Clin Research Co.ord At IQVIA Life sciences graduate
Job Description
IQVIA™ is the leading human data science company focused on
helping healthcare clients find unparalleled insights and better solutions for
patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a
broad range of solutions that harness the power of healthcare data, domain
expertise, transformative technology, and advanced analytics to drive
healthcare forward.
Conduct site/trial feasibility to identify & select the
right site and investigator for the study
Ensure timely compilation of all essential documents &
assist in regulatory package preparation, timely submission, follow up with
site EC to resolve any queries, and obtain approvals
Ensuring site setup according to protocol, review patient
data base & pre-screening, identify physician network
Coordinate for Clinical Trial Supplies receipt,
accountability & storage
Prepare site team for study initiation visit and coordinate
with monitor for the visit
Assist in the process of administering the informed consent
to the potential objects and discussing in detail the patient information sheet
Ensure that site documentation remains current, accurate and
complete
Coordinate for lab samples collection and logistics; review
of lab reports and update PI
Review & implement appropriate recruitment/referral
activities for active enrolment at sites
Ensure CRF Completion and query resolution on specified
timelines
Coordinate in conduct of monitoring visits and audits (Internal
or External)
Ensure that monitoring/audit related findings are resolved
within the timelines
Ensure patient follow up visit and visit compliance; manage
patient related reimbursement; site related payment
Drug receipt, accountability, storage, dispensing and related
documentation
Ensure adherence to protocol guideline, regulations, ethical
guidelines
Coordinate and ensure timely reporting to all stakeholders
Maintain study log(s) & study manuals
Assist monitor with the site closeout activities
Manage final reconciliation of Clinical Trial Supplies and
archival of study documents at sites
Qualification: Life sciences graduate
Eligibility criteria:
Good verbal & written English communication skills
Must speak, read & write regional language
Basic knowledge of MS word & excel
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