Clinical Research Job at Biomérieux in the USA
The Clinical Research Scientist role is a high-impact R&D position responsible for leading global clinical studies and executing the company’s clinical evidence generation program. This opportunity is available in Hazelwood, Missouri, with additional locations in Salt Lake City, Utah, and Durham, North Carolina. The Clinical Research Job at Biomérieux Careers in the USA focuses on clinical trial leadership, regulatory compliance, cross-functional collaboration, and strategic study execution within a competitive global healthcare environment.
Job Details:
- Job Title: Clinical Research Scientist
- Department: Scientific / R&D
- Primary Location: Hazelwood, Missouri
- Additional Locations: Salt Lake City, Utah; Durham, North Carolina
- Employment Type: Full-time
- Salary Range: $80,000 – $116,700 (eligible for variable annual bonus)
About the Company:
bioMérieux is a global leader in in vitro diagnostics, committed to scientific excellence and patient-centric innovation. The company collaborates with cross-functional teams and global stakeholders to deliver high-quality clinical evidence and advance healthcare solutions worldwide.
BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers committed to diversity, compliance, and ethical standards.
Educational Requirements for the Clinical Research Scientist Role:
- Bachelor’s degree in a scientific or healthcare discipline (required)
- 2+ years of professional experience in clinical trial management (preferably in diagnostics or medical devices)
- Certifications such as ACRP-CP or ACRP-PM (preferred)
Key Responsibilities:
- Lead execution of clinical studies from study synopsis to data lock and final report as a Clinical Research Scientist at Biomérieux Careers
- Develop and finalize clinical protocols aligned with regulatory and scientific objectives
- Mentor Associate Clinical Research Scientists
- Collaborate with Regulatory Affairs, Quality Assurance, Biostatistics, CROs, and other stakeholders
- Manage study budgets, timelines, enrollment strategies, and resourcing in this Clinical Research Job
- Develop study execution, risk mitigation, monitoring, and communication plans
- Contribute to abstracts, posters, clinical study reports, and scientific publications
- Oversee study start-up, site initiation, enrollment, monitoring, and close-out
- Manage site selection, activation, monitoring, and data integrity
- Conduct site qualification, monitoring, and close-out visits
- Manage IRB/EC documentation and clinical trial agreements
- Maintain electronic trial master file (eTMF) systems
- Ensure adherence to SOPs and regulatory requirements in this Clinical Research Job
- Support SOP review and continuous improvement initiatives
- Identify and mitigate risks throughout the trial lifecycle
- Ensure quality plans are implemented
- Oversee electronic data capture (EDC) systems
- Manage vendor contracts, budgets, and performance at Biomérieux Careers
- Ensure inspection readiness and regulatory compliance
Skills Required:
- Strong knowledge of ICH/GCP and global regulatory frameworks (FDA, CE-Mark IVD Directives, CAP, CLIA, WHO)
- Proven leadership and stakeholder management skills
- Experience in contract and budget negotiation
- Expertise in CTMS, EDC, and eTMF systems
- Strong presentation and communication skills
- Advanced MS Office proficiency
- Ability to manage multiple projects, timelines, and budgets
- Strategic planning and risk mitigation capabilities
Benefits of the Clinical Research Job:
BioMérieux offers a competitive Total Rewards package including:
- Medical, dental, and vision plans with telemedicine options
- Company-provided life and accidental death insurance
- Short and long-term disability insurance
- Retirement plan with employer contribution and match
- Adoption assistance
- Wellness programs
- Employee Assistance Program
- Commuter benefits
- Voluntary benefit offerings
- Discount programs
- Parental leave
