Clinical Research Oversight Specialist

4 weeks ago


Adelaide, South Australia Pharmiweb Full time
Job Title: Clinical Research Oversight Specialist

As a Clinical Research Oversight Specialist at Pharmiweb, you will be responsible for developing and implementing comprehensive oversight monitoring plans tailored to our organization's specific clinical trials and research activities.

Key Responsibilities:

  • Develop oversight monitoring plans to ensure protocol compliance and data accuracy.
  • Perform onsite and remote oversight monitoring visits to assess monitoring visit report review and oversight.
  • Implement quality control measures and risk management strategies to proactively identify and mitigate potential risks.
  • Prepare comprehensive oversight monitoring reports summarizing findings, recommendations, and corrective actions for management and regulatory agencies.
  • Provide support for local partnerships with internal and external stakeholders to enable country-focused delivery and execution of the R&D pipeline.

Requirements:

  • Bachelor's Degree (or equivalent) with 6-8 years of relevant healthcare experience in the pharma or clinical research industry.
  • Scientific background and experience in Oncology, Infectious Diseases/Vaccines, and Rare Diseases.
  • Proficiency with medical terminology and working knowledge of Local Regulations and ICH/GCP Guidelines.
  • Excellent record-keeping skills and attention to detail.
  • Experience conducting Site Selection, Initiation, Routine Monitoring, and Close Out Visits both remotely and on-site.

What We Offer:

  • Competitive salary and benefits package.
  • Opportunities for professional growth and development.
  • Diverse and inclusive work environment.

How to Apply:

Please visit our careers website to learn more about this opportunity and to submit your application.



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