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Senior Cd Proj Sppt Assistant

1+ years
Not Disclosed
10 July 16, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title: Senior Clinical Project Support Assistant

Location: Thane, India
Work Mode: Hybrid
Experience Required: Minimum 1 year
Job Type: Full-time
Salary Range: Not specified


Job Summary

IQVIA is hiring a Senior Clinical Project Support Assistant in Thane to assist project managers with end-to-end study lifecycle operations. This hybrid role involves document management, vendor coordination, and support for connected device applications used in clinical trials. Ideal for candidates with at least 1 year of experience in clinical research administration and strong proficiency in Microsoft Office tools.


Key Responsibilities

  • Maintain and update study trackers and communicate progress to sponsors.

  • Support document preparation and access management for connected device applications.

  • Coordinate translation requests for patient/site documents with external vendors.

  • Create, manage, and periodically review Trial Master Files for accuracy and completeness.

  • Assist in uploading documentation on logistics systems and coordinate with the logistics team.

  • Participate in project archival activities and ensure documentation integrity.

  • Train and mentor junior team members or new joiners.

  • Respond to vendor queries and perform cost analysis and rate evaluation.

  • Track and report project metrics and manage customer satisfaction surveys.


Required Skills & Qualifications

  • High School Diploma or equivalent (preferred); relevant experience accepted in lieu of formal education.

  • Minimum of 1 year of relevant experience in clinical project support.

  • Proficiency in Microsoft Excel and Word.

  • Strong communication skills and ability to collaborate with cross-functional teams.

  • Organized, detail-oriented, and able to manage multiple administrative tasks.


Perks & Benefits

  • Hybrid work flexibility (office and remote blend)

  • Opportunity to work in global clinical trial operations

  • Continuous learning and development support

  • Inclusive and collaborative work environment

  • Career advancement within a global CRO


About the Company

IQVIA is a global leader in healthcare analytics, technology solutions, and clinical research services. With expertise in connected health and data-driven innovation, IQVIA enables the pharmaceutical and healthcare industries to improve outcomes and advance medical innovation.


Work Mode

Hybrid – Flexibility to work from home and on-site in Thane, India.


Call-to-Action

If you're ready to make an impact in global clinical research operations, apply now to join IQVIA’s world-class team as a Senior Clinical Project Support Assistant.