ONSITE - Charlottesville, Virginia 22911
DIRECT HIRE
Clinical Research Coordinator
Job Description
Responsibilities/ Job Duties:
- Obtaining vital signs and ECGs;
- May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
- Screening of patients for study enrollment;
- Patient consents;
- Patient follow-up visits;
- Documenting in source clinic charts;
- Entering data in EDC and answers queries;
- Requesting and tracking medical record requests;
- Updating and maintaining logs, chart filings;
- Maintaining & ordering study specific supplies;
- Scheduling subjects for study visits and conducts appointment reminders;
- Building/updating source as needed;
- Conducting monitoring visits and resolves issues as needed in a timely manner;
- Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
- Filing SAE/Deviation reports to Sponsor and IRB as needed;
- Documenting and reporting adverse events;
- Reporting non-compliance to appropriate staff in timely manner;
- Maintaining positive and effective communication with clients and team members;
- May assist with study recruitment, patient enrollment, and tracking as needed;
- Maintaining confidentiality of patients, customers and company information, and;
- Performing all other duties as requested or assigned.
- Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
- Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;
- May set up, train and maintain all technology needed for studies.
Minimum Education and Experience Qualification Requirements:
2+ years of experience as a Clinical Research Coordinator
Schedule/ Shift:
Monday to Thursday 7:30AM-5:30PM, Friday 8AM-12PM
40 Hours per week
