Scientist, Protein Design
Moderna · Cambridge, MA +1 more
ResearchFull-time$109k–$175kCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
What they're looking for
- Minimum 5 years of trial coordination experience in clinical research industry
- Bachelor's degree in science-based subject; advanced degree preferred
- Understanding of FDA and ICH GCP guidelines for clinical study conduct
- Solid knowledge of drug development processes
- Project management skills with excellent organizational abilities
- Strong verbal and written communication skills
- Experience in global clinical trial settings
What you'll be doing
- Manage assigned clinical trials to ensure quality, compliance, and timely delivery of all deliverables
- Oversee feasibility processes and coordinate with internal teams on study execution and timelines
- Draft and maintain site materials including training documentation and support resources
- Monitor clinical data entry, review periodic data quality, and support data review meetings
- Ensure trial compliance with Moderna and ICH/GCP standards across multiple global regions
Privacy & handoff
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