Associate, Clinical Operations (RID00214)

Experience Level: 1-10 years

Required Qualifications: Undergraduate degree or equivalent professional experience Experience operationalizing clinical study protocols, amendments, observational research studies, and registries Professional experience within biotech, pharmaceutical, CRO, clinical site, or consulting environments Knowledge of GCP, ICH, HIPAA, GDPR, FDA requirements, and clinical research regulations Experience managing multiple research projects, vendors, sponsors, sites, and stakeholders simultaneously Working knowledge of EDC, ePRO, EHR, and clinical research technologies Strong written and verbal communication skills and proficiency with Microsoft Office (Word, Excel, PowerPoint)

What You'll Do: Support studies from startup through closeout Manage sponsor, site, and vendor relationships Participate in protocol design discussions and implementation planning Develop IRB submission packages, training materials, caregiver/site manuals, and operational documentation Lead or support Site Initiation Visits (SIVs), site training, and central rater training Partner with Data Management, Product Management, and Technical Delivery teams Support UAT and product launches

Nice to Have: Digital health or mobile application experience Experience in rare diseases, gene therapy, or long-term follow-up studies Knowledge of clinical drug development pathways, including Phase I-III studies and registries Diversity, equity and inclusion are valued at Red Nucleus and we believe we have a shared responsibility to provide equal opportunity and foster an inclusive spirit. We do not discriminate on the basis of race, color, national origin, religion, caste, sexual orientation, gender, age, marital status, veteran status, or disability status.