...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 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...
...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 ...
...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...
...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...
...Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise... ...Editing their own projects and conducting peer ...
...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...
