Remotely
gcpclinical researchoncologyregulatory compliancesite managementrisk based monitoringmonitoringich guidelines
Job Description
📋 Description
- Considered as the Primary Sponsor point of contact for the investigative site. Advanced level of
- Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical
- Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure
- Superior understanding of site engagement and ability to customize site engagement strategy for
- Superior level of competency connecting the study protocol, scientific principles and clinical
- Possesses advanced level of competency to mentor and train less experienced CRAs on various aspects
🎯 Requirements
- Appropriate tertiary qualification in health related disciplines (e.g., Medical, Scientific
- Minimum of 3 years of clinically related experience, of which a period of 2 years is preferable in
- Knowledge of appropriate therapeutic area indications with the ability to understand and apply
- Superior knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP
- Demonstrate advanced communication skills and superior cross-functional collaboration skills among
- Demonstrate superior planning and organizational skills and the ability to work effectively and
🎁 Benefits
- Comprehensive package of benefits including paid time off (vacation, holidays, sick)
- This job is eligible to participate in our short-term incentive programs.
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