Michigan Pain Consultants (ProCare Pain Solutions) is seeking a full-time Clinical Trial Associate (CTA) for their Wyoming Clinic. We offer employees competitive wages, paid holidays, and paid time off. Employees can expect no night, weekend, or holiday shifts. In addition, full-time employees are eligible for a free high deductible plan after 90 days and a generous 401k profit sharing plan after one year of service.

Position Summary:

The Clinical Trial Associate (CTA) is a licensed medical professional. The CTA helps support the Research Department by collaborating with assigned physician investigators, research teams, and clinical trial subjects. It is a hands-on position for patient care and education. Protocol knowledge, adherence, and documentation are at the core of this position, and therefore the candidate must be able to think critically and be extremely thorough and accurate. Specialty procedure scheduling and patient education are key components for this position.

Minimum Qualifications:

Licensed Practical Nurse
Strong medical/science background
2 years of clinical patient care
Experience working with project teams
Excellent written and verbal skills
Excellent attention to detail and ability to think critically
Self-motivated, efficient and able to work autonomously
Positive interpersonal skills
Strong IT skills

Preferred Qualifications:

2 years of clinical patient care in chronic pain management
Knowledge of GCP/FDA/ICH regulations
Demonstrated thorough and accurate documentation
Phlebotomy experience
Specialty procedure experience (i.e. spinal cord stimulator implants)

Primary Responsibilities:

  • Ensure adherence to regulations, protocol, and company SOPs and processes
  • Perform various hands-on clinical tasks such as ECGs, BPs, and blood draws
  • Support study coordinators and physician investigators
  • Manage patient enrollment data in designated clinical tracking systems and according to protocol timelines
  • Manage investigational medications according to protocol and ensure accurate and timely documentation
  • Package clinical trial samples per protocol and coordinate shipments accordingly
  • Process clinical trial product shipments according to protocol and timelines
  • Participate in monitor and/or FDA site reviews
  • Schedule and educate patients for specialty procedures
  • Represent company and assigned practice(s) in a positive and professional manner