Remote TIME Operations Manager: Clinical Trials

Tempus

Illinois

On-site

USD 65,000 - 110,000

Full time

14 days+

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Benefits offered by this job

Benefits package
Incentive compensation
Remote work option

Job summary

Tempus is seeking a TIME Operations Manager to oversee study start-up and execution within our clinical trials network. You will maintain collaborations with pharmaceutical partners and CROs, drive on-time deliverables, and ensure quality across sites from start-up to closure.

The role requires a Bachelor's degree and 5+ years of complex trial experience, with strong FDA/GCP knowledge. Remote work from Illinois with competitive compensation and a comprehensive benefits package.

Qualifications

  • 5+ years of experience working with complex clinical trials in site, sponsor, or CRO settings.
  • In-depth knowledge of FDA regulations, GCP, site start-up, trial budgets, IRB submission, and pharma operations.
  • Strong collaboration, customer service, and problem-solving skills.

Responsibilities

  • Maintain and expand collaborations with pharmaceutical partners/CROs for rapid study start-up.
  • Oversee delivery execution for a subset of pharma clients with focus on quality and timelines.
  • Manage daily study activities from start-up through closure ensuring customer satisfaction and growth.
  • Leverage clinical trial development knowledge to prep trials for Tempus network sites.
  • Collaborate with site operations, medical affairs, pathology, bioinformatics and data science to deliver key results.

Skills

Clinical trial experience
Regulatory knowledge
Attention to detail

Education

Bachelor's Degree in a relevant field

Job description

Tempus is seeking a TIME Operations Manager to oversee study start-up and execution within our clinical trials network. You will maintain collaborations with pharmaceutical partners and CROs, drive on-time deliverables, and ensure quality across sites from start-up to closure.

The role requires a Bachelor's degree and 5+ years of complex trial experience, with strong FDA/GCP knowledge. Remote work from Illinois with competitive compensation and a comprehensive benefits package.

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