JOB SUMMARYThe 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 tasks as requested and needed.RESPONSIBILITIES
- Provide support (e.g. data entry, filing, QC, etc.) to CRU personnel and other Clinilabs personnel as requested and needed.
- Assist in the entry of patient visit data into databases, ensuring the completeness and integrity of source documents and case report forms (CRFs).
- Develop and maintain good communications and working relationships with Clinilabs' project team members as well as Sponsors, CRO, vendor, and clinical site project team members.
- Manage and track project timelines and quality issues.
- Provide entry status reports.
- Reading and understanding study protocols.
- Communicate with all operational departments regarding project status/issues.
- Follow and ensure compliance with current Good Clinical Practices (cGCPs).
- Adhere to corporate policies and procedures.
- Other duties as assigned.
Salary may vary depending on individual skills, relevant experience, and geographic location. For positions based in New York City, the salary range is up to $24 per hour. Requirements
- The position requires at least a high school diploma or equivalent, but individuals with college degrees and advanced degrees are preferred.
- Must have related experience for at least two years.
- Must possess excellent clerical, strong computer, and good interpersonal skills.
- Must be able to provide accurate documentation of produced work.