Senior CRA I - Remote Clinical Trial Monitor

7252 Syneos Health Chile S.A.

Chile

Remote

CLP 20.088.000 - 26.784.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Syneos Health Chile S.A. is seeking a Sr CRA I for sponsor-dedicated work in Chile, home-based. The role focuses on monitoring clinical studies, ensuring data integrity and regulatory compliance, and collaborating with cross-functional teams to support trial execution.

The candidate should have a bachelor's degree, 3-5 years of clinical research experience, familiarity with GCP, and CCRP or equivalent certification preferred. This is a full-time, home-based position in Chile.

Qualifikationen

  • Bachelor's degree in a related field.
  • 3-5 years of experience in clinical research or related field.
  • In-depth knowledge of clinical trial processes and regulations.
  • Strong analytical and problem-solving skills.
  • Excellent communication and interpersonal skills.

Aufgaben

  • Conduct on-site and remote monitoring of clinical research studies to ensure compliance with clinical practices.
  • Develop tools and templates for monitoring reports and site visit checklists.
  • Contribute to design and delivery of processes, programs, and policies for trials.
  • Manage and direct work of junior staff and oversee day-to-day trial site activities.
  • Ensure accurate documentation and timely reporting of trial data for regulatory submissions.
  • Collaborate with data management, biostatistics, and regulatory teams to support trials.
  • Identify and resolve issues related to trial conduct and data integrity.
  • Provide training and mentorship to junior staff on monitoring techniques.

Kenntnisse

Analytical thinking
Communication
Independent worker

Ausbildung

Bachelor's degree
CCRP certification preferred

Tools

CTMS

Jobbeschreibung

Syneos Health Chile S.A. is seeking a Sr CRA I for sponsor-dedicated work in Chile, home-based. The role focuses on monitoring clinical studies, ensuring data integrity and regulatory compliance, and collaborating with cross-functional teams to support trial execution.

The candidate should have a bachelor's degree, 3-5 years of clinical research experience, familiarity with GCP, and CCRP or equivalent certification preferred. This is a full-time, home-based position in Chile.

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