Associate Director/Director, Clinical Scientist jobs in United States
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Kymera Therapeutics · 2 days ago

Associate Director/Director, Clinical Scientist

Kymera Therapeutics is a clinical-stage biotechnology company focused on developing targeted protein degradation therapies to improve patient lives. The Associate Director/Director, Clinical Scientist will serve as a key player in clinical trial design and execution, ensuring scientific integrity and compliance with regulatory standards in the field of immunology.

BiotechnologyHealth CareMedicalTherapeutics
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Growth Opportunities
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H1B Sponsor Likelynote

Responsibilities

Serve as the study level Clinical Scientist in immunology, actively participating in program team meetings, Vendor meetings, and data/safety monitoring committees
Support the design of clinical trial protocols, synopses, and amendments, ensuring scientific integrity and alignment with regulatory standards
Conduct clinical data reviews, including safety monitoring activities, to ensure patient safety data accuracy and accuracy
Collaborate with Translational Medicine to embed bioanalytical sampling (e.g., PK/PD, biomarker assays) into trial protocols; ensure data flow to functional groups for analysis
Prepare and review essential documents such as medical monitoring plans, statistical analysis plans (SAPs), informed consent forms, and clinical study reports, supporting regulatory submissions
Work within a matrix environment, collaborating with medical directors, regulatory affairs, translational medicine, clinical operations, statistics, and other departments to drive clinical development programs forward
Data review and cleaning, review protocol deviations, monitor data, query resolution, analyze trends, and prepare clinical study reports and regulatory submission materials
Present data and information to external investigators and internal stakeholders, contributing to meetings with governance bodies and regulatory authorities

Qualification

Clinical ScientistImmunological diseasesClinical trial protocolsRegulatory requirementsMedical writingPharmaceutical clinical developmentProblem-solvingCollaboration

Required

Bachelor's or advanced degree (MSc, PharmD, MD, PhD) in Life Sciences, Pharmacology, or related field
4+ years in pharmaceutical clinical drug development, with experience in global clinical trials and program execution
Proficiency in immunological diseases (e.g. Atopic dermatitis, Asthma) including an understanding of disease biology and treatment landscapes
In-depth understanding of clinical development processes, regulatory requirements, and guidelines (FDA, EMEA, ICH, GCP)
Strong problem-solving abilities and excellent medical writing skills

Benefits

Eligibility for annual bonus
Equity participation
Comprehensive benefits

Company

Kymera Therapeutics

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Kymera Therapeutics is a biotechnology company that specializes in the field of targeted protein degradation.

H1B Sponsorship

Kymera Therapeutics has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (5)
2024 (2)
2023 (4)
2022 (3)
2021 (3)

Funding

Current Stage
Public Company
Total Funding
$1.96B
Key Investors
Biotechnology Value FundAtlas Venture
2025-12-10Post Ipo Equity· $602M
2025-06-26Post Ipo Equity· $250.8M
2024-08-19Post Ipo Equity· $225M

Leadership Team

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Nello Mainolfi
Founder, President and Chief Executive Officer
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Jeremy Chadwick
Chief Operating Officer
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Company data provided by crunchbase