Project Associate Clinical Trials at Syngene

Project Associate Clinical Trials – Life Science/Pharmacology – Bangalore | Syngene Careers

Apply now for Project Associate Clinical Trials at Syngene, Bangalore. Openings for MSc Life Science/Pharmacology graduates with 1–3 years’ experience.

In today’s competitive healthcare and life sciences industry, securing a position at a global leader like Syngene International Ltd. can be a career-defining move. If you are a postgraduate in Life Sciences or Pharmacology with a passion for clinical operations, this Project Associate – Clinical Trials role in Bangalore offers a strong platform to grow your expertise in clinical research, regulatory compliance, and trial management.

Company Overview

Founded in 1993, Syngene International Ltd. is one of India’s leading contract research, development, and manufacturing organizations (CRDMO). With a strong global presence, Syngene partners with some of the world’s top pharmaceutical, biotechnology, and specialty chemical companies including Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife.

Syngene is home to over 4,200 scientists, working across discovery, development, and manufacturing services, supporting end-to-end R&D. Its mission is to help clients accelerate time-to-market, reduce innovation costs, and improve global healthcare outcomes.

Job Role & Responsibilities

As a Project Associate – Clinical Trials, you will play a key role in ensuring smooth clinical operations and regulatory compliance. Your responsibilities will include:

• Assisting Clinical Project Managers (CPMs) and Clinical Research Associates (CRAs) in maintaining site compliance and project tracking systems.
• Supporting clinical teams with documentation, distribution, archiving, and reporting activities.
• Preparing and handling Clinical Trial Supplies while maintaining accurate tracking records.
• Managing and coordinating Case Report Forms (CRFs), data queries, and clinical data flow.
• Acting as a central communication hub between internal teams, vendors, and investigators.
• Supporting Quality Assurance (QA) during audits by providing access to Trial Master Files (TMFs).
• Coordinating translations of study-related documents in collaboration with translation agencies.
• Performing administrative tasks that support clinical trial execution.

This position is best suited for detail-oriented professionals who can manage cross-functional coordination, documentation accuracy, and regulatory adherence.

Eligibility / Qualifications

To qualify for the Project Associate – Clinical Trials position at Syngene, you must have:

• Education: Master’s degree in Life Sciences, Pharmacology, Biotechnology, or related fields. Relevant courses include MSc Life Sciences, MSc Pharmacology, MSc Biotechnology, MSc Clinical Research.
• Experience: 1–3 years in clinical research or clinical operations.
• Technical Skills:
  • Strong knowledge of ICH-GCP guidelines and Indian regulatory frameworks.
  • Proficiency in MS Word, Excel, and PowerPoint.
  • Experience in preparing SOPs (Standard Operating Procedures).
  • Familiarity with internal and external audits.
• Behavioral Skills: Strong English communication skills, integrity, and teamwork.

Location & Salary

• Job Location: Bangalore, India
• Salary: Competitive, based on experience and qualifications (industry standards for Clinical Research roles typically range between ₹4.5 LPA to ₹7.5 LPA for candidates with 1–3 years of experience).

Application Process

Interested candidates can apply directly through Syngene’s official career portal:

👉 Apply Here

Note: Early applications are encouraged as interviews are conducted on a rolling basis. Apply today to secure your spot!

Why Join Syngene?

• Work with global pharma and biotech leaders on cutting-edge projects.
• Gain exposure to international regulatory standards and advanced trial methodologies.
• Build a career in a fast-growing organization recognized for innovation and quality.
• Inclusive workplace culture with equal opportunity policies.

FAQs

1. Who can apply for the Project Associate Clinical Trials role at Syngene?
Candidates with a Master’s in Life Sciences, Pharmacology, or Biotechnology and 1–3 years’ experience in clinical operations are eligible.

2. What skills are required for this position?
Knowledge of ICH-GCP, regulatory guidelines, MS Office tools, SOP preparation, and audit handling are essential.

3. What is the expected salary range?
While Syngene does not disclose salaries publicly, typical ranges for similar positions in Bangalore are between ₹4.5 – ₹7.5 LPA.

4. Where is this job located?
The position is based at Syngene International’s Bangalore facility.

5. How do I apply?
Applications must be submitted via Syngene’s official careers page: Apply Here

Summary Table

Call-to-Action:
Don’t miss the opportunity to build a career with a global leader in life sciences research. Apply before the deadline to secure your place at Syngene International!