Novartis Released Job Openings On 24/05/2022.Novartis is a global healthcare company based in Switzerland that provides solutions to address the evolving needs of patients worldwide.Eligibility for the Clinical Data Manager as follows.
Vacancy Details:
Novartis Recruiting University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree with 3 years experience in Drug Development with at least 2 years in Clinical Data Management for Clinical Data Manager Position.Complete Details for the Clinical Data Manager as follows.
Important Details :
- Location : Hyderabad
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 24/05/2022
- 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
- As Clinical Data Manager (CDM) provide data management input on Clinical Trial teams. May have the role of TDM on small low complexity trials . Performs DM activities for start up of a study including preparing the eCRF, CCG’s where needed, Data Handling plan (DHP) Data Review Plan (DRP) and performing user acceptance testing (UAT) as applicable
- Manage local lab set up for the Clinical Database as applicable
- Under supervision ensures consistency of assigned trials with program level standards
- Understands third party data requirements and begins to gather an understanding of new technologies that may be used in the course of clinical trials
- Performs ongoing review of all data generated from the clinical study including Third party and local lab data as well as SAE reconciliation where applicable
- Ensures activities that are performed are done with quality and understanding of the process. Verifies and tracks eCRF completion including Query resolution and provides data status updates as needed
- With support from the Trial Data Manager develops proposals to resolve issues that may occur during the running of assigned trials. With support from the Trial Data Manager gives input into Study Specification worksheets should assigned trials need to be outsourced
- Has a working knowledge of FDA and ICH guidelines. Has proven ability to use the tools available to generate listings for data review and where necessary provides these to the study teams. Generates the study status reports for use at Clinical trial team meetings
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