MiRus is an innovative healthcare company with a growing portfolio of cardiovascular and orthopedic products and deep proprietary technology in both implants and procedural solutions. MiRus was started by a team of experienced entrepreneurs with a history of creating disruptive technologies and very successful, highly valued companies.

We offer competitive compensation, options, and full benefits.

Job Summary

We are seeking a skilled Data Scientist to join our team supporting a pivotal TAVR clinical trial. The role focuses on managing, analyzing, and interpreting complex clinical datasets to ensure data integrity, quality, and regulatory compliance. The Data Scientist will work closely with clinical teams, biostatisticians, and CRAs to support trial endpoints, reporting, and submission-ready datasets.

Responsibilities

♦ Develop, maintain, and manage clinical trial datasets in alignment with trial protocols.
♦ Perform data cleaning, validation, and quality checks to ensure integrity and compliance.
♦ Support statistical analysis, data visualization, and generation of trial reports.
♦ Collaborate with clinical teams and CRAs to resolve data queries and clarify endpoints.
♦ Ensure datasets meet regulatory standards (CDISC, SDTM, ADaM) for FDA/EMA submissions.
♦ Build dashboards or analytics tools to monitor trial progress and outcomes.
♦ Apply advanced analytics or modeling techniques to explore trends, patient outcomes, or predictive insights.
♦ Document processes, assumptions, and analysis methods according to GCP and internal SOPs.

Key Qualifications

♦ Advanced degree in Data Science, Biostatistics, Computer Science, or related field.
♦ Experience in clinical trial data management; preferably in cardiology or medical device trials.
♦ Strong programming skills in SAS, R, Python, and database management (SQL, Oracle, Medidata, REDCap).
♦ Familiarity with CDISC standards (SDTM, ADaM) and FDA/EMA regulatory requirements.
♦ Experience with data visualization and reporting tools (Tableau, Power BI, or similar)
♦ Strong problem-solving skills and ability to interpret complex clinical datasets.
♦ Excellent communication and collaboration skills with cross-functional teams.

Requirements

♦ Ability to work onsite full-time.
♦ Prior experience working in regulated clinical trial environments (GCP, FDA).
♦ Strong attention to detail and ability to document all analyses for regulatory review.
♦ Comfortable working in a fast-paced, high-stakes clinical trial setting.
♦ Ability to collaborate effectively with clinicians, statisticians, and project teams.

Benefits:

MiRus offers competitive compensation, options, full benefits, and relocation assistance.
♦ 401(k)
♦ Dental insurance
♦ Vision insurance
♦ Disability insurance
♦ Employee assistance program
♦ Flexible spending account or Health Savings Account
♦ Health insurance
♦ Life insurance
♦ Paid time off

Schedule:

♦ Monday to Friday (8am – 5pm)

Work Location:

♦ Marietta, GA
♦ Position may require domestic travel up to 10%, however this is an in-house position.

Interested ?Please complete the contact information below and submit your resume to mirusHR@mirusmed.com