BioSpace
Overview
Join to apply for the Medical Director role at BioSpace. The Maze Clinical Sciences team is looking for a mission-driven Medical Director to play a central role in advancing our clinical development programs. We’re seeking a passionate and committed professional to join our team on a mission to turn groundbreaking genetic discoveries into life-saving medicines. As a Medical Director, you will provide medical oversight and drive the execution of early-stage clinical trials in renal and cardiometabolic diseases, with a focus on our APOL1 program. You’ll also contribute to the development of our broader pipeline, including precision medicines for other forms of chronic kidney disease and phenylketonuria. This position reports to the Senior Medical Director. You’ll thrive in this role if you bring scientific curiosity, collaborative spirit, and clinical leadership. You will work cross-functionally to design, conduct, and analyze key clinical studies, including first-in-human and proof-of-concept trials, helping to shape the future of Maze’s clinical programs. Your impact will be highly visible and integral to our mission. Responsibilities
Serve as medical monitor and provide medical oversight for the APOL1 proof-of-concept study and other early development studies for other clinical stage assets at Maze. Lead the execution and analysis of clinical trials for the APOL1 program. Author and review clinical-regulatory documents, including study protocols, amendments, informed consents, study reports, and statistical analysis plans (SAPs). Develop and deliver scientific presentations and communications for internal and external stakeholders, including investigators, academic partners, and advocacy groups. Engage with scientific thought leaders and patient advocacy groups to gather insights, shape clinical development plans, and build awareness of Maze’s pipeline. Partner with Clinical Operations to select and engage study investigators and sites, ensuring strong professional relationships and close collaborations. Collaborate on the identification, selection, and oversight of vendors and CROs to support clinical program needs. Serve as a functional representative on cross-functional teams, providing clinical development insights and contributing to strategic discussions and planning. Leadership Competencies
Communication and Influence
Builds communication channels across Maze for sharing information Influences Senior Management decisions through persuasive arguments Respectfully addresses differing opinions leading to support of decision
Teamwork and Collaboration
Champions partnerships and connections across Maze Proactively addresses issues that could result in breakdown of team relationships Spotlights team and individual contributions in public forums
Execution and Results
Addresses gaps and leverages strengths to get best results Maintains a steadying presence and clarifies priorities during change Anticipates and removes barriers that put functional/corporate goals at risk
Develop Others and Self
Removes barriers to staff development and empowers them to make their own decisions Stays current on industry trends and keeps direct-reports prepared and responsive
What We’re Looking For
MD (or equivalent) or MD/PhD with 3+ years of industry experience in drug development. Board eligibility/certification and clinical experience in internal medicine, pediatrics or surgery (nephrology or cardiometabolic disease expertise preferred). Experience as a clinical study medical monitor in early-stage and/or registration-enabling clinical programs Experience in relationship-building with investigators and other key external stakeholders, such as patient advocacy groups Experience in clinical trial design, execution, and data interpretation Experience working in cross-functional teams representing the clinical development function Experience working with CRO partners Experience in developing and reviewing scientific publications, study protocols, investigator brochures, and other clinical-regulatory documents A collaborative, proactive, and ethical mindset, with a commitment to scientific excellence and patient impact Willingness to travel domestically and internationally (up to 20%) for vendor visits, conferences, regulatory meetings, and advisory boards. About Maze Therapeutics
Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing the power of human genetics to develop novel, small molecule precision medicines for patients living with renal, cardiovascular and related metabolic diseases, including obesity. The company’s pipeline is led by two wholly owned lead programs, MZE829 and MZE782. Maze is based in South San Francisco. Our People
Maze is comprised of a team of passionate and creative professionals committed to discovering and delivering transformative medicines to patients suffering from both rare and common genetic diseases. We foster a culture that encourages vision, initiative and the development of talent, with a supportive work environment that inspires creative thinking and freedom of expression. Our Core Values
Further Together – Our path is paved with challenges, but with resilience and a team-first mentality, we’ll achieve our mission. Impact Obsessed – We embrace the bold, take calculated risks, and learn from our mistakes to improve the lives of others. Stand True – Our integrity is foundational; it guides us no matter the obstacle. Compensation and Benefits
The expected annual salary range for employees located in the San Francisco Bay Area is $279,000 - $341,000. This position is eligible for an annual performance bonus. Maze offers a comprehensive benefits package including medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) with employer match, and generous holiday and PTO policy. Salary determinations depend on experience, skills, and location, and may be modified in the future.
