Collaborate with various teams within Tempus, to execute key deliverables including site operations, medical affairs, pathology, bioinformatics and data science.
Identify risks to assigned studies and work with internal and external partners to resolve issues
Qualifications
Occasional Travel required (will vary by project)
Bachelor's Degree and 4+ years of experience in working with complex clinical trials from a site, sponsor or CRO perspective
Highest level knowledge of FDA regulations, GCP, study start-up, clinical trial agreements, trial budgets, IRB submission and pharma operations
Collaborative team player
Exceptional customer service skills and strong interpersonal and problem solving skills
Proven track record of setting and achieving high personal standards of performance
Highly organized and systematic, superb attention to detail, and ability to complete tasks with a high degree of accuracy and an eye towards process improvement
Flexible and adaptable; ability to work independently in a fast-paced environment
Preferred Qualifications
Experience with rapid site activation
Experience with a research networks
Clinical research project management experience
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$65,000-$100,000
The expected salary range may vary for other locations. Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.