仕事内容

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: [email protected]

Clinical Scientist