Collecting interest
IND / FDA Submissions Specialist
IND preparation, eCTD familiarity, and FDA correspondence.
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
- No
- Conflict review
- Standard disclosure
- Reviewed by
- Regulatory & QA
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:
- Writing sample
- Portfolio (if applicable)
- IND submission example (redacted)
What we’ll ask you
Not box-checking — genuine protection of participants and integrity. 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.
- Walk us through how you'd think about whether a botanical study triggers IND requirements, and how you'd handle the uncertainty there.
- Describe a time you held a line on participant protection, quality, or regulatory compliance when it was inconvenient or unpopular.
- How do you approach an IRB submission, a reportable event, or a CAPA so it genuinely protects participants rather than just satisfies a checklist?
- Tell us about your regulatory, IRB/HRPP, or quality experience and the most consequential issue you handled. (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.