Clinical Research Associate – Oncology Trials (Travel)

Worldwide

Italia

In loco

EUR 42.000 - 60.000

Tempo pieno

14 giorni+
Generatore di candidature

Una candidatura apposita per questa offerta — un curriculum e una lettera di presentazione personalizzati, perfettamente in linea con l'annuncio.

Supera i filtri ATS

Descrizione del lavoro

Worldwide Clinical Trials is seeking a seasoned Clinical Research Associate to work across diverse therapeutic areas including Neuroscience, Oncology, and Cardiovascular. You will monitor sites, ensure protocol adherence, and support TMF processes while collaborating with a global team.

The role requires 2+ years as a CRA, a 4-year degree or RN/BSN, and willingness to travel. Strong English communication and data quality focus are essential to succeed in this team-oriented environment.

Competenze

  • Strong communication skills and teamwork abilities.
  • Experience as a Clinical Research Associate is required.
  • Willingness to travel and work in diverse therapeutic areas.
  • Background in Oncology and Hematology is preferred.

Mansioni

  • Qualify, initiate, monitor, manage sites and close-out visits.
  • Mentor and guidance to junior CRAs and site staff.
  • Document site visit findings with clear reports.
  • Train site staff on protocol adherence as needed.
  • Review safety information and informed consent.
  • Perform source data verification for data accuracy and patient safety.
  • Review CRFs and assist with data query resolution.
  • Prepare TMF filings and site-related documentation.
  • Ensure IP receipt, accountability, and destruction where applicable.
  • Conduct accompanied site visits for training and assessment.

Conoscenze

Interpersonal skills
English communication
Organizational skills
Independence
MS Office/CTMS/EDC proficiency

Formazione

4-year university degree or RN/BSN in Nursing

Strumenti

Microsoft Office
CTMS
EDC Systems

Descrizione del lavoro

Worldwide Clinical Trials is seeking a seasoned Clinical Research Associate to work across diverse therapeutic areas including Neuroscience, Oncology, and Cardiovascular. You will monitor sites, ensure protocol adherence, and support TMF processes while collaborating with a global team.

The role requires 2+ years as a CRA, a 4-year degree or RN/BSN, and willingness to travel. Strong English communication and data quality focus are essential to succeed in this team-oriented environment.

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