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Responsibilities:
- Lead risk-based monitoring implementation and manage study-specific plans and central data review.
- Present monitoring analysis to teams and clients and handle issues in cross-functional settings.
Qualifications:
- College degree or equivalent education and experience in clinical study leadership.
- Strong communication, leadership, and independent work abilities; centralized monitoring experience is a plus.
- Proficiency in English, MS Office, and understanding of clinical trial processes and risks.
Opportunity:
- This role is crucial and growing in the CRO industry, offering frontline work and a global project view.
- It involves setting foundations for risk-based models and ensuring patient safety and data integrity.
PSI
PSI is a leading Contract Research Organization (CRO) delivering quality and on-time clinical research services across various therapeutic indications. It is a stable yet innovative company with almost 30 years of market experience.