Clinical Research Coordinator- Part Time

Redbock, an NES Fircroft company, is seeking a part-time Clinical Research Coordinator to support an ongoing clinical study. The role coordinates patient visits, study start-up activities, source documentation, clinical supplies, data entry, adverse-event follow-up, and compliance with protocol and GCP requirements.

Pharmaceutical

• Biotechnology
• Consulting
• Medical Device
• Insider Connection @Redbock - an NES Fircroft company
• 2 email credits available today
• Beyond your network
• Cathy Zeier
• Principal Recruitment Consultant
• From your previous company
• & 2 connections
• Previously@undefined and...

Responsibilities

• Contact patients to schedule study visits, confirm appointments, and ensure visit completion
• Properly handle source documents and make necessary corrections to 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

Preferred

• Medical device experience
• Redbock is a consultancy that delivers customized resourcing solutions to pharmaceutical, biotechnology, medical device and diagnostics companies.
• Cupertino, California, USA
• http://redbock.com/
• H1B Sponsorship
• Data Powered by
• Distribution of Different Job Fields Receiving Sponsorship
• Represents job field similar to this job
• Customer Service and Support
• Engineering and Development
• Legal and Compliance
• Management and Executive
• Trends of Total Sponsorships
• *2026
• (4)
• 2025
• (8)
• 2024
• (5)
• 2023

Qualifications

• 1–3 years experience as a Clinical Research Coordinator with a life science organization
• Experience working with human research participants and clinical trial data collection
• Strong proficiency with EDC systems and general clinical trial technology
• Tech-savvy with the ability to quickly learn new systems, software, and processes
• Comfortable reviewing data/files, navigating study documentation, and locating information independently
• Clinical documentation and data management experience and training on best practices
• Excellent written, verbal, and interpersonal communication skills
• Ability to work independently, efficiently, and ramp up quickly in a fast-paced environment
• Medical device experience
• 1–3 years experience as a Clinical Research Coordinator with a life science organization.

Required skills

• Clinical Research Coordination, Human Research Participant Management, Clinical Trial Data Collection, Electronic Data Capture (EDC) Systems, Clinical Documentation, Clinical Data Management, Medical Device Research

Preferred skills

• Medical device experience, Cupertino, California, USA, http://redbock.com/, H1B Sponsorship, Data Powered by, Distribution of Different Job Fields Receiving Sponsorship, Represents job field similar to this job, Customer Service and Support, Engineering and Development, Legal and Compliance, Management and Executive, Trends of Total Sponsorships, *2026, (4), 2025, (8), 2024, (5), 2023, (1), 2022, 2021, 2020, (9), Growth Stage, Total Funding, unknown, 2018-06-20, Acquired, Company data provided by

Experience

• 1-3 years