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Summit Therapeutics Jobs (NOW HIRING)

Summit Therapeutics

Sr. Commercial Attorney, Transactions

$142K - $194K/yr

Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs.

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How much do summit therapeutics jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for summit therapeutics in the United States is $16.41, according to ZipRecruiter salary data. Most workers in this role earn between $13.46 and $18.27 per hour, depending on experience, location, and employer.

How much does a director at Summit Therapeutics make?

A director at Summit Therapeutics typically earns between $120,000 and $180,000 annually, depending on experience, location, and specific responsibilities. Compensation may also include bonuses, stock options, and benefits common in the biotech industry.

How many employees does Summit Therapeutics have?

Summit Therapeutics is a biotechnology company that employs approximately 100 to 200 staff members. The exact number can vary as the company grows or restructures, and it typically includes research, development, and administrative personnel.

What is the difference between Summit Therapeutics vs Clinical Research Associate?

AspectSummit TherapeuticsClinical Research Associate
CredentialsBachelor's degree in life sciences, relevant certificationsBachelor's degree, often with clinical research certifications
Work EnvironmentPharmaceutical company, research labs, clinical trial sitesClinical trial sites, pharmaceutical companies, CROs
Industry UsageDrug development, biotech researchMonitoring clinical trials, ensuring compliance

Both Summit Therapeutics and Clinical Research Associates work within the pharmaceutical and biotech industries, focusing on drug development and clinical trials. While Summit Therapeutics is a company specializing in developing therapies, Clinical Research Associates are professionals who monitor and manage clinical trials across various organizations. The roles share similar credentials and work environments, but their focus differs: Summit Therapeutics is a company, whereas Clinical Research Associates are individual professionals involved in trial oversight.

What is happening with Summit Therapeutics?

Summit Therapeutics is a biopharmaceutical company focused on developing treatments for rare and serious diseases. The company is engaged in ongoing research and clinical trials, and updates on its progress are typically shared through press releases and investor reports.

What does Summit Therapeutics do?

Summit Therapeutics is a biopharmaceutical company focused on developing treatments for rare and serious diseases, particularly in the field of infectious and genetic disorders. Employees in this company typically work in research, clinical development, or regulatory roles, often requiring scientific expertise and knowledge of drug development processes.
What cities are hiring for Summit Therapeutics jobs? Cities with the most Summit Therapeutics job openings:
What states have the most Summit Therapeutics jobs? States with the most job openings for Summit Therapeutics jobs include:
Infographic showing various Summit Therapeutics job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 96% Full Time, 1% Part Time, and 1% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $34,140 per year, or $16.4 per hour.

Senior Medical Science Liaison (KS, MO, OK, AR)

Summit Therapeutics

Kansas City, MO • On-site

Full-time

Posted 18 days ago

Job description

About Summit:
Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.
Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including:
Non-small Cell Lung Cancer (NSCLC)
  • HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
  • HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
  • HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.

Colorectal Cancer (CRC)
  • HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.

Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China's National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
This role will support (KS, MO, OK, AR)!
Overview of Role:
The Regional Medical Science Director (also referred to as MSL) is a field based scientific expert that strategically supports the scientific and business objectives of cancer therapeutic areas across the product life cycle. MSLs are the primary communicators of Summit Therapeutics science within a specific geography with healthcare professionals. MSLs are the field scientific experts on Immuno-Oncology and treatment options within this therapeutic area. They combine strong business acumen, clinical expertise, market awareness, and serve as a conduit of information to a cross functional customer base internally within Summit Therapeutics. Based on therapeutic needs and product life cycles, teams may focus on certain responsibilities, including clinical development and pipeline support.
Role and Responsibilities:
  • Develop, execute and maintain high impact territory plans, including HCP and Investigator engagement plans in alignment with therapeutic area medical and scientific objectives with a focus on quality.
  • Support clinical development and research initiatives across development at the request of R&D to include, but not limited to, site evaluation and identification, recruitment, investigator meetings, external expert identification, and involving experts to generate scientific data including investigator-sponsored trials.
  • Identify, gain access to, and develop professional customer centric based relationships with external experts in Immuno-Oncology within assigned geography.
  • Provide education relative to disease state, therapeutic landscape and Summit Therapeutics products across the product lifecycle to healthcare providers and researchers.
  • Participate, monitor, and provide insights to Summit from relevant scientific meetings in relevant geography.
  • Continuously maintain self-education on market issues/trends, product knowledge, and new therapeutic areas of interest as it pertains to specific business responsibilities, including creating awareness and relationships for Summit Therapeutics in the Medical community.
  • Actively participate in relevant team meetings, organizational activities, and Country-driven medical affairs activities (e.g. advisory boards, Masterclasses, Round-tables)
  • Create, maintain, and collaborate in relationships with Cross-Functional partnerships, as appropriate, to develop and execute Account plans designed to support and meet shared scientific or business objectives.
  • All other duties as assigned

Experience, Education and Specialized Knowledge and Skills:
  • Doctoral degree in the health sciences from an accredited university required (MD, PhD, PharmD, or equivalent). Significant clinical and/or industry experience in oncology and cancer therapeutic area may be accepted in lieu of education requirements.
  • A minimum of 5+ years of solid tumor cancer experience
  • Greater than or equal to 5+ years of clinical, scientific/research, or industry related experience or equivalent preferred.
  • A minimum of 2+ years as a Medical Science Liaison required.
  • Previous pharmaceutical industry experience within relevant scientific discipline preferred.
  • The MSL must possess and be able to demonstrate past achievements in:
    • Understanding, analyzing and communicating complicated scientific concepts and data.
    • Building credible relationships with prominent HCPs.
    • Ability to independently identify and translate corporate needs into an action plan that will achieve objectives.
    • Self-motivation to achieve and exceed goals.
    • Problem solving and analytic skills.
    • Critical thinking.
    • Ability to work independently.
  • An essential requirement of the position is to meet health care industry representative (HCIR) credentialing requirements to gain entry into facilities and organizations that in your assigned territory. These HCIR credentialing requirements may include, but are not limited to, background checks, drug screens, and proof of immunization/vaccination for various diseases.
  • Other requirements:
    • Must be willing to travel up to 75% of the time.
    • Proficient user of standard MS Office suite (e.g., Word, Excel), experience using electronic document management systems, and document review tools desirable
    • Strong computer and database skills
    • Attention to detail, accuracy and confidentiality.
    • Clear and concise oral and written communication skills
    • Excellent organizational skills
    • Must be able to effectively multi-task and manage time-sensitive and highly confidential documents.
    • Prioritize conflicting demands.
    • Work in a fast-paced, demanding and collaborative environment

This is the pay for this position
Pay Transparency
$200,000-$235,000 USD
Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit's Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.
Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

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