Clinical Data Vacancies at IQVIA | BSc Biological Science Candidates Apply Now
IQVIA is looking for an experienced Clinical Data Specialist to join our team in Bengaluru, India. In this hybrid role, you will oversee critical data management tasks for global clinical trials, supporting digital and electronic Clinical Outcome Assessment (eCOA) processes. If you have a background in clinical data management and want to be part of a team transforming global health through data, this opportunity is for you.
About The Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Job Overview
Provide comprehensive data management expertise to eCOA Data Management to provide efficient, quality da
ta management products that meet customer needs. Provide support in operational eCOA Data Management activities to the eCOA Data Team Lead (DTL) or operate in a specific eCOA DM task (e.g., lead of a task on a megatrial, data reconciliation, and monitoring).Essential Functions
- Serve as Data Operations Coordinator (DOC) for several global clinical trials or serve in a leadership role for a specific data management task.
- With minimal guidance, serve as back-up for the Data Operations Coordinator or Data Team Lead.
- Provide specific eCOA or Clinical DM task or technology expertise.
- Manage the delivery of projects through the full data management process life cycle.
- With minimal guidance, manage project timelines and quality issues.
- Determine resource needs, and identify and justify out-of-scope.
- Provide comprehensive data management expertise (including all operations tasks).
- Perform comprehensive quality control procedures.
- Independently bring project solutions to the eCOA DM team.
- Communicate ideas for process improvement.
- Assist in developing and implementing new technology.
- Understand and comply with core operating procedures and working instructions.
- Meet objectives as assigned.
- Develop and maintain good communications and working relationships with eCOA DM and project teams.
- Interact with eCOA DM team members to negotiate timelines and responsibilities.
Qualifications and Experience
- Bachelor’s Degree in Clinical, biological, or mathematical sciences, or related field, or nursing qualification required.
- Working knowledge of SAS software is a plus, but not required.
- 3 years of related experience, including clinical trials experience in a function similar to data management.
- Equivalent combination of education, training, and experience.
- Thorough knowledge of the data management process.
- Knowledge of medical terminology, pharmacology, anatomy, and/or physiology.
- Previous experience and proven competence in managing the delivery of a project through the whole data management study life-cycle.
- Comprehensive understanding of the clinical drug development process.
- Excellent organizational, communication, and data management skills (detail-oriented).
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
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