Clinical Medical Writer — CSR & Regulatory Docs

PSI CRO; United States; Sur place; USD 70 000 - 90 000; Plein temps

Résumé du poste

A leading global clinical research organization is seeking experienced professionals for medical writing roles. Candidates should have a bachelor's or master's degree in biomedical or life sciences, along with at least 2 years of experience in medical and regulatory writing. The role involves writing, editing, and reviewing clinical documentation, collaborating with project teams, and ensuring quality control. This is an opportunity to showcase your skills within a supportive and dynamic work environment.

Qualifications

• Minimum 2 years of experience in medical and/or regulatory writing.
• Experience with clinical documentation and data.
• Knowledge of FDA, ICH regulations.

Responsabilités

• Write and review clinical documentation.
• Finalize clinical study report narratives.
• Perform quality control reviews of documents.
• Collaborate with teams on patient safety narratives.

Connaissances

Medical writing

Regulatory writing

Clinical documentation

Quality Control

Formation

Bachelor's or Master's degree in biomedical or life sciences

Description du poste

A leading global clinical research organization is seeking experienced professionals for medical writing roles. Candidates should have a bachelor's or master's degree in biomedical or life sciences, along with at least 2 years of experience in medical and regulatory writing. The role involves writing, editing, and reviewing clinical documentation, collaborating with project teams, and ensuring quality control. This is an opportunity to showcase your skills within a supportive and dynamic work environment.