Job requirement for Clinical Data Associate in Glenmark Pharma
Glenmark is a leading player in the discovery of new molecules both NCEs (new chemical entity) and NBEs (new biological entity) with eight molecules in various stages of clinical development. The company has a significant presence in branded generics markets across emerging economies including India. Its subsidiary, Glenmark Generics Limited has a fast growing and robust US generics business. The subsidiary also markets APIs to regulated and semi-regulated countries. Glenmark employs nearly 6000 people in over 80 countries. It has twelve manufacturing facilities in four countries and has five R&D centres.
Post: Clinical Data Associate
Perform QC of the data under the Supervision of CDC.
Understands and comply with ICH-GCP, core operating procedures and work instructions.
Filing of Study related documents.
Perform other duties as directed by the LDM or Functional Manager.
Develop and maintain good communications and working relationships with CDM team.
Performs Tracking of CRFs/DCFs.
Performs Scanning & Indexing, Filing and printing of CRFs.
Reconciliation and acknowledgement of CRFs received.
Performs First pass entry.
Updating Status report.
Assist CDC in filing and printing of DCFs.
Maintain quality and timeliness of assigned work.
Basic understanding of GCP and ICH guidelines
Perform Data entry in an efficient manner
Ability to comply with company policies and procedures
Basic Understanding of Data Management Practices
Experience: 1-4 years
Education: B.Pharm, B.Sc - Biochemistry, Chemistry, Microbiology
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
Apply/Send resume at, email@example.com
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