Ground every answer in facts on this page and the original listing. We never invent Glassdoor-style reviews or salaries that are not in our data.
Strong fit if you have senior clinical data management experience, comfort directing CROs (not only executing data entry), and early-phase study fluency. Less fit if you want pure remote work (listing is non-remote) or lack vendor-oversight depth.
As Senior Data Manager, CRO Oversight for early-phase studies through Eliassen Group, expect to own clinical data integrity across CRO partners: review EDC/data plans, chase query aging and protocol deviations, align vendors on SDTM/CDISC readiness, and escalate risk to study leads before database lock.
Role-aligned skills (no cert list supplied): early-phase clinical data management, CRO vendor oversight, EDC/query management, protocol and data-management plan review, and cross-functional escalation with clinical operations. No certification costs in DATA.
No. The listing marks remote as off; location is Frankfort, Franklin County, Kentucky.
Eliassen places and supports technology and life-sciences talent; this title points to clinical data leadership with CRO oversight on early-phase work.
None in the provided DATA—no salary bands, Glassdoor/Indeed ratings, or occupation wage stats.
Website: eliassen.com
Public cache only — not an employee review.
Eliassen Group - Senior Data Manager, CRO Oversight, Early Phase Studies - Frankfort, Franklin County Role Overview The Eliassen Group is seeking a Senior Data Manager to provide operational support across multiple early-phase clinical studies. This role will oversee Contract Research Organization (CRO) oversight and ensure the integrity of data management processes. Day-to-Day Responsibilities Provide comprehensive CRO oversight for early-phase clinical trials, ensuring adherence to regulatory standards and quality control measures. Manage and maintain accurate data records, ensuring compliance with Good Clinical Practice (GCP) guidelines. Collaborate with cross-functional teams to ensure timely and efficient study execution. Develop and implement data management strategies that support the overall success of clinical trials. Ensure all data is properly documented and stored in a secure, compliant manner. Requirements Minimum 8 years of experience as a Data Manager or related role within the pharmaceutical or biotechnology industry. Proven track record in CRO oversight for early-phase clinical studies. Strong understanding of GCP and regulatory requirements. Excellent communication, organizational, and problem-solving skills. PMP certification is a plus but not required. Working at Eliassen Group Eliassen Group offers a dynamic work environment with opportunities for professional growth. Our client values collaboration, innovation, and integrity in all aspects of their operations. Ready to Apply? To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.
Generated for personal interview prep · 2026-08-03 UTC · getajob.ai