Career Opportunities at IQVIA: Clinical Process Associate Roles
Join IQVIA - Leading the Way in Clinical Research
IQVIA, a global leader in advanced analytics, technology solutions, and contract research services, is seeking talented professionals for the role of Clinical Process Associate in Mumbai. If you have a background in clinical trials and are passionate about advancing healthcare, this is your chance to join a dynamic team dedicated to improving patient outcomes.
Open Positions and Qualifications
Clinical Process Associate
Location: Mumbai (Local candidates preferred)
Experience: 6 months to 1 year
Mode of Work: Hybrid
Qualification: Experience in clinical trials coordination, CRC skills
Key Responsibilities:
- Clinical Trials Coordination: Assist in the planning, coordination, and execution of clinical trials. Ensure compliance with regulatory requirements and study protocols.
- Data Management: Collect, verify, and enter data accurately. Maintain and update clinical trial databases.
- Patient Interaction: Liaise with patients to ensure they understand the trial process and adhere to the study protocols.
- Documentation: Prepare and maintain study documentation, including informed consent forms, case report forms, and regulatory submissions.
- Quality Assurance: Ensure adherence to Good Clinical Practice (GCP) guidelines and standard operating procedures (SOPs).
Skills Required
- Clinical Research Coordination (CRC): Experience in coordinating clinical trials and managing patient interactions.
- Technical Skills: Proficiency in using clinical trial management software and electronic data capture systems.
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Clinical Process Associate Jobs at IQVIA[/caption]
How to Apply
Interested candidates are encouraged to apply by sending their updated resumes to Navitha Gouli at
navitha.gouli@iqvia.com.
https://pharmastuff.org.in/job/clinical-process-associate-jobs-at-iqvia
