Tempus

TIME Operations Manager

Tempus$65K — $100K *
US-AnywhereRemote in Illinois, US
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree and 4+ years of experience in clinical trials (site, sponsor, CRO perspective)
  • Expertise in FDA regulations, GCP, clinical trial agreements, and IRB submissions
  • Strong collaborative team player with exceptional customer service skills
  • Effective interpersonal and problem-solving abilities
  • Track record of high personal performance standards
  • Highly organized with superb attention to detail
  • Flexibility and adaptability to work independently in a fast-paced environment

Responsibilities

  • Maintain and expand collaborations with pharmaceutical partners and CROs
  • Oversee execution of deliverables for pharma clients, focusing on quality
  • Manage day-to-day studies within the TIME network from start to closure
  • Prepare a portfolio of trials for network of sites using clinical trial knowledge
  • Assist in creating innovative tactics and strategies for cancer clinical trials
  • Collaborate with various teams to execute key deliverables
  • Identify risks to studies and coordinate with partners for issue resolution

Benefits

  • Full range of benefits including medical coverage
  • Incentive compensation opportunities
  • Potential for restricted stock units
  • Supportive work culture focused on innovation and collaboration
  • Opportunity for professional growth in a dynamic environment
Full Job Description
What you'll do:
  • Maintain and expand collaborations with pharmaceutical partners/CROs to employ an innovative approach to rapid study start-up
  • Oversee the execution of deliverables for a subset of pharma clients with a focus on quality and expeditious timelines
  • Manage the day-to-day execution of studies within the TIME network from study start up through closure ensuring customer satisfaction and ability for continued growth of Tempus business
  • Utilize knowledge of clinical trial development and study start-up to get a portfolio of trials ready for our network of sites
  • Assist team in creation of innovative tactics, processes, tools, systems, and strategies to continually accelerate the completion of cancer clinical trials
  • 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


#LI-DA1

$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.

About Tempus

Tempus is a technology company that has built an operating system to battle cancer. The company enables physicians to deliver personalized cancer care for patients through its interactive analytical and machine learning platform. Tempus provides genomic sequencing services and analyzes molecular and therapeutic data to empower physicians to make real-time, data-driven decisions. The company also offers research services to enable discovery of new therapeutic targets and clinical services that support clinical trial design and monitoring. Tempus was founded in 2015 by Eric Lefkofsky and has raised over $8 billion in funding to date.
Learn more about Tempus
Size
1,001 employees
Industry
Founded
2015

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