CTA Job Opportunity at IQVIA | Apply Now
CTA job seekers looking for opportunities in clinical research can explore this exciting Clinical Trial Assistant position with IQVIA. This full-time, home-based role in Mexico City offers professionals with life sciences backgrounds the opportunity to support global clinical trials, contribute to study documentation, and work with one of the world’s leading clinical research organizations. If you are interested in IQVIA careers, a remote job, or a job in Mexico, this opportunity could be an excellent fit.
- Job Position: Clinical Trial Assistant (CTA)
- Location: Mexico, North America
- Job ID: R1549528
About the Company
IQVIA careers offer opportunities with one of the world’s leading providers of clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company creates intelligent connections that accelerate the development and commercialization of innovative medical treatments, helping improve patient outcomes and population health worldwide.
CTA Job Description
CTA job responsibilities involve performing daily administrative activities in conjunction with Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams to ensure complete and accurate Trial Master File delivery. The Clinical Trial Assistant will support study documentation, maintain compliance-related records, assist with clinical trial administration, and help ensure project timelines are met.
Qualifications
CTA job applicants should meet the following requirements:
Education
Experience
- 1 year of clinical research experience as an Intern or Study Coordinator.
Skills and Knowledge
- Fluent conversational English.
- Computer skills including working knowledge of Microsoft Word, Excel, and PowerPoint.
- Written and verbal communication skills with a 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.
- Awareness of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
- Knowledge of applicable protocol requirements as provided in company training.
CTA Job – Key Responsibilities
CTA Job responsibilities include supporting clinical research teams and maintaining study documentation.
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams with accurately updating and maintaining clinical documents and systems, including Trial Master Files (TMF).
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to standard operating procedures.
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU teams with preparation, handling, and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Assist with the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.
- Act as a central contact for the clinical team regarding designated project communications, correspondence, and associated documentation.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
Why Consider IQVIA for this CTA Job?
IQVIA careers provide professionals with opportunities to contribute to innovative healthcare solutions while working in a collaborative and globally recognized environment. Benefits of joining IQVIA include:
- Exposure to global clinical research projects.
- Professional development opportunities.
- Flexible home-based work environment.
- Experience working with industry-leading clinical research professionals.
- Opportunity to support the development of innovative medical treatments.