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Join to apply for the Medical Director role at BioSpace. The Maze Clinical Sciences team is looking for a mission-driven Medical Director to play a central role in advancing our clinical development programs. We’re seeking a passionate and committed professional to join our team on a mission to turn groundbreaking genetic discoveries into life-saving medicines. As a Medical Director, you will provide medical oversight and drive the execution of early-stage clinical trials in renal and cardiometabolic diseases, with a focus on our APOL1 program. You’ll also contribute to the development of our broader pipeline, including precision medicines for other forms of chronic kidney disease and phenylketonuria. This position reports to the Senior Medical Director. You’ll thrive in this role if you bring scientific curiosity, collaborative spirit, and clinical leadership. You will work cross-functionally to design, conduct, and analyze key clinical studies, including first-in-human and proof-of-concept trials, helping to shape the future of Maze’s clinical programs. Your impact will be highly visible and integral to our mission. Responsibilities
Serve as medical monitor and provide medical oversight for the APOL1 proof-of-concept study and other early development studies for other clinical stage assets at Maze. Lead the execution and analysis of clinical trials for the APOL1 program. Author and review clinical-regulatory documents, including study protocols, amendments, informed consents, study reports, and statistical analysis plans (SAPs). Develop and deliver scientific presentations and communications for internal and external stakeholders, including investigators, academic partners, and advocacy groups. Engage with scientific thought leaders and patient advocacy groups to gather insights, shape clinical development plans, and build awareness of Maze’s pipeline. Partner with Clinical Operations to select and engage study investigators and sites, ensuring strong professional relationships and close collaborations. Collaborate on the identification, selection, and oversight of vendors and CROs to support clinical program needs. Serve as a functional representative on cross-functional teams, providing clinical development insights and contributing to strategic discussions and planning. Leadership Competencies
Communication and Influence
Builds communication channels across Maze for sharing information Influences Senior Management decisions through persuasive arguments Respectfully addresses differing opinions leading to support of decision
Teamwork and Collaboration
Champions partnerships and connections across Maze Proactively addresses issues that could result in breakdown of team relationships Spotlights team and individual contributions in public forums
Execution and Results
Addresses gaps and leverages strengths to get best results Maintains a steadying presence and clarifies priorities during change Anticipates and removes barriers that put functional/corporate goals at risk
Develop Others and Self
Removes barriers to staff development and empowers them to make their own decisions Stays current on industry trends and keeps direct-reports prepared and responsive
What We’re Looking For
MD (or equivalent) or MD/PhD with 3+ years of industry experience in drug development. Board eligibility/certification and clinical experience in internal medicine, pediatrics or surgery (nephrology or cardiometabolic disease expertise preferred). Experience as a clinical study medical monitor in early-stage and/or registration-enabling clinical programs Experience in relationship-building with investigators and other key external stakeholders, such as patient advocacy groups Experience in clinical trial design, execution, and data interpretation Experience working in cross-functional teams representing the clinical development function Experience working with CRO partners Experience in developing and reviewing scientific publications, study protocols, investigator brochures, and other clinical-regulatory documents A collaborative, proactive, and ethical mindset, with a commitment to scientific excellence and patient impact Willingness to travel domestically and internationally (up to 20%) for vendor visits, conferences, regulatory meetings, and advisory boards. About Maze Therapeutics
Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing the power of human genetics to develop novel, small molecule precision medicines for patients living with renal, cardiovascular and related metabolic diseases, including obesity. The company’s pipeline is led by two wholly owned lead programs, MZE829 and MZE782. Maze is based in South San Francisco. Our People
Maze is comprised of a team of passionate and creative professionals committed to discovering and delivering transformative medicines to patients suffering from both rare and common genetic diseases. We foster a culture that encourages vision, initiative and the development of talent, with a supportive work environment that inspires creative thinking and freedom of expression. Our Core Values
Further Together – Our path is paved with challenges, but with resilience and a team-first mentality, we’ll achieve our mission. Impact Obsessed – We embrace the bold, take calculated risks, and learn from our mistakes to improve the lives of others. Stand True – Our integrity is foundational; it guides us no matter the obstacle. Compensation and Benefits
The expected annual salary range for employees located in the San Francisco Bay Area is $279,000 - $341,000. This position is eligible for an annual performance bonus. Maze offers a comprehensive benefits package including medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) with employer match, and generous holiday and PTO policy. Salary determinations depend on experience, skills, and location, and may be modified in the future.
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