Offer summary

Qualifications:

Bachelor’s degree in a biological program from an accredited institution., One or more years of experience in clinical research and project management., Strong verbal and written communication skills, with attention to detail., Proficient in Microsoft Office and able to work independently..

Key responsabilities:

Provide administration for home nurse visits and coordinate with Clinical Project Managers.

Manage logistics for supplies and investigational products for studies.

Act as the primary point of contact for low risk/complexity projects and liaise with stakeholders.

Oversee nurse activities, ensure documentation accuracy, and contribute to process improvements.

Job description

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!

In addition to performing duties associated with the Clinical Project Coordinator I role, the CPC II will be established as a project lead for low risk/complexity projects.

Qualifications

Bachelor’s degree from an accredited four-year college or university in a biological program.
One or more years of experience in the clinical research industry or equivalent.
One or more years of experience in project management.
Ability to work independently as a project coordinator or project lead with minimal project manager guidance.
Detail oriented.
Excellent verbal and written communication skills.
Proficient in Microsoft Office suite.
Ability to travel up to 10% of time

Essential Functions/Areas of Accountability

Clinical Project Coordinator – Provide administration for home nurse visits within a matrixed team of Clinical Project Managers on multiple projects.
Supply/IP Logistics - Stocks, maintains, ships and tracks supplies and investigational product for ongoing studies as needed.
Nurse Scheduling Logistics - Staffs, coordinates and confirms visits for study nurses.
Database Management - Manage internal and external clinical databases. Process study expenses.
Documentation - Request and deliver documentation to internal and external cross-functional teams including nurses, study sites, sponsors, vendors, suppliers, CROs, pharmacies and laboratories.
Project Lead – Function as the primary point of contact for low risk/complexity projects and act as central liaison for all project stakeholders.
Nurse Monitoring - Provide oversight and support for nurses on assigned projects. Review and approve nurse activities for payment.
Risk mitigation – Identify and mitigate risks while establishing and documenting corrective actions.
Training - Deliver material to nurses and sites through audio/visual presentations.
Contributor to Quality - Contribute to continuous improvement of all processes, protocols and SOPs.
Review source documents for accuracy.
Perform additional duties and responsibilities as necessary.

The typical base pay range for this role is USD $58,240 - $83,200 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.

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