Join a Top Workplace!!  A multi-year award winner of the Star Tribune Top Workplace designation, Dermatology Consultants is proud to be celebrating its 75th year in business. Founded in 1949, we are a thriving private dermatology practice with 21 physicians and 4 clinic locations in the East Metro.

The Clinical Research Coordinator (CRC) is responsible for the coordination and management of dermatology clinical research studies under the direction of the Director of Quality, Compliance & Research with oversight from the Principal Investigator (PI). The CRC must be able to effectively coordinate multiple studies concurrently and appropriately prioritize tasks across assigned studies and responsibilities.

Dermatology Consultants offers employees:

• Competitive Salary
• No Evenings or Weekends
• Discounts on Cosmetic Services (including Botox, laser hair removal, facials and more)
• Generous Company-funded 401K and Profit Sharing
• Paid Time Off and Paid Holidays
• Free Parking
• Continuing Education (CEUs) and CPR certification
• Company-sponsored Wellness program

Duties:

• Provide support, coordination, and leadership for research studies that may involve industry, FDA or government sponsored studies for Phase 1-4 clinical trials
• Ensure smooth, accurate progress of studies from site initiation through study completion and post-study closure
• Support subject recruitment and screening in collaboration with Principal Investigator(s) and facilitate continued study participation
• Manage and track all subject related information utilizing designated study tools (i.e. EDC, regulatory binders etc.)
• Develop standard operating procedures (SOPs) and ensure compliance with all study protocols
• Abstract data from medical records and other sources
• Identify, document, and assist with Institutional Review Board (IRB) mandated reporting and review

Minimum Qualifications:

• Bachelor’s degree (healthcare field preferred) or a combination of related education and healthcare employment experience totaling four years.
• Familiarity with clinical study regulations and guidance (i.e., ICH-GCP and trial master file regulations)
• Ability to work independently, make decisions, problem solve, and prioritize duties across multiple clinical studies
• Strong interpersonal, written, and verbal communication skills with a history of working collaboratively as part of a team
• Proficiency with Microsoft O365 (Outlook, Excel, Word, etc.) and Electronic Medical Record (EMR) systems

Preferred Qualifications:

• Previous experience conducting clinical research including screening and recruiting participants; obtaining informed consent; data entry and database management; regulatory management
• Current (non-expired) Good Clinical Practice (GCP) training documentation or current GCP training is required within the first 3 weeks of employment.

Schedule: ~24 hours/week, day shift

Dermatology Consultants, P.A. is an Equal Opportunity Employer