Medical Director or Senior Medical Director

Kymera Therapeutics•Watertown, MA

5d•$300,000 - $380,000

About The Position

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. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years.

Requirements

MD or MD/PhD and substantial clinical development experience in developing medicines for dermatologic indications.
Minimum of 4 years of experience in clinical drug development, of which at least 2 years of experience is working on dermatologic indications or in programs with dermatologic endpoints.
Experience interacting with global regulatory agencies (e.g., FDA, EMA) and preparing briefing documents for regulatory submissions.
Proven track record in designing and executing clinical trials (Phase I–III) and contributing to successful regulatory interactions.
Strong understanding of translational science, biomarkers, and mechanistic drug development.
Demonstrated ability to lead cross-functional teams and manage multiple programs in parallel.
Entrepreneurial mindset and passion for advancing first-in-class therapies in a collaborative, science-driven environment.
Excellent leadership, communication, and collaborative skills; ability to thrive in a fast-paced, matrixed environment.

Responsibilities

Serve as the clinical lead for one or more studies within the STAT6 program.
Integrate translational and biomarker data into clinical strategy to refine patient selection and endpoint development.
Lead the design and implementation of clinical studies, ensuring scientific rigor and patient safety.
Collaborate with external partners, academic institutions, and consortia to advance the scientific and clinical development strategy.
Provide medical leadership to cross-functional teams, including development sub-teams and clinical study teams.
Provide medical oversight during clinical trial conduct, including safety monitoring, data review, and protocol amendments as needed.
Contribute to the development of clinical and regulatory documents (protocols, IBs, CSRs, regulatory submissions).
Contribute to hiring, coaching, and development of clinical development talent.
Represent Kymera in scientific, regulatory, and clinical forums, including interactions with KOLs, investigators, and advisory boards.