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Senior Manager, Clinical Data Management

6+ years
Not Disclosed
10 May 17, 2025
Job Description
Job Type: Full Time Education: BA/BS 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 Manager, Clinical Data Management
Location: Manila (Homebased)
Job ID: 2025-117610
Department: Clinical Data Management, Clinical Data Scientist Lead, Clinical Systems, Data Standards Consultant
Organization: ICON Strategic Solutions
Mode: Remote


Role Summary:
The Senior Manager, Clinical Data Management will be responsible for ensuring high-quality and timely data management deliverables across the company’s clinical study portfolio. Working under the Data Management Lead, this role involves oversight of in-house and outsourced data management activities, strategic vendor coordination, and active participation in cross-functional collaboration to support clinical and regulatory goals.


Key Responsibilities:

  • Lead data management activities for internal and outsourced clinical trials.

  • Provide vendor oversight across global programs and serve as the point of contact for data deliverables.

  • Represent Data Management in Clinical Sub-teams and drive alignment between ICON and CROs.

  • Guide setup and validation of study tools (e.g., EDC, IRT, ePRO, eCOA).

  • Oversee data quality plans: edit checks, reconciliation guidelines, coding, lock plans.

  • Manage data review processes, including query management, and database locks.

  • Ensure TMF documents are inspection-ready and archived.

  • Lead resolution of escalated risks and issues across cross-functional stakeholders.

  • Track budgets and timelines for Data Management vendors; provide accurate forecasts.

  • Champion process improvements and support continuous development of operational standards.

  • Act as subject matter expert in clinical data management, CDISC standards, and regulatory compliance.


Candidate Profile:

  • Education: Bachelor’s degree (BS/BA) in health/life sciences or technology-related fields.

  • Experience:

    • Minimum 6+ years in clinical data management or related drug development roles.

    • Experience managing large global development programs.

    • Familiarity with all clinical trial phases and cross-functional clinical operations.

    • Expert understanding of FDA/ICH regulations, CDISC, and GCP standards.

    • Strong project management and vendor oversight experience.

    • Budget management and strategic forecasting experience.

  • Skills:

    • Technologically adept with EDC, data review platforms, and eClinical tools.

    • Strong leadership, decision-making, and risk mitigation skills.

    • Effective communicator across functions and vendors.


Benefits at ICON:

  • Competitive salary structure.

  • Generous annual leave and retirement benefits.

  • Comprehensive health insurance for you and your family.

  • Access to 24/7 Global Employee Assistance Programme (TELUS Health).

  • Flexible benefit options including childcare vouchers, gym memberships, and health assessments.

  • Life assurance coverage.

  • Commitment to inclusion, equity, and accessible working environments.


Note:
If you require a reasonable accommodation during the recruitment process or have a medical condition impacting your application, please reach out through:

https://careers.iconplc.com/reasonable-accommodations