Job Overview
Compensation
Type:
Hourly
Rate:
Range $22.50 - $30.00
Benefits
Health Insurance
Dental Insurance
Paid Time Off
401(k) Plan
Professional development opportunities
Flexible work schedules
Job Description
Innovo Research is a leading clinical research organization dedicated to advancing medical science through well-managed and ethically conducted clinical trials. Renowned for its commitment to patient safety and scientific excellence, Innovo Research collaborates with top-tier Principal Investigators and healthcare professionals to bring innovative treatments from concept to reality. With a focus on compliance with all human research subject regulations, Innovo Research ensures the integrity and quality of clinical research studies across multiple therapeutic areas. The company is known for fostering a collaborative and professional environment where clinical research staff and study participants alike are treated with the utmost respect and... Show More
Job Requirements
- Bachelor’s degree or equivalent
- Experience in clinical research coordination
- Knowledge of human research subject regulations
- Ability to perform clinical functions such as phlebotomy
- Experience managing multiple concurrent clinical trials
- Strong organizational and communication skills
- Ability to comply with regulatory standards and SOPs
Job Qualifications
- Bachelor’s degree in a relevant field such as nursing, life sciences, or clinical research
- Proven experience in clinical research coordination
- Strong knowledge of human research subject regulations and guidelines
- Demonstrated ability to manage multiple studies simultaneously
- Excellent communication and interpersonal skills
- Experience with IRB submission processes and regulatory documentation
- Proficiency in clinical trial management systems and data entry
- Ability to perform clinical procedures including phlebotomy and vital signs monitoring
- Capability to mentor and train junior staff
Job Duties
- Assist with mentoring and training clinical research staff
- Perform clinical functions such as phlebotomy and vital signs monitoring when warranted
- Liaise with agencies, pharmaceutical companies, laboratories, vendors, equipment, and supply companies
- Manage multiple concurrent trials including screening, recruiting, enrollment, scheduling, protocol-related procedures, data entry, and IRB submissions
- Develop strong working relationships and maintain effective communication with study team members
- Support collection and review of essential study documents and reports
- Facilitate pre-study, site qualification, study initiation, monitoring visits, and study close-out activities
- Collect, process, and ship laboratory specimens
- Comply with Innovo, Clinic, and Sponsor policies, SOPs, and applicable regulatory requirements
Job Qualifications
Experience
Expert Level (7+ years)
Job Location
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