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    CRA – Clinical Research Associate | Syngene | Bangalore

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    Syngene

    CRA – Clinical Research Associate | Syngene | Bangalore

    Apply for CRA (Clinical Research Associate) role at Syngene in Bangalore. 3–5 years’ experience required. Life Science/Pharmacology graduates.


    Are you passionate about advancing clinical research and contributing to global healthcare innovations? Syngene International Ltd. is inviting applications for the position of Clinical Research Associate (CRA) in Bangalore. This is an excellent opportunity for life science professionals with hands-on experience in clinical research to grow with one of India’s leading CROs trusted by top global pharma and biotech companies.


    Company Overview

    Syngene International Ltd., incorporated in 1993, is a globally recognized, innovation-driven Contract Research Organization (CRO). With over 4,200 scientists, Syngene partners with leading pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical companies worldwide. Clients include industry giants such as Bristol-Myers Squibb, Amgen, Merck KGaA, GSK, Baxter, and Herbalife. The company’s mission is to accelerate R&D productivity, reduce time-to-market, and lower the cost of innovation while ensuring world-class compliance and quality.


    Job Role & Responsibilities

    As a Clinical Research Associate (CRA), you will play a pivotal role in ensuring the smooth conduct of clinical studies, site management, and compliance with international standards.

    Key responsibilities include:

    • Performing site selection, initiation, monitoring, and close-out visits in line with SOPs, ICH-GCP, and regulatory guidelines.
    • Managing site activities for assigned clinical protocols and therapeutic areas.
    • Delivering protocol-related and study-specific training to site staff.
    • Ensuring compliance, quality, and integrity of trial data.
    • Addressing quality issues by implementing Corrective and Preventive Actions (CAPA).
    • Tracking regulatory approvals, Ethics Committee submissions, subject recruitment, CRF completion, and query resolution.
    • Maintaining accurate documentation including monitoring reports, follow-up letters, and action plans.
    • Assisting Clinical Project Managers in study tool development, team coordination, and project documentation.
    • Preparing for and supporting both internal and external audits.

    Eligibility / Qualifications

    To apply for this CRA role at Syngene, candidates must meet the following criteria:

    • Education: Master’s degree in Life Science, Pharmacology, Clinical Research, or related fields. Eligible courses include M.Sc. Pharmacology, M.Sc. Biotechnology, M.Sc. Biochemistry, M.Pharm Pharmacology, M.Sc. Clinical Research.
    • Experience: Minimum 3–5 years in core clinical research activities.
    • Technical Skills:
      • Strong knowledge of ICH-GCP guidelines and Indian regulatory requirements.
      • Proficiency in MS Office tools (Word, Excel, PowerPoint).
      • Knowledge of SOP development and compliance.
      • Experience in audit preparedness and facing regulatory inspections.
    • Behavioral Skills:
      • Strong communication skills in English.
      • Conflict resolution, stress management, empathy, and patience.

    Location & Salary

    • Job Location: Bangalore, India
    • Department: Clinical Operations – Discovery Services
    • Work Schedule: Full-time, 40 hours per week (IST)
    • Salary: Competitive package aligned with industry standards, commensurate with qualifications and experience.
    CRA – Clinical Research Associate | Syngene | Bangalore
    CRA – Clinical Research Associate | Syngene | Bangalore

    Application Process

    Interested candidates can apply online through Syngene’s career portal: Apply Here

    Applicants are encouraged to submit:

    • Updated resume
    • Cover letter highlighting clinical research experience
    • Relevant certifications and training documents

    Why Join Syngene?

    • Work with global pharma leaders and contribute to breakthrough discoveries.
    • Grow your career in an internationally accredited CRO.
    • Access to continuous professional development and structured learning.
    • Be part of a collaborative and innovation-driven team.

    FAQs

    1. What is the minimum experience required for this CRA role at Syngene?
    A minimum of 3–5 years in core clinical research activities is required.

    2. Can freshers apply for the CRA position?
    No. This role requires prior experience in clinical research operations.

    3. What qualifications are accepted for this role?
    A Master’s degree in Life Science, Pharmacology, Biotechnology, Biochemistry, M.Pharm, or related fields is mandatory.

    4. What does a CRA do at Syngene?
    A CRA ensures site selection, initiation, monitoring, compliance, and data integrity in clinical trials.

    5. Where is the job location?
    The position is based in Bangalore, India.

    6. Is remote work possible for this role?
    No, this is an on-site position within the Clinical Operations department.

    7. What is the salary range?
    Syngene offers a competitive compensation package in line with candidate expertise and market standards.


    Call to Action

    Don’t miss this opportunity to build your career with one of India’s leading CROs! Apply now and take the next step in your clinical research journey.
    👉 Apply before the position closes


    Summary Table

    Company Syngene International Ltd.
    Vacancies Clinical Research Associate (CRA)
    Required Education M.Sc. Life Sciences, M.Sc. Pharmacology, M.Pharm, M.Sc. Clinical Research, M.Sc. Biotechnology
    Experience 3–5 years in clinical research

    To apply for this job please visit careers.syngeneintl.com.

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