Remote Contract Medical Writer for Clinical Trials

Ergclinical; Idaho; Remote; USD 83,000 - 124,000; Full time

Benefits offered by this job

Remote work

Job summary

Ergclinical is seeking a Contract Medical Writer to support writing and editing of protocols, investigator brochures, clinical study reports, and IND submissions for Phase I–IV trials. You will help develop corporate practices for document handling and ensure regulatory compliance across study documents, with strong collaboration across multiple functions.

Ideal candidates have at least 5 years in medical writing, experience with regulatory submissions, and knowledge of GCP/ICH guidelines, SOP

Qualifications

• BS/BA in a health-related or life science field; Master’s preferred.
• Minimum 5 years of medical writing experience.
• Experience designing and analyzing clinical studies.
• CRO industry experience preferred.

Responsibilities

• Collaborate with cross-functional teams including Regulatory Operations and Project Management.
• Develop and maintain study protocols and writing templates.
• Lead preparation of regulatory documents and trial reports (IND, protocols, CRFs).
• Ensure documentation complies with regulatory requirements (GCP/ICH).
• Coordinate activities per SOPs and manage project timelines.

Skills

Medical writing

Clinical trials documentation

Regulatory guidelines (GCP/ICH)

Project coordination

Microsoft Office

Education

BS/BA in life sciences or health-related field

Master’s degree preferred

Tools

Microsoft Office

Job description

Ergclinical is seeking a Contract Medical Writer to support writing and editing of protocols, investigator brochures, clinical study reports, and IND submissions for Phase I–IV trials. You will help develop corporate practices for document handling and ensure regulatory compliance across study documents, with strong collaboration across multiple functions.

Ideal candidates have at least 5 years in medical writing, experience with regulatory submissions, and knowledge of GCP/ICH guidelines, SOP