...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.
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...- Perform core medical monitoring activities for multiple assigned studies, including input into study design, protocol and regulatory approval strategy,
- Prepare and execute successful SEC Presentation in CDSC...
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...
...Key responsibilities include, but are not limited to: accountability for the operational delivery of clinical study to time, quality, and budget (eg, country selection, diversity, patient engagement strategy, recrui...
...to ensure that all assets are properly cataloged in the asset management system (in use or not)
Work with our logistics warehouse to ship and reclaim hardware as requested
Process disposal shipments, ensuring a...
...Job Description :
1) Should be a medical doctor - preferably with MD in Pharmacology
2) 4+ years- experience in handling Phase 2/Phase 3 clinical trials in India
3) Manage the CRO team for all clinical ...
...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...
...business information and concepts into dynamic, impactful eLearning content.
Editing their own projects and conducting peer review of co-workers projects, as well as conducting quality checks for technical issues...