Collecting interest
Pharmacovigilance / Safety Specialist
Adverse-event reporting, MedDRA coding, and safety narratives under GCP/safety training.
Paid or volunteer, your choice. Every position can be filled as paid work or offered as volunteer service. If you would like to help the cause, you are welcome to volunteer your time in any capacity.
- Compensation
- Paid or volunteer
- Participant-facing
- No
- Credential required
- No
- Training before activation
- Yes
- Conflict review
- Standard disclosure
- Reviewed by
- Clinical leadership
What your application includes
- Profile & contact
- Clinical-trial experience
- Conflict-of-interest disclosure
- Document uploads
What to have ready
A CV or résumé is part of every profile. For this role, also have:
- GCP / HSP training certificate
- Research certifications (SOCRA / ACRP, if any)
- Safety narrative sample (redacted)
What we’ll ask you
These roles exist to protect participants even against the study's own momentum. Everyone also answers a few shared questions on research integrity and why this work. You answer these in your private portal after verifying your email — a reviewer reads them, and they’re never scored by a machine.
- How do you think about a stopping rule? What evidence would make you halt or pause a study, and how do you protect your independence in that judgment?
- How do you handle a sponsor, PI, or institution that resists a safety recommendation you believe is right?
- What financial, professional, or personal ties might affect your independence in this role, and how would you manage them?
- Tell us about your adverse-event or safety-monitoring experience, especially a case where your judgment changed a study's course. (optional)
Never upload Social Security numbers, tax or bank details, or patient records. Herbal Trials does not sell supplements, make efficacy claims, or provide medical advice, and does not endorse any substance. Candidate substances remain unverified until studied.