Senior Clinical Data Science Manager

hace 4 días

Bogotá, Bogotá D.E., Colombia ICON A tiempo completo
About ICON

ICON plc is a world-leading healthcare intelligence and clinical research organization. Our mission is to shape the future of clinical development by fostering an inclusive environment that drives innovation and excellence.

We are committed to developing our employees in a continuous learning culture where every experience adds to your professional development.

We strive to provide you with a comprehensive and competitive total reward package that comprises an excellent level of base pay, variable pay, and recognition programs.

Job Description

This Principal Clinical Data Science Lead role is part of the Early Phase Data Management department and is responsible for managing data management teams, studies, and programs under the general direction of the Senior Manager/Director of Data Management.

The successful candidate will provide planning estimates for project scope, schedule, and resource requirements, ensuring that studies are properly managed and delivered on time and within budget.

They will work closely with Clinical Operations, Biostatistics, SAS Programming, Medical Writing, and Quality Assurance to ensure that data collected during trials is managed according to corporate standards and meets regulatory guidelines for data integrity.

Responsibilities

The Principal CDSL will manage multiple fast-moving early phase studies or programs of studies to ensure project objectives are met within agreed timelines and to a high level of quality.

Key responsibilities include:
  • Reviewing project contracts to ensure out-of-scope work is managed efficiently.
  • Managing overall project budgets, taking responsibility for cost control, timelines, and project quality.
  • Negotiating with clients and/or external customers/departments regarding timelines and key deliverables.
  • Traveling (approximately 15%) domestically and/or internationally.

Requirements

To be successful in this role, the ideal candidate will have:
  • 6+ years of clinical data management experience (in a Clinical Research Organization or Pharmaceutical company).
  • 3+ years of experience leading studies with key responsibilities for study set-up and close-out tasks.
  • Experience with Phase I studies is strongly preferred, but not required.
  • Experience with Rave is strongly preferred, but must have experience with at least one of ICON's preferred CDMS.
  • Highly computer literate, including strong Microsoft Office skills.
  • Excellent communication and interpersonal skills.
  • Strong client relationship management skills.
  • Excellent organizational and planning skills as well as a demonstrated aptitude for project management.
  • Bachelor's degree or local equivalent in a scientific field and/or equivalent experience.

Benefits

We offer a range of benefits designed to support you and your family's well-being and career development, including:
  • Various annual leave entitlements.
  • Health insurance offerings tailored to your needs.
  • Competitive retirement planning options.
  • Global Employee Assistance Programme.
  • Life assurance.
  • Flexible country-specific optional benefits.

Why Choose ICON?

We are committed to building a diverse culture that rewards high performance and nurtures talent. We believe in providing an inclusive and accessible environment for all candidates and employees.

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