IQVIA Life Science Clinical Research Coordinator Job Vacancy

IQVIA Life Science Clinical Research Coordinator Job Vacancy

Life sciences candidates are encouraged to apply for a Clin Research Coord position that is vacant and available at IQVIA. IQVIA Life Science Clinical Research Coordinator Job Vacancy. For more details on the Job description, responsibilities and such, check out all the details posted below.

Job Title: Clin Research Coord

Job ID: R1126154

Location(s):

• Bangalore, India
• Coimbatore, India

Job Description:

• 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 set up according to the protocol, review patient database & 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 the 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 a regional language
• Basic knowledge of MS word & excel

Apply Online

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