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Centralized Clinical Trial Manager

0-2 years
Not Disclosed
10 Sept. 24, 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

Job Category:

Clinical Research / Clinical Operations

Location:

Bangalore, India – Office or Home-based (Hybrid/Remote)

Employment Type:

Full-Time

Job Requisition ID:

JR135179

Application Deadline:

October 20, 2025


Company Overview:

ICON plc is a global healthcare intelligence and clinical research organization focused on innovation, excellence, and inclusivity. The company supports clinical development by providing advanced insights, centralized monitoring, and quality oversight to improve patient safety and trial outcomes.


Job Purpose:

The Centralized Clinical Trial Manager oversees centralized monitoring activities for clinical trials, ensuring compliance with protocols and regulatory standards, optimizing trial quality, and supporting patient safety. The role involves managing data-driven insights, collaborating with cross-functional teams, and contributing to continuous improvement of trial processes.


Primary Responsibilities:

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

  • Collaborate with clinical operations, data management, and biostatistics teams to identify risks and ensure proactive trial management.

  • Ensure study compliance with regulatory requirements and protocols via real-time data review and monitoring.

  • Monitor site performance, patient safety, and data quality using centralized analytics.

  • Coordinate with cross-functional teams to optimize clinical trial execution and process improvements.


Qualifications & Experience:

  • Bachelor’s degree in Life Sciences, Healthcare, or related field (advanced degree preferred).

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

  • Strong understanding of risk-based monitoring approaches and trial data oversight.

  • Excellent analytical, organizational, and project management skills.

  • Effective communication and interpersonal skills to collaborate across diverse teams.


Skills & Competencies:

  • Data review and interpretation for clinical trials.

  • Risk-based monitoring implementation and oversight.

  • Multitasking and managing multiple studies simultaneously.

  • Collaboration and stakeholder management.

  • Strong attention to detail and problem-solving skills.


Benefits:

  • Competitive salary and annual leave entitlements.

  • Comprehensive health insurance options for employees and family.

  • Retirement planning support and life assurance.

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

  • Flexible country-specific optional benefits (childcare vouchers, gym discounts, subsidized travel, health assessments, etc.).


Inclusion & Accessibility:

  • ICON is committed to providing an inclusive and accessible workplace free from discrimination or harassment.

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

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