Excelya is seeking a Quality Control Specialist (Medical Writing) for a remote, part-time position based in India. This role offers an exciting opportunity to contribute to clinical research through meticulous editing and quality control of medical and regulatory documents.
Responsibilities of the Role
As a Quality Control Specialist, your primary responsibilities will include:
- Document Review & Editing
- Review and edit various medical and clinical regulatory documents such as clinical study protocols, informed consent forms, clinical evaluation reports, and journal manuscripts.
- Ensure compliance with Excelya’s SOPs and client-specific guidelines.
- Quality Control Activities
- Verify accuracy in data, references, grammar, and formatting across documents.
- Check for consistency within and across documents, ensuring appropriate links and compliance with industry guidelines.
- Collaboration
- Provide quality review feedback to medical writers and other team members.
- Resolve QC findings through clear communication and teamwork.
Qualifications Required
- A university graduate in life sciences or an equivalent field. Post-graduate studies are an advantage.
- 1–5 years of experience as a QC Specialist, Editor, or Medical Writer in clinical regulatory documents.
- Proficiency in ICH regulations, CONSORT, STROBE, and PRISMA guidelines.
Essential Skills
- Advanced English language proficiency (written and verbal).
- Strong analytical and data interpretation skills.
- Attention to detail and a strong work ethic.
- Intellectual curiosity, creativity, and adaptability to dynamic environments.
