Instagram
youtube
Facebook

Senior Cd Proj Sppt Assistant

1+ years
Not Disclosed
10 July 8, 2025
Job Description
Job Type: Full Time 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

 

Senior Clinical Development Project Support Assistant

Location: Thane, India (Remote/Home-based)
Job Type: Full-Time
Work Mode: Remote


Job Summary:

IQVIA is seeking a highly organized Senior Clinical Development Project Support Assistant to provide end-to-end support to Project Managers throughout the lifecycle of global clinical studies. This is a fully remote role ideal for professionals with 1+ year experience in project coordination, documentation, or trial support in the healthcare or pharmaceutical industry.


Key Responsibilities:

  • Prepare study trackers and update project sponsors regularly

  • Assist with compiling clinical study documentation under Project Manager guidance

  • Manage access requests and biannual reviews for Connected Devices applications and databases

  • Coordinate vendor activities for translation of site/patient materials

  • Upload project documentation to clinical logistics systems

  • Maintain and audit Trial Master Files (TMF) for accuracy and completeness

  • Liaise with the Logistics team for site setup and related deliverables

  • Support project archival activities and documentation lifecycle

  • Mentor junior support staff and assist in onboarding new team members

  • Respond to vendor queries and assist with cost analysis

  • Conduct vendor rate analysis and proposal tracking

  • Administer and analyze Customer Satisfaction Surveys

  • Maintain and update internal/external project metrics


Required Skills & Qualifications:

  • High School Diploma or equivalent (Bachelor’s degree preferred)

  • Minimum 1 year of relevant clinical or project support experience

  • Proficiency in Microsoft Office (Excel, Word)

  • Strong communication, coordination, and organizational skills

  • Ability to manage documentation workflows and project timelines

  • Collaborative team player with a proactive attitude

  • Prior experience with Trial Master Files or clinical logistics systems a plus


Perks & Benefits:

  • 100% Remote working flexibility

  • Opportunity to support global clinical development operations

  • Exposure to advanced digital health and connected device platforms

  • Professional development and cross-functional learning opportunities

  • Inclusive and collaborative work culture


Company Overview:

IQVIA is a global leader in clinical research, real-world data, and healthcare technology solutions, serving the life sciences industry. The company empowers healthcare advancement through data-driven innovation to improve patient care and research delivery.


Work Mode:

Remote / Home-based – Flexible location across India.


Call-to-Action:

Ready to grow your career in clinical trial operations with a leading CRO? Apply now and become part of IQVIA’s mission to drive smarter healthcare.