Clinical Project Coordinator I, Execution
About The Position
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! EmVenio 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.
Requirements
- 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.
Nice To Haves
- 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.
Responsibilities
- Staff, coordinate and confirm visits for study nurses.
- Manage internal and external clinical databases.
- Process study expenses.
Benefits
- Medical
- Dental
- Vision
- 401(k)
- Company Paid Short Term Disability
- Flexible Spending Account (FSA)
- Health Savings Account (HSA)
- Paid Time Off
- Voluntary Benefits
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
1,001-5,000 employees
