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Sun Pharma Hiring – Clinical Trial Associate| Mumbai

ByPharma Hiring Hub

Sun Pharmaceutical Industries Ltd, one of India’s leading pharmaceutical companies, is hiring for the role of Clinical Trial Associate (CTA) at its Mumbai location. This opportunity is suitable for candidates with a Life Sciences degree and 0–2 years of experience who are looking to start or grow their career in clinical research and trial operations.

Sun pharma clinical trial associate

🏢 About Company

Sun Pharmaceutical Industries Ltd. (Sun Pharma) is one of India’s largest and most trusted pharmaceutical companies, with a strong presence in global markets. The company develops, manufactures, and markets high‑quality generic and specialty medicines used by patients worldwide.

Sun Pharma is known for its work across multiple therapeutic areas, including cardiology, neurology, dermatology, oncology, diabetology, and gastroenterology. In addition to marketed products, the company invests heavily in research and development, supporting clinical trials and innovation to ensure safe and effective medicines.

📊 Job Overview

  • Position: Clinical Trial Associate
  • Department: Clinical Research
  • Location: Mumbai,India
  • Experience: 0 to 2 years
  • Qualification: Bachelor or Master degree in Lifescience
  • Job Type: Full-Time
  • Last Date of application: Not provided

📋 Key Responsibilities –Clinical Trial Associate

  • Assist in maintaining clinical study documents, including protocols, informed consent forms (ICF), case report forms (CRFs), and study reports.
  • Organize and maintain electronic and paper‑based study files, ensuring documents are accurate, complete, and up to date.
  • Provide general administrative support to the clinical research team.
  • Assist with scheduling meetings, preparing meeting agendas and minutes, and coordinating travel arrangements when required.
  • Support the preparation and submission of regulatory documents to Ethics Committees (EC) and Regulatory Authorities.
  • Help maintain compliance with Good Clinical Practice (GCP) guidelines and applicable local regulatory requirements.
  • Assist in tracking site invoices, monitoring the payment process, and maintaining related records.
  • Support vendor code generation and help track vendor‑related activities for clinical studies.

🎓 Qualification required

  • Bachelor or Masters degree in Lifescience
  • Candidate with Postgraduate Diploma in Clinical research
  • relevant work experience preffered
  • Candidate must be comfortable communicating in English, both spoken and written, as this role involves regular documentation and communication.

🧠 Required Skills

  • Ability to track invoices, payments, and vendor details accurately.
  • Willingness to learn and adapt in a fast‑paced clinical research environment.
  • Ability to work independently as well as in a team.
  • Professional attitude with respect for confidentiality and data integrity.

⭐ Job Role Insight

The Clinical Trial Associate (CTA) role is an important support position in Sun Pharma’s clinical research team. In this role, you help ensure that clinical studies run smoothly, correctly, and in compliance with regulations.

You will mainly support the team by handling study documentation, coordinating with clinical sites, vendors, and internal teams, and assisting with regulatory submissions. Accuracy and organization are very important because the documents you manage are reviewed by ethics committees, regulatory authorities, and auditors.

🎯 Who Should Apply

  • Life Sciences degree such as B.Pharm, M.Pharm, B.Sc, or M.Sc.
  • fresher or have up to 2 years of experience in clinical research or a related field.
  • interested in clinical trials, research documentation, and study coordination.

💰 Salary & Work Model Insight

  • Salary: 4 – 5 LPA, Salary may vary based as per experience and role
  • Work Model: This role follows a office‑based model in Mumbai, depending on project needs.

💡 Preparation Tips

  • Revise GCP (Good Clinical Practice) basics — you should at least know:
    • Why GCP exists
    • How it protects patients and data
  • Understand simple clinical trial terms like:
    • Protocol
    • Informed Consent (ICF)
    • CRF (Case Report Form)
    • Ethics Committee (EC)

🔗 Application Process

Interested candidates should apply only through the official company career website using the link provided below.

Application Link

Important Disclaimer: This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

❓FAQ – Clinical Trial Associate

1. What does a Clinical Trial Associate do?

Managing study documents
Assisting with regulatory submissions
Coordinating with study sites, teams, and vendors
Supporting day‑to‑day clinical research activities

2. Will I interact with sites and vendors?

Yes. You may coordinate with:
Clinical sites
Internal study teams
Vendors (for invoices, codes, and tracking)

3. What career growth can I expect from this role?

Clinical Research Associate (CRA)
Clinical Operations Executive
Project Coordinator
Regulatory or Clinical Operations roles

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