Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

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.