Clinical Scientist

Job summary

This contract role is for a Clinical Scientist supporting clinical and post-market work for medical device products. It is suited to early-career candidates with 0 to 2 years of relevant experience who want exposure to clinical research, data evaluation, quality processes, and regulatory compliance.

Responsibilities

• Assist with post-market surveillance activities and evaluations of product performance.
• Examine clinical, quality, and complaint data to identify patterns and insights.
• Help prepare documentation required for clinical and regulatory purposes.
• Contribute to product investigations and trend analysis efforts.
• Work closely with teams across Clinical, Quality, Regulatory, and Engineering functions.
• Take part in risk assessments and compliance-related initiatives.
• Keep records accurate, organized, and up to date.

Qualifications

• A bachelor's degree in Biomedical Engineering, Biotechnology, Life Sciences, Public Health, Pharmacy, or a closely related discipline is required.
• 0 to 2 years of experience in clinical research, medical devices, pharmaceuticals, quality, or regulatory affairs is preferred.
• Working knowledge of FDA regulations and medical device quality systems is needed.
• Strong skills in analysis, communication, and documentation are expected.
• Comfort using Microsoft Office Suite is required.
• The role calls for the ability to work independently as well as within a cross-functional team.

Additional information

This position is based in the USA and is fully remote. The contract duration is 12+ months. Interested candidates should be able to support clinical and post-market activities for medical device products.

Contact

Recruiter: Abhiram, United Consulting Hub
Email: abhiram@unitedconsultinghub.com