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Clinical Trial Manager

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ICON
2-12+ years
Not Disclosed
Bangalore, India
10 Feb. 27, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Clinical Trial Manager

Location: Bangalore, India
Work Model: Office-Based
Job Type: Full-Time
Job Requisition ID: JR144479
Industry: Clinical Research / Clinical Operations

ICON plc, a global leader in healthcare intelligence and clinical research, is seeking an experienced Clinical Trial Manager (CTM) to lead end-to-end clinical trial execution. This role is office-based and requires expertise in clinical operations, project management, and cross-functional coordination to ensure high-quality, timely delivery of study milestones.

Role Overview

As a Clinical Trial Manager at ICON, you will oversee all operational aspects of clinical trials, including site selection, start-up, monitoring, and close-out activities. You will collaborate with investigators, site teams, vendors, and global study teams to ensure compliance with protocols, SOPs, and regulatory standards, while maintaining patient safety and data integrity.

Key Responsibilities

  • Lead and manage local trial operations in accordance with protocol, GCP, and SOP requirements.

  • Oversee site selection, initiation, monitoring, and close-out activities, ensuring quality and compliance.

  • Serve as primary liaison with investigators, site teams, vendors, and global study teams.

  • Drive performance metrics, site monitoring excellence, and risk mitigation strategies.

  • Ensure inspection readiness and support audits and regulatory inspections.

  • Provide guidance and mentorship to Clinical Research Associates (CRAs) to maintain robust monitoring standards.

  • Identify operational risks and proactively implement corrective actions to maintain study timelines.

Required Experience & Skills

  • 12+ years in Clinical Operations with significant on-site monitoring experience.

  • 2–3 years of project management or study leadership experience.

  • Strong knowledge of ICH-GCP, regulatory guidelines, and clinical trial processes.

  • Proven experience in Oncology, Cardiology, or Pulmonology clinical trials.

  • Excellent communication, stakeholder management, and problem-solving skills.

  • Ability to manage high-pressure situations, tight timelines, and complex operational challenges.

What ICON Offers

  • Competitive salary with global career growth opportunities.

  • Comprehensive benefits including health insurance, retirement planning, life assurance, and wellness programs.

  • Flexible work environment supporting professional development and work-life balance.

  • Access to global networks, professional training, and continuous learning opportunities.

  • Inclusive, diverse, and collaborative culture emphasizing innovation and excellence.

ICON is an equal opportunity employer committed to providing a workplace free from discrimination and harassment. All qualified applicants will receive consideration regardless of race, color, religion, gender, sexual orientation, disability, or other protected status.

This position offers a strategic opportunity for experienced clinical operations professionals to lead complex clinical trials, ensure regulatory compliance, and drive operational excellence. Apply now to advance your career with ICON.