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Clinical Research Associate II

Job in Fort Worth, Tarrant County, Texas, 76102, USA
Listing for: Placements24
Full Time position
Listed on 2026-10-02
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 21000 - 34000 USD Yearly USD 21000.00 34000.00 YEAR
Job Description & How to Apply Below

About the Role

Our client is seeking a diligent and detail-oriented Clinical Research Associate II to join their growing pharmaceutical team in George . This role is essential for ensuring the successful execution of clinical trials, adhering to strict regulatory guidelines and company protocols. You will be responsible for monitoring clinical trial sites, ensuring data integrity, and working closely with investigators and study staff to maintain participant safety and study compliance.

This position offers a significant opportunity to contribute to groundbreaking medical research within the picturesque setting of the Western Cape , supporting the development of innovative therapies that improve health outcomes.

Key Responsibilities
  • Monitor clinical trial sites to ensure compliance with protocol, Good Clinical Practice (GCP) , and regulatory requirements.
  • Verify the accuracy, completeness, and consistency of clinical data through source data verification.
  • Manage investigational product accountability and ensure proper storage and handling.
  • Serve as the primary point of contact for assigned trial sites, addressing site staff queries and issues.
  • Prepare and present study status updates to internal stakeholders and clinical operations management.
  • Conduct site initiation, interim monitoring, and close-out visits as per the clinical monitoring plan in George .
Requirements
  • Bachelor's degree in a life science, nursing, or related field.
  • Minimum of 3 years of experience as a Clinical Research Associate or in a similar role.
  • Thorough understanding of clinical trial processes , ICH-GCP guidelines, and regulatory requirements.
  • Proficiency in using electronic data capture (EDC) systems and clinical trial management systems (CTMS).
  • Strong organizational skills, attention to detail, and ability to manage multiple priorities.
  • Excellent interpersonal and communication skills, with the ability to build rapport with site personnel.
Benefits
  • Competitive annual salary and performance incentives.
  • Comprehensive health and wellness benefits package.
  • Generous paid time off and company holidays.
  • Professional development opportunities and training programs.
  • A supportive and collaborative work environment in the beautiful George area.
Position Requirements
10+ Years work experience
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