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Clinical Trial Manager I/ Ii

Syneos Health
2+ years
Not Disclosed
Pune, Pune city, India
8 May 19, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Clinical Trial Manager I / II

Company

Syneos Health

Location

Pune, Maharashtra, India

Job ID

25108578

Job Type

Full-time (Clinical Trial Management / Clinical Research)


Company Overview

Syneos Health is a fully integrated life sciences services organization focused on accelerating drug development and commercialization. The company partners with pharmaceutical and biotech innovators to improve clinical research efficiency and patient outcomes globally.


Role Summary

The Clinical Trial Manager (CTM I/II) is responsible for overseeing clinical trial site operations, ensuring compliance with regulatory requirements, Good Clinical Practice (GCP), and study protocols. The role involves managing site performance, supporting clinical monitoring activities, and ensuring data integrity and patient safety across assigned clinical trial sites.


Key Responsibilities

1. Site Management & Monitoring

  • Conduct site qualification, initiation, monitoring, and close-out visits (on-site or remote)

  • Evaluate site performance and recommend corrective actions when required

  • Ensure compliance with ICH-GCP, regulatory guidelines, and company SOPs

2. Patient Safety & Compliance

  • Verify informed consent processes are properly executed and documented

  • Assess patient safety risks, protocol deviations, and pharmacovigilance issues

  • Ensure confidentiality of patient data is maintained

3. Data Integrity & Documentation

  • Perform source document verification (SDV)

  • Ensure accurate and complete case report form (CRF) data entry

  • Manage query resolution and ensure timely closure

  • Review Investigator Site File (ISF) and reconcile with Trial Master File (TMF)

4. Investigational Product (IP) Management

  • Verify IP storage, dispensing, accountability, and reconciliation

  • Ensure compliance with blinding/randomization requirements

  • Support IP return, labeling, and regulatory handling

5. Communication & Reporting

  • Document monitoring activities (trip reports, follow-up letters, communication logs)

  • Act as liaison between sponsor teams, investigators, and site staff

  • Participate in investigator meetings and sponsor meetings

6. Project & Study Support

  • Support patient recruitment and retention strategies

  • Ensure site readiness for audits and inspections

  • Track study milestones, timelines, and deliverables

  • Adapt to changing project priorities under guidance of Lead CRA

7. Systems & Technology Use

  • Use clinical data management and electronic data capture (EDC) systems

  • Ensure compliance with electronic systems and tracking tools


Additional Responsibilities (Real-World / Late Phase Studies)

  • Support full study lifecycle from site selection to close-out

  • Conduct chart abstraction and real-world data collection

  • Collaborate with medical science liaisons and country teams

  • Support sponsor affiliates and local operational teams


Required Qualifications

  • Bachelor’s degree or Registered Nurse (RN) in a relevant field (or equivalent experience)

  • Knowledge of ICH-GCP guidelines and regulatory requirements

  • Strong computer and digital system skills

  • Excellent communication, interpersonal, and presentation skills

  • Willingness to travel up to 75%


Preferred Skills

  • Clinical research or monitoring experience

  • Strong understanding of clinical trial processes and documentation

  • Ability to manage multiple sites and competing priorities

  • Attention to detail and strong analytical skills


Job Level Summary

Clinical Trial Manager I / II Responsibilities

  • Manage clinical trial site operations and ensure protocol compliance

  • Coordinate between investigators, sponsors, and internal teams

  • Ensure timely execution of monitoring and reporting activities

  • Support budget, timelines, and operational delivery of studies

Scope of Work

  • Individual contributor role with technical expertise

  • May oversee limited staff or processes (≤2 employees)

  • Works on complex clinical research tasks with moderate supervision

  • Contributes to study execution and operational decision-making


Work Environment

  • Global clinical research organization

  • High-compliance, regulated environment

  • Requires collaboration across multiple stakeholders and geographies