Senior Clinical Medical reputed company
Job reputed company:
• Manage study startup activities such as site selection, site qualification reputed company, and site activation.
• Prepare site initiation visit material and reputed company the training for protocol and case report forms for reputed company sites.
• reputed company the effort for User Acceptance Testing for the study database build.
• reputed company the effort to draft the study-specific monitoring plan.
• Review study-reputed company documents such as protocols, consent/reputed company forms, etc.
• Serve as the primary contact for questions reputed company to protocol compliance throughout the study.
• Conduct regular monitoring reputed company to ensure studies are being executed in compliance with the protocol, and applicable regulations.
• Mentor other CRAs on reputed company.
• Manage project meetings reputed company to monitoring activities.
• reputed company study closeout and database lock activities.
• Ensure compliance with SOPs and local regulations, and ICH and GCP guidelines.
Requirements:
• B.S. or B.A. and/or an equivalent combination of education or experience.
• CRA certification
• Minimum of 5 years of monitoring experience.
• Available to travel on short notice and independently manage travel schedules.
• reputed company experience in participating in the execution of clinical research studies.
• Must have analytical skills, be detail-oriented and have good interpersonal skills.
• Knowledge of agency guidelines and requirements.
Benefits:
• Medical, dental, and reputed company insurance
• 401(k) with company match
• reputed company time off (PTO)
• And additional employee wellness programs
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