Helping people gain better

Our Clinical Research Department specializes in Phase II-IV clinical, observational, and device trials.

We are currently seeking LVNs and/or RNs to fill Clinical Research Coordinator roles at our Central Austin office.  Working under the supervision of the Principal Investigator(s), Site Director/Operations Director and Study Coordinator(s), this position will coordinate the conduct of clinical research trials from study start-up through close-out procedures.

Key duties include:

• 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 (sponsor, site, CRO, IRB/IEC correspondence), and prepares source documents including study and subject information folders
• Completes study start-up through close-out procedures:
  • recruitment and patient enrollment
  • informed consent process
  • pre-screening, screening, and study visits in conjunction with Physician/Investigator
  • documentation of patient progress in response to investigative agents
  • coordination of monitor visits source documents and case report forms
  • as needed, oversee preparation of physician orders to ensure protocol compliance
  • maintain communication with physician regarding study requirements, dose modifications, and adverse events
• Other related duties as assigned

Requirements:

• At least 2 years of progressive experience in the medical field
• Excellent multi-tasking and organizational skills. Able to excel in a fast-paced environment.
• Exceptional interpersonal and communication skills.
• Must be self-sufficient, detail-oriented, and able to identify problems and solve them.
• Must be able to handle confident information and meet objectives in compliance with all legal, regulatory, and protocol guidelines

Preferred:

• Prior experience in the pharmaceutical industry or in a clinical research setting; Working knowledge of research methodology/medical terminology.
• Experience with e-MDs, InForm System, Medidata Rave, or similar

Position is full-time (40 hours per week). Salary: dependent on experience