Clinical Research Coordinator 227013
We are looking to add a CRC to our growing team- if you enjoy a collaborative environment and are looking for a company with a ton of room for growth- join our team! We offer a competitive salary and great benefits!
Qualified candidates will have at a minimum 3-4 years of experience working in therapeutic clinical trials.
Responsibilities include :
- Maintaining thorough knowledge of study-specific inclusion / exclusion criteria
- Performing safety and efficacy assessments per protocol
- Vital signs, EKGs, and other assessments as assigned
- Accurate and timely completion of source documents recording participant’s participation in the study
- Communicate closely with all departments to ensure study visits are coordinated in compliance with protocol and GCP guidelines
- Assist investigators in the collection of information from participants regarding AEs, concomitant medications, and other changes throughout participation
- Responsible for timely data entry and query resolution
- Timely reporting of study events (SAEs, protocol deviations, etc.)
- Following subjects through study completion and creating a follow-up care plan with a physician, study subject, and primary care provider;
- Ensuring preparation for and facilitating of all study monitoring visits and following up promptly with monitor follow-up letters
- Prompt and professional communication with sponsors, representatives, and other study-related parties
- Maintaining professional and appropriate interactions with study subjects, caregivers, sponsors, and all other study-related personnel, and staff members
- Interacting with nursing / unit staff on a daily basis as applicable to ensure communication and accurate completion of source through daily chart review
- Keeping CTM informed of study status and any study-related issues
- Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials
Clinical Research Coordinator 227013
Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials. Qualified candidates will have at a minimum 3-4 years of experience working in therapeutic clinical trials. ...
Clinical Research Coordinator 227013
Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials. Qualified candidates will have at a minimum 3-4 years of experience working in therapeutic clinical trials. ...
Clinical Research Coordinator - 227013
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