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Senior Associate, Senior Data Manager, Clinical Data Sciences

Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Argentina
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Associate, Senior Data Manager, Clinical Data Sciences (Clinical Data Management): Leading data management activities for clinical trials with an accent on database design, data review, query management, and submission readiness. Focus on coordinating study deliverables, coaching junior Data Managers, maintaining data quality, and meeting study milestones.

Location: Buenos Aires, Argentina — Complejo LUMINA Office Park; hybrid work with 2–3 days per week in the hirify.global office or as required by business needs

Company

hirify.global develops medicines and supports healthcare decisions through scientifically robust clinical evidence and medical expertise.

What you will do

  • Lead data management activities for one or more clinical trials, including data acquisition standards, database design, clinical data collection tools, and EDC systems.
  • Develop and maintain Data Management Plans, conduct data review and query management, and oversee data cleaning, processing, access, visualization, and metrics reporting.
  • Manage database release and submission-related activities while ensuring study milestones are delivered on time and to the required quality.
  • Coordinate daily data management activities and allocate study resources appropriately.
  • Coach junior Data Managers and peer-review study deliverables for quality control.
  • Maintain high-quality, contemporaneous CDS documentation in the Trial Master File and contribute to continuous improvement and cross-study learning.

Requirements

  • At least 3 years of data management experience and a bachelor’s degree.
  • Knowledge of clinical development, all phases of clinical trials, GCP, FDA, ICH, GCDMP, and related regulatory requirements.
  • Experience with commercial clinical data management systems and/or EDC products; Inform experience is preferred.
  • Familiarity with MedDRA and WHO-Drug, plus proficiency in Microsoft Office.
  • Strong verbal and written communication skills, including the ability to communicate remotely.
  • Experience with resource management, timelines, and quality control is preferred.

Nice to have

  • Master’s degree and relevant pharmaceutical industry experience.
  • Experience with data visualization tools such as Spotfire or J-Review.
  • Awareness of regulatory requirements and relevant data standards.
  • Strong analytical, problem-solving, organizational, and time-management skills.
  • Experience using generative AI tools such as ChatGPT or Microsoft Copilot responsibly to improve productivity and outcomes.

Culture & Benefits

  • Work in a healthcare-focused environment supporting the safe and effective use of medicines.
  • Collaborate with Clinical Data Scientists and study teams to achieve operational excellence.
  • Contribute to shared lessons learned and continuous improvement across clinical studies.
  • Equal employment opportunity is provided without discrimination based on legally protected characteristics.

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