IQVIA, a leading global healthcare intelligence provider, is on a mission to drive advancements in healthcare by combining advanced analytics, technology, and deep industry expertise. As a trusted partner to the pharmaceutical, biotechnology, and healthcare sectors, IQVIA is dedicated to delivering high-quality, impactful solutions that improve patient outcomes and optimize healthcare systems worldwide.
Job Responsibilities
As a Document QC Specialist at IQVIA, you will play a crucial role in ensuring the accuracy, quality, and compliance of the Trial Master Files (TMF) and other clinical documents. Your key responsibilities will include:
- Performing quality control (QC) of TMF documents to ensure compliance with internal and external standards.
- Ensuring that documents are appropriately indexed, organized, and maintained in a structured and easily accessible manner.
- Identifying and resolving discrepancies or issues within clinical trial documentation.
- Supporting teams in maintaining up-to-date TMF repositories.
- Working closely with project teams to ensure that all documents meet regulatory and client-specific requirements.
Qualifications
To be considered for the Document QC Specialist role at IQVIA, candidates should possess the following qualifications:
- Experience: 1-2 years of experience in TMF/Document QC, ideally within a clinical trial or healthcare environment.
- Education: A bachelor’s degree in Life Sciences, Healthcare, or related fields is preferred.
- Knowledge: Familiarity with TMF standards and document management systems is essential.
Key Skills
In addition to the required qualifications, the following skills will enhance your success in this role:
- Attention to Detail: Strong focus on maintaining document accuracy and compliance.
- Organizational Skills: Ability to effectively manage multiple tasks and prioritize effectively.
- Communication Skills: Clear communication skills, both written and verbal, to collaborate with cross-functional teams.
- Problem-Solving: Ability to identify discrepancies and resolve issues efficiently.
How to Apply
If you are ready to make a significant impact on the future of healthcare, we invite you to apply for the Document QC Specialist position at IQVIA. This role is based in Pune, Thane, or Bangalore, and offers a dynamic and office-based work environment.
To apply:
- Prepare your updated resume.
- Send it to subudhi.bhanuja@iqvia.com.