- Work with source document staff on development and QC of study specific documents.
- Coordinate initiation meeting with all pertinent staff.
- Review clinic schedule for adequate staff coverage of all protocol activities and communicate any concerns to Clinic Manager.
- Consult with pharmacy technician for drug handling, dispensing, dosing time and dosing intervals.
- Review sample collection and processing instructions with Phlebotomists to ensure all requirements are followed.
- Participate in dosing of study participants.
- Prepare adverse event summary for Client Services.
- Conduct and coordinate check-in procedures for study.
- Verify documentation of all study activities.
- QC all case report forms for accuracy within specified time frame.
- Compute participant payments based on completed study participation.
- Communicate pertinent study observations to the Principal Investigator and management.
- Complete tables for final report.
- Must have Flexible work schedule, able to work 10-12 hour shifts, evenings and regular weekends as needed.
- Associates Degree or equivalent, or Nursing qualification. At least 3 years work experience in a medical or clinical research setting.
- One year of supervisory/management experience. Strong leadership/management skills will be responsible for directly supervising clinical staff and study participants.
- Prefer previous research experience.
Country: USA, State: Nevada, City: Las Vegas, Company: Novum Pharmaceutical Research Services, Inc..
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