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Freshers CRA Job Openings at Sascan Meditech Pvt. Ltd.
If you’re looking to begin your career in clinical research with a strong industry-focused role, the Freshers CRA Job Openings at Sascan Meditech Pvt. Ltd. update is a valuable opportunity to explore. This position is ideal for candidates aiming to gain hands-on experience in clinical trials, medical device validation, and patient-centric research workflows—making it a standout choice for fresh graduates entering the clinical domain in 2025.
Job Title: Clinical Research Associate – Medical Device
Company: Sascan Meditech Pvt. Ltd.
Location: Thiruvananthapuram, Kerala
Experience: 0–1 years
Salary: ₹30,000 per month
Position Type: Full-time (On-site)
Eligibility: Female candidates only
Role Summary
Sascan Meditech is seeking a dedicated Clinical Research Associate (CRA) to support the
design, development, and clinical validation of cutting-edge optics-based medical devices.
The ideal candidate will possess a solid understanding of clinical validation protocols, strong
multitasking capabilities, and an entrepreneurial mindset suited for a fast-paced startup
environment. The role involves managing multi-centric clinical studies for gynecological
oncology devices and working closely with cross-functional teams to ensure successful trial
execution.
Key Responsibilities
Clinical Validation & Study Management
• Design, develop, and review clinical validation documents, including study protocols
and Investigator’s Brochures, in alignment with IEC standards.
• Coordinate and manage multi-centric clinical trials for gynecological oncology
devices.
• Perform statistical analysis, data interpretation, and preparation of study reports.
• Oversee trial workflows including patient recruitment, monitoring, and record
management.
• Support regulatory submissions and facilitate approvals from ethics committees and
hospitals.
Site Coordination & Collaboration
• Conduct clinical site visits for device testing, workflow assessment, and optimization.
• Liaise closely with clinical teams to understand requirements and ensure seamless
trial execution.
• Collaborate with engineering, R&D, and quality teams to support clinical study
objectives.
Qualifications
• Master’s degree in Biomedical Engineering, Biotechnology, Pharmacy, or related
fields.
• 0–2 years of experience in medical device R&D or clinical research.
• Strong communication, presentation, and scientific documentation skills.
• Ability to work independently and collaboratively within cross-functional teams.
Desirable Skills
• Experience in clinical research, pilot/pivotal trials, or hospital-based studies.
• Familiarity with ISO 13485:2015 and medical device regulatory pathways (e.g.,
CDSCO).
• Knowledge of scientific writing, data analysis, and study management tools.
• Strong clinical aptitude and a commitment to continuous learning.
CLICK HERE TO APPLY ONLINE
