Remote Contract Senior Clinical Research Associate

Actalent

Phoenix (AZ)

Remote

USD 96,000 - 131,000

Full time

11 days ago

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Benefits offered by this job

Medical, dental & vision
401(k) retirement plan
Life Insurance
PTO (paid time off)

Job summary

Actalent is seeking a Clinical Research Associate (CRA) for a 6-month renewable contract to hire. The role allows 100% remote work with 60-80% travel across the United States. The CRA will monitor sites, ensure protocol and regulatory compliance, and maintain trial documentation per ICH-GCP.

Therapeutic background is accepted across disciplines. The ideal candidate has a life sciences degree (or RN) with 2+ years as a clinical research monitor, strong data management skills, and excellent

Qualifications

  • Bachelor's degree in a life sciences field or RN certification.
  • Minimum 2+ years as a clinical research monitor.
  • Valid driver's license where applicable.
  • Strong ICH-GCP knowledge and regulatory understanding.
  • Proficient in MS Office and CTMS usage.

Responsibilities

  • Monitor investigator sites using risk-based monitoring and RCA.
  • Ensure data accuracy via source data review and CRF checks.
  • Maintain trial documentation and regulatory compliance.
  • Escalate deficiencies and coordinate resolutions.
  • Maintain site communications and progress reporting to Clinical Team Manager.
  • Support investigator meetings and identify potential sites.
  • Ensure essential documents are complete per ICH-GCP.

Skills

Clinical monitoring
2+ years CRA experience
Medical terminology
ICH-GCP
Communication
Time management
Independent work

Education

Bachelor's degree in life sciences
Registered Nursing certification

Tools

MS Office
CTMS
Regulatory documentation tools

Job description

Actalent is seeking a Clinical Research Associate (CRA) for a 6-month renewable contract to hire. The role allows 100% remote work with 60-80% travel across the United States. The CRA will monitor sites, ensure protocol and regulatory compliance, and maintain trial documentation per ICH-GCP.

Therapeutic background is accepted across disciplines. The ideal candidate has a life sciences degree (or RN) with 2+ years as a clinical research monitor, strong data management skills, and excellent

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