Proclinical is seeking a Remote Medical Writer for a leading biopharmaceutical company located.
Must be eligible to work in the US.
Job Responsibility
- Perform quality control (QC) review of clinical study reports and other documents written by other Medical Writers.
- Work with colleagues from various functional areas in Clinical Development, Clinical Operations, Medical Science, Medical Affairs, Regulatory, and Program Management to ensure high quality clinical and regulatory documents are prepared and submission ready, including protocols, study reports, investigator brochures, etc. according to company and agency guidelines in order to support drug development under strict timelines.
- Work effectively with company document management system and related tools, templates, and procedures in order to ensure efficient production and publishing of documents and dossiers.
If you are having difficulty in applying or if you have any questions, please contact Janelle Jones at (+1) 267– 297– 3257 or j.jones@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
Proclinical Staffing is an equal opportunity employer.