Experienced Clinical Research Coordinator | Minimum 5 years of experience required.
Encore Medical Research of Boynton Beach LLC.
Behavioral Health Market Context
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Benefits
Paid Time OffHealth InsuranceDental Coverage
Job Description
dinator for our Boynton Beach office. Join our energetic team today! Enjoy working in a great environment. We offer competitive compensation and benefits.
Job Responsibilities:
• Must comply with the highest GCP standards
• Perform informed consent process to subjects
• Perform delegable protocol assessments to subjects
• Completion and revision of progress notes
• Enter subject data in a CTMS system
• Perform vital signs, weight, and blood pressure assessments
• Perform blood draws
• Strict compliance with ALCOA guidelines
• Limited recruitment activities
• Assist with monitoring procedures
• Data entry on EDC systems
Requirements:
• Must be fluent in English and Spanish and be able to write clearly in English and Spanish.
• A minimum of 5 years of experience as a Clinical Research Coordinator is required.
• Must hold a current Medical Assistant or Phlebotomy license in the State of Florida
• Must have completed GCP / ICH and IATA trainings and hold up-to-date certifications.
• Must have outstanding phone and customer service skills
• Experienced with Microsoft Office
• Must be willing to work with patients with COVID-19
• Previous experience with Dermatology and Endocrinology studies is highly preferred.
• Experience with the most common EDC , IWRS and IRT Systems is required.
Job Type: Full-time
Job Type: Full-time
Pay: From $30.00 per hour
Benefits:
• Dental insurance
• Health insurance
• Paid time off
• Parental leave
• Professional development assistance
• Referral program
• Tuition reimbursement
• Vision insurance
Work Location: In person
Job Responsibilities:
• Must comply with the highest GCP standards
• Perform informed consent process to subjects
• Perform delegable protocol assessments to subjects
• Completion and revision of progress notes
• Enter subject data in a CTMS system
• Perform vital signs, weight, and blood pressure assessments
• Perform blood draws
• Strict compliance with ALCOA guidelines
• Limited recruitment activities
• Assist with monitoring procedures
• Data entry on EDC systems
Requirements:
• Must be fluent in English and Spanish and be able to write clearly in English and Spanish.
• A minimum of 5 years of experience as a Clinical Research Coordinator is required.
• Must hold a current Medical Assistant or Phlebotomy license in the State of Florida
• Must have completed GCP / ICH and IATA trainings and hold up-to-date certifications.
• Must have outstanding phone and customer service skills
• Experienced with Microsoft Office
• Must be willing to work with patients with COVID-19
• Previous experience with Dermatology and Endocrinology studies is highly preferred.
• Experience with the most common EDC , IWRS and IRT Systems is required.
Job Type: Full-time
Job Type: Full-time
Pay: From $30.00 per hour
Benefits:
• Dental insurance
• Health insurance
• Paid time off
• Parental leave
• Professional development assistance
• Referral program
• Tuition reimbursement
• Vision insurance
Work Location: In person
Qualifications
- •Must be fluent in English and Spanish and be able to write clearly in English and Spanish
- •A minimum of 5 years of experience as a Clinical Research Coordinator is required
- •Must hold a current Medical Assistant or Phlebotomy license in the State of Florida
- •Must have completed GCP / ICH and IATA trainings and hold up-to-date certifications
- •Must have outstanding phone and customer service skills
- •Experienced with Microsoft Office
- •Must be willing to work with patients with COVID-19
- •Experience with the most common EDC , IWRS and IRT Systems is required
Benefits
- •Enjoy working in a great environment
- •We offer competitive compensation and benefits
- •Pay: From $30.00 per hour
- •Dental insurance
- •Health insurance
- •Paid time off
- •Parental leave
- •Professional development assistance
- •Referral program
- •Tuition reimbursement
- •Vision insurance
Responsibilities
- •Must comply with the highest GCP standards
- •Perform informed consent process to subjects
- •Perform delegable protocol assessments to subjects
- •Completion and revision of progress notes
- •Enter subject data in a CTMS system
- •Perform vital signs, weight, and blood pressure assessments
- •Perform blood draws
- •Strict compliance with ALCOA guidelines
- •Limited recruitment activities
- •Assist with monitoring procedures
- •Data entry on EDC systems
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