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Data Manager I (Clinical Trials)

Формат работы
remote (только Costa_rica)
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
CR
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
Data Manager I (Clinical Trials) (Clinical Data Management): Managing clinical trial data collection, cleaning, reconciliation, database lock, and delivery with an accent on data quality, compliance, and Sponsor collaboration. Focus on defining data processing requirements, maintaining audit-ready documentation, coordinating data transfers and validation, and ensuring timely study deliverables.

Location: Remote in Costa Rica

Company

hirify.global, part of Thermo Fisher Scientific, develops regulated technology that helps generate better clinical evidence and improve patient outcomes.

What you will do

  • Act as the primary Data Management contact for Sponsors and internal teams throughout the study lifecycle.
  • Manage clinical trial data collection, cleaning, reconciliation, database lock, routine data runs, and final data delivery.
  • Develop and maintain Data Management Plans, study-specific processing requirements, edit checks, and data quality standards.
  • Lead data transfer specifications, sample data files, transfer approvals, and coordination with programming teams on validation activities.
  • Maintain audit-ready documentation, including data transfer agreements, Data Correction Requests, and client communications.
  • Conduct status meetings, provide study metrics, manage escalations, and identify out-of-scope requests for Project Management review.

Requirements

  • Bachelor’s degree in Life Sciences or a related field preferred.
  • At least 2 years of Data Management or related experience, preferably in clinical research.
  • Strong understanding of clinical trial processes and data management principles.
  • Strong organizational, interpersonal, time-management, problem-solving, and communication skills.
  • Ability to manage multiple priorities, meet deadlines, and collaborate with Sponsors, programmers, project teams, and other stakeholders.
  • Excellent written and verbal English communication skills required.

Nice to have

  • Prior client-facing experience.
  • Exposure to SAS and/or SQL.
  • Knowledge of CDISC SDTM standards.

Culture & Benefits

  • Competitive compensation.
  • Health, dental, and vision coverage.
  • Retirement savings plan with company contribution.
  • Paid time off and company holidays.
  • Work focused on supporting clinical science and helping deliver life-changing therapies to patients faster.

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