Regulatory and Start Up Specialist

Precision for Medicine(1 month ago)

RemoteFull TimeJunior$56,680 - $76,037 (estimated)Regulatory Affairs

About this role

The Regulatory and Start Up Specialist at Precision for Medicine supports regulatory activities and site start-up efforts to ensure timely site activation and compliance with international and local clinical trial regulations. The role coordinates submissions to Competent Authorities and Ethics Committees, maintains project trackers and regulatory intelligence, and partners with clinical teams and sites. This position contributes to document management, translation coordination, and audit readiness to enable the conduct of clinical trials in oncology and rare diseases.

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Required Skills

Regulatory Submissions
Site Activation
Authority Interaction
Project Tracking
Document Review
Consent Customization
Translation Coordination
Budget Negotiation
Contract Negotiation
Audit Readiness

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Qualifications

Bachelor's Degree in Life Sciences
Registered Nurse (RN)
Pharmacy Qualification
MD
PhD
PharmD
RAC Certification
Masters in Regulatory Science

About Precision for Medicine

precisiongroupcompanies.com

The site is currently a placeholder that immediately redirects to /lander and contains no public content describing the company. Presuming it's a web-focused startup, it likely offers a SaaS platform to help businesses build high-converting landing pages and marketing funnels. Typical offerings would include a drag-and-drop page builder, A/B testing, analytics, and integrations with CRMs and email platforms to drive lead generation. Customers would be small-to-medium businesses and marketing teams seeking easy onboarding, template libraries, and conversion optimization tools.

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