Worldwide Clinical Trials
Worldwide Clinical Trials
Worldwide Clinical Trials is a global contract research organization that supports pharmaceutical and biotechnology companies throughout the drug development lifecycle. With more than 30 years of experience, the company provides clinical monitoring, data management, patient recruitment, and regulatory consulting across therapeutic areas including oncology, cardiology, and rare diseases. Its approach combines broad clinical trial expertise with personalized support and tailored solutions for complex studies.

In-House Clinical Research Associate I - Romania Remote

Supports clinical trial site data quality, safety reporting, and regulatory documentation. Works remotely on clinical operations for Worldwide Clinical Trials.

Description

  • Maintain the quality of data submitted by study sites and support timely data delivery
  • Coordinate appropriate reporting and follow-up for safety events managed by site personnel
  • Compile complete regulatory and ethics submission packages, including IRB approval, informed consent, and laboratory certification
  • Update site documentation as needed for filing in the Trial Master File (TMF)
  • Conduct feasibility assessments and identify potential study sites when requested
  • Work remotely with clinical operations teams, sponsors, and site personnel

Requirements

  • Demonstrated strength in interpersonal, verbal, and written communication
  • Ability to work effectively as part of a remote team
  • Strong customer orientation and professional communication with sponsor contacts
  • Working knowledge of Microsoft Office, CTMS, and EDC systems
  • A four-year college program focused on life sciences is preferred but not mandatory
  • A two-year college program or equivalent education and training, plus one year of clinical research or related experience
  • Fluency in English and Romanian, plus one of German, French, Italian, Spanish, or Polish

Benefits

  • Equal employment opportunity is provided without regard to race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or any other category protected by applicable law

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