Clinical Trial Monitor
1 month ago
Parexel Clinical Trial Monitor
Parexel is seeking a highly skilled Clinical Trial Monitor to join our team. As a Clinical Trial Monitor, you will be responsible for ensuring the smooth conduct of clinical trials at investigator sites.
Key Responsibilities- Ensure regulatory compliance with ICH-GCP and local regulations
- Conduct site visits and monitoring activities to ensure data integrity and subject safety
- Verify informed consent and ensure confidentiality of subject data
- Manage site-level activities and communication to ensure project objectives are met
- Collaborate with site staff and other stakeholders to resolve issues and ensure audit readiness
- Provide guidance on Good Clinical Practice and regulatory requirements
- Bachelor's degree or RN in a related field or equivalent combination of education, training, and experience
- Minimum 1 year experience as a clinical monitor with demonstrated experience of monitoring (virtual or onsite)
- Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
- Excellent communication, presentation, and interpersonal skills
- Ability to manage required travel of up to 75% on a regular basis
- Demonstrated experience of utilizing systems like Siebel CTMS, eTMF, eISF (Florence)
- Proficiency in local language preferred. English is required
About Parexel
Parexel is a leading global biopharmaceutical services company. We provide a comprehensive range of services to help our clients succeed in the development and delivery of innovative new treatments.
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