Lab Data Coordinator
iqviaNew York (NY)
Lab Data Coordinator
Posted 10 days ago
iqviaNew York (NY)
Clinical Research CoordinatorsResearch and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)
SENIORITY
Junior
About the role
Job TitleEssential 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
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
Fresh graduates are welcome to apply.
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 Microsoft Office, especially Excel.
General understanding of medical and clinical research.
Before you apply
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A number in mind
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Your notice period
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