing support for New and Existing Produc...

Title: Sr Regulatory Writer R&D Location: Park Ridge, NJ area Schedule: M-F Full Time Type: Direct Hire Responsibilities: Our client is seeking Regulatory writing support for New and Existing Produc...

Title: Sr Regulatory Writer R&D Location: Park Ridge, NJ area Schedule: M-F Full Time Type: Direct Hire Responsibilities: Our client is seeking Regulatory writing support for New and Existing Produc...

Title: Sr Regulatory Writer R&D Location: Park Ridge, NJ area Schedule: M-F Full Time Type: Direct Hire Responsibilities: Our client is seeking Regulatory writing support for New and Existing Produc...

Title: Sr Regulatory Writer - R&D. Works closely with clinical development teams, including clinical scientists, clinical affairs, regulatory affairs, biostatistics, physicians, and medical affairs, t...

Title: Sr Regulatory Writer - R&D. Works closely with clinical development teams, including clinical scientists, clinical affairs, regulatory affairs, biostatistics, physicians, and medical affairs, t...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

Drafts eCTD written and tabulated summaries, investigator brochure content, FDA briefing packages, and other agency related technical documents, in collaboration with Regulatory teams. Works closely w...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Senior Writer will lead and drive the technical (CMC) writing to accelerate the development of small molecules, combination drug/device products, and other innovative materials for areas with high...

Title: Sr Regulatory Writer - R&D. Our client is seeking Regulatory writing support for New and Existing Product Development (NPD/EPD) pipeline for products in the drug (OTC, DIN, NHP), medical device...

Title: Sr Regulatory Writer - R&D. Coordinating reporting needs with project teams, regulatory strategies, and product development timelines. Works closely with clinical development teams, including c...

Title: Sr Regulatory Writer - R&D. Coordinating reporting needs with project teams, regulatory strategies, and product development timelines. Drafts eCTD written and tabulated summaries, investigator ...

Title: Sr Regulatory Writer - R&D. Coordinating reporting needs with project teams, regulatory strategies, and product development timelines. Drafts eCTD written and tabulated summaries, investigator ...

Title: Sr Regulatory Writer – R&D Location: Park Ridge, NJ area Schedule: M-F Full Time Type: Direct Hire Responsibilities: Our client is seeking Regulatory writing support fo...

Title: Sr Regulatory Writer – R&D Location: Park Ridge, NJ area Schedule: M-F Full Time Type: Direct Hire Responsibilities: Our client is seeking Regulatory writing support fo...

Drafts eCTD written and tabulated summaries, investigator brochure content, FDA briefing packages, and other agency related technical documents, in collaboration with Regulatory teams. Works closely w...

Drafts eCTD written and tabulated summaries, investigator brochure content, FDA briefing packages, and other agency related technical documents, in collaboration with Regulatory teams. Works closely w...

Title: Sr Regulatory Writer – R&D. Our client is seeking Regulatory writing support for New and Existing Product Development (NPD/EPD) pipeline for products in the drug (OTC, DIN, NHP), m.

Title: Sr Regulatory Writer – R&D. Our client is seeking Regulatory writing support for New and Existing Product Development (NPD/EPD) pipeline for products in the drug (OTC, DIN, NHP), m.

Title: Sr Regulatory Writer - R&D. Drafts eCTD written and tabulated summaries, investigator brochure content, FDA briefing packages, and other agency related technical documents, in collaboration wit...

Title: Sr Regulatory Writer - R&D. Our client is seeking Regulatory writing support for New and Existing Product Development (NPD/EPD) pipeline for products in the drug (OTC, DIN, NHP), medical device...

Nonclinical Regulatory Document and Scientific Writer,. Assist with quality review of DMPK reports that are generated by DMPK scientists by fully reviewing the raw data outputs/electronic notebooks an...

Assist with quality review of DMPK reports that are generated by DMPK scientists by fully reviewing the raw data outputs/electronic notebooks and ensuring validity and quality of reported data in the ...

POSITION Nonclinical Regulatory Document and Scientific Writer. Assist with quality review of DMPK reports that are generated by DMPK scientists by fully reviewing the raw data outputs/electronic note...

Join our team as a Nonclinical Regulatory Document and Scientific Writer, where you'll be a key player in authoring, reviewing, and tracking regulatory documents. Job Title: Nonclinical Regulatory Doc...

Join our team as a Nonclinical Regulatory Document and Scientific Writer, where you'll be a key player in authoring, reviewing, and tracking regulatory documents. Job Title: Nonclinical Regulatory Doc...

POSITION Nonclinical Regulatory Document and Scientific Writer. Assist with quality review of DMPK reports that are generated by DMPK scientists by fully reviewing the raw data outputs/electronic note...