Clinical Research Scientist

BIOMERIEUX, INC.

SALT LAKE CITY, UT

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JOB DETAILS

LOCATION

SALT LAKE CITY, UT

POSTED

30+ days ago

Description

The Clinical Research Scientist leads the execution of the clinical studies that make up the company's clinical evidence generation program. In this role, you will execute clinical studies and/or programs worldwide in accordance with strategy, project plans, approved budget and resource allocations following applicable regulatory and standard operating procedures.

The Clinical Research Scientist collaborates closely with cross-functional teams, including Medical Scientists, Biostatistics and Data Management, Medical Writers, and Marketing to generate impactful clinical evidence that supports the company's strategy. This role is crucial in maintaining our commitment to scientific excellence and patient-centric approaches within the competitive global healthcare landscape.
This position can also be located in Durham, North Carolina
Primary Duties

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Contributes to the development and leads the implementation of study strategy with internal stakeholders
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Contributes to the development of the study synopsis
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Leads the development of study plan for non-registrational studies (Simple)
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Leads the development of BIR/CIR study protocols for non-registrational studies (Simple)
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Review IIR study protocols
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Lead site selection activities
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Serves as Global Medical Affairs point of contact with external resources and contacts at various management levels concerning clinical operations or scheduling of specific phases of clinical studies
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Functionally responsible for all clinical monitoring activities throughout study
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Manages clinical study agreements
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Manages the coordination of logistics and training needed to execute studies
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Outline and communicate safety issues and planned mitigations in collaboration with internal stakeholders
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Assures clear external/internal team communication, process documentation, and compliance with BMX and departmental processes along with GCP
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Contributes to the assessment of processes and establishing plans for improvements
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Manages IIR study execution / follow-up with little to no supervision
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Define and manage study budget
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Accountable for the delivery of documentation to meet study milestones
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Coordinates the creation of the study database/CRF and reviews data/analysis with cross-functional teams
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Contributes to or leads the development of study abstract and/or poster in collaboration with internal stakeholders
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Contributes to peer-reviewed journal publication of study results in collaboration with internal stakeholders
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All other duties as assigned.
Experience

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Bachelor's degree in a life science field (biology, chemistry, medical/clinical laboratory technologist etc.) required
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Master's or PhD preferred
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5+ years of experience conducting in vitro diagnostics and/or medical device clinical research with responsibilities for managing all major aspects of strategic planning, organization, implementation and delivery of clinical studies.

Experience with the management of timelines, deliverables, and milestones
Experience with budget oversight, risk mitigation, and clinical data review
Understands the US and European Medical Testing environments and relevant professional societies and guidelines (e.g. FDA, CE-Mark IVD Directives, CAP, CLIA, WHO, IASLC, ASCCP, etc.)
Proven track record of writing clinical study plans and study protocols
Knowledge, Skills and Abilities

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Strong computer skills including word processing and use of spreadsheets. Skills with database and project ma
nagement software desirable.
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Demonstrate ability to work collaboratively with various stakeholders in a highly matrixed global environment
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Good communication skills

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About the Company

BIOMERIEUX, INC.

Scientific and technological innovation is at the heart of bioMérieux's strategy. A world leader in the field of in vitro diagnostics for 50 years, <span itemprop="name">bioMérieux</span> designs, develops, produces, and markets diagnostic systems for medical and industrial applications. bioMérieux's solutions (reagents, instruments, software, and services) are used to determine the source of disease and contamination to improve patient health and ensure consumer safety.

To fulfill its mission to improve public health worldwide, bioMérieux is present in more than 150 countries through 41 subsidiaries. Its world headquarters are located in the Lyon area in France.

We are committed to creating an optimal work environment that fosters teamwork, emphasizes training and offers international career development opportunities.

Equal Opportunity Employer/Affirmative Action Employer M/F/Vet/Disability

INDUSTRY

Biotechnology/Pharmaceuticals

FOUNDED

1963

WEBSITE

http://www.biomerieux-diagnostics.com/