FDA Submissions Specialist Needed

Posted 4 weeks ago

Worldwide

Summary

We are seeking an experienced professional to assist with FDA submissions for new drug and medical device human trials. The ideal candidate will have a strong background in interfacing with the FDA and providing guidance on regulatory compliance. Responsibilities include preparing and submitting regulatory documents, ensuring compliance with FDA regulations, and communicating effectively with FDA representatives. If you have a proven track record in this field, we would love to hear from you.

Less than 30 hrs/week
Hourly
1-3 months
Duration
Intermediate
Experience Level
$50.00
-
$100.00
Hourly
Remote Job
Ongoing project
Project Type

Skills and Expertise

Mandatory skills

Article Writing

Content Writing

Nice-to-have skills

Blog Writing

Creative Writing

Activity on this job

Proposals:20 to 50
Last viewed by client:4 weeks ago
Interviewing:
4
Invites sent:
7
Unanswered invites:
1

About the client

Member since Apr 8, 2021

United States
Jasper2:42 AM
$7.2K total spent
3 hires, 1 active
198 hours

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