Worldwide Clinical Trials
Worldwide Clinical Trials
Worldwide Clinical Trials farmatsevtika va biotexnologiya kompaniyalarini dori vositalarini ishlab chiqish jarayonining barcha bosqichlarida qo‘llab-quvvatlaydigan global shartnoma asosidagi tadqiqot tashkilotidir. 30 yildan ortiq tajribaga ega kompaniya onkologiya, kardiologiya va noyob kasalliklar kabi turli terapevtik yo‘nalishlarda klinik monitoring, ma’lumotlarni boshqarish, bemorlarni jalb qilish va tartibga solish bo‘yicha konsalting xizmatlarini taqdim etadi. Uning yondashuvi keng qamrovli klinik tadqiqotlar tajribasini murakkab tadqiqotlar uchun shaxsiylashtirilgan yordam va moslashtirilgan yechimlar bilan birlashtiradi.

Clinical Data Associate II - Argentina Remote

Clinical Data Associate II role with Worldwide Clinical Trials focused on clinical trial data cleaning, reconciliation, testing, and documentation. This full-time remote position is open to candidates based in Argentina.

Tavsif

  • Clean clinical trial data, including reviewing and closing queries, to maintain data quality and support study timelines.
  • Inspect database pages to detect issues and maintain accurate, complete clinical trial records.
  • Compile and share study-specific data management metrics with internal and external stakeholders.
  • Execute User Acceptance Testing (UAT) for electronic data capture (EDC) databases.
  • Review reconciliations involving third-party vendor data and assist with discrepancy resolution.
  • Complete Database Quality Assessment (DQA) reviews.
  • Assess SAS listings and data checks, then take appropriate action on resulting queries and findings.
  • Assemble end-of-study media and documentation for trial archiving.
  • Submit completed study records to the Trial Master File.

Talablar

  • Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, a related field, or equivalent relevant experience.
  • At least one year of relevant industry experience in clinical research, data management, or a related area.
  • Professional proficiency in English.
  • Experience cleaning clinical data and reviewing and closing queries.
  • Experience reviewing database pages and identifying data issues.
  • Experience developing study-specific data management metrics.
  • Experience performing User Acceptance Testing (UAT) on EDC databases.
  • Experience reconciling data from third-party vendors.
  • Experience conducting Database Quality Assessment (DQA) reviews.
  • Experience evaluating SAS listings and data checks.
  • Experience preparing end-of-study media and archival documentation.
  • Experience submitting final study documentation to the Trial Master File.

Imtiyozlar

  • Equal opportunity employment.
  • A diverse and inclusive workplace.
  • A work environment that encourages collaboration and creativity.
  • Supportive, closely connected teams.
  • Accessible leadership.
  • The opportunity to collaborate with global teams across multiple time zones.

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