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Clinical Research Quality Control Associate at Clinilabs LLC
Eatontown, New Jersey, United States -
Full Time

Start Date

Immediate

Expiry Date

04 Mar, 26

Salary

25.0

Posted On

04 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Data Entry, Clerical Skills, Computer Skills, Interpersonal Skills, Documentation, Communication, Quality Control, Project Management, Good Clinical Practices, Study Protocols, Filing, Tracking, Team Collaboration, Database Management, Source Document Integrity, Case Report Forms

Industry

Research Services

Description
Description JOB SUMMARY The 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. TRAVELING Between Corporate New York site and New Jersey sites, as needed. The salary for this position ranges from $24 to $25 per hour. Final compensation is based on skills, experience, location, and overall expertise. 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.
Responsibilities
The Clinical Research Quality Control Associate is responsible for data entry tasks related to various studies and assisting Clinical Research Unit personnel with various tasks. This includes ensuring the completeness and integrity of source documents and case report forms, managing project timelines, and communicating with operational departments regarding project status.