Clinical Research Coordinator (Part-Time)

Overview

Our client needs a Part-Time (20-30 hours per week) Clinical Research Coordinator (CRC) to support an ongoing study. This role is responsible for patient-facing coordination, study start up, source documentation, data management, and handling clinical supplies. The ideal candidate is highly organized, comfortable engaging with patients, and experienced in EDC-based clinical trial support. 2-3 days onsite per week in Pleasanton, CA required.

Key Responsibilitie

• sContact patients to schedule study visits, confirm appointments, and ensure visit completion
• .Properly handle source documents and make necessary corrections paper based documents
• .Track, prepare, and handle clinical supplies going in and out to patients
• .Conduct remote evaluations and distribute patient surveys per protocol requirements
• .Perform timely and accurate data entry into EDC and resolve data queries
• .Follow up on adverse events, collect relevant information, and escalate as needed
• .Maintain clear, professional communication with patients, investigators, and internal teams
• .Ensure compliance with protocol, GCP, and study documentation requirements

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Qualificatio

• ns1-3 years experience as a Clinical Research Coordinator with a life science organization (preferable medical device
• ).Strong comfort interacting with patients via phone, video, and electronic tool
• s.Proficiency with EDC systems and general clinical trial technolog
• y.Excellent written, verbal, and interpersonal communication skill
• s.Clinical documentation and data management experience and training on best practice
• s.Ability to work independently and learn quickly in a fast-paced environmen