IQVIA Careers in Clinical Data Management
About IQVIA
IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services to the life sciences and healthcare industries. With a commitment to innovation and improving patient outcomes, IQVIA leverages data-driven insights to accelerate the development and commercialization of innovative medical treatments. Our mission is to create intelligent connections that enhance the quality of care and drive population health improvements worldwide.
Current Job Opening: Clinical Data Management
IQVIA is currently seeking qualified professionals for the position of Clinical Data Management at our Hyderabad location. This role is crucial in ensuring the accuracy and quality of clinical data, which is vital for the success of our research and clinical trials.
Position Name:
- Clinical Data Management
Organization:
- IQVIA
Qualifications Required
Candidates should hold a Bachelor’s or Master’s degree in Pharmacy (B.Pharm, M.Pharm), Pharm.D, M.Sc, B.Sc, or Life Sciences, with a minimum of 2 years of relevant experience.
Job Location:
- Hyderabad
Salary:
- ₹25,000 – ₹35,000 / month
Experience Required:
- Minimum 2 years of experience in Clinical Data Review tasks.
Key Responsibilities
- Protocol Review: Understand and review protocols along with relevant data review documents (e.g., Protocol Data Review Plan, Data Quality Management Plan).
- Clinical Data Review: Review clinical data listings and manage the resolution of data discrepancies.
- Data Cleaning: Perform data cleaning as per the defined Clean Patient Group, including the freezing and locking of CRFs/fields.
- Coordination: Coordinate with the Data Management Lead for study deliverables and manage the review of loaded external data.
- Discrepancy Management: Track data load, address discrepancies, and coordinate with external data vendors for resolution.
- Documentation: File appropriate documents in eTMF as per the eTMF master plan.
Must-Have Skills
- Good knowledge of clinical data management activities.
- Expertise in clinical data listings review and Vendor Data reconciliation, including Local lab review.
- Strong understanding and expertise in Query Management.
- Experience in performing User Acceptance Testing (UAT) for data review listings.
- Experience in freezing and locking of CRFs.
- Knowledge and experience with EDC systems (Medidata RAVE preferred).
- Excellent oral and written communication skills.
- Proficiency in Veeva Vault documentation.
Nice-to-Have Skills
- Knowledge of ICH-GCP guidelines and regulatory guidelines/regulations.
- Familiarity with third-party reconciliations like SAE Reconciliation, Protocol Deviation, and Questionnaire review.
- Basic understanding of study build aspects like CRF design and Edit Check build for efficient data review.
- Ability to perform UAT of screens and edit checks for appropriate discrepancy management.
- Understanding of the roles and responsibilities of all key stakeholders across projects.
- Effective communication skills with cross-functional teams.
- General knowledge of clinical research, including Investigator site processes.
- Basic understanding of 21 CFR Part 11 and data privacy as they apply to data handling and the use of computer systems in clinical research.
Why Join IQVIA?
IQVIA offers a dynamic and collaborative work environment where innovation and creativity are encouraged. We provide opportunities for professional growth and development while working on projects that have a global impact on healthcare. Joining IQVIA means becoming part of a team that is dedicated to making a difference in the lives of patients around the world.
How to Apply
If you meet the qualifications and have the required experience, we encourage you to apply for this exciting opportunity. Join us at IQVIA and contribute to our mission of improving patient outcomes and population health worldwide.
To Apply: Please visit the IQVIA careers page and submit your application.
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