Duties
- Coordinate and oversee clinical research studies from start to finish
- Collect and record patient data, including vital signs, medical history, and medication information
- Assist with patient recruitment and screening for clinical trials
- Schedule and coordinate study visits and procedures for participants
- Ensure compliance with study protocols and regulatory requirements
- Perform blood sampling and phlebotomy as needed
- Collaborate with investigators and research team members to analyze data and interpret results
- Maintain accurate and complete documentation of study activities
- Assist with the preparation of research reports and presentations
Experience
- Bachelor’s degree in a related field (e.g., life sciences, nursing, public health)
- Previous experience working as a Clinical Research Coordinator or in a similar role preferred
- Knowledge of medical terminology and clinical trial processes
- Familiarity with statistical software for data analysis
- Strong attention to detail and ability to accurately collect and record data
- Excellent organizational skills and ability to manage multiple tasks simultaneously
- Strong communication skills, both written and verbal, to effectively interact with patients, investigators, and other research team members
- Ability to work independently as well as part of a team in a fast-paced environment
Note: This job description is not intended to be all-inclusive. The employee may perform other related duties as assigned by their supervisor.
Job Type: Full-time
Pay: $20.00 - $27.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Relocation assistance
• Vision insurance

Work Location: In perso

Please refer the Job description for details