Require Clinical trial researcher in Jaipur. Candidate must have knowledge of MS Word, Excel and some basic formulas. Must be presentable and good behaviour is required to interact with patients.
Participants are provided with information about the clinical trial.
The content of the informed consent is explained.
Reporting of adverse events or drug reactions.
report suspected misconduct.
Protect the integrity and confidentiality of records and data during the clinical study
Assuring timely completion of studies.
Monitoring data for safety and efficacy trends by reviewing clinical data.
Writing clinical reports upon completion or termination of studies.
Preparing manuscripts for technical journals and making presentations at scientific meetings.
Liaising with doctors, scientists and health professionals and meeting with colleagues.