Summary

This role is responsible for the design, execution, oversight, and monitoring of internal and external clinical studies that support product development and evidence generation for Lingo. The individual develops study protocols, executes clinical research activities, and ensures the accurate analysis, interpretation, and documentation of study results. They contribute to the development and implementation of clinical strategies that advance product innovation and support regulatory and commercialization objectives. As a subject matter expert in metabolic health, the role provides scientific leadership and expertise across the organization, partnering with cross-functional teams to drive informed decision-making. The individual also translates complex scientific concepts into clear, actionable insights and effectively communicates scientific principles, study findings, and clinical evidence to a broad range of stakeholders, including research and development, regulatory, medical, quality, commercial teams, and executive leadership. This is a unique role that goes across both the Clinical Affairs and Medical Affairs teams at Lingo. This position is an onsite role based in Alameda, CA.

Job description

The Opportunity

This role is responsible for the design, execution, oversight, and monitoring of internal and external clinical studies that support product development and evidence generation for Lingo. The individual develops study protocols, executes clinical research activities, and ensures the accurate analysis, interpretation, and documentation of study results. They contribute to the development and implementation of clinical strategies that advance product innovation and support regulatory and commercialization objectives. As a subject matter expert in metabolic health, the role provides scientific leadership and expertise across the organization, partnering with cross-functional teams to drive informed decision-making. The individual also translates complex scientific concepts into clear, actionable insights and effectively communicates scientific principles, study findings, and clinical evidence to a broad range of stakeholders, including research and development, regulatory, medical, quality, commercial teams, and executive leadership. This is a unique role that goes across both the Clinical Affairs and Medical Affairs teams at Lingo. This position is an onsite role based in Alameda, CA.

What You'll Work On

Leads the design, execution, monitoring, and analysis of internal and external clinical studies to support product development and evidence generation.
Provides scientific leadership and subject matter expertise in metabolic health, guiding research initiatives and cross-functional decision-making.
Collaborates closely with Medical Affairs, Marketing, Product Development, Regulatory Affairs, and other cross-functional stakeholders to support business and scientific objectives.
Develops, implements, and maintains clinical research operating procedures to ensure compliance, quality, and consistency across studies.
Participates in cross-functional product development and commercialization teams, providing scientific and clinical insights throughout the product lifecycle.
Ensures the successful and timely completion of clinical studies, directly impacting product development milestones, regulatory objectives, and product launch timelines.
Communicates clinical and scientific findings effectively to technical and non-technical stakeholders, translating complex data into actionable insights.

Required Qualifications

Bachelor's Degree or an equivalent combination of education and experience.
Min 8+ years relevant experience, in conducting clinical trials.
Experience in communicating science to a variety of internal and external stakeholders.

Preferred Qualifications

MS, PharmD or Ph.D. strongly preferred.

Requirements

Bachelor's Degree or an equivalent combination of education and experience
Min 8+ years relevant experience in conducting clinical trials
Experience in communicating science to a variety of internal and external stakeholders
MS, PharmD or Ph.D. strongly preferred

Benefits

Medical coverage
Retirement savings plan
Tuition reimbursement
Student debt program
Education benefit

Company overview

Abbott Laboratories is a global healthcare technology leader founded in 1888 and headquartered in Chicago, Illinois. As an international medtech and pharmaceutical company, Abbott operates in approximately 160 countries worldwide with a workforce of over 115,000 employees. The company is organized into four major business segments: Medical Devices (48% of revenue), Diagnostics (20%), Nutritional Products (19%), and Established Pharmaceutical Products (12%). Abbott's medical devices portfolio includes revolutionary technologies such as the FreeStyle Libre continuous glucose monitoring system for diabetes management, cardiovascular devices like the MitraClip and TriClip for heart valve repair, and neuromodulation systems for chronic pain management. The company's diagnostics division pioneered breakthrough tests including the first licensed HIV blood test in 1985. With a rich history spanning over 135 years, Abbott has consistently been recognized as one of Fortune's World's Most Admired Companies since 1984 and continues to drive innovation in healthcare technology to help people live healthier, fuller lives.