What are the responsibilities and job description for the Clinical Research Coordinator position at Redbock - an NES Fircroft company?
Overview
Our client needs a 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.
Key Responsibilities
- Contact 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.
Qualifications
- 1-3 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 tools.
- Proficiency with EDC systems and general clinical trial technology.
- Excellent written, verbal, and interpersonal communication skills.
- Clinical documentation and data management experience and training on best practices.
- Ability to work independently and learn quickly in a fast-paced environment