Clinical Research Associate
Behavioral Health Market Context
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Benefits
Dental CoverageHealth Insurance
Job Description
Work: Play a key role in conducting clinical trials that are at the forefront of healthcare. Your contributions will ensure that trials are compliant with regulatory standards and that data integrity is maintained.
• Collaborative Environment: You will be a vital part of a cross-functional team, working alongside some of the brightest minds in the industry. Build lasting connections with site personnel, researchers, and key stakeholders.
• Professional Growth: With opportunities for continuous learning and development, you’ll be encouraged to propose solutions that streamline processes and improve efficiency.
Your Role Includes:
• Driving the success of clinical trials by supporting and coordinating study startup activities.
• Performing thorough remote monitoring visits and generating comprehensive reports.
• Cultivating strong relationships with site personnel and internal partners to enhance site enrollment and performance.
• Assisting with site remediation activities to uphold the highest standards of quality.
Qualifications We’re Seeking:
• Education: Bachelor’s Degree or Equivalent in Life Sciences or Nursing is a must!
• Experience: Bring 3-4 years of clinical research experience (either as a CRC or CRA), with a solid understanding of quality assurance/control and regulatory compliance.
• Skills: Familiarity with electronic data capture is preferred. A clinical research certification (ACRP or SoCRA) is a bonus!
Perks of Joining Us:
• Enjoy a comprehensive benefits package after just 90 days of employment.
• Get ready for a secure future with our 401(k) plan featuring company match after 1 year of service.
• Be part of an AI-driven organization that enhances human decision-making and fosters innovation!
If you’re a proactive individual looking to make a significant impact in clinical research, we want to hear from you!
INDKL
Pay: $60.00 per hour
Benefits:
• 401(k)
• Dental insurance
• Health insurance
• Vision insurance
Work Location: In person
• Collaborative Environment: You will be a vital part of a cross-functional team, working alongside some of the brightest minds in the industry. Build lasting connections with site personnel, researchers, and key stakeholders.
• Professional Growth: With opportunities for continuous learning and development, you’ll be encouraged to propose solutions that streamline processes and improve efficiency.
Your Role Includes:
• Driving the success of clinical trials by supporting and coordinating study startup activities.
• Performing thorough remote monitoring visits and generating comprehensive reports.
• Cultivating strong relationships with site personnel and internal partners to enhance site enrollment and performance.
• Assisting with site remediation activities to uphold the highest standards of quality.
Qualifications We’re Seeking:
• Education: Bachelor’s Degree or Equivalent in Life Sciences or Nursing is a must!
• Experience: Bring 3-4 years of clinical research experience (either as a CRC or CRA), with a solid understanding of quality assurance/control and regulatory compliance.
• Skills: Familiarity with electronic data capture is preferred. A clinical research certification (ACRP or SoCRA) is a bonus!
Perks of Joining Us:
• Enjoy a comprehensive benefits package after just 90 days of employment.
• Get ready for a secure future with our 401(k) plan featuring company match after 1 year of service.
• Be part of an AI-driven organization that enhances human decision-making and fosters innovation!
If you’re a proactive individual looking to make a significant impact in clinical research, we want to hear from you!
INDKL
Pay: $60.00 per hour
Benefits:
• 401(k)
• Dental insurance
• Health insurance
• Vision insurance
Work Location: In person
Qualifications
- •Education: Bachelor’s Degree or Equivalent in Life Sciences or Nursing is a must!
- •Experience: Bring 3-4 years of clinical research experience (either as a CRC or CRA), with a solid understanding of quality assurance/control and regulatory compliance
- •A clinical research certification (ACRP or SoCRA) is a bonus!
Benefits
- •Impactful Work: Play a key role in conducting clinical trials that are at the forefront of healthcare
- •Enjoy a comprehensive benefits package after just 90 days of employment
- •Get ready for a secure future with our 401(k) plan featuring company match after 1 year of service
- •Pay: $60.00 per hour
- •401(k)
- •Dental insurance
- •Health insurance
- •Vision insurance
Responsibilities
- •Your contributions will ensure that trials are compliant with regulatory standards and that data integrity is maintained
- •Collaborative Environment: You will be a vital part of a cross-functional team, working alongside some of the brightest minds in the industry
- •Build lasting connections with site personnel, researchers, and key stakeholders
- •Professional Growth: With opportunities for continuous learning and development, you’ll be encouraged to propose solutions that streamline processes and improve efficiency
- •Driving the success of clinical trials by supporting and coordinating study startup activities
- •Performing thorough remote monitoring visits and generating comprehensive reports
- •Cultivating strong relationships with site personnel and internal partners to enhance site enrollment and performance
- •Assisting with site remediation activities to uphold the highest standards of quality
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