Astria Therapeutics, Inc.
Medical Director, Clinical Development
Astria Therapeutics, Inc., Boston, Massachusetts, us, 02298
Overview
Astria Therapeutics is dedicated to bringing hope with life-changing therapies to patients and families affected by allergic and immunological diseases. Astria’s pipeline includes our lead program, Navenibart, a monoclonal antibody inhibitor of plasma kallikrein in clinical development for the treatment of hereditary angioedema, as well as STAR-0310, an OX40 monoclonal antibody antagonist currently in pre-clinical development for atopic dermatitis (AD) and being explored for other allergic and immunological diseases.
Astria is seeking a creative individual who is driven by patients and science to advance our pipeline. The Medical Director, Clinical Development will report to the VP, Late Clinical Development and be responsible for supporting clinical development, functioning as the medical lead and Astria medical monitor for clinical trials, and working with cross-functional multidisciplinary study teams on clinical trial strategy, design, and execution. The ideal candidate will have deep expertise in immunology and/or dermatology (rendering a thorough understanding of target and disease biology), as well as experience as a medical monitor in early- to late-stage clinical trials.
Responsibilities
Provide medical, disease-specific expertise into specific clinical research activities.
Support the design of trials and develop protocols, Investigational Brochures, and other key study documents in conjunction with other functional areas; ensure alignment of protocols across a program
Review and analyze patient and clinical trial data to identify trends, ensure data integrity, and support informed medical decision-making.
Support start-up activities (informed consent forms, eCRF design, etc.) related to the assigned clinical studies
Serve as Astria medical monitor, working closely with the CRO, clinical operations, and pharmacovigilance on study execution including but not limited to safety reporting, point of escalation for medical monitoring, development and execution of the CRO Medical Monitoring Plan
Work closely with cross-functional colleagues, including, but not limited to, clinical operations, regulatory, biostatistics, and data management, to ensure timely and flawless execution of the clinical plan
Partner with medical affairs to build and maintain strong relationships with Principal Investigators, including support of Advisory and Scientific Boards, as well as publications
Serve as primary Astria medical point of contact for sites and PIs for the assigned studies, as applicable
Qualifications
Ability to work a hybrid schedule of 2-3 days a week in our Boston office.
MD / DO or equivalent
2+ years’ experience as a medical monitor and/or medical director
2+ years’ of industry or clinical experience in one of the following: Immunology, dermatology, rare disease, allergy, rheumatology, pediatrics
Experience designing mid- and late-phase clinical trials and comfortability with advanced clinical trial design and statistical methodologies
Experience with executing clinical trials either as a medical monitor or as an investigator.
Capable of analyzing patient and clinical trial data to identify trends, ensure data integrity, and support informed medical decision-making
Capable of analyzing research data and publications; working knowledge of biostatistics; working knowledge of GCP, scientific and clinical research methods and clinical study design
Highly organized, outcome-oriented, self-motivated performer; demonstrates creativity, determination and ownership.
Team player with a growth mindset, can-do attitude and willingness to learn from others
Effective oral and written communication skills with an ability to present to a variety of stakeholders and tailor message accordingly
Excellent interpersonal skills, ability to develop important relationships with key stakeholders across a variety of disciplines, good conflict management and negotiation skills
Ability to travel up to 15%, domestic and international
About Astria and Culture At Astria, we are committed to building a team where every Astrian endorses the idea that people bring their authentic self to work. We embrace a patients-first, people-always culture which strives to ensure all Astrians and our collaborators have a sense of belonging and receive the support they need to thrive.
We invest in our people through our words, our actions, and our values. We are working to develop and implement initiatives that promote inclusion and belonging throughout the organization and foster a culture of openness, respect, and collaboration, where all voices are heard, and everyone is valued for their unique perspectives and contributions.
At Astria, people are our greatest asset, and by fostering an inclusive environment, we all shine brighter. Together we can bring our passion and compassion to the work of delivering life-changing therapies to patients, families, and communities.
Job Details
Seniority level: Director
Employment type: Full-time
Job function: Science
Industries: Biotechnology Research and Pharmaceutical Manufacturing
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Astria is seeking a creative individual who is driven by patients and science to advance our pipeline. The Medical Director, Clinical Development will report to the VP, Late Clinical Development and be responsible for supporting clinical development, functioning as the medical lead and Astria medical monitor for clinical trials, and working with cross-functional multidisciplinary study teams on clinical trial strategy, design, and execution. The ideal candidate will have deep expertise in immunology and/or dermatology (rendering a thorough understanding of target and disease biology), as well as experience as a medical monitor in early- to late-stage clinical trials.
Responsibilities
Provide medical, disease-specific expertise into specific clinical research activities.
Support the design of trials and develop protocols, Investigational Brochures, and other key study documents in conjunction with other functional areas; ensure alignment of protocols across a program
Review and analyze patient and clinical trial data to identify trends, ensure data integrity, and support informed medical decision-making.
Support start-up activities (informed consent forms, eCRF design, etc.) related to the assigned clinical studies
Serve as Astria medical monitor, working closely with the CRO, clinical operations, and pharmacovigilance on study execution including but not limited to safety reporting, point of escalation for medical monitoring, development and execution of the CRO Medical Monitoring Plan
Work closely with cross-functional colleagues, including, but not limited to, clinical operations, regulatory, biostatistics, and data management, to ensure timely and flawless execution of the clinical plan
Partner with medical affairs to build and maintain strong relationships with Principal Investigators, including support of Advisory and Scientific Boards, as well as publications
Serve as primary Astria medical point of contact for sites and PIs for the assigned studies, as applicable
Qualifications
Ability to work a hybrid schedule of 2-3 days a week in our Boston office.
MD / DO or equivalent
2+ years’ experience as a medical monitor and/or medical director
2+ years’ of industry or clinical experience in one of the following: Immunology, dermatology, rare disease, allergy, rheumatology, pediatrics
Experience designing mid- and late-phase clinical trials and comfortability with advanced clinical trial design and statistical methodologies
Experience with executing clinical trials either as a medical monitor or as an investigator.
Capable of analyzing patient and clinical trial data to identify trends, ensure data integrity, and support informed medical decision-making
Capable of analyzing research data and publications; working knowledge of biostatistics; working knowledge of GCP, scientific and clinical research methods and clinical study design
Highly organized, outcome-oriented, self-motivated performer; demonstrates creativity, determination and ownership.
Team player with a growth mindset, can-do attitude and willingness to learn from others
Effective oral and written communication skills with an ability to present to a variety of stakeholders and tailor message accordingly
Excellent interpersonal skills, ability to develop important relationships with key stakeholders across a variety of disciplines, good conflict management and negotiation skills
Ability to travel up to 15%, domestic and international
About Astria and Culture At Astria, we are committed to building a team where every Astrian endorses the idea that people bring their authentic self to work. We embrace a patients-first, people-always culture which strives to ensure all Astrians and our collaborators have a sense of belonging and receive the support they need to thrive.
We invest in our people through our words, our actions, and our values. We are working to develop and implement initiatives that promote inclusion and belonging throughout the organization and foster a culture of openness, respect, and collaboration, where all voices are heard, and everyone is valued for their unique perspectives and contributions.
At Astria, people are our greatest asset, and by fostering an inclusive environment, we all shine brighter. Together we can bring our passion and compassion to the work of delivering life-changing therapies to patients, families, and communities.
Job Details
Seniority level: Director
Employment type: Full-time
Job function: Science
Industries: Biotechnology Research and Pharmaceutical Manufacturing
#J-18808-Ljbffr