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Ecoa Data Team Lead

5-8 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

 

Job Title: eCOA Data Team Lead

Location: Bengaluru, India
Work Mode: Hybrid
Experience Required: 5–8 years in clinical data management, with at least 1 year as CDM project lead
Job ID: R1474595
Company: IQVIA


Job Summary

IQVIA is seeking an experienced and motivated eCOA Data Team Lead to manage end-to-end delivery of data management services for clinical trials. This role involves leading global clinical data management projects, ensuring high-quality, timely deliverables aligned with sponsor expectations. The ideal candidate brings a strong understanding of the drug development lifecycle, project management, and eCOA systems integration. This is a hybrid role based in Bengaluru.


Key Responsibilities

  • Gather and interpret study setup requirements from stakeholders

  • Oversee validation of new device integrations with minimal guidance

  • Conduct regular data cleaning activities ensuring accuracy and quality

  • Monitor project timelines, deliverables, and quality compliance

  • Support training of new team members and junior staff

  • Lead internal study meetings and represent DM in audits and sponsor calls

  • Track project progress, identify risks, and propose corrective measures

  • Collaborate with programming teams on process innovation and automation

  • Participate in SOP development and adherence

  • Communicate proactively with line managers and cross-functional teams


Required Skills & Qualifications

  • Bachelor’s degree in Pharmacy or equivalent field (preferred)

  • 5–8 years of direct clinical data management experience

  • At least 1 year of experience as a CDM project lead

  • Advanced proficiency in MS Excel, Word, Outlook

  • In-depth understanding of drug development lifecycle and clinical research processes

  • Excellent English communication skills (verbal and written)

  • Strong leadership, organizational, and problem-solving abilities


Perks & Benefits

  • Opportunity to work with a global leader in clinical research

  • Hybrid working model for flexibility and work-life balance

  • Access to cutting-edge tools and global clinical trial technologies

  • Collaborative, diverse, and supportive work culture

  • Career development programs and internal mobility


About the Company

IQVIA is a global leader in clinical research services and healthcare intelligence, serving life sciences and pharmaceutical industries worldwide. With a strong focus on innovation, IQVIA accelerates the development of life-saving medical solutions and improves patient outcomes through data-driven insights and technology-enabled services.


Work Mode

Hybrid – Combination of on-site (Bengaluru) and remote work


Call to Action

Ready to lead impactful clinical data management projects with IQVIA?
Apply now to take your career forward in global healthcare innovation.