Description
We are seeking a Clinical Research Quality Control Specialist to join our team in Beijing, China. This is a full-time position.
Essential Functions
- Perform quality control (QC) of project databases and requisition forms against sponsor protocols and requirements.
- Collaborate with cross-functional teams to ensure QC reviews align with current processes and quality standards.
- Work with Set-up Managers, Project Managers, and Set-up Coordinators to resolve issues identified during QC reviews.
- Maintain adherence to QC timelines to meet client needs.
- Analyze quality trends and identify opportunities for training and process improvements.
- Ensure global consistency in study set-up processes with QC counterparts.
- Participate in external and internal audits as required.
- Adhere to ICH E6 Guideline for Good Clinical Practice.
Qualifications
- Bachelor's degree in a science-related field.
- Minimum 2 years of experience in the clinical or research industry, including 1 year of set-up-related or project management experience.
- Strong interpersonal skills for interacting with senior stakeholders and sponsor organization members.
- High attention to detail, with a track record of achievement in roles such as Set-up Manager or Project Manager.
- Proficiency in Microsoft Office, Q Squared Solutions systems, and ELVIS.
- Understanding of medical and clinical research terminology.
- Ability to work in a fast-paced, deadline-driven environment.
- Excellent organizational, operational, written, and verbal communication skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
What We Offer
- Competitive salary and benefits package.
IQVIA is committed to integrity in our hiring process and maintains a zero-tolerance policy for candidate fraud.