Clinical Project Coordinator I

Put your talents to work at PCM! Whether you work in our Home Care, Clinical Research, Impairments, or Catastrophic Care division, you will support our mission to deliver care and other services that enhance the quality of life of our clients. Be a part of our dynamic client-focused team and make a difference in your career!

PCM TRIALS provides quality, in-home clinical trial visits for various Sponsors and CROs. We're the only company that hires, trains, certifies, tests, and manages our own Certified Mobile Research Nurses (CMRNs). Our mission is to bring clinical trial visits to subjects wherever they may be to increase convenience and compliance with study protocols.

Be part of a team who fully embrace our values and key behaviors

• We work as a team
• We do the right thing
• We figure it out
• We pursue growth
• We take ownership
  
  

Why work for PCM TRIALS?

• Contribute to advancements of truly life changing treatments
• Help in creating a better way to meet the needs of patients
• Work with a pioneer in the industry and gain valuable insight from leaders in DCT
  
  

Summary

We are seeking Clinical Project Coordinators to assist Clinical Project Managers with the administration of mobile clinical research visits to patients. This position is available as a remote option.

Qualifications

• Bachelor’s degree from an accredited four-year college or university in a biological or life sciences program.
• Previous work experience in a clinical or research setting.
• Detail oriented, excellent verbal, and written communication skills.
• Proficient in Microsoft Office products.
• Ability to work out of normal business hours up to 5% of time.
  
  

Preferred

• Previous experience in quality checking of clinical source documentation.
• Coordination and scheduling logistics for investigational products and biological specimens.
• Requesting and delivering documentation to internal and external cross-functional teams including nurses, study sites, sponsors, vendors, suppliers, CROs, pharmacies, and laboratories.
• Staff, coordinate and confirm visits for study nurses.
• Manage internal and external clinical databases.
• Process study expenses.
  
  

The typical base pay range for this role is USD $52,000 - $72,800 per year.

Individual base pay depends on various factors, in addition to primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience, skills and other market-based factors.

Available Benefits Include

• Medical
• Dental
• Vision
• 401(k)
• Company Paid Short Term Disability
• Flexible Spending Account (FSA)
• Health Savings Account (HSA)
• Paid Time Off
• Voluntary Benefits
  
  

Please contact Carson Moreira-Rego at (866) 776-0127 x387 or at Carson.Moreira-Rego@procasemanagement.com today to learn more about our opportunities where you can make a difference in your own career!

Professional Case Management is an Equal Opportunity Employer.