Are you looking for rewarding clinical trial jobs in India? ClinTrek Research Pvt. Ltd., a Bangalore-based Contract Research Organization (CRO), is hiring a Clinical Trial Assistant/Associate (CTA) to join their growing team. This full-time, on-site position in Bengaluru, Karnataka, offers an excellent opportunity for freshers and early-career professionals in the pharma and life sciences fields to kickstart their careers. Posted just 4 hours ago on February 20, 2025, this job has already attracted 91 applicants, so act fast—applications are no longer being accepted directly, but you can still explore similar opportunities on Pharmabharat.org, your go-to platform for pharma jobs in India.
About ClinTrek Research Pvt. Ltd.
ClinTrek Research Pvt. Ltd. is a dynamic start-up CRO dedicated to delivering high-quality clinical trials that drive medical advancements. With a mission to support global pharmaceutical, biotechnology, and medical device companies, ClinTrek provides end-to-end clinical trial solutions, including project management, data management, regulatory support, and more. Their commitment to ethical, efficient, and compliant research makes them a trusted name in the industry. Joining ClinTrek means being part of a team that’s shaping the future of healthcare.
Job Role: Clinical Trial Assistant/Associate
The Clinical Trial Assistant/Associate role is office-based and pivotal in ensuring the seamless execution of clinical trials. This position involves supporting clinical operations, managing documentation, and coordinating with trial sites and regulatory authorities. If you’re detail-oriented, proactive, and eager to contribute to groundbreaking research, this could be the perfect pharma job for you.
Key Responsibilities
- Trial Documentation & Compliance: Maintain and organize essential trial documents like regulatory submissions and ethics approvals, ensuring adherence to ICH-GCP, CDSCO, and DCGI guidelines.
- Site Coordination: Serve as a communication link between research sites, investigators, and sponsors.
- Regulatory Support: Assist in preparing submissions for ethics committees and regulatory bodies.
- Logistics & Supply Management: Manage investigational products and trial supplies across sites.
- Data Management: Support CRAs in data verification and trial progress tracking.
- Administrative Support: Handle scheduling, contracts, budgets, and study trackers for project managers.
This role requires collaboration with Clinical Research Associates, Project Managers, and Data Management teams, making it a fantastic opportunity to build a strong foundation in clinical research.
Qualifications & Skills
- Education: Master’s degree in Clinical Research, Life Sciences, Pharmacy, or Biotechnology.
- Experience: 0-2 years in clinical research (CRO, pharma, or hospital settings preferred). Freshers with a solid academic background are welcome.
- Knowledge: Familiarity with ICH-GCP guidelines and Indian clinical trial regulations (CDSCO/NDCT).
- Technical Skills: Proficiency in MS Office and Clinical Trial Management Systems (CTMS) is a plus.
- Soft Skills: Strong communication, multitasking, and organizational abilities.
Why Choose This Job?
The pharmaceutical industry is booming, and clinical trial jobs are in high demand. ClinTrek Research offers a fast-paced, learning-focused environment where you can grow your career. Bengaluru, a hub for pharma and biotech innovation, adds to the appeal of this role. Whether you’re a fresher or have some experience as a Clinical Research Coordinator (CRC), this position provides hands-on exposure to global clinical trial processes.
Send your resume or drop an email to careers@clintrek.com
