Hybrid CRA: Trials & Data Oversight

Placements24

United States

Hybrid

USD 35,000 - 53,000

Full time

48 hours ago
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Benefits offered by this job

Competitive salary
Medical and retirement benefits
Bonus structure
Professional development opportunities
Hybrid work arrangement

Job summary

Placements24 is seeking a dedicated Clinical Research Associate to strengthen the clinical operations team. The role, based in a hybrid setting in Gauteng, ZA, involves ensuring trial protocols and regulatory compliance, data integrity, and effective coordination with site staff and investigators.

Ideal candidates bring 3+ years of CRA experience, strong GCP/ICH knowledge, and the ability to travel up to 40%. Join a team focused on advancing new therapies and maintaining rigorous trial standards.

Qualifications

  • Bachelor's degree as required in Life Sciences, Nursing, Pharmacy, or related field.
  • Minimum of 3 years in a Clinical Research Associate or similar role.
  • Strong understanding of GCP, ICH guidelines, and local regulatory requirements.
  • Proven experience in site monitoring, data review, and regulatory document management.

Responsibilities

  • Monitor clinical trial sites to ensure adherence to protocol, GCP, and regulatory requirements.
  • Verify accuracy, completeness, and integrity of clinical data collected at study sites.
  • Manage site initiation, interim monitoring visits, and close-out activities.
  • Act as primary point of contact for study sites and address queries or issues.
  • Prepare and submit essential regulatory documents and reports.
  • Oversee drug accountability and investigational product management at sites.
  • Maintain TMF documentation.
  • Collaborate with investigators, site staff, and internal project teams to progress trials.

Skills

GCP & ICH knowledge
CTMS proficiency
EDC proficiency
Site monitoring
Data review
Regulatory document management
Communication & teamwork
Travel readiness 30-40%

Education

Bachelor's degree in Life Sciences/Nursing/Pharmacy or related field

Tools

CTMS
EDC

Job description

Placements24 is seeking a dedicated Clinical Research Associate to strengthen the clinical operations team. The role, based in a hybrid setting in Gauteng, ZA, involves ensuring trial protocols and regulatory compliance, data integrity, and effective coordination with site staff and investigators.

Ideal candidates bring 3+ years of CRA experience, strong GCP/ICH knowledge, and the ability to travel up to 40%. Join a team focused on advancing new therapies and maintaining rigorous trial standards.

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