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AdventHealth · 1 day ago

Clinical Research Data Coordinator I Oncology

Altamonte Springs, FL

Full-time

Onsite

New Grad, Entry Level

$44K/yr - $81K/yr

AdventHealth is a community-focused organization committed to uplifting individuals in body, mind, and spirit. They are seeking a Clinical Research Data Coordinator I Oncology to obtain and manage protocol-required information, assist with data collection and reporting, and ensure compliance with research guidelines.

Health CareHospitalOnline Portals

Responsibilities

Obtains essential protocol-required information as outlined by the approved study protocol and within contractual obligations

Assists with the identification, collection, and reporting of protocol deviations, adverse events, and serious adverse events in accordance with ICH, CFR, GCP, and protocol-specific guidelines

Ensures PI signatures on eCRFs and ensures all study investigators complete applicable EDC training

Contributes to tasks related to site monitor visits and/or audits conducted by the institution, industry sponsors, the FDA, and other authorities

Corresponds with personnel at external institutions to ensure timely and specified data acquisition

Onboards and precepts new team members

Manages accurate and timely retrieval and electronic data entry submission of protocol-driven data points to relevant research sponsors/organizations

Abstracts and records essential physical and test data from internal and external sources

Maintains a tracking system of study participants at relevant time points

Conducts follow-up visits and data searches to maintain smooth operational flow

Prepares and provides participant status reports to leadership as requested

Completes and maintains sponsor training and certifications on protocol-specific Electronic Data Capture (EDC) systems and portals

Contributes to ongoing research activities by meeting with study sponsor monitors, CRCs, and Principal Investigators to review study data and resolve data queries

Other duties as assigned