Job Overview
Provide comprehensive clinical lab data expertise as part of a team to develop and maintain Laboratory Data Management (LDM) tasks for the studies awarded to IQVIA Laboratories and meets the external client data reporting needs. May be required to support the development of new systems and processes related to the electronic data transfer process, or the configuration of business rules and master data in study and laboratory information systems.  Understand and comply with core standard operating procedures and working instructions.

Essential Functions

Capable of taking up, independently or providing inputs for, Python programming activities pertaining to ongoing study requirements or any other adhoc projects in the department

Create and/or review all appropriate data management documents

Understand and comply with core standard operating procedures and working instructions

Develop and maintain good communications and working relationships with LDM team. Serve as back-up for other Data Team Leads

Interact with internal and external team members to negotiate timelines and responsibilities

Train and mentor junior staff in DM expertise

Ensure service and quality meet agreed upon timelines and deliverables in data transmission agreements. Ensure quality checks performed on data files before transmission and obtain peer-review where required. Review own work for accuracy and completeness

Record all evidence of the data transmission process from data file definition to closure of study

Ensure that all specification and design documentation are filed and stored according to company policy

Ensure the internal and external customer queries are timely addressed and resolved effectively

Multiple communication styles and skill to effectively broker, audience specific [peers, senior team members, internal/external customers] business and interpersonal relationships that lead to positive outcomes and successful business results

Perform other duties as directed by the functional manager

Qualifications

High School Diploma or equivalent

2+ years of relevant work experience or equivalent combination of education, training and experience.

Self-driven.

Keen attention to detail to anticipate, address and/or escalate issues, with aptitude to embrace and be conduit for change.

Analytical skills as well as ability to proactively identifying process improvements which reduce operational costs and maintain quality.

Quality conscious with high degree of ethics and integrity carrying out duties in accordance to laws, regulatory standards, and with company policies and procedures.

Computer proficiency including word processing, spreadsheet and Power Point applications.

General understanding of medical, clinical research.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.