Rapid-Launch Clinical Trials Operations Lead

Tempus AI; Illinois; On-site; USD 65,000 - 110,000; Full time

Job summary

Tempus AI is seeking a TIME Operations Manager to drive rapid study start-up and ongoing delivery for pharma partners within the Tempus network. You will oversee day-to-day study execution from startup to closure, ensure quality and timelines, and collaborate across clinical operations, medical affairs, pathology, and data science.

The ideal candidate has a BA/BS and 5+ years of clinical trial experience, strong FDA regulatory knowledge, and superb organizational and communication skills.

Qualifications

• Bachelor's Degree and 5+ 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 with strong interpersonal and problem solving skills.
• Proven track record of achieving high personal performance standards.
• Highly organized with attention to detail and focus on process improvement.
• Flexible and able to work independently in a fast-paced environment.

Responsibilities

• 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

Skills

FDA regulations & GCP

Clinical trial operations

Project management

Interpersonal skills

Attention to detail

Independent work

Education

Bachelor's Degree

Job description

Tempus AI is seeking a TIME Operations Manager to drive rapid study start-up and ongoing delivery for pharma partners within the Tempus network. You will oversee day-to-day study execution from startup to closure, ensure quality and timelines, and collaborate across clinical operations, medical affairs, pathology, and data science.

The ideal candidate has a BA/BS and 5+ years of clinical trial experience, strong FDA regulatory knowledge, and superb organizational and communication skills.