Manager, Research Studies

Position Summary

The Manager, Research Studies leads the day-to-day planning and execution of assigned studies prioritized by the ASH Research Collaborative and its Research Networks. The position manages studies working with Network investigators, industry, government, foundations, and other external or internal parties and helps ensure that each study is delivered in accordance with the approved scope, protocol, budget, timeline, data requirements, and applicable research and privacy requirements.

Working under the direction of the Deputy Director, Data Hub, the Manager collaborates with investigators, participating sites, patient and community participants, internal teams, contractors, funders, and other partners throughout the study lifecycle. The position manages research workflows, IRB and consent requirements, study start-up, site implementation, study documentation, data quality coordination, issue resolution, funder deliverables, and closeout activities. The Manager works closely with other ASH RC teams to support successful study execution.

Essential Duties and Responsibilities Research Study Planning and Execution Lead day-to-day management of assigned research studies from planning and start-up through execution, dissemination, and closeout. Translate approved study concepts, protocols, scopes of work, and funding commitments into actionable project plans, timelines, milestones, responsibilities, and deliverables. Monitor progress against protocol requirements, contractual deliverables, budgets, and timelines; identify risks early and implement or escalate corrective actions. Facilitate study meetings, document decisions and actions, and ensure timely follow-through.

Manage one or more assigned studies and priorities while maintaining visibility into workload, dependencies, and resource needs. Protocol, Regulatory, and Research Compliance Orchestrate development, review, and implementation of study protocols, research plans, data collection requirements, and study materials. Manage IRB submissions, reliance arrangements, continuing reviews, amendments, reportable events, and study closeout requirements in conjunction with investigators, sites, and designated regulatory partners. Oversee informed consent and authorization processes when applicable, including development of materials, site training, documentation expectations, and issue resolution.

Maintain complete and current study documentation, including approvals, training records, decisions, deviations, and required reports. Track protocol deviations, noncompliance, and other study issues; coordinate assessment, documentation, corrective actions, and required reporting. Ensure study activities are conducted in accordance with approved protocols, contracts, ASH RC policies, research ethics, HIPAA, data use agreements, and applicable regulatory requirements. Escalate compliance, participant safety, privacy, or data integrity concerns promptly to the appropriate leaders and experts…

Read the full posting