Remote Clinical Research Associate II – Dermatology

Premier Research International

España

Ibrido

EUR 42.000 - 68.000

Tempo pieno

2 giorni fa
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Descrizione del lavoro

Premier Research International in Madrid is seeking a Clinical Research Associate II to join our Clinical Monitoring team. You will deliver quality monitoring reports, manage TMF/eTMF, and ensure data integrity across dermatology trials in I-IV phases.

The role offers remote/hybrid/office options from Madrid, with approximately six days on-site per month and country-wide monitoring requirements. A healthcare-related undergraduate degree with 2+ years in clinical trials is expected.

Competenze

  • Undergraduate degree in a clinical, science, or health-related field or equivalent work experience.
  • Previous clinical research experience required.
  • At least 2+ years' experience in clinical trials and independent monitoring.
  • Experience working in Dermatology therapy area preferred.

Mansioni

  • Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines.
  • Maintains submission of expenses according to travel and expense requirements within company guidelines.
  • Monitors (remote, onsite, or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with country regulations.
  • Plans day to day activities for monitoring of a clinical study and sets priorities per site.
  • Prepares for and conducts on-site qualification, study initiation, interim monitoring, and close-out monitoring visits at investigator sites as required by the clinical monitoring plan.
  • Maintains TMF/eTMF as defined by the organization's processes per filing guidelines.

Conoscenze

Clinical monitoring
Data integrity
Regulatory compliance
Dermatology experience

Formazione

Undergraduate degree in clinical, science, or health-related field

Descrizione del lavoro

Premier Research International in Madrid is seeking a Clinical Research Associate II to join our Clinical Monitoring team. You will deliver quality monitoring reports, manage TMF/eTMF, and ensure data integrity across dermatology trials in I-IV phases.

The role offers remote/hybrid/office options from Madrid, with approximately six days on-site per month and country-wide monitoring requirements. A healthcare-related undergraduate degree with 2+ years in clinical trials is expected.

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