Clinical Trial Associate Dr. Reddy Laboratories
Job Overview
| Position | Clinical Trial Associate |
|---|---|
| Location | Hyderabad, India |
| Experience Required | 1 – 3 Years |
| Education Qualification | B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences, Biology, Biotechnology, Biochemistry, or Diploma in Clinical Research |
| Salary | ₹4.5 – 6 LPA |
| Application Mode | Online Application |
About Dr. Reddy’s Laboratories
Dr. Reddy’s Laboratories Ltd. is a leading global pharmaceutical company, known for its dedication to affordable and innovative healthcare solutions. Operating across 66 countries, the company has over 24,000 employees and aims to impact 1.5 billion patients by 2030. With a strong focus on integrity, transparency, and respect, Dr. Reddy’s promotes diversity and inclusion, aiming to create a positive social and environmental impact. Clinical Trial Associate Dr. Reddy Laboratories
Key Responsibilities of a Clinical Trial Associate (CTA)
As a CTA at Dr. Reddy’s, you will support clinical studies and assist the Clinical Operations Department by ensuring smooth and compliant trial processes. Key responsibilities include:
- Administrative Support: Provide day-to-day administrative support to the clinical operations team.
- Document Review & Quality Control: Review study documentation, including Informed Consent Forms (ICF) and study plans, to ensure regulatory compliance.
- Study Metrics & Tracking: Maintain study trackers, tools, and reports; track Investigator and third-party payments.
- eTMF Management: Submit study documents to the eTMF, assist with audits, and address any findings.
- Study Oversight: Support clinical monitoring oversight, coordinate Investigator Meetings, and assist in preparing clinical site contracts.
- Communication & Coordination: Engage with clinical sites, manage team meetings, and document agendas and minutes. Clinical Trial Associate Dr. Reddy Laboratories
Qualifications and Skills
Educational Background
- Required: Graduate or Master’s degree in pharmacy, life sciences, biology, biotechnology, biochemistry, or a diploma in clinical research.
Experience
- Required: 1-3 years of experience in clinical trials, with knowledge of clinical operations and regulatory standards.
Technical Skills
- Knowledge of Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.
- Proficiency with Electronic Data Capture (EDC) systems.
- Advanced skills in MS Office for document and report generation.
Behavioral Skills
- Strong communication and interpersonal skills for effective collaboration.
- Project management abilities to handle multiple tasks efficiently.
- Analytical mindset with keen attention to detail.
- Passion for delivering impactful results.
Why Join Dr. Reddy’s?
Dr. Reddy’s Laboratories offers a unique opportunity to work with a globally recognized pharmaceutical leader committed to innovation and accessibility in healthcare. Employees benefit from a diverse, inclusive work environment and the chance to impact lives worldwide. As a CTA, you will have the opportunity to grow professionally and contribute to meaningful clinical research. Clinical Trial Associate Dr. Reddy Laboratories
How to Apply
Qualified candidates are encouraged to apply online, submitting their resume to highlight relevant experience and qualifications. Join Dr. Reddy’s Laboratories and be a part of a visionary team dedicated to global healthcare solutions.
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