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Job Functions, Duties, Responsibilities and Position Qualifications:

The Clinical Research Project Manager will be responsible and accountable for the successful management of multiple service and product lines with primary emphasis on ARI's Research Service Division. The CRSPM will work in tandem with the other Project Managers, Lab Technicians/ Technologists and multiple Principal Investigators to oversee project fulfillment progress by managing day to day Clinical Research Coordinator (CRC) activity and Operations in the Research Laboratory in Las Vegas, NV. In addition, the CRSPM will also be responsible for managing site responses to client study related inquiries, provide extensive updates as well as collaborate on other client or project related issues. The CRSPM will be a key member of the ARI Management Team and collaborate on all issues and opportunities impacting ARI and provide meaningful input as necessary to further the company's endeavors and help achieve its goals.

• Participate in the processes associated with the evaluation, budgeting, administration, contracting, scheduling and orchestration of diagnostic validation protocols relevant to ARI's Research Services Division.
• Become familiar with all active study specifications and criteria associated with each and every active ARI Study. Prior to initiation of study, assist in introducing the studies to the assigned CRCs and Techs and making sure that all Study requirements, specifications and timelines are fully understood.
• Understand and manage associated costs related to ARI projects and product procurement and distribution. Conduct margin analysis of prospective projects to determine if project meets ARI profitability criteria.
• Work in tandem with Quality Assurance to assure the consistent quality output of ARI service and product lines.
• Manage the flow of data submitted by the assigned CRCs into the ARI electronic project management tool. Ensure that all live counts are up to date and ensure that all project data is entered accurately and in accordance with all specifications.
• Coordinate multiple Studies over multiple locations and travel to study locations as required and as necessary to assist in the implementation of protocols and to conduct Study oversight.
• Personally assume specific project management responsibilities as needed and required to ensure timely completion of active studies leading to successful attainment of ARI Goals and Objectives.
• Work with Project Managers, PIs and CRCs in providing timely responses to client new project inquiries and requests.
• Assist in the training and on-boarding of new (ARI and non-ARI) CRCs in the assigned geography. Work with the Management team to design and implement a training program resulting in equipping new CRCs with the knowledge, skills and resources necessary to operationalize ARI activities in their respective site locations.
• Help coordinate and lead weekly CRC Project Review Conference calls to review progress, compliance with specifications, project timing and address issues or concerns.
• Work with the Quality Operations Coordinator in assisting in the establishment and revisions of Standard Operating Procedures necessary to conduct daily business.
• Help to establish and monitor all Study related files and forms across the ARI network to ensure compliance with all IRB, CAP and related Federal Regulations. Assist in the establishment and maintenance of Study Site Regulatory Binders to be kept at each participating ARI site.

• Med-tech degree or certification required. BA/BS science related degree preferred.

• CRT must have a minimum of 2 years' experience in a CLIA and CAP accredited Laboratory and demonstrate competency in all assigned areas. Experience or knowledge of clinical chemistry, histology, cytology and pathology strongly desired.

• Experience with Ventana BenchMark ULTRA and Dako Autostainer Link 48 instrumentation.

• Working knowledge and able to work with highly detailed clinical research protocols.

• Good communications skills
• Familiar with Microsoft Office programs.
• Well versed in medical terminology relevant to the field of pathology.
• Experienced Laboratory Instrument Operator for multiple platforms.
• Ability to understand and abide by FDA Good Clinical Practice Guidelines.

• Must be able to have access to a vehicle.
• Must be able to travel 30% - 40%.

• Must exhibit excellent leadership skills.
• Good computer skills. Especially Excel.
• Comfortable in a laboratory and hospital pathology environment
• Compassionate and caring with respect to communicating with cancer patients.

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Sonic Healthcare USA is an equal opportunity employer that celebrates diversity and is committed to an inclusive workplace for all employees. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, age, national origin, disability, genetics, veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.