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Senior Manager, Data Management (LATAM)

3 weeks, 5 days ago
Mexico
Full-time
Lead
Program Manager
Project and Program Management
Apply Now
Precision Medicine Group

Precision Medicine Group

Precision Medicine Group specializes in precision medicine, utilizing targeted expertise and data insights to accelerate drug development and enhance the commercialization of next-generation medical products for the pharmaceutical and life sciences ind...

Pharmaceuticals
251-1K
Founded 2012
View All Jobs 106

Description

  • Manage the day-to-day activities of the Data Management function in line with SOPs, regulatory directives, and study-specific plans.
  • Lead, supervise, develop, and mentor data managers while supporting hiring, performance feedback, and evaluations.
  • Oversee planning, implementation, and execution of contracted data management activities across multiple projects and clients.
  • Serve as a point of contact for internal teams and sponsors, coordinating communication, continuity, and responsiveness.
  • Review RFPs, proposals, change orders, and project estimates, including support for contractual and financial aspects of projects.
  • Track and manage project timelines, deliverables, quality, budget, and resource needs.
  • Oversee CRF specification development, database build activities, UAT, edit checks, and clinical database quality.
  • Ensure completeness of data management documentation for the Trial Master File and compliance with SOPs and industry regulations.
  • Coordinate training for project team members and clinical research personnel on study-specific tools, processes, and reporting.
  • Liaise with sponsors, vendors, and cross-functional stakeholders to resolve issues, manage risks, and support data-related deliverables.

Requirements

  • Minimum 8 years of data management experience and 3 years of line management experience.
  • Bachelor’s degree with direct clinical trial experience in a CRO or pharmaceutical environment.
  • Experience managing people in a scientific or clinical background preferred.
  • Proficiency in Microsoft Office: Word, Excel, PowerPoint, and Outlook.
  • Ability to handle a variety of clinical research tasks with strong organizational and communication skills.
  • Professional written and spoken English proficiency.
  • Experience using clinical database management systems.
  • Broad knowledge of drug, device, and/or biologic development and effective data management practices.
  • Preferred experience in a clinical, scientific, or healthcare discipline.
  • Preferred experience with MedDRA and WHODrug medical coding, CDISC standards, and oncology and/or orphan drug programs.

Benefits

  • Remote work arrangement indicated by the #LI-REMOTE posting tag.
  • Opportunity to work across multiple countries in Latin America, including Mexico, Brazil, Argentina, Colombia, Chile, and Peru.
  • Equal Opportunity Employer status with accommodations available for applicants with disabilities.
  • Privacy protections for applicant data, including a separate CA Privacy Notice for California applicants.

Interested in this position?

Apply directly on the company website

Apply Now

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