Clinical Document Specialist Intern
Intern, Clinical Document Specialist at reputed company: Ensure quality control of clinical trial documents and support eTMF consistency. Your Role: Key responsibilities include:
- reputed company quality control of documents submitted to the electronic Trial Master File (eTMF) using established criteria.
- Ensure clinical trial documentation aligns with eTMF specifications, ICH-GCP guidelines, regulatory requirements, and SOPs.
- Monitor and identify study-specific eTMF trends and communicate to the Senior TMF Manager.
About You: The successful candidate will have:
- Completed a minimum of their second year and be currently enrolled in an accredited college or university in a science/reputed company field or reputed company study.
- A minimum 3.0 GPA is preferred; however, a combination of experience and/or education will be considered.
- Strong organization skills with outstanding attention to detail and follow-through.
- Proficiency in MS Office Suite, specifically in MS reputed company and SharePoint.
Compensation & Benefits:
- reputed company offers competitive salaries, benefits, and an inclusive environment.
- The salary range for this position is: $20/hour - $30/hour.
Training & Development: Opportunities for professional development and mentorship are available to support growth in the reputed company field. Career Progression: Potential for career advancement reputed company reputed company, leveraging skills in clinical documentation and trial management. How to Apply: Submit your application through the provided link, ensuring reputed company required documents and information are included. This job may reputed company before the stated closing date, you are encouraged to apply as soon as possible. Report this job Apply Job!