Director, Clinical Data Management (Oncology)

Location: Remote - Any State US

Salary: $220,000–$230,000 per year, plus performance-based bonus and equity.

Company

hirify.global is a biopharmaceutical company developing novel therapeutic candidates to address unmet needs in oncology and improve quality of life and survival for people with cancer.

What you will do

• Lead study-level clinical data management activities for one or more oncology clinical trials across the full data lifecycle.
• Develop and maintain data management plans, CRF completion guidelines, edit check specifications, and data transfer specifications.
• Oversee CRF design, eCRF programming, database setup, data review, query management, data cleaning, and interim and final database lock activities.
• Coordinate the integration and reconciliation of external data sources, including central laboratory, imaging, biomarker, and third-party data.
• Collaborate with Clinical Operations, Biostatistics, Medical, Regulatory Affairs, CROs, technology vendors, and external data management partners.
• Lead data working groups, support process and SOP improvements, contribute to regulatory inspections and audits, and mentor or manage team members as the organization grows.

Requirements

• Must be based in the United States; the role is remote across any US state.
• Bachelor’s degree in life sciences, data science, statistics, mathematics, computer science, health informatics, or a related field; an advanced degree is preferred.
• At least 8 years of clinical data management experience in biotech, pharmaceutical, or CRO organizations.
• At least 3 years of experience managing people, vendors, and functional teams.
• Strong working knowledge of clinical data systems, preferably Medidata Rave, and CDISC standards including SDTM and CDASH.
• Experience with third-party vendor oversight, outsourced data management, GCP, ICH, and relevant regulatory guidelines.

Nice to have

• Experience in a small biotech or startup environment.
• Familiarity with imaging, genomics, and digital endpoints in oncology trials.
• Experience supporting regulatory submissions such as NDA or BLA filings.
• Experience implementing data review tools, R Shiny apps, ePRO, wearables, or standardized data review workflows.

Culture & Benefits

• Fast-paced, hands-on environment requiring adaptability, accountability, and strategic thinking.
• Opportunity to contribute to high-impact oncology clinical trials and build improved data management processes.
• Competitive base salary, annual performance bonus, and equity plans.
• Unlimited vacation and 10 sick days annually.
• Medical, dental, and vision coverage, plus a 401(k) with company matching.