Senior Clinical Research Associate I - Remote

Actalent

Houston (TX)

Remote

USD 81,000 - 86,000

Full time

11 days ago

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Benefits offered by this job

Medical, dental & vision
401(k) retirement plan
Paid travel and lodging
Fully remote contract

Job summary

Actalent is seeking a Senior Clinical Research Associate I for a 6‑month contract (renewable) based out of Houston, TX. The role is fully remote with substantial travel, supporting diverse trials under ICH‑GCP guidelines.

On-site visits may be required to ensure protocol adherence and data integrity. The position emphasizes site monitoring, data quality, and collaboration with sponsors and project teams in a global clinical research environment.

Qualifications

  • Bachelor’s degree in a life sciences field required.
  • Minimum of 2 years’ experience as a clinical research monitor.
  • Valid driver’s license for travel as needed.
  • Excellent knowledge of ICH‑GCP guidelines and regulatory requirements.
  • Strong written and spoken English skills.

Responsibilities

  • Monitor trials remotely and on-site and manage sites.
  • Apply risk‑based monitoring and corrective actions.
  • Perform SDR/SDV and CRF reviews for data integrity.
  • Track and ensure regulatory documentation and site payments.
  • Communicate findings and results to study team and sponsors.
  • Support investigator meetings and site trainings.

Skills

Bachelor’s degree life sciences
2+ years CRA experience
Valid driver’s license
ICH‑GCP knowledge
Strong English
CTMS proficiency
Microsoft Office

Education

Bachelor’s degree in life sciences
Registered Nursing certification

Tools

CTMS
Microsoft Office

Job description

Actalent is seeking a Senior Clinical Research Associate I for a 6‑month contract (renewable) based out of Houston, TX. The role is fully remote with substantial travel, supporting diverse trials under ICH‑GCP guidelines.

On-site visits may be required to ensure protocol adherence and data integrity. The position emphasizes site monitoring, data quality, and collaboration with sponsors and project teams in a global clinical research environment.

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