Piper Companies
Clinical Research Associate
Piper Companies, Las Vegas, Nevada, us, 89105
Zachary Piper Solutions
is seeking a
Clinical Research Associate
to join a large CRO located in
Las Vegas
to travel regionally for site support and monitoring. The Clinical Research Associate will conduct On-Site monitoring for multiple research locations supporting
Oncology
trials.
This job opens for applications on 01/07/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Responsibilities of the Clinical Research Associate include
: •Travel to multiple sites within the West Coast and Midwest Market. •Collaborate with sites to develop and track recruitment plans ensuring project needs are met. •Provide protocol and study training to sites. •Oversee regulatory submissions, enrollment, CRF completion and data query resolution. •Ensure all site documents are filed in the TMF and ISF per GCP/ICH guidelines. •Mentor clinical staff through co-monitoring and training visits.
Qualifications for the Clinical Research Associate include: •1-3+ years of experience in on-site monitoring for oncology clinical trials. •1.5 years of Phase 1 oncology. •Proficient in GCP and ICH guidelines •Excellent computer skills including Microsoft Office Suite. •Effective communication, organizational, and problem-solving skills •Experience working within a large CRO preferred over Academia experience.
Compensation for the Clinical Research Associate: •Salary Range $100,000 - 120,000 Depending on experience •Full Comprehensive Benefits, Medical, Dental and Vision coverage
KEYWORDS
Clinical Research Associate, Site Monitor, Clinical, Clinical Research, Oncology, Clinical Trial Associate, CRO, Industry, Patient Recruitment, Site Support, TMF, Trial Master File ETMF, GCP, FDA,CRA, Clinical Research Training, Informed Consent, Healthcare, Health and Medical, Life Science, Cancer Research, Oncology Research, L-TH1, L-DNP, #Pando, Travel
is seeking a
Clinical Research Associate
to join a large CRO located in
Las Vegas
to travel regionally for site support and monitoring. The Clinical Research Associate will conduct On-Site monitoring for multiple research locations supporting
Oncology
trials.
This job opens for applications on 01/07/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Responsibilities of the Clinical Research Associate include
: •Travel to multiple sites within the West Coast and Midwest Market. •Collaborate with sites to develop and track recruitment plans ensuring project needs are met. •Provide protocol and study training to sites. •Oversee regulatory submissions, enrollment, CRF completion and data query resolution. •Ensure all site documents are filed in the TMF and ISF per GCP/ICH guidelines. •Mentor clinical staff through co-monitoring and training visits.
Qualifications for the Clinical Research Associate include: •1-3+ years of experience in on-site monitoring for oncology clinical trials. •1.5 years of Phase 1 oncology. •Proficient in GCP and ICH guidelines •Excellent computer skills including Microsoft Office Suite. •Effective communication, organizational, and problem-solving skills •Experience working within a large CRO preferred over Academia experience.
Compensation for the Clinical Research Associate: •Salary Range $100,000 - 120,000 Depending on experience •Full Comprehensive Benefits, Medical, Dental and Vision coverage
KEYWORDS
Clinical Research Associate, Site Monitor, Clinical, Clinical Research, Oncology, Clinical Trial Associate, CRO, Industry, Patient Recruitment, Site Support, TMF, Trial Master File ETMF, GCP, FDA,CRA, Clinical Research Training, Informed Consent, Healthcare, Health and Medical, Life Science, Cancer Research, Oncology Research, L-TH1, L-DNP, #Pando, Travel