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Cta-Clinops

Syngene
Syngene
1-3 years
Not Disclosed
Bangalore, India
10 March 10, 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

Job Title: Clinical Trial Assistant (CTA) – Clinical Operations
Company: Syngene International Ltd.
Location: Bangalore, India
Department: Clinical Operations – T&CR
Division: Discovery Services
Job Type: Full-Time
Experience Required: 1–3 Years in Clinical Trial Coordination, Clinical Research, or Clinical Operations

About Syngene International
Syngene International Ltd. is a leading innovation-driven contract research, development, and manufacturing organization (CRDMO) offering integrated scientific services from early discovery to commercial supply. With extensive expertise across multiple therapeutic areas, Syngene partners with global pharmaceutical, biotechnology, and healthcare companies to accelerate research and development programs.

At Syngene, safety, compliance, and operational excellence are core priorities. The organization emphasizes strong adherence to environmental health and safety standards, regulatory compliance, and high-quality scientific research practices across all operations.

Role Overview
The Clinical Trial Assistant (CTA) – Clinical Operations supports the clinical study team in the coordination and administration of clinical trial activities. This role works closely with Clinical Study Managers (CSM) and Clinical Research Associates (CRA) to ensure efficient documentation management, regulatory submissions, study tracking, and communication with trial sites and vendors.

The CTA plays a key role in maintaining trial documentation, ensuring inspection readiness, and supporting the smooth execution of clinical trials in compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.

Key Responsibilities

Clinical Trial Documentation Management

  • Maintain and update Trial Master Files (TMF) and Investigator Site Files (ISF) to ensure compliance with regulatory requirements.

  • Organize, track, and archive essential clinical trial documents including study protocols, informed consent forms, approvals, and correspondence.

  • Conduct regular quality checks to ensure completeness and accuracy of clinical documentation.

Clinical Trial Coordination

  • Support Clinical Study Managers and Clinical Research Associates in planning and tracking clinical trial activities.

  • Assist with scheduling investigator meetings, site initiation visits, monitoring visits, and study close-out visits.

  • Help track Case Report Forms (CRFs), clinical queries, and clinical data flow during the study lifecycle.

Regulatory and Ethics Committee Support

  • Assist in the preparation and submission of study documents to regulatory authorities and ethics committees.

  • Track regulatory approvals and study start-up milestones.

  • Maintain accurate records related to regulatory submissions and approvals.

Communication and Stakeholder Coordination

  • Serve as a central communication point between internal teams, clinical trial sites, and external vendors.

  • Coordinate communication related to study activities, updates, and documentation.

  • Work with translation agencies to ensure study documents are translated and back-translated as required.

Clinical Systems and Data Tracking

  • Update and maintain information in clinical trial management systems (CTMS).

  • Maintain study logs including site contact lists, enrollment logs, and essential document trackers.

  • Support study status reporting activities including data entry tracking and protocol deviation monitoring.

Clinical Trial Supply Management

  • Assist with coordination and documentation of clinical trial supplies and investigational product shipments to study sites.

  • Track inventory and reconcile study supplies with site reports.

Audit and Inspection Support

  • Assist in preparing documentation required for internal audits and regulatory inspections.

  • Support quality assurance teams by providing Trial Master Files during internal or external audits.

Administrative and Operational Support

  • Perform administrative tasks to support the clinical study team and project operations.

  • Submit project-related timesheets and maintain project documentation as required.

Safety, Compliance, and Quality Standards

  • Follow all environmental health and safety (EHS) guidelines and organizational safety protocols.

  • Ensure compliance with Good Clinical Practice (GCP), company Standard Operating Procedures (SOPs), and regulatory requirements.

  • Support quality and compliance initiatives across clinical operations.

Educational Qualifications

  • Master’s degree in Pharmacy (M.Pharm), Pharmaceutical Sciences, or Life Sciences.

  • PharmD, BAMS, BDS, MDS, BHMS, or equivalent life sciences qualification may also be considered.

Experience Requirements

  • 1–3 years of experience in clinical research, clinical trial coordination, or clinical operations.

  • Experience as a Clinical Research Coordinator (CRC) or similar clinical trial support role is preferred.

Required Skills and Competencies

  • Good understanding of clinical trial processes and documentation management.

  • Knowledge of Good Clinical Practice (GCP) guidelines and clinical research regulations.

  • Strong organizational and documentation management skills.

  • Excellent communication and interpersonal skills.

  • Ability to work in a dynamic and fast-paced research environment.

  • Strong attention to detail and ability to manage multiple priorities.

Technical Skills

  • Familiarity with Clinical Trial Management Systems (CTMS) and electronic trial documentation systems.

  • Proficiency in Microsoft Office tools including Word, Excel, and PowerPoint.

  • Experience maintaining trial master files and study tracking systems.

Work Environment
This is an office-based role located in Bangalore and requires close collaboration with clinical operations teams, study sites, and external vendors to support clinical trial execution.

Job Location
Bangalore, India.