Clinical Process Associate vacancies at IQVIA

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.

How to Apply

Interested candidates are encouraged to apply by sending their updated resumes to Navitha Gouli at navitha.gouli@iqvia.com.