Senior Clinical Research Associate (scra)

Labcorp

United States
Base: $115k - $140k annually; bonus/equity: not sp...
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Good clinical practice (gcp) guidelines
Ensure subject safety
Data integrity
** Labcorp is seeking a fully remote Senior Clinical Research Associate (SCRA) to oversee the planning and execution of clinical trials, ensuring compliance with regulatory standards and Good Clinical Practice (GCP) guidelines. The ideal candidate should have significant experience in clinical research, particularly with electronic data capture systems, and possess strong organizational and communication skills. **

Job Summary

  • The SCRA ensures the successful planning, coordination, and execution of clinical trials, fundamentally contributing to groundbreaking advancements in laboratory diagnostics and patient care.
  • This role is essential in verifying that clinical trials are conducted in adherence to stringent regulatory standards, Good Clinical Practice (GCP) guidelines, and ethical norms.
  • Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.

Matching Summary

Match Score: 75

** Labcorp is seeking a fully remote Senior Clinical Research Associate (SCRA) to oversee the planning and execution of clinical trials, ensuring compliance with regulatory standards and Good Clinical Practice (GCP) guidelines. The ideal candidate should have significant experience in clinical research, particularly with electronic data capture systems, and possess strong organizational and communication skills. **

Salary

Base: $115k - $140k annually; Bonus/Equity: Not specified; Benefits: Comprehensive benefits package

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) guidelines
  • ensure subject safety
  • data integrity
  • electronic data capture (EDC) systems
  • Microsoft Office Suite

Nice-to-have

  • improve health and improve lives
  • advancing care
  • groundbreaking advancements

Key Requirements

  • Bachelor’s degree
  • 5 or more years of experience as a Clinical Research Associate
  • 3 or more years of experience with electronic data capture (EDC) systems
  • 3 or more years of experience with Microsoft Office Suite
  • Ability to travel for on-site monitoring visits

Work Rights

Not specified

Tailored Resume

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