What are the responsibilities and job description for the Clinical Research Coordinator position at Nira Medical?
Central Texas Neurology Consultants is seeking an experienced Clinical Research Coordinator (CRC) to manage Neurology studies. Responsibilities include, but are not limited to EDC data entry, scheduling, chart preparation, conducting rating scales, collecting vital signs, blood draws, and ECGs.
Key duties include but not limited to :
- Responsible for the integrity and overall quality of assigned clinical research trials
- Serves as the primary contact for study subjects and sponsors, communicating daily as needed.
- Reviews study protocols and brochures; creates study document binder and prepares source documents including study and subject information folders.
- Attend sponsor meeting as needed for assigned protocols.
- Oversee sponsor database process.
- Completes study procedures including :
- Pre-screening, screening, and study visits in conjunction with Physician / Investigator (may include vital signs, performing EKG's, phlebotomy, processing specimens and shipping to labs).
- Documentation of patient progress in response to investigative agents.
- Coordination of monitor visits with patients.
- Completion of source documents and case report forms.
- Oversee preparation of physician orders to ensure protocol compliance as needed.
- Maintain communication with physician regarding study requirements, dose modifications, and adverse events.
- Upkeeps all trial regulator documentation.
- Maintain high level of understanding of the ICH / GCP guidelines.
- Perform other related duties as assigned
Qualifications
Preferred :
What We Offer
