Description
We are seeking a Clinical Data Acquisition Specialist to join our team in Bengaluru, India.
As a Clinical Data Acquisition Specialist, you will be responsible for performing study set-up activities and technical development of Electronic Data Capture (eDC) solutions and associated tools for one or more clinical studies.
Key responsibilities include:
- Providing input to study design, clinical protocol, study planning, and review of study documents
- Coordinating review, revision, and approval of study specification documents and key vendor deliverables
- Developing and delivering high-quality eDC applications and associated documents, including forms, data validation checks, and data extraction
- Providing reports, status updates, feedback, and raising risks and advice to Study Data Managers
- Ensuring quality control of deliverables
- Providing input to process improvements, new processes, training, quality assessments, audits, and inspections related to Data Acquisition
- Performing after-action reviews to share learnings and propose improvements for the future
Requirements:
- 5+ years of data acquisition experience or related job experience in Clinical Research or Information Systems
- Extensive working knowledge of GxP, ICH requirements, internal processes, and external regulations that govern drug development
- Experience with eDC solutions (Inform, Rave, Veeva CDMS Vault) and ePro solutions
- Knowledge of multiple programming languages (PL/SQL, SAS, Python, C#, etc.)
Benefits:
- Opportunity to work with a global biopharma company
- Collaborative and dynamic work environment
- Professional development and growth opportunities
At GSK, we are committed to creating an inclusive environment where our people can thrive and focus on what matters most.
For more fresh new jobs, check out yubhub.co.