Clinical Research Specialist

Draper, UT

About Novamind

Novamind Inc. (CSE:NM, OTC:NVMDF, FSE:HN2) is a leading mental health company enabling safe access to psychedelic medicine through a network of clinics and clinical research sites. Novamind provides ketamine-assisted psychotherapy and other novel treatments through its network of integrative mental health clinics and operates a full-service contract research organization specialized in clinical trials and evidence-based research for psychedelic medicine.

About Cedar Psychiatry

At Cedar Psychiatry…Healing Happens Here! Join our team and play an integral role in helping individuals achieve mental wellness. Cedar Psychiatry is a growing mental health practice with multiple outpatient clinics that provides advanced, cutting-edge psychedelic drug therapies. As well as, Transcranial Magnetic Stimulation (TMS), individualized therapy including holistic approaches, medical management services and more. Cedar Psychiatry also has an esteemed team of medical professionals dedicated to the clinical research in the use of psychedelic-assisted psychotherapy. This research is changing the future of how we treat mental illnesses. It’s pretty exciting here at Cedar and we’d love for you to join our team!

Cedar Psychiatry values diversity and strives to create an inclusive work environment. We respect and celebrate individuals for their differences and encourage applicants from all backgrounds to apply.

About the Role

We are looking for someone who is highly motivated, organized, and able to work independently to join our team. This Clinical Research Coordinator position will need to have the ability to float between Murray Clinical Research and Draper Clinical Research locations.

Key Responsibilities

  • Coordinating and performing responsibilities related to research participants including pre-screening, scheduling, overseeing patient visits, and obtaining informed consent
  • Preparing, submitting, and maintaining IRB regulatory documents
  • Ensuring quality data and compliance to the protocol
  • Entering data into EDC systems
  • Conducting ECG’s
  • Performing blood draws
  • Packaging and shipping labs
  • Obtaining medical history
  • Documenting, reporting, and tracking AE’s and SAE’s
  • Preparing for site visits or audits from sponsors and/or other agencies
  • Ordering supplies
  • Maintaining various logs including temperature, screening and enrollment, etc.

Minimum Qualifications

  • 1-2 years experience as a Clinical Research Coordinator required
  • Must have High School Diploma or GED
  • Bachelor’s Degree preferred
  • CCRC credential preferred
  • Phlebotomist Certification ideal

Job Type: Full-time

Excellent benefit package including health, dental, vision, and life insurance, 401(k) with employer match, PTO, Holiday Pay, and Flexible Savings Account. Must pass post-offer, pre-employment background check. Benefits dependent on hours worked.

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