Clinical Research Coordinator
Welcome to the Latest Job Vacancies Site 2025 and at this time we would like to inform you of the Latest Job Vacancies from the IQVIA with the position of Clinical Research Coordinator which was opened this.
If this job matches your qualifications, please send your application directly through our latest Job site. Indeed, every job is not easy to apply because it must meet several qualifications and requirements that we must meet in accordance with the standard criteria of the Company who are looking for potential candidates to work. Good job information Clinical Research Coordinator below matches your qualifications.
- Provide clinical research support to investigators to prepare for and execute assigned research studies, including: review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data;
- Attend all relevant study meetings;
- Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research;
- Recruit and screen patients for clinical trials and maintain subject screening logs;
- Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits;
- Design and maintain source documentation based on protocol requirements;
- Schedule and execute study visits and perform study procedures;
- Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness;
- Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics;
- Monitor subject safety and report adverse reactions to appropriate medical personnel;
- Correspond with research subjects and troubleshoot study-related questions or issues;
- Participate in “huddles” to confirm daily study tasks are assigned to team members and are executed to the expected standards;
- Assist with study data quality checking and query resolution;
- Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring;
- Record, report and interpret study findings appropriately to develop a study-specific database;
- Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards;
- Provide training to new investigator site staff members on study-specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records;
- Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies;
- Assist research site with coverage planning related to staffing and scheduling for research projects.
- Bachelor's Degree;
- High School Diploma or equivalent;
- 3 years' relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training and experience;
- Working knowledge of clinical trials;
- Working knowledge of the principles of Good Clinical Practices (GCP);
- In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules;
- Skill in carrying out required clinical procedures such as intravenous catheter insertion and spirometry testing;
- Good skill in using MS Windows and Office applications such as Access, Outlook and Word;
- Excellent interpersonal skills;
- Ability to pay close attention to detail;
- Ability to establish and maintain effective working relationships with coworkers, managers and clients;
- Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
How to Submit an Application:
After reading and knowing the criteria and minimum requirements for qualifications that have been explained from the Clinical Research Coordinator job info - IQVIA Buenos Aires, Buenos Aires above, thus jobseekers who feel they have not met the requirements including education, age, etc. and really feel interested in the latest job vacancies Clinical Research Coordinator job info - IQVIA Buenos Aires, Buenos Aires in 2025-06-05 above, should as soon as possible complete and compile a job application file such as a job application letter, CV or curriculum vitae, FC diploma and transcripts and other supplements as described above, in order to register and take part in the admission selection for new employees in the company referred to, sent via form this bottom.
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