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Centralized Clinical Trial Manager

0-2 years
Not Disclosed
10 Sept. 19, 2025
Job Description
Job Type: Full Time 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

Job Title

Centralized Clinical Trial Manager

Location: Bangalore / Remote (Office or Home-based, India)
Time Type: Full-time
Posted: 2 Days Ago
Application Deadline: October 20, 2025
Job Requisition ID: JR135179


About ICON

ICON plc is a global leader in healthcare intelligence and clinical research, committed to shaping the future of clinical development.

  • ICON fosters an inclusive, diverse, and innovative environment.

  • The organization focuses on enhancing trial quality, patient safety, and the development of innovative therapies.


Role Overview

The Centralized Clinical Trial Manager will oversee centralized monitoring activities of clinical trials, ensuring effective coordination of data-driven insights to enhance trial quality and patient safety. This role involves collaboration with cross-functional teams to ensure study compliance and efficient trial execution.


Key Responsibilities

  • Lead centralized monitoring activities, including data review and risk-based monitoring.

  • Collaborate with clinical operations, data management, and biostatistics teams to identify and manage potential risks.

  • Ensure study compliance with regulatory requirements and protocols.

  • Provide oversight on site performance, patient safety, and data quality using centralized data insights and analytics.

  • Coordinate cross-functional teams to ensure efficient trial execution and support continuous process improvements.


Qualifications

  • Bachelor’s degree in life sciences, healthcare, or related field (advanced degree preferred).

  • Experience in clinical trial management, centralized monitoring, or data management.

  • Solid understanding of risk-based monitoring approaches.

  • Strong analytical skills and proficiency in clinical trial data review and interpretation.

  • Excellent organizational and project management skills, capable of handling multiple studies and meeting deadlines.

  • Effective communication and interpersonal skills, with the ability to collaborate across diverse teams.


Benefits at ICON

  • Competitive salary and additional benefits.

  • Various annual leave entitlements.

  • Health insurance plans suitable for employees and families.

  • Retirement planning offerings.

  • Global Employee Assistance Programme (TELUS Health) with 24-hour access to professionals for well-being support.

  • Life assurance and flexible optional benefits, including childcare vouchers, gym discounts, travel subsidies, bike purchase schemes, and health assessments.


Diversity & Inclusion

  • ICON is committed to a discrimination-free and inclusive workplace.

  • Equal consideration for all applicants, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

  • Reasonable accommodations are available for applicants with medical conditions or disabilities.


Encouragement to Apply

  • Applicants are encouraged to apply even if they do not meet all requirements.

  • Current ICON employees should follow internal application procedures.