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Lead Clinical Data Manager (Remote)

5-10 years
USD $68,500 – $217,100
10 Oct. 29, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Position: Lead Clinical Data Manager (Remote)

Location: Durham, North Carolina (Home-Based)
Job ID: R1496394
Employment Type: Full-Time
Available Locations:
Anaheim (CA), Atlanta (GA), Austin (TX), Boston (MA), Charleston (SC/WV), Charlotte (NC), Chicago (IL), Dallas (TX), Jacksonville (FL), Jersey City (NJ), Las Vegas (NV), Miami (FL), Myrtle Beach (SC), New York (NY), Norfolk (VA), Oakland (CA), Orlando (FL), Philadelphia (PA), Portland (ME/OR), Raleigh (NC), Richmond (VA), San Diego (CA), San Francisco (CA), Tampa (FL), Virginia Beach (VA), and other remote locations across the U.S.


Overview

IQVIA is expanding its Clinical Data Management (CDM) division and seeking experienced Lead Clinical Data Managers for both FSP (Functional Service Provider) and Sponsor-Agnostic delivery models.
This role offers the opportunity to manage global clinical trials end-to-end, ensure data integrity, and drive excellence in data management delivery across diverse therapeutic areas.
💻 This is a fully remote position — all required equipment will be provided.


Key Responsibilities

Data Management Leadership

  • Lead data management for complex, global clinical trials from study setup to database lock.

  • Serve as the primary client contact for all data management deliverables and communications.

  • Oversee serious adverse event (SAE), pharmacokinetic (PK), and external data reconciliation.

  • Manage database design, testing, and deployment using industry-standard EDC systems.

Project Oversight & Delivery

  • Oversee timelines, budgets, and resource allocation to meet project milestones and client expectations.

  • Ensure quality, accuracy, and regulatory compliance across all deliverables.

  • Monitor project progress and proactively resolve issues or delays.

Team Mentorship & Development

  • Mentor and guide junior CDM staff, providing technical leadership and best practice training.

  • Promote process efficiency, data quality, and operational consistency across projects.

  • Collaborate cross-functionally with biostatistics, clinical operations, and programming teams.

Process Improvement & Compliance

  • Drive continuous process improvement initiatives within CDM teams.

  • Ensure compliance with ICH-GCP, SOPs, and sponsor-specific data management standards.

  • Support internal/external audits and regulatory inspections.


Qualifications

Education

  • Bachelor’s degree in Life Sciences, Health Sciences, Clinical Research, Biological Sciences, or Mathematics (required).

Experience

  • Minimum 10 years of clinical data management experience, with 5+ years in a Lead CDM role.

  • Proven success in managing large-scale, global clinical trials (1000+ patients).

  • Hands-on expertise with EDC systems such as Medidata Rave, Oracle InForm, or equivalent.

  • Strong knowledge of GCP, ICH guidelines, and clinical research processes.

  • Prior job titles may include:

    • Clinical Data Manager

    • Senior Clinical Data Manager

    • Lead Data Manager

    • Principal Data Manager

    • Data Management Project Manager

Core Skills

  • Exceptional leadership and organizational skills.

  • Strong communication, analytical, and problem-solving abilities.

  • Ability to manage multiple complex projects simultaneously.


Compensation & Benefits

  • Base Pay Range: USD $68,500 – $217,100 (annualized)

    • Actual pay depends on qualifications, experience, and location.

  • Eligible for bonuses, incentive plans, and additional compensation packages.

  • Comprehensive benefits include:

    • Medical, dental, and vision coverage (effective Day 1)

    • 401(k) with company match

    • Life insurance and discretionary PTO

    • Career growth opportunities, mentoring, and global mobility options


Recruitment Process

  1. Recruiter Video Chat – 20 minutes

  2. Hiring Manager Interview – 1 hour (via MS Teams)

Offer decisions are typically made within one week of the final interview.


Why Join IQVIA

IQVIA is a global leader in clinical research services, data analytics, and healthcare technology.
We connect data, science, and innovation to accelerate the development of life-changing medical treatments and improve global health outcomes.

🌐 Learn more: https://jobs.iqvia.com


Equal Opportunity Employer

IQVIA provides equal employment opportunities to all applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic.
📄 More Info: https://jobs.iqvia.com/eoe


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