Laboratory Project Services Coordinator (R1112961) in Buenos Aires, Argentina at IQVIA™

Date Posted: 1/14/2020

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Job Description

Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation, Q2 Solutions uses its global experience and scientific expertise to transform science and data into actionable medical insights that help customers improve human health.  A joint venture of IQVIA (formerly QuintilesIMS) and Quest Diagnostics, Q2 Solutions combines the best of each parent organization’s clinical trials laboratory services capabilities to fulfill its mission of treating each sample as if a life depends on it.


. Perform generic, routine study duties and tasks that are applicable across designated projects and Protocol phases, including but not limited to: receipt of site lists, entering site data into the database, ordering laboratory kits, and monitoring the day to day running of designated projects (i.e. patient specimen management receipt, pending lab analysis, and test result approvals and reports.

. Ensure outputs are delivered in line with organizational standards and client expectations.

. Maintain project documentation files that provide project status and escalation.

. Work through Protocol questions, issues, escalations and changes with relevant senior coordinators (e.g. study specific) and managers.

. Update and maintain internal databases with generic project information and input project specific information, as directed.

. Liaise with other departments and support services (e.g. Laboratory) in order to expedite testing of patient’s laboratory specimens.

. Keep Project Managers and other relevant staff informed of any issues that may affect the smooth running of the project.

. Develop solutions for routine project related issues and problems, within a limited scope.

. Participate in local and global improvement projects as defined by the relevant process improvement management team.

. Participate in internal audits, as required.

. May have occasional, limited contact with study Sponsor(s) (e.g. exchanging factual information).


. Good organizational and operational skills

. Good accuracy and attention to detail skills

. Good written and verbal communication skills including good command of English language

. Computer proficiency in word processing and spreadsheet applications

. Demonstrated ability to work in a fast-paced, high stress environment highly desirable

. Ability to establish and maintain effective working relationships with coworkers and managers.

Job ID: R1112961