Atlas Venture
About Kymera Therapeutics
Kymera is a clinical stage biopharmaceutical company focused on discovering and developing novel small molecule therapeutics that selectively degrade disease-causing proteins by harnessing the body’s own natural protein degradation system.
Job Description Who we are:
Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. We are deploying TPD to targets inaccessible with conventional therapeutics. Since our founding in 2016, we have advanced the first degrader into the clinic for immunological diseases and are building an industry-leading pipeline of oral small molecule degraders. Recognized as one of Boston’s top workplaces, we are committed to innovation and impact.
How we work:
PIONEER:
We are courageous, resilient, and rigorous in our mission.
COLLABORATE:
We value trust, transparency, and shared goals.
BELONG:
We embrace diversity, curiosity, and inclusivity.
How you’ll contribute:
The Senior Director, Medical Affairs, reporting to the Vice President, Medical Affairs, will develop and execute medical strategies, including data generation, scientific publications, advisory boards, and congress planning. This role involves collaboration with internal teams (R&D, Commercial, Regulatory) and external healthcare professionals, KOLs, and scientific organizations to ensure impactful, compliant medical engagement.
Review and interpret clinical data, communicate findings, and develop impactful initiatives.
Drive scientific publication strategies, including manuscripts, abstracts, and posters.
Provide medical expertise for clinical trial design, safety, regulatory compliance, and educational materials.
Lead medical strategy at scientific congresses, including planning and KOL engagement.
Oversee medical research activities, grants, sponsorships, and collaborations.
Coordinate with internal and external stakeholders for logistics and deliverables.
Develop internal training to enhance scientific knowledge.
Support corporate strategy and business development with medical insights.
Skills and experience:
Advanced degree (MD, PharmD, PhD) in a relevant scientific or clinical discipline; immunology experience preferred.
Minimum 10+ years in medical affairs within pharma or biotech.
Experience in data dissemination strategies based on clinical data and market needs.
Understanding of clinical research methodologies and scientific communication.
Knowledge of clinical trial design, drug development, and regulatory processes.
Strong business acumen, especially in immunology/inflammation markets.
Familiarity with digital channels for healthcare education and engagement.
Understanding of regulatory and compliance standards.
Leadership, project management, and strategic skills.
Excellent communication and interpersonal skills.
Kymera Therapeutics is an equal opportunity employer committed to diversity and inclusion. All applicants will be considered without regard to legally protected characteristics.
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Job Description Who we are:
Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. We are deploying TPD to targets inaccessible with conventional therapeutics. Since our founding in 2016, we have advanced the first degrader into the clinic for immunological diseases and are building an industry-leading pipeline of oral small molecule degraders. Recognized as one of Boston’s top workplaces, we are committed to innovation and impact.
How we work:
PIONEER:
We are courageous, resilient, and rigorous in our mission.
COLLABORATE:
We value trust, transparency, and shared goals.
BELONG:
We embrace diversity, curiosity, and inclusivity.
How you’ll contribute:
The Senior Director, Medical Affairs, reporting to the Vice President, Medical Affairs, will develop and execute medical strategies, including data generation, scientific publications, advisory boards, and congress planning. This role involves collaboration with internal teams (R&D, Commercial, Regulatory) and external healthcare professionals, KOLs, and scientific organizations to ensure impactful, compliant medical engagement.
Review and interpret clinical data, communicate findings, and develop impactful initiatives.
Drive scientific publication strategies, including manuscripts, abstracts, and posters.
Provide medical expertise for clinical trial design, safety, regulatory compliance, and educational materials.
Lead medical strategy at scientific congresses, including planning and KOL engagement.
Oversee medical research activities, grants, sponsorships, and collaborations.
Coordinate with internal and external stakeholders for logistics and deliverables.
Develop internal training to enhance scientific knowledge.
Support corporate strategy and business development with medical insights.
Skills and experience:
Advanced degree (MD, PharmD, PhD) in a relevant scientific or clinical discipline; immunology experience preferred.
Minimum 10+ years in medical affairs within pharma or biotech.
Experience in data dissemination strategies based on clinical data and market needs.
Understanding of clinical research methodologies and scientific communication.
Knowledge of clinical trial design, drug development, and regulatory processes.
Strong business acumen, especially in immunology/inflammation markets.
Familiarity with digital channels for healthcare education and engagement.
Understanding of regulatory and compliance standards.
Leadership, project management, and strategic skills.
Excellent communication and interpersonal skills.
Kymera Therapeutics is an equal opportunity employer committed to diversity and inclusion. All applicants will be considered without regard to legally protected characteristics.
#J-18808-Ljbffr