Clinical Research Coordinator/Nurse/Study Manager Job in Las Vegas 89121, Nevada Us
We are still growing strong.
For over 25 years, Novum Pharmaceutical Research Services has been a world leader in the conduct of clinical trials and equivalency studies for the generic, pharmaceutical, and biotechnology industries.
Last year alone the FDA approved over 40 products for marketing where Novum had designed, conducted and reported the studies in the marketing application. We have completed over 2,000 studies with over 36,000 participants for more than 200 pharmaceutical companies.
Clinical Research Coordinator/Nurse/Study Manager
Novum Pharmaceutical Research Services is a specialist Contract Research Organization that offers study services to the generic, pharmaceutical, biotechnology industries and other Clinical Research Organizations. For over 25 years, Novum has been a world leader in the conduct of clinical trials and equivalency studies. We have completed over 2,000 studies with over 36,000 participants for more than 200 pharmaceutical companies.
Our people are our biggest asset!
Position Summary
Coordinate and oversee all aspects necessary for clinical study progression, according to the study protocol and Standard Operating Procedures (SOP’s).
Responsibilities
- 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.
Qualifications
- Must have Flexible work schedule, able to work 10-12 hour shifts, evenings and regular weekends as needed.
- Associate’s 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.
Excellent benefits package including; health, dental and vision benefits, 2 weeks’ paid time off, paid holidays, 401(k) program, life insurance, disability insurance, flexible spending account and more!!!
*****If you would like to be part of a successful team where your ideas are important, please forward your cover letter, resume and salary requirements. EOE******