Clinical Research Associate (CRA): Monitoring & Site Oversight

Placements24

Netherlands

Hybrid

EUR 60,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Competitive salary plus incentives
Health, dental, and vision insurance
Paid time off and holidays
Company car or travel allowance

Job summary

Placements24 is seeking an experienced Pharmaceutical Clinical Research Associate (CRA) to support ongoing clinical trials, mainly in the Randburg area. You will monitor sites to ensure protocol adherence, data integrity, and regulatory compliance while serving as the liaison between sponsor and sites.

Travel and remote administrative tasks are part of the role. The ideal candidate has a life sciences background, 3+ years CRA experience, and strong communication and organizational skills to

Qualifications

  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field.
  • Minimum 3 years of CRA experience in pharma.
  • Strong knowledge of GCP and regulatory requirements.
  • Experience across phases I–IV of clinical trials.
  • Strong monitoring and data verification skills.
  • Willingness to travel frequently and communicate effectively.

Responsibilities

  • Conduct site initiation, monitoring, and close-out visits per protocol and SOPs.
  • Ensure GCP and regulatory compliance for trials.
  • Verify accuracy and completeness of trial data at sites.
  • Manage study site activities and support investigators and staff.
  • Prepare and submit monitoring visit reports promptly.
  • Oversee collection and management of essential trial documents.

Skills

GCP knowledge
Regulatory compliance
Travel readiness
Data integrity

Education

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

Job description

Placements24 is seeking an experienced Pharmaceutical Clinical Research Associate (CRA) to support ongoing clinical trials, mainly in the Randburg area. You will monitor sites to ensure protocol adherence, data integrity, and regulatory compliance while serving as the liaison between sponsor and sites.

Travel and remote administrative tasks are part of the role. The ideal candidate has a life sciences background, 3+ years CRA experience, and strong communication and organizational skills to

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