Sr. Clinical Research Qc Associate

JOB SUMMARY

The Senior Clinical Research Quality Control Associate is responsible for data entry tasks related to the various studies as well as assisting Clinical Research Unit (CRU) personnel and other Clinilabs personnel with other various task as requested and needed.

RESPONSIBILITIES

• Provide support (e.g. data entry, filing, QC, etc…) to CRU personnel and other Clinilabs personnel ad requested and needed.
• Assist in entry of patient visit data into databases, ensuring the completeness and integrity of source documents and case report forms (CRFs).
• Provide entry status reports.
• Communicate with all operational departments regarding project status/issues.
• Reading and understanding study protocols.
• Develop and maintain good communications and working relationship with Clinilabs’ project team members as well as Sponsors, CRO, vendor, and clinical site project team members.
• Adhere to corporate policies and procedures.
• Other duties as assigned
• Manage and track project timelines and quality issues.
• Follow and ensure compliance with current Good Clinical Practices (cGCPs).

TRAVELING

Between Corporate New York site and New Jersey sites, as needed.

• Must be able to provide accurate documentation of produced work.
• Must have related experience for at least five years.
• The position requires at least a high school diploma or equivalent, but individuals with college degrees and advanced degrees are preferred
• Must possess excellent clerical, strong computer and good interpersonal skills.