Job Description
Job Description
First Assistant – Problem-Solver & Key Support
Role Overview
Thet Assistant is the person , ensuring smooth study operations, compliance, and patient safety. This role requires a task-oriented, problem-solving mindset, not prior experience. The ideal candidate is proactive, detail-oriented, and eager to learn.
Key Responsibilities
Study Execution & Oversight
- Ensure all study tasks are completed on time & correctly.
- Support the PI in daily trial operations and problem-solving.
- Verify that protocols & study procedures are followed correctly.
Regulatory Compliance & Documentation
- Keep the Regulatory Binder & essential documents updated.
- Ensure investigational drug accountability & compliance.
- Assist in audit preparation & monitor visits.
Patient Safety & Data Integrity
- Ensure proper informed consent and protocol adherence.
- Monitor and document adverse events & safety reports.
- Maintain accurate & ALCOA+ compliant data.
Communication & Site Coordination
- Be the main problem solver & point of contact for staff, sponsors, and monitors.
- Respond quickly to monitor queries & site issues.
- Assist in scheduling, reports, and resolving study challenges.
Who Should Apply?
✅ No prior experience needed – we train the right person.
✅ Must be organized, detail-oriented & great at problem-solving.
✅ Comfortable handling challenges & working in a fast-paced environment.
✅ Interested in clinical research & regulatory processes.
Why Join?
Work directly with the PI & industry experts.
Gain fast-track training & career growth in clinical trials.
Learn how to manage trials, compliance & study operations.
This is a high-impact role for someone who wants to grow fast in clinical research without prior experience—we’re looking for intelligence, problem-solving, and strong attention to detail!