ICBio Job Vacancy For Any Life Science Background
Qualification:Any Life Science Background
Experience:2 to 3 Years Experience in Clinical Trial
Job Description
1) Perform site/center related study activities according to the study protocols.
2) Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
3) Responsible for the safety and proper conduct throughout the trial.
4) Verifying that the investigator follows the approved protocol and all GCP procedures.
5) Adverse events, concomitant medications, and inter current illness are reported in accordance with the protocol on the CRF's.
6) Collects documents needed to initiate the study and submit to the sponsor.
7) Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.
8)Day to day updating of all study related activities status to the CRO/Project Manger.
9) Assists the PI in submission of accurate and timely closeout documents to applicable regulatory agencies and the sponsoring agency in accordance with regulations and sponsoring agency policies and procedures.
Send CVs to hrd@icbiocro.com
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