Michigan Pain Consultants (ProCare Pain Solutions) is hiring a full time Clinical Trial Study Coordinator! 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 also eligible for a generous 401k profit sharing plan after one year of service!

Position Summary:
The Clinical Trial Study Coordinator (SC) is a certified or licensed medical professional. The SC helps support the Research Department by collaborating with assigned physician investigators, research teams, and clinical trial subjects. Protocol knowledge, adherence, and documentation are at the core of this position, and therefore the candidate must be a critical thinker as well as extremely thorough and accurate.

Minimum Qualifications:

  • Registered Nurse or Licensed Practical Nurse Certification or licensure in health-related field
  • Strong medical/science background
  • 2 years of clinical patient care
  • Experience working with project teams, and work with individuals at different levels
  • 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:

  • RN, BSN
  • 2 years of clinical patient care in chronic pain management
  • Knowledge of GCP/FDA/ICH regulations
  • Demonstrated thorough and accurate documentation
  • Phlebotomy experience

Primary Responsibilities:

  • Ensure adherence to regulations, protocol, and company SOPs and Manage and track all clinical trial documents including protocol and subject documents
  • Perform various hands-on clinical tasks such as ECGs, BPs, and blood draws
  • Support 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 lab 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
  • Represent company in a positive and professional manner

Varies; dependent upon clinical trials and necessary training. All locations in West Michigan