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Clin Process Assoc - India

2+ years
Not Disclosed
10 April 17, 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

 


Clin Process Assoc – India

Department: Clinical Operations
Location: Bengaluru, Karnataka
Job Type: Full-Time
End Date to Apply: 25th April 2025

Job Overview:
Provide project-related assistance for assigned projects, sites, and project teams. Ensure that all work is conducted in accordance with SOPs, policies, good clinical practices, applicable regulatory requirements, and meets quality and timeline metrics.

Essential Functions:

  • Perform processes and tasks that result in high-quality deliverables completed according to service level agreements (SLAs) and within project timelines.

  • Tasks may be assigned to either Start-Up studies or Maintenance studies.

  • Establish and maintain effective project/site communications.

  • Create and maintain relevant project documents.

  • Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines, and project plans with project-specific information.

  • Review, evaluate, and recommend modifications to designated processes.

  • Participate in document management (creation, review, maintenance, storage, as applicable).

  • Participate in study team meetings and implement action items.

  • Collaborate with the project lead/team members in creation/review of study documents.

  • Set quality standards and review deliverables to the same for process tasks.

  • Work on visit tracking in CTMS for investigator payments, Vendor Setup QC’s, PV Batch Review, Passthrough invoice Batch Review, and associated tasks.

  • Provide and revoke access as necessary.

  • Review ATP (Authorization to Proceed) trainings.

  • Coordinate with translation vendors.

  • Understand contracts and enable excellent output quality for processing teams.

  • Ensure effective and efficient coordination between the operations team (PM/RSU/Clinical/IPA) for visit/passthrough batch query resolutions.

  • Work effectively in a deadline-oriented environment and manage SLAs (TAT, productivity, quality).

  • Respond to ad-hoc requests for data/information/analysis.

  • Provide general administrative support for projects, tracking various activities.

  • Responsible for indexing.

  • May act as a buddy for new hires and serve as an SME for the team.

Qualifications:

  • Bachelor's Degree (preferred).

  • Life Sciences graduates with a minimum of 2 years of relevant experience (preferred).

About IQVIA:
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more: IQVIA Careers

Location: Bengaluru, India