
Senior Clinical Research Monitor
1 day ago
We are seeking a Clinical Research Associate II to conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
Responsibilities- Conduct on-site and remote monitoring of clinical research studies to ensure adherence to GCP guidelines and regulatory requirements.
- Develop and implement quality assurance tools, procedures, and processes to ensure efficient monitoring.
- Collaborate with cross-functional teams to support clinical trial operations and optimize study outcomes.
- Ensure accurate and timely documentation of monitoring activities and findings.
- Bachelor's degree in a related field or equivalent experience.
- Minimum of 2-4 years of experience in clinical research monitoring with a strong focus on GCP compliance.
- Excellent knowledge of GCP guidelines and regulatory requirements, as well as effective communication and interpersonal skills.
- Ability to work independently, manage multiple priorities, and adapt to changing project needs.
The successful candidate will be measured on their ability to:
- Ensure high-quality monitoring and reporting.
- Meet or exceed project timelines and milestones.
- Collaborate effectively with cross-functional teams.
- Adhere to company policies and procedures.
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