Clinical Research Oversight Specialist
3 days ago
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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