Senior Clinical Research Associate
Behavioral Health Market Context
Apply Nowvia Piper Companies
Benefits
Paid Time OffDental CoverageHealth Insurance
Job Description
g activities across multiple study
• Responsible for both remote and on-site monitoring and study activation
• Participate in the development of study tools, protocols, and clinical trial documentation
• Some travel required once travel bands are lifted
Qualifications for the Senior Clinical Research Associate:
• 3-5 years performing on-site monitoring and hands on experience with EDC Systems
• Experience with Oncology is highly advantageous
• Organization to perform monitoring duties across multiple sites is a must
Compensation for the Senior Clinical Research Associate:
• Salary Range: $115,000-125,000
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays
#LI-SR1
• Responsible for both remote and on-site monitoring and study activation
• Participate in the development of study tools, protocols, and clinical trial documentation
• Some travel required once travel bands are lifted
Qualifications for the Senior Clinical Research Associate:
• 3-5 years performing on-site monitoring and hands on experience with EDC Systems
• Experience with Oncology is highly advantageous
• Organization to perform monitoring duties across multiple sites is a must
Compensation for the Senior Clinical Research Associate:
• Salary Range: $115,000-125,000
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays
#LI-SR1
Qualifications
- •3-5 years performing on-site monitoring and hands on experience with EDC Systems
- •Experience with Oncology is highly advantageous
- •Organization to perform monitoring duties across multiple sites is a must
Benefits
- •Salary Range: $115,000-125,000
- •Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays
Responsibilities
- •The Senior Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization
- •Conduct site and study visits and perform all site monitoring activities across multiple study
- •Responsible for both remote and on-site monitoring and study activation
- •Participate in the development of study tools, protocols, and clinical trial documentation
- •Some travel required once travel bands are lifted
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