Experienced Clinical Research Associate - Full-service

SyneosHealth

Multiple Locations
Base: not specified; bonus/equity: eligibility to ...
Fully remote
Ich-gcp and regulatory compliance
Clinical site monitoring and management
Source document and data verification
Syneos Health is a leading fully integrated biopharmaceutical solutions organization focused on accelerating customer success by placing the customer and patient at the center of clinical development

Job Summary

  • Syneos Health is a leading fully integrated biopharmaceutical solutions organization focused on accelerating customer success by placing the customer and patient at the center of clinical development.
  • The Clinical Research Associate role involves comprehensive site management activities including qualification, monitoring, data verification, investigational product oversight, and ensuring regulatory compliance.
  • Employees benefit from a supportive culture that promotes career development, diversity, competitive benefits including health coverage, 401k match, stock purchase plans, and flexible paid time off.

Matching Summary

Syneos Health is a leading fully integrated biopharmaceutical solutions organization focused on accelerating customer success by placing the customer and patient at the center of clinical development.

Salary

Base: Not specified; Bonus/Equity: Eligibility to earn commissions/bonus based on performance; Benefits: Medical, Dental, Vision, 401k match, Employee Stock Purchase Plan, flexible PTO and sick time

Skills & Requirements

Must-have

  • ICH-GCP and regulatory compliance
  • Clinical site monitoring and management
  • Source document and data verification
  • Investigational product handling and reconciliation
  • Electronic data capture compliance
  • Subject recruitment and retention support
  • Up to 75% travel requirement

Nice-to-have

  • Career development and progression opportunities
  • Supportive and engaged line management
  • Diversity and inclusion culture
  • Collaboration with cross-functional teams
  • Audit readiness and preparation
  • Use of new technologies in clinical monitoring
  • Training junior staff

Key Requirements

  • Bachelor’s degree or RN in related field
  • Knowledge of Good Clinical Practice/ICH Guidelines
  • Excellent communication and interpersonal skills
  • Ability to manage up to 75% travel
  • US work authorization compliance
  • Experience with real world late phase studies (optional)

Work Rights

Must comply with site access medical and personal information requirements

Tailored Resume

Cover Letter