Freelance Clinical Oversight Monitor

vor 2 Wochen

Lugano, Tessin, Schweiz Proclinical Vollzeit

Responsibilities

  • Monitor clinical studies to ensure compliance with applicable regulations and standards.
  • Perform comonitoring qualityled, onsite visits with the assigned monitoring team.
  • Provide support to CRAs and investigational site personnel to ensure data integrity is maintained during all facets of the study maintenance.
  • Develop and maintain relationships with key stakeholders including CRO, principal investigators, and other external parties.
  • Undertake motivational calls to support patient recruitment boosting activity.
  • Analyse data from clinical trials and ensure accuracy and integrity.
  • Provide guidance and support to study teams as needed.

Requirements:

  • Bachelor's Degree in a scientific discipline (e.g. biology, chemistry).
  • 5+ years of experience in clinical research.
  • 9+ years of experience in site management and onsite monitoring (CRA experience).
  • Strong understanding of Good Clinical Practices (GCP) and the EMA.
  • Excellent interpersonal, communication, and problemsolving skills.
  • Ability to work independently and as part of a team.
  • Ability to multitask and manage multiple projects.
  • Proficiency in MS Office Suite.
  • Willing to travel regionally up to 40%.


Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

LI-RN1

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