Posted:11 hours ago|
Platform:
On-site
Full Time
● Delegated duties of the clinical trials
● Maintenance of the trial master files
● Involved in the consent process and documentation
● Randomization and allocation, Electronic data capture
● Prepare the documents for SAE reporting, if any
● Reviewing scientific literature and attending conferences to stay current with advances in clinical research
● Preparing reports on study results and submitting them to colleagues and supervisors
● Reviewing data from clinical trials to ensure that study procedures were followed accurately
● Coming up with new ideas for research projects that can be conducted within the department or company
● Participating in research projects related to pharmacokinetics and pharmacodynamics
● Preparing publications, presentations or working reports; and
● Performing other research and administrative duties as assigned
● Participate with the PI and study team to identify and prioritize the development of systems and infrastructure to maintain research quality and compliance
Occasional travel to attend sponsor study training meetings as required
Job Type: Full-time
Pay: ₹70,000.00 - ₹72,000.00 per month
SRM Institute of Science and Technology
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