Part-Time Clinical Research Coordinator — Data & Patient Care

Redbock - an NES Fircroft company; Pleasanton (CA); On-site; USD 34,000 - 50,000; Part time

Job summary

Redbock - an NES Fircroft company is seeking a part-time Clinical Research Coordinator in Pleasanton, CA, to support an ongoing study. You will coordinate patient-facing activities, manage start-up tasks, handle source documentation, and oversee data entry and supply logistics.

The ideal candidate has 1–3 years as a CRC, experience with human subjects and data collection, and strong EDC/system skills. This role emphasizes independent work, reliability, and clear communication in a fast-paced

Qualifications

• 1–3 years experience as a Clinical Research Coordinator in life sciences.
• Experience with human research participants and clinical trial data collection.
• Strong proficiency with EDC systems and clinical trial technology.
• Tech-savvy with the ability to quickly learn new systems, software, and processes.
• Excellent written, verbal, and interpersonal communication.
• Ability to work independently, efficiently, and ramp up quickly in a fast-paced environment.
• Medical device experience preferred, but not required.

Responsibilities

• Schedule study visits with patients and confirm appointments.
• Manage source documents and correct paper-based records.
• Track and handle clinical supplies for patients.
• Conduct remote evaluations and distribute patient surveys per protocol.
• Enter data into the EDC and resolve data queries.
• Follow up on adverse events and escalate as needed.
• Maintain professional communication with patients, investigators, and internal teams.
• Ensure compliance with protocol, GCP, and study documentation.

Skills

CRC coordination

Data management

Communication

Independent work

Tech-savvy

Tools

EDC systems

Job description

Redbock - an NES Fircroft company is seeking a part-time Clinical Research Coordinator in Pleasanton, CA, to support an ongoing study. You will coordinate patient-facing activities, manage start-up tasks, handle source documentation, and oversee data entry and supply logistics.

The ideal candidate has 1–3 years as a CRC, experience with human subjects and data collection, and strong EDC/system skills. This role emphasizes independent work, reliability, and clear communication in a fast-paced