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Senior Clinical Trial Monitor
2 months ago
Company Overview: AL Solutions collaborates with a dynamic Biotech organization committed to excellence in clinical research.
Position Summary: We are in search of a skilled Senior Clinical Trial Monitor to supervise and evaluate clinical studies at research sites.
Key Responsibilities:
- Conduct site assessments to ensure adherence to protocols and gather data.
- Perform verification of source documents and review data integrity.
- Guarantee the completion of study records and regulatory submissions.
- Establish strong connections with site staff and principal investigators.
- Resolve site-related challenges that may affect study execution.
- Assist in the selection and qualification of study sites.
- Work in conjunction with Data Management for precise data reporting.
- Remain informed on industry standards and regulations.
Qualifications:
- Bachelor's degree in a scientific or healthcare-related field.
- A minimum of 2 years of experience as a Clinical Research Associate in a contract research organization or pharmaceutical environment.
- Familiarity with ICH-GCP guidelines and regulatory standards.
- Experience in site monitoring and conducting visits.
- Excellent communication and interpersonal abilities.
- Detail-oriented and organized with the capacity to manage multiple tasks.
- Proficient in computer applications and data management systems.
- Willingness to travel to research sites as needed.
Benefits:
401k
Competitive Salary
And additional perks