Senior Cta

ICON Clinical Research, LP

Competitive salary; not specified; various annual ...
Bachelor's degree in life sciences or clinical research
Solid understanding of clinical trial processes
Strong knowledge of good clinical practice guidelines
The role involves supporting the management and monitoring of clinical trial sites to ensure compliance with study protocols and regulatory requirements

Job Summary

  • The role involves supporting the management and monitoring of clinical trial sites to ensure compliance with study protocols and regulatory requirements.
  • ICON offers a competitive salary along with a range of benefits including health insurance, retirement planning, and global employee assistance programs.
  • Candidates will collaborate with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle.

Matching Summary

The role involves supporting the management and monitoring of clinical trial sites to ensure compliance with study protocols and regulatory requirements.

Salary

Competitive salary; Not specified; Various annual leave entitlements; Health insurance offerings; Retirement planning offerings

Skills & Requirements

Must-have

  • Bachelor's degree in life sciences or clinical research
  • Solid understanding of clinical trial processes
  • Strong knowledge of Good Clinical Practice guidelines
  • Experience in site management or clinical monitoring
  • Excellent analytical skills and attention to detail

Nice-to-have

  • Ability to mentor junior staff members
  • Exceptional communication and interpersonal skills
  • Collaborative approach with cross-functional teams
  • Proven track record in project management
  • Commitment to fostering an inclusive environment

Key Requirements

  • Bachelor's degree in relevant field
  • Relevant clinical research experience
  • Understanding of GCP guidelines

Work Rights

Not specified

Tailored Resume

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