Clinical Research Associate (FullTime)

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Summary

• Assist with the management of multiple research grants and 3b/4 clinical trial activities
• Ordering and maintaining clinical supplies for grant studies
• Tracks grant study progress and maintains accurate tracking systems
• Reviews, calculates, and facilitates, the issuance of investigator grant payments
• Participate in clinical team meetings to offer suggestions or recommendations for timely and successful completion of grant and 3b/4 studies
• Assist the Regional Monitors with Pre-Study, Initiation, interim monitoring, and close-out visits for 3b/4 studies
• Assist with budget processing for 3b/4 studies
• Interact with Clinical Safety CRAs to ensure accurate reporting of safety-related 3b/4 clinical trials
• Interact with Clinical, Marketing, Regulatory, and alliance partners on Medical Strategy initiatives
• Support Sr. VP, Medical Directors on other clinical/scientific projects as needed

Qualifications

• Bachelors degree in a medical/scientific field
• Minimum of 2 years clinical research experience in the pharmaceutical industry
• Exercises good clinical judgement and demonstates professional conduct when interacting with Investigational site personnel
• Strong organizational skills with attention to detail and accuracy
• Strong written and oral communications skills