Associate Data Team Lead

Posted 2 Days Ago
Be an Early Applicant
Mexico City
Mid level
Healthtech
The Role
The Clinical Data Manager is responsible for managing data activities in Phase I-III clinical trials, ensuring compliance with relevant guidelines, and completing trials on time and within budget. Responsibilities include serving as the primary representative on project teams, reviewing clinical trial documents, participating in UAT, and training vendors. The role requires a minimum of 4-6 years of data management experience and includes collaboration with Clinical Database Programmers.
Summary Generated by Built In

Job Overview

The Clinical Data Manager (CDM) is responsible for managing data activities for Phase I-III clinical trials, ensuring compliance with ICH/Good Clinical Practices (GCP) and other relevant guidelines. The CDM ensures trials are completed on time, within budget, and with the highest quality.

Key Responsibilities:

  • Serve as the primary data management representative on multidisciplinary project teams.

  • Communicate key clinical data management metrics (e.g., data entry status, query resolution, and aging) and determine appropriate actions with the study team.

  • Review, develop, and write clinical trial documents and manuals, including Case Report Forms, Edit Checks, Data Management Plans, Clinical Data Review Plans, and eCRF Completion Guidelines.

  • Participate in User Acceptance Testing (UAT) and Quality Control (QC) as needed.

  • Collaborate with Clinical Database Programmers to develop Data Flow Charts, Data Transfer Specifications, and Import Guidelines.

  • Assist with training sites and third-party vendors on CDM-related topics.

  • Provide data review training and guidance to Senior Clinical Data Coordinators supporting the trials.

  • Perform data review and discrepancy resolution as needed.

  • Archive trials and associated documentation upon completion.

  • Ensure adherence to Good Clinical Practice and all applicable local and international regulations.

Qualifications

  • Minimum of 4-6 years of data management experience, with 2-3 years of leading studies independently preferred.

  • Experience from startup through database lock, with at least 2-3 startups and 2-3 database locks.

  • Experience with Oracle Inc.'s Inform EDC system is preferred.

  • Oncology and/or inflammatory therapeutic area experience is preferred.

  • Project management experience within Data Management is preferred.

  • Experience with Electronic Data Capture (EDC) systems is required.

  • Bachelor’s degree but individuals with commensurate experience will be considered.

  • Work history at a Clinical Research Organization (CRO) or CRO management experience in data management is preferred.

#LI-Remote

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

Top Skills

Oracle Inc.'S Inform Edc
The Company
Bangalore, Karnataka
61,500 Employees
On-site Workplace
Year Founded: 2016

What We Do

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.

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