Veeda Lifesciences looking for Clinical Data Management Associate

Veeda Lifesciences is a global contract research organization (CRO) offering comprehensive clinical, preclinical, and bioanalytical services to support the development of innovative, biosimilar, and generic drugs. With a presence across multiple regions, Veeda provides expertise in preclinical R&D, BA/BE studies, bioanalytical services, and early to late-phase clinical trials (Phase I-IV). Renowned for scientific excellence, regulatory compliance, and ethical practices, Veeda ensures high-quality research through continuous investment in people, processes, and technology.

Post : Clinical Data Management Associate

Position Summary
The Clinical Data Management Associate is responsible for providing expert skills as part of the clinical data management team within the Data Management and Statistics Department to ensure that efficient and quality data management products are produced in accordance with customer requirements. The core responsibility of this role is to ensure that the clinical data review, query review and resolution is in track with the study timelines while maintaining the quality and integrity of the clinical trial data.

Responsibilities :
- Manages the delivery of projects through the full data management process life cycle by fulfilling the following (including but not limited to):
• annotated CRF development, o management of queries and warnings,
• processing of external data,
• reporting,
• SAE reconciliation,
• update of data in the eCRF.
• coding (e.g.. development and validation of codes, oversight of the coding library), o coding review (e.g.. MedDRA. CTCAE. WHO or Sponsor dependent), o validation or participation in the UAT, o development of eCRF guidelines, o . Review the SAS program outputs queries

Provides input to the management of :
• eCRF development according to Sponsor needs and protocol specifications o Project timelines o Quality issues o Resource management
- Performs presentations of data management activities
- Manages comprehensive data management tasks pertaining to the documented project specifications
- Provides data management expertise and data management process improvement input to the reporting Lead Clinical Data Manager or the Principal Clinical Data Manager
- Complies with the Company's Quality and Information Security Management Systems and applicable national and international legislation, including legislation for data protection

Candidate Profile
• Up to 2 years of experience in specialized data management skills (e.g.. CRF design. SAE reconciliation, central laboratory, and/or new technologies) in a CRO. a pharmaceutical or equivalent organization

Skills Required : coding review (e.g., MedDRA, CTCAE, WHO or Sponsor dependent), update of data in the eCRF, annotated CRF development.