Clinical Research Liaison

Illinois, United States

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Not SpecifiedCompensation

Entry Level & New Grad, Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Healthcare, Life Sciences, Clinical ResearchIndustries

Requirements

Candidates must possess a Bachelor's Degree and at least 3 years of experience in oncology and/or clinical trials, with a deep understanding of study start-up processes. Strong persuasive, strategic, and motivational skills are essential, along with a proven track record of high personal performance. The role requires exceptional organizational skills, meticulous attention to detail, persistence, resilience, strong relationship-building abilities, and advanced written and oral communication, analytical, interpersonal, and problem-solving skills. Regular travel, up to 40%, is also required.

Responsibilities

The Clinical Research Liaison will serve as the primary point of contact for research and care teams regarding TIME trial activities, maintaining regular communication with targeted accounts. Responsibilities include building relationships with key client stakeholders, drafting and executing strategic operational plans to meet JIT standards, and providing ongoing education about clinical trial access. The liaison will also participate in research steering committees, collaborate with internal teams to execute key deliverables, and utilize knowledge of oncology and clinical trials to identify site resource gaps and onboard sites. Additionally, they will assist in creating innovative tactics to ease site burden, incorporate client feedback into product improvements, contribute to marketing collateral, attend relevant conferences, and perform associated administrative activities, including oversight of program coordinators.

Skills

oncology

clinical trials

site management

stakeholder engagement

study start-up

research operations

cross-functional collaboration

education and training

real-world evidence

protocols and SOPs

communication

project coordination

Tempus

AI-driven healthcare data analysis platform

About Tempus

Tempus focuses on enhancing patient outcomes through the use of data and artificial intelligence in healthcare. The company offers a platform that analyzes medical data to provide insights for physicians, helping them make better treatment decisions. This platform also aids pharmaceutical and biotech companies in drug development by identifying new targets and assessing treatment effectiveness. For patients, Tempus identifies personalized therapy options, particularly in cancer care, where their research has shown increased opportunities for tailored treatments. They have developed a pan-cancer organoid platform and a liquid biopsy assay for profiling circulating tumor DNA. Tempus generates revenue by charging healthcare providers and companies for access to their platform and insights, setting them apart from competitors by their focus on personalized medicine and extensive cancer research.

Chicago, IllinoisHeadquarters

2015Year Founded

$894.9MTotal Funding

IPOCompany Stage

AI & Machine Learning, Biotechnology, HealthcareIndustries

1,001-5,000Employees

Benefits

Relocation Assistance

Company Equity

Performance Bonus

Risks

Competition from partners like Genialis may lead to conflicts of interest.

Ambry Genetics acquisition could pose financial risks if synergies aren't realized.

Technical challenges may arise in integration with Flatiron's OncoEMR platform.

Differentiation

Tempus uses AI to analyze clinical and molecular data for precision medicine.

Their platform aids in personalized treatment decisions for cancer patients.

Tempus collaborates with biotech firms to enhance drug development using real-world data.

Upsides

Increased AI adoption in healthcare boosts Tempus' partnerships and collaborations.

Acquisition of Ambry Genetics expands Tempus' genetic testing capabilities.

Integration with Flatiron's OncoEMR enhances precision in cancer treatment plans.

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