Ssu Cra I

ICON Clinical Research, LP

Mexico
Competitive salary; benefits include annual leave,...
**
Site start-up activities and feasibility assessments
Drafting and reviewing informed consent forms
Knowledge of ich-gcp guidelines and local regulations
** ICON Clinical Research is seeking a Site Start-Up Clinical Research Associate (SSU CRA I) in Mexico for a hybrid role. The ideal candidate will manage study start-up activities, ensuring compliance and collaboration with clinical stakeholders while benefiting from a supportive, inclusive company culture. **

Job Summary

  • The role involves working independently to coordinate study start-up and monitoring activities while ensuring accurate status reporting.
  • Candidates must support site identification, feasibility assessments, and regulatory submissions in line with sponsor requirements.
  • ICON offers a competitive salary, health insurance, retirement planning, and a global Employee Assistance Programme focused on well-being.

Matching Summary

Match Score: 75

** ICON Clinical Research is seeking a Site Start-Up Clinical Research Associate (SSU CRA I) in Mexico for a hybrid role. The ideal candidate will manage study start-up activities, ensuring compliance and collaboration with clinical stakeholders while benefiting from a supportive, inclusive company culture. **

Salary

Competitive salary; Benefits include annual leave, health insurance, retirement planning, and life assurance; Additional flexible country-specific benefits available

Skills & Requirements

Must-have

  • Site start-up activities and feasibility assessments
  • Drafting and reviewing Informed Consent Forms
  • Knowledge of ICH-GCP guidelines and local regulations
  • Experience with clinical study monitoring and documentation
  • Advanced English communication skills

Nice-to-have

  • Strong interpersonal and stakeholder management skills
  • Ability to work independently in fast-paced environments
  • Collaborative relationship building with investigators
  • Detail-oriented approach to data integrity
  • Willingness to conduct on-site field visits

Key Requirements

  • Proven experience in clinical research and site start-up
  • Background as CTA Lead, Senior CTA, or CTA with regulatory experience
  • Solid knowledge of ICH-GCP guidelines
  • Availability for 1-2 on-site field visits

Work Rights

Not specified

Tailored Resume

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