BioSpace
Associate Director of Clinical Data Management
BioSpace, Salt Lake City, Utah, United States, 84193
Associate Director of Clinical Data Management
Join as the Associate Director of Clinical Data Management at BioSpace, leading end‑to‑end Clinical Data Management activities across multiple studies and programs.
In This Role, You Will
Lead end‑to‑end Data Management activities, manage outsourced programs, and oversee vendor deliverables.
Represent Data Management in Clinical Study Meetings and align expectations with CROs and Recursion.
Coordinate EDC setup, database migrations, UAT, and system integration for IRT, ePRO, and other platforms.
Establish Vendor Oversight Plans and conduct Data Quality Reviews to harmonize processes across studies.
Serve as SME for data standardization, CRF development, and integration plans, providing metrics and solutions for data handling.
Develop and maintain Data Management documents: CDMP, CCGs, Data Review Plans, edit checks, listing checks, integration specs, transfer specs, reconciliation plans, coding guidelines, and lock checklists.
Ensure data collection meets SDTM requirements and collaborates on data flow design across EDC and non‑EDC sources.
Maintain trial master file activities and manage external Data Management budgets.
Support clinical Data Management SOPs, work instructions, and compliance with GCP, regulatory guidelines, and CDM guidance.
Experience You’ll Need
Bachelor’s degree in science, mathematics, or computer science.
12+ years of experience in the biopharmaceutical industry with proven asset management and people leadership.
Experience managing external data and third‑party vendors.
Strong knowledge of regulations and guidelines governing clinical trials.
Excellent written and verbal communication with ability to work collaboratively.
Working Location & Compensation This position can be based at or near our offices in Salt Lake City or New York City.
Annual base: $189,000 – $244,000 USD for U.S. candidates.
Eligible for annual bonus, equity, and a comprehensive benefits package.
The Values We Hope You Share
We act boldly with integrity, take calculated risks while upholding ethics.
We care deeply, showing up, speaking honestly, and taking action.
We learn actively, adapt rapidly, and embrace iteration.
We move with urgency to accelerate patient impact.
We take ownership and accountability, enabling trust and autonomy.
We are One Recursion – collaborating with trust, clarity, humility, and impact.
More About Recursion Recursion (NASDAQ: RXRX) is a clinical‑stage TechBio company decoding biology to radically improve lives through its unique OS platform spanning data, machine learning, and experimental scale.
Recursion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected under applicable law.
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In This Role, You Will
Lead end‑to‑end Data Management activities, manage outsourced programs, and oversee vendor deliverables.
Represent Data Management in Clinical Study Meetings and align expectations with CROs and Recursion.
Coordinate EDC setup, database migrations, UAT, and system integration for IRT, ePRO, and other platforms.
Establish Vendor Oversight Plans and conduct Data Quality Reviews to harmonize processes across studies.
Serve as SME for data standardization, CRF development, and integration plans, providing metrics and solutions for data handling.
Develop and maintain Data Management documents: CDMP, CCGs, Data Review Plans, edit checks, listing checks, integration specs, transfer specs, reconciliation plans, coding guidelines, and lock checklists.
Ensure data collection meets SDTM requirements and collaborates on data flow design across EDC and non‑EDC sources.
Maintain trial master file activities and manage external Data Management budgets.
Support clinical Data Management SOPs, work instructions, and compliance with GCP, regulatory guidelines, and CDM guidance.
Experience You’ll Need
Bachelor’s degree in science, mathematics, or computer science.
12+ years of experience in the biopharmaceutical industry with proven asset management and people leadership.
Experience managing external data and third‑party vendors.
Strong knowledge of regulations and guidelines governing clinical trials.
Excellent written and verbal communication with ability to work collaboratively.
Working Location & Compensation This position can be based at or near our offices in Salt Lake City or New York City.
Annual base: $189,000 – $244,000 USD for U.S. candidates.
Eligible for annual bonus, equity, and a comprehensive benefits package.
The Values We Hope You Share
We act boldly with integrity, take calculated risks while upholding ethics.
We care deeply, showing up, speaking honestly, and taking action.
We learn actively, adapt rapidly, and embrace iteration.
We move with urgency to accelerate patient impact.
We take ownership and accountability, enabling trust and autonomy.
We are One Recursion – collaborating with trust, clarity, humility, and impact.
More About Recursion Recursion (NASDAQ: RXRX) is a clinical‑stage TechBio company decoding biology to radically improve lives through its unique OS platform spanning data, machine learning, and experimental scale.
Recursion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected under applicable law.
#J-18808-Ljbffr