Clinical Research Coordinator

5 days ago


Fatih, Istanbul, Turkey IQVIA Argentina Full time
Job Overview
Clinical Research Coordinators play a vital role in the success of clinical trials. At IQVIA Argentina, we seek an experienced Senior Clinical Trial Assistant to join our team and contribute to the delivery of high-quality trial results.

The ideal candidate will possess strong administrative skills, excellent communication abilities, and a keen eye for detail. As a key member of our research operations team, you will be responsible for ensuring seamless trial execution, maintaining accurate records, and providing exceptional support to our clients.

Key Responsibilities
  1. Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up teams with accurately updating and maintaining clinical documents and systems that track site compliance and performance within project timelines.
  2. Collaborate with clinical teams on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to scope of work and standard operating procedures.
  3. Assist with periodic review of study files and completeness.
  4. Collaborate with CRAs and RSU on the preparation, handling, and distribution of Clinical Trial Supplies and maintenance of tracking information.
  5. Coordinate the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.
  6. Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
  7. Act as a mentor for less experienced Clinical Trial Assistants (CTAs).
  8. Assist with training and onboarding of new CTAs.
  9. May serve as subject matter expert for business processes.
  10. May lead CTA study teams.
  11. May assist with interviewing and screening of potential new team members.
  12. May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
  13. May participate in departmental quality or process improvement initiatives.
Requirements
  1. Bachelor's degree in Life Sciences or related field.
  2. Equivalent combination of education, training, and experience.
  3. Minimum two years clinical research experience strongly preferred, including previous experience as a CTA.
  4. Proficiency in Microsoft Office applications, particularly Word, Excel, and PowerPoint.
  5. Effective written and verbal communication skills, including good command of the English language.
  6. Effective time management and organizational skills.
  7. Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  8. Knowledge of applicable clinical research regulatory requirements, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  9. Knowledge of applicable protocol requirements.
About Us
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.

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