LogoFresh Jobs Ahead
Worldwide Clinical Trials
Worldwide Clinical Trials
1.001 – 5.000 Angajați
Sponsor pentru viza H1BAsistență medicalăConsultanțăLogistică
Worldwide Clinical Trials este o organizație globală de cercetare clinică pe bază de contract, care sprijină companiile farmaceutice și de biotehnologie pe parcursul întregului ciclu de dezvoltare a medicamentelor. Cu o experiență de peste 30 de ani, compania oferă servicii de monitorizare clinică, gestionare a datelor, recrutare a pacienților și consultanță de reglementare în domenii terapeutice precum oncologia, cardiologia și bolile rare. Abordarea sa combină expertiza vastă în studiile clinice cu sprijin personalizat și soluții adaptate studiilor complexe.
LinkedIn
Locurile de muncă ale companiei

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.

ARArgentinaRemoteNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăAsociatGeneral

Descriere

  • 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.

Cerințe

  • 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.

Beneficii

  • 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.

Locuri de muncă similare