Are you a passionate professional with a background in life sciences or clinical research? Sova, a leading name in the healthcare and clinical research industry, is excited to announce a job opening for the position of Clinical Trial Associate (CTA) in Gurugram. This is a full-time role perfect for individuals with 1-3 years of experience in clinical research and a strong understanding of ICH-GCP guidelines and FDA regulations. If you’re looking to advance your career in the pharmaceutical and clinical research sector, this could be your next big opportunity!
About Sova
Sova is a trusted name in the healthcare and clinical research domain, dedicated to improving patient outcomes through innovative research and development. With a focus on excellence and compliance, Sova has established itself as a leader in conducting clinical trials and delivering high-quality results. Joining Sova means becoming part of a dynamic team that values professionalism, innovation, and collaboration.
Job Overview: Clinical Trial Associate (CTA)
Location: Gurugram
Job Type: Full-time
Experience Required: 1-3 years
Industry: Pharmaceutical/Clinical Research
Key Responsibilities:
As a Clinical Trial Associate (CTA) at Sova, you will play a crucial role in supporting clinical trial operations. Your responsibilities will include:
- Assisting in the planning, implementation, and management of clinical trials.
- Ensuring compliance with ICH-GCP guidelines, FDA regulations, and other clinical research standards.
- Maintaining accurate trial documentation and records.
- Coordinating with investigators, sponsors, and other stakeholders.
- Supporting site management and monitoring activities.
- Contributing to the preparation of clinical trial reports and regulatory submissions.
Eligibility Criteria:
To be considered for the Clinical Trial Associate (CTA) role, candidates must meet the following requirements:
- Educational Qualification: Bachelor’s degree in life sciences, healthcare, or a related field.
- Experience: 1-3 years of experience in clinical research, preferably in a CTA or similar role.
- Knowledge: Strong understanding of ICH-GCP guidelines, FDA regulations, and other clinical research standards.
- Certification: Certification in clinical research (e.g., ACRP, SOCRA) is a plus.
How to Apply:
If you meet the eligibility criteria and are excited about this opportunity, we encourage you to apply! Submit your updated CV to divjyot.kaur@sova.health. Don’t miss this chance to join a leading organization in the clinical research industry.
