Syngene Hiring CTA – Clinical Operations (Clinical Trial Assistant)

Syngene Hiring CTA – Clinical Operations (Clinical Trial Assistant) | Clinical Research Job in Bangalore

Syngene International Ltd is currently hiring for the position of CTA – Clinical Operations (Clinical Trial Assistant) in the Clinical Operations – T&CR department. The role is based in Bangalore, India, and is ideal for candidates with a background in clinical research or life sciences who want to build a career in pharmaceutical clinical trials and clinical study management support.

This opportunity is suitable for professionals with experience as a Clinical Research Coordinator (CRC) or those who have worked in clinical trial conduct and documentation management. The CTA – ClinOps role supports Clinical Study Managers (CSM) and Clinical Research Associates (CRA) by maintaining clinical trial documentation, managing Trial Master Files, supporting regulatory submissions, and ensuring smooth coordination of clinical trial activities.

Professionals joining this role will gain hands‑on exposure to global clinical trial operations, regulatory documentation processes, investigational product management, and clinical data tracking systems used in pharmaceutical research.

Company Overview

Syngene International Ltd is an innovation‑driven contract research, development, and manufacturing organization (CRDMO). The company provides integrated scientific services that support pharmaceutical, biotechnology, and healthcare companies from early drug discovery through clinical development and commercial manufacturing.

Headquartered in India, Syngene collaborates with global pharmaceutical companies to accelerate drug discovery and clinical development programs. The organization provides expertise across discovery services, clinical research support, biologics manufacturing, and regulatory compliance.

Safety, scientific integrity, and operational excellence are core principles at Syngene. The company promotes a workplace culture that prioritizes environment, health, and safety (EHS) standards while maintaining the highest quality practices in clinical and laboratory operations.

Employees at Syngene work in collaborative scientific environments that encourage innovation, accountability, and continuous professional development within the life sciences and pharmaceutical research industry.

Job Role and Responsibilities

The CTA – Clinical Operations role focuses on supporting clinical trial management activities and maintaining documentation systems that ensure regulatory compliance and operational efficiency across clinical research projects.

Key responsibilities include:

• Supporting Clinical Study Managers and Clinical Research Associates in tracking clinical trial progress and site performance
• Maintaining and updating Trial Master Files (TMF) and Investigator Site Files (ISF)
• Filing, tracking, and archiving essential clinical trial documents including protocols, approvals, and consent forms
• Performing quality checks on study documentation to ensure accuracy and audit readiness
• Assisting with regulatory submissions to ethics committees and regulatory authorities
• Tracking regulatory approvals and clinical study start‑up milestones
• Supporting planning and scheduling of investigator meetings, site initiation visits, monitoring visits, and close‑out visits
• Coordinating communication between clinical teams, research sites, vendors, and internal departments
• Managing study communications and distributing project updates to team members and research sites
• Supporting management of Case Report Forms (CRFs), clinical data queries, and clinical data flow
• Entering and tracking clinical study data in clinical trial management systems (CTMS)
• Maintaining logs such as screening logs, enrollment logs, and site contact trackers
• Coordinating shipment of clinical trial supplies and investigational products to study sites
• Tracking investigational product inventory and reconciling supplies with site records
• Preparing documentation required during audits and regulatory inspections
• Supporting Quality Assurance teams during Trial Master File reviews and internal audits
• Maintaining training records and ensuring adherence to Good Clinical Practice (GCP) and regulatory guidelines

This role plays an essential part in ensuring clinical trial documentation, study coordination, and regulatory compliance across pharmaceutical clinical development programs.

Eligibility and Qualifications

Candidates interested in this clinical operations role should meet the following educational and professional requirements.

Required Education

Candidates should have postgraduate or undergraduate qualifications in healthcare or life sciences.

Relevant courses include:

M.Pharm, M.Sc Life Sciences, PharmD, BAMS, BDS, MDS, BHMS, Biotechnology, Biochemistry, Microbiology, Clinical Research, Pharmacology, Biomedical Sciences

Experience

• Experience working as a Clinical Research Coordinator (CRC) or in clinical trial operations is preferred
• Experience supporting clinical documentation, study coordination, or clinical site management activities

Required Skills

• Good communication and interpersonal skills
• Ability to work effectively in fast‑paced clinical research environments
• Strong organizational and documentation management skills
• Ability to prioritize multiple tasks and meet strict project timelines
• Team collaboration and stakeholder coordination skills
• Problem solving ability and proactive approach to project coordination

Candidates with knowledge of Trial Master File management, clinical trial documentation processes, and regulatory compliance standards will have an advantage.

Location and Salary

Job Location: Bangalore, India

The role will be based within Syngene’s clinical operations environment and involves coordination with internal research teams and external clinical trial sites.

Salary details for this position have not been publicly disclosed by the company and may vary depending on experience, qualifications, and previous exposure to clinical trial operations.

Application Process

Candidates interested in this clinical research job opportunity can apply through the official Syngene careers portal.

Apply here:

https://careers.syngeneintl.com/job/CTA-ClinOps/1357990266/

Applicants are advised to apply only through the official website to ensure authenticity and avoid recruitment scams.

Frequently Asked Questions

What does a Clinical Trial Assistant (CTA) do?

A Clinical Trial Assistant supports clinical research teams by managing trial documentation, maintaining Trial Master Files, coordinating study activities, and assisting with regulatory submissions.

Who can apply for this role?

Candidates with life sciences or healthcare degrees such as M.Pharm, PharmD, M.Sc Life Sciences, BDS, BAMS, BHMS, or Biotechnology can apply.

Is prior clinical research experience required?

Experience as a Clinical Research Coordinator or in clinical trial operations is preferred for this role.

What systems are commonly used in this role?

Clinical Trial Assistants often work with Trial Master File systems, clinical trial management systems (CTMS), and electronic documentation platforms used in pharmaceutical research.

How can I apply for this job?

Candidates can submit their application through the official Syngene careers website using the link provided in this article.

Job Summary

Company	Syngene International Ltd
Vacancies	CTA – Clinical Operations (Clinical Trial Assistant)
Required Education	M.Pharm, M.Sc Life Sciences, PharmD, BAMS, BDS, MDS, BHMS, Biotechnology, Biochemistry, Microbiology, Clinical Research, Pharmacology, Biomedical Sciences
Experience	Clinical Research Coordinator (CRC) or clinical trial operations experience preferred

Tagged as: Pharma Jobs in Bangalore