Job Description:
Clinical Research Associate (CRA) will be responsible for conducting clinical studies, managing & monitoring of study sites in accordance with SOPs, ICH-GCP (International Clinical Harmonization-Good Clinical Practice) and local regulations. CRA will manage multiple projects, support Project Team and report directly to Clinical Project Manager.
This candidate will also be responsible to coordinate all necessary activities required to set up a study,toparticipate in the start-up process including reviewing protocols, reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings and study specific training meetings, to meet the planned study timelines and to generate high quality data.
Qualifications,
We are looking for preferably experienced candidates to become a team member for clinical studies.
A successful candidate should have: