Job Title: Clinical Research Coordinator
Location: Bengaluru, India
Employment Type: Full-time
Job ID: R1460978
Company Overview:
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. We aim to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
Job Overview:
The Clinical Research Coordinator will perform a variety of clinical procedures to collect, record, report, and interpret data on patients enrolled in clinical studies, ensuring adherence to study protocols, standard operating procedures (SOPs), and Good Clinical Practices (GCP). The role also involves assisting with daily workload planning.
Essential Functions:
Study Support:
Provide clinical research support to investigators for study preparation and execution.
Review study protocols, Case Report Forms (CRFs), study-specific documents, and data capture systems.
Attend all relevant study meetings and assist with regulatory/ethics documentation submission (FDA and other regulatory bodies).
Patient Management:
Recruit and screen patients for clinical trials, maintaining subject screening logs.
Orient patients to the study, explaining the purpose, procedures, and protocol.
Documentation & Data Management:
Design and maintain source documentation based on protocol requirements.
Schedule and execute study visits, performing necessary procedures.
Collect and maintain accurate study data, ensuring quality control for content, accuracy, and completeness.
Handle lab testing and analysis, ensuring proper specimen collection and logistics.
Safety & Communication:
Monitor patient safety and report adverse reactions to appropriate medical personnel.
Communicate with research subjects, addressing study-related questions or issues.
Assist with study data quality checking and resolving queries.
Clinical Procedures:
Perform complex clinical procedures such as ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring.
Study Monitoring & Staff Training:
Assist in verifying that study objectives are met on time, within budget, and according to protocol.
Provide training to new site staff on study-specific topics and requirements.
Assist with study monitoring visits, audits, and regulatory inspections.
Qualifications:
Education:
Bachelor’s Degree (Required) or High School Diploma (Required)
Experience:
3+ years of relevant work experience in a clinical environment or medical setting (e.g., medical assistant, nurse, laboratory technician).
Skills & Knowledge:
Working knowledge of clinical trials and Good Clinical Practices (GCP).
Proficiency in MS Windows and Office applications (Access, Outlook, Word).
In-depth knowledge of departmental and study-specific SOPs, consent forms, and study schedules.
Skill in clinical procedures (e.g., intravenous catheter insertion, spirometry testing).
Excellent attention to detail, interpersonal, and communication skills.
Certifications/Licenses:
Applicable certifications and licenses as required by company, country, state, and/or regulatory bodies.
About IQVIA:
IQVIA is committed to helping improve global health by accelerating the development and commercialization of innovative medical treatments. We leverage data, technology, and advanced analytics to make intelligent connections that improve patient outcomes.
For more information, visit IQVIA Careers.
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