Clinical Research Nurse – RN – IMA Clinical Research – San Antonio, TX

IMA Clinical Research is seeking an experienced Clinical Research Nurse – RN for the Diagnostics Research Group – DXRG location in San Antonio, TX!

The Clinical Research Coordinator or Clinical Research Nurse is responsible for managing the facilitation of clinical trials in collaboration with the investigative team.

Duties Include but are not limited to

• Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols.
• Basic understanding of SOPs and ensure they are adhered to in the conduct of the clinical research study.
• Acquire detailed knowledge of the protocol and procedures associated with each clinical research study.
• Maintain familiarity with each clinical research study?s requirements and apply all applicable regulations accurately.
• Effectively communicate with clinical research sponsors, CROs, monitors CRAs, IRBs, laboratories, and clinical personnel within the research industry.
• Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research study.
• Notify Investigator, monitor CRA of any adverse events or serious adverse events per the protocol.
• Follow ALCOA principles to complete all required documentation in a legible and timely fashion – including data entry – and that all necessary documents are appropriately signed and dated.
• Possess a willingness to assume responsibility for tasks outside of your current role and to work flexible hours as needed.

Other Skills and Abilities

• Additional duties and responsibilities may be assigned as needed.
• Team player – effective participant as a team member and can demonstrate significant positive participation on successful teams.
• Strong follow through skills and ability to proactively identify and solve problems, demonstrated initiative is imperative.
• Must have strong communication skills, speak, and listen respectfully with the public, physicians, and co-workers.
• Must be proficient in Microsoft Office Word and Excel, CRIO – preferred, will train – and databases used in research environment.
• Possess the ability to work well under pressure, multi-task, and manage deadlines.
• Able to adapt to a changing environment and demonstrates a make it happen attitude.
• Exhibits professionalism in negotiating sensitive issues.