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Clinical Research Coordinator

Headlands Research
Location
Springfield, Missouri
Posted
16 days ago
Department
Clinical: Clinical Research Coordinators
What they actually want (must-haves)
  • Bachelor's degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP
  • Strong interpersonal, verbal, and written communication skills
  • Organized, detail-oriented, and capable of managing multiple priorities
  • Proficient in Microsoft Office and other clinical research systems
  • Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures
Nice to have
  • Previous experience as a Clinical Research Coordinator
  • Industry-sponsored trial experience
  • Familiarity with electronic data capture (EDC), IVRS, and other trial platforms
  • Vaccine study experience
What the job really is

As a Clinical Research Coordinator at Headlands Research, you will manage and execute Phase I-IV clinical studies, ensuring compliance with FDA regulations and GCP/ICH guidelines. Your daily tasks will include coordinating clinical trials, conducting subject visits, maintaining regulatory documentation, and collaborating with various stakeholders. This role is onsite in Springfield, MO, and offers a structured schedule with no nights or weekends.

Benefits
  • Health insurance (medical, dental, and vision)
  • Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA)
  • Paid Time Off (PTO)
  • 401(k) plan with company match
  • Annual performance incentives
  • Company holidays
Things to weigh
  • Onsite work only; no remote or hybrid options available
  • Fast-paced environment may not suit everyone
  • No mention of salary or specific performance metrics for incentives
Job score3.2/5
Benefits3/5
Freshness4/5
Career value4/5
Role clarity5/5
Pay transparency0/5

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