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Role Description

We’re hiring a Clinical Data & Operations Manager to join Ro’s Scientific Affairs team—a small, high-impact group of physicians, scientists, and data experts shaping how clinical credibility is built in modern healthcare.

You’ll work at the intersection of clinical science, data, and operations—combining hands-on study execution with rigorous data review and analytics. Your work will support sponsor-facing monitoring, source data verification, and reporting, ensuring studies meet the highest standards of quality, transparency, and regulatory rigor.

You’ll collaborate closely with physicians, PhDs, and clinical experts who care deeply about scientific integrity and patient impact. Together, you’ll generate evidence that fills critical gaps left by traditional trials and informs how therapies are evaluated and used in real-world care. Operating within GCP, sponsor expectations, and regulatory frameworks, you’ll play a key role in translating high-quality data into insights that are trusted and actionable.

This is a role for someone who wants more than operational excellence alone—it’s an opportunity to contribute to evidence that is consequential. Your work will influence partners, practitioners, and internal leadership, and help strengthen Ro’s position as an evidence-driven leader in healthcare innovation.

If you’re motivated by rigor, impact, and the chance to help define how real-world evidence is generated and applied at scale, this role was built for you.

Qualifications

• Bachelor’s degree in health sciences, life sciences, statistics, data science, or a related field, or equivalent experience
• 5-7 years of experience in clinical research, research operations, or data operations within a pharmaceutical company, contract research organization (CRO), or pharma-sponsored research environment
• Hands-on experience supporting sponsor monitoring, SDV, or data reconciliation activities
• Strong working knowledge of SQL and experience querying relational databases for study monitoring and validation
• Familiarity with GCP, ICH guidelines, and sponsor expectations for data quality and documentation
• Strong analytical, documentation, and communication skills

Requirements

• Experience supporting RWE, observational studies, or post-marketing research for pharmaceutical sponsors
• Experience building or validating dashboards in BI tools (e.g., Hex)
• Experience working with safety data, lab data, EHR-derived data, or patient-reported outcomes
• Prior experience interacting directly with sponsors, CROs, or monitors during audits or data reviews
• Completion of required GCP and human subjects protection training prior to study involvement, with re-certification as required

Benefits

• Full medical, dental, and vision insurance + OneMedical membership
• Healthcare and Dependent Care FSA
• 401(k) with company match
• Flexible PTO
• Wellbeing + Learning & Growth reimbursements
• Paid parental leave + Fertility benefits
• Pet insurance
• Student loan refinancing
• Virtual resources for mindfulness, counseling, and fitness