IQVIA
Clin Research Coord Life sciences graduate
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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