Syngene CRA Jobs 2026 | Specialist Clinical Trials & Site Monitoring Jobs in Bangalore
Are you seeking Syngene Careers Bangalore or a Clinical Research Associate Job in Bangalore? Innovation-driven global CRDMO Syngene International is hiring a Specialist – Clinical Trials (CRA) for its Clinical Operations division.
This clinical study site monitoring position is ideal for experienced professionals holding a postgraduate degree in Life Sciences or Pharmacology who have hands-on experience conducting site selections, SIVs, monitoring visits, and GCP documentation checks. To draft a resume summarizing your site management milestones, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Syngene International Limited |
| Position | Specialist – Clinical Trials (CRA) |
| Job Location | Bangalore, Karnataka, India |
| Department | Clinical Operations |
| Employment Type | Full-Time |
| Experience Required | Experienced CRA (Prior site monitoring experience) |
| Qualifications | Master’s Degree in Life Sciences or Master's in Pharmacology |
| Expected Salary | ₹7,00,000 – ₹12,00,000 per annum (CTC) |
💼 Key Responsibilities
- Site Monitoring Visits: Perform site selection, initiation, monitoring, and close-out visits in accordance with GCP guidelines and SOPs.
- Site Management: Liaise with investigators and site coordinators to manage study progress, subject recruitment, and documentation.
- Protocol Training: Administer protocol training and study-related workflows to investigators and clinical site staff.
- Data Validation: Review Case Report Forms (CRFs), identify clinical inconsistencies, and resolve queries within database systems.
- CAPA Actions: Investigate study quality issues with the Clinical Project Manager, supporting CAPA implementation.
- Documentation: Prepare comprehensive monitoring reports, follow-up letters, and site compliance files.
- Safety Standards: Ensure all clinical research activities comply with Syngene's Environmental, Health & Safety (EHS) policies.
To learn how experienced CRA salaries compare to pharmacovigilance drug safety associates and medical writing specialist structures, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Experience
- Education: Master’s degree in Life Sciences (Biotech, Biochemistry, Genetics, etc.) or a Master’s degree in Pharmacology.
- Experience: Hands-on Clinical Research Associate (CRA) experience and practical knowledge of clinical research operations.
- Guidelines Knowledge: Deep understanding of ICH-GCP guidelines, trial monitoring methodologies, site activation, and IRB/IEC submissions.
- Skills: Excellent site management, communication, time management, technical writing, and problem-solving skills.
For postgraduates evaluating clinical trial monitoring careers compared to laboratory research chemistry tracks, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Syngene?
- Opportunity to work on international, multi-phase clinical trial programs.
- Collaborate with global biopharmaceutical and healthcare leaders.
- Strong scientific research infrastructure with structured career development paths.
- Excellent organizational safety culture and continuous GCP training.
To test your understanding of clinical protocols, GCP guidelines, and adverse event safety profiles before your technical interviews, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Clinical Trials Specialist vs Healthcare IT
Specialists in Clinical Trials conduct site inspections, verify ICF records, and audit CRF compliance to manage global drug studies, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Syngene CRA Candidates
- List Therapeutic Areas: Detail the specific clinical areas (e.g. oncology, immunology, cardiology) where you have monitored sites.
- Quantify Site Experience: Mention the number of active sites, investigators, or monitors you coordinated in your previous roles.
- Highlight Audits: Detail if you have successfully managed health authority inspections (FDA, EMA) or sponsor-led quality audits.
💬 Syngene Clinical Trials Specialist Interview Questions
- Q1. What are the key tasks performed during a Site Initiation Visit (SIV)?
Answer Guidance: During an SIV, the CRA trains the investigator and study staff on the protocol, reviews the Investigator Site File (ISF), confirms study drug storage parameters, verifies investigator pharmacy setups, and reviews the electronic CRF entries. - Q2. How do you handle a Protocol Deviation discovered during a monitoring visit?
Answer Guidance: I document the deviation in my monitoring report, discuss it immediately with the principal investigator to find the root cause, implement corrective training, and escalate the event to the Clinical Project Manager and IRB according to safety guidelines. - Q3. Explain the basic purpose of an Informed Consent Form (ICF) audit.
Answer Guidance: The ICF audit ensures that every subject gave voluntary consent before any study-specific procedures began, the document is signed and dated by the patient and the investigator, and the most recent Ethics Committee-approved version was utilized.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Syngene's official careers board. Click the button below to apply:
Apply Online – Syngene Careers Portal❓ Frequently Asked Questions
Q. What is the educational eligibility for this Syngene CRA opening?
Candidates must hold a Master’s degree in Life Sciences or a Master’s degree in Pharmacology.
Q. Is this position for entry-level candidates?
No, Syngene requires candidates to have practical, hands-on experience as a Clinical Research Associate (CRA).
Q. Where is this job based?
This is a full-time position located at Syngene's office in Bangalore, Karnataka.
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