Company: Thermo Fisher Scientific
Experience: 1-3 years | Salary: INR 5-7 Lakhs
Education: B.Pharm, M.Pharm, M.Sc, B.Sc, Pharm.D
Location: Work From Home
Description:
Join our Clinical Research Services team at Thermo Fisher Scientific, supporting safety and regulatory document coordination with precision and confidentiality.
Responsibilities:
| Responsibilities | Details |
|---|---|
| Review safety and regulatory documents | Ensure accurate processing and timely uploads to electronic trial master files. |
| Maintain document quality and confidentiality | Track data, redact sensitive information, and ensure compliance with IT security standards. |
| Coordinate project meetings and facilitate communication | Ensure effective collaboration and support project-specific training and audit readiness. |
| Manage project expenses and budget | Oversee expenses, manage translations, and ensure cost-efficiency while adhering to budget parameters. |
| Archive regulatory documents and submissions | Contribute to seamless information flow and compliance by archiving essential documents and submissions accurately. |