Clinical Research Coordinator
5 days ago
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
- 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.
- 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.
- Assist with periodic review of study files and completeness.
- Collaborate with CRAs and RSU on the preparation, handling, and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Coordinate the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
- Act as a mentor for less experienced Clinical Trial Assistants (CTAs).
- Assist with training and onboarding of new CTAs.
- May serve as subject matter expert for business processes.
- May lead CTA study teams.
- May assist with interviewing and screening of potential new team members.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
- May participate in departmental quality or process improvement initiatives.
- Bachelor's degree in Life Sciences or related field.
- Equivalent combination of education, training, and experience.
- Minimum two years clinical research experience strongly preferred, including previous experience as a CTA.
- Proficiency in Microsoft Office applications, particularly Word, Excel, and PowerPoint.
- Effective written and verbal communication skills, including good command of the English language.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Knowledge of applicable clinical research regulatory requirements, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Knowledge of applicable protocol requirements.
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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