...Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the... ...the sector, and you'll be helping shape an industry.
...
Perform duplicate search, intake, and triage of the received source documents such as Spontaneous, Literature, Regulatory and clinical trials as per agreed timelines.
Possess thorough knowledge of regulatory updates.
Awareness and understandin...
1.1 To appoint Principal Analytical Investigator during the preparation of study protocol or method validation protocol. 1.2 To identify the Principal Analytical Investigator for method development, method validation projects.
1.3 To identify the P...
...Call for JRF Position in SERB Funded Project
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Applications are invited for the position of Junior Research Fellow (JRF) for a project funded by the SERB under the Start-up Research Grant (SRG).
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Name/T...
...development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries around the world....
...The Medical Writer is in charge of producing medical writing deliverables (both regulatory and medical communication documents) with experienced and well-defined input.
The Medical Writer will draft the medical d...
...Position: Risk Investigator - AML& Surveillance (Stock Broking Transaction Monitoring & Reporting)
About the Team: -
Embark on... ...closely with other members of the Trust & Safety, Com...
...approved medicine.
Summarized Profile:
As a Project Support Coordinator you will provide administrative and technical support to... ...client and/or internal meetings with completion an...
1.1 To appoint Principal Analytical Investigator during the preparation of study protocol or method validation protocol.
1.2 To identify the Principal Analytical Investigator for method development, method validation projects.
1.3 To identify the Pri...
