AstraZeneca Released Job Openings On 10/09/2022.AstraZeneca is an exciting global, innovation-driven biopharmaceutical company. We’re inspired by what science can do.Application form link provided at the end of post.
Vacancy Details:
AstraZeneca Recruiting University or college degree in the life sciences or related subject, pharmacy, nursing or equivalent relevant degree for Senior Clinical Data Manager Position.Complete Details for the Senior Clinical Data Manager as follows.
Important Details :
- Location :Bengaluru
- No of Vacancies:NA
- Details of Salary:NA
- Opening date for online Application: 10/09/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
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Job Description/Skills Required
Responsible for coordination of the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM processes, standards and technology. May act as a Core member of Global Study Team (GST) and may lead studies with less complexities. Collaborates with DM vendors and liaise with a variety of departments on a local and/or global level to ensure each study is run in accordance to the specifics of the model. Maintains Business Continuity for CDM processes and standards including integrity of the clinical database for the relevant studies. May work under direction of an experienced Principal Project Data Manager
Typical Accountabilities
- Coordinate the Clinical Data management deliverables on assigned studies depending on the relevant model and DM Vendor. Takes accountability and serves as the first line of contact at the study level.
- Demonstrates leadership and operational knowledge in the planning and delivery of CDM deliverables at a study level potentially under mentorship from a Principle Project Data Manager.
- Communicates and collaborates effectively with all study level team members. Primary point of contact for DM vendor and provides guidance and supervision to Lead Data Manager/DM Team Lead working on the study (CRO or in-house).
- Oversight of the day to day operational aspects of CDM for assigned studies; Responsible to identify risks and collaborate with the DM Vendor to mitigate the risk.
- Understands therapeutic area, indication or program specific data capture standards and AZ standards.
- Provide input into CDM related activities associated with regulatory inspections/audits for assigned studies.
- Responsible for compliance to Trial Master File requirements relating to DM Vendor
- Support Senior Leaders to oversee CDM Vendor performance, depending on relevant model. Review, assess and manage DM Vendor delivery against important metrics, budget and overall performance. Oversees vendor timelines and breakthrough deliverables for the assigned studies. Ensures DM Vendor billing is accurate and gives recommendations for payment of invoices.
- Drive adherence to AZ CDM standards and processes for data quality and consistency of data capturing for assigned studies.
- Demonstrates willingness to take on ad hoc activities consistent with current or experience in support of CDM.
- Mentoring junior Clinical Data management colleagues
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