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Ctm I / Ctm Ii – Clinical Trial Management

Syneos Health
Syneos Health
2+ years
Not Disclosed
Remote, India, India
1 May 8, 2026
Job Description
Job Type: Full Time Education: None Skills: Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding

CTM I / CTM II – Clinical Trial Management
Location: India (Remote Opportunity)
Company: Syneos Health
Job ID: 25107742
Job Type: Full-Time
Industry: Clinical Research / Clinical Trial Management / Pharmaceutical Operations


About the Company

Syneos Health is a globally recognized biopharmaceutical solutions organization focused on accelerating customer success across clinical development, medical affairs, and commercialization. The company combines scientific expertise, operational excellence, and innovative healthcare solutions to help pharmaceutical and biotechnology organizations deliver therapies faster and more efficiently.

Operating across more than 110 countries with a workforce of over 29,000 professionals, Syneos Health is committed to improving patient outcomes through advanced clinical research and technology-driven solutions.


Job Overview

Syneos Health is hiring experienced professionals for the role of CTM I / CTM II (Clinical Trial Management). The selected candidate will oversee clinical trial management activities, site management operations, monitoring deliverables, and cross-functional coordination to ensure successful execution of global clinical studies.

This remote opportunity is ideal for candidates with strong clinical trial management experience, vendor management expertise, and a solid understanding of GCP, regulatory compliance, and risk-based monitoring strategies.


Key Responsibilities

  • Oversee site management, clinical monitoring, and central monitoring activities throughout the clinical trial lifecycle
  • Ensure patient safety, protocol compliance, regulatory adherence, and data integrity
  • Manage site interactions from activation through closeout activities
  • Support patient recruitment, investigator payments, and site engagement activities
  • Identify and assess protocol execution risks and mitigation strategies using Risk Assessment and Categorization Tools (RACT)
  • Review study scope, budgets, protocols, and operational deliverables
  • Monitor project timelines, quality metrics, and budget-related risks
  • Escalate operational risks and out-of-scope requests to project leadership
  • Participate in key project meetings, including Kick-Off Meetings and study discussions
  • Serve as an escalation point for investigator site communication and issue resolution
  • Collaborate with Study Start-Up, Data Management, Patient Recruitment, Pharmacovigilance, and Quality Assurance teams
  • Develop and maintain Clinical Monitoring Plans (CMPs), study tools, and operational templates
  • Ensure CTMS dashboards, EDC systems, ePROs, IWRS/IVRS, and monitoring systems are properly configured and maintained
  • Coordinate protocol-specific and operational training for study teams
  • Oversee CRA and Central Monitor resource allocation, study assignments, and operational performance
  • Review monitoring documentation, visit reports, monitoring letters, and study correspondence
  • Support inspection readiness, audit preparation, and quality compliance activities
  • Assist with corrective action planning and risk mitigation strategies
  • Support database lock and study milestone completion activities

Required Qualifications

  • Bachelor’s degree in:
    • Life Sciences
    • Pharmacy
    • Biotechnology
    • Nursing
    • Healthcare-related disciplines
  • Registered Nurse (RN) qualification or equivalent clinical experience may also be considered
  • Strong understanding of:
    • Clinical trial management
    • GCP and ICH Guidelines
    • Site management
    • Risk-based monitoring
    • Clinical operations and regulatory compliance