participants to determine eligibility into study in line with study protocol and SOPs Recruit and obtain informed consent from eligible participants, in line with study protocol, SOPs and Good Clinical Practice manage and maintain quality data for research and operations purposes. Capture data into study databases e
participants to determine eligibility into study in line with study protocol and SOPs Recruit and obtain informed consent from eligible participants, in line with study protocol, SOPs and Good Clinical Practice manage and maintain quality data for research and operations purposes. Capture data into study databases e
participants to determine eligibility into study in line with study protocol and SOPs Recruit and obtain informed consent from eligible participants, in line with study protocol, SOPs and Good Clinical Practice manage and maintain quality data for research and operations purposes. Capture data into study databases e
participants to determine eligibility into study in line with study protocol and SOPs Recruit and obtain informed consent from eligible participants, in line with study protocol, SOPs and Good Clinical Practice manage and maintain quality data for research and operations purposes. Capture data into study databases e
participants to determine eligibility into study in line with study protocol and SOPs Recruit and obtain informed consent from eligible participants, in line with study protocol, SOPs and Good Clinical Practice manage and maintain quality data for research and operations purposes. Capture data into study databases e
participants to determine eligibility into study in line with study protocol and SOPs Recruit and obtain informed consent from eligible participants, in line with study protocol, SOPs and Good Clinical Practice manage and maintain quality data for research and operations purposes. Capture data into study databases e
data collection as per protocol and Standard Operating Procedures and study targets Location: VIDA – resolve them accordingly Any other duties assigned in line with requirements for research studies Availability
data collection as per protocol and Standard Operating Procedures and study targets Location: VIDA – resolve them accordingly Any other duties assigned in line with requirements for research studies Availability
Faculty with a legal framework within which to operate the research and other activities necessary to appropriate training and development opportunities in line with role requirements Play an active role in the the clinical team adheres to the set standard operating procedures in the conduct of clinical trials and
Faculty with a legal framework within which to operate the research and other activities necessary to appropriate training and development opportunities in line with role requirements Play an active role in the the clinical team adheres to the set standard operating procedures in the conduct of clinical trials and