Tempus

Associate Medical Director / Medical Director, Clinical Development

Maryland, United States

Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Healthcare, Biotechnology, Pharmaceuticals, Medical ResearchIndustries

Associate Medical Director/Medical Director, Clinical Development

Employment Type: Full-time

Position Overview

Tempus is seeking an Associate Medical Director/Medical Director, Clinical Development to join its Medical Science team. This role is crucial for driving clinical development plans for new precision medicine products, such as genomic assays and algorithmic diagnostics. If you are passionate about precision medicine and advancing the healthcare industry, this is an opportunity to leverage AI's impact on clinical care.

Responsibilities

  • Drive Clinical Development plans for new precision medicine products through their entire lifecycle, including clinical validation, clinical utility studies, and post-market data review across various oncology indications.
  • Provide medical expertise and subspecialty clinical context for development and delivery.
  • Design and conduct studies, including documentation and data analysis.
  • Lead and collaborate with multidisciplinary teams in a matrix environment, including biostatistics, R&D scientists, bioinformatics, operations, legal, business development, scientific communications, marketing, regulatory, and more.
  • Deliver clinical/scientific presentations and publications for medical audiences, including conferences.
  • Engage in collaborations with external clinical research centers and investigators.

Requirements

  • MD degree or equivalent, with advanced training in Oncology preferred.
  • 5 years of clinical research experience, including experience in biotechnology/pharmaceutical, clinical research organization, or primary investigator academic research settings.
  • Ability to work collaboratively in a team environment and lead cross-functional teams.
  • Strong analytical thinking, strategic thinking, implementation, and research skills.
  • Goal-oriented, self-motivated, and driven to make a positive impact in healthcare.
  • Ability to thrive in a fast-paced environment with adaptability to changing priorities.
  • Experience with site engagement and operations in clinical research settings.
  • Strong communication skills, including oral and written communication.
  • Innovative thinker regarding clinical development and study execution.

Preferred Skillsets

  • Understanding of or interest in genomics, molecular diagnostics, data, artificial intelligence, machine learning, bioinformatics/clinical informatics, real-world evidence, clinical innovation, or novel technologies in drug discovery and clinical development.
  • Previous experience with:
    • Leading teams, including planning and timely organization of clinical development plan components, clinical trial development, and cross-functional work.
    • Precision medicine, drug development, medical devices, or diagnostics development.
    • Medical monitoring, study design and documents, and trial oversight and conduct.
    • Good Clinical Practice (GCP) and other regulations governing research, health authority responses, and interactions.
    • Clinical practice guidelines, device and/or drug approvals, and label expansions.
    • Planning and management of investigator meetings, advisory boards, and other scientific committees.
    • Clinical partnerships, consulting, and/or client-facing experience.
  • Peer-reviewed publications.

Location

  • Chicago, IL
  • New York, NY
  • Redwood, CA

Company Information

Tempus is 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.

Skills

Genomic assays
Algorithmic diagnostics
Clinical validation
Clinical utility studies
Data analysis
Study design
Multidisciplinary collaboration
Scientific communication
Regulatory knowledge
Oncology expertise

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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