
Biotechnology company.
Senior Scientist, Biomarkers
Company Overview:
Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types.
Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology & oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit www.primemedicine.com.
We are seeking a Senior Scientist, Biomarkers Key Responsibilities Biomarker Strategy & Scientific Leadership
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Lead fluid biomarker strategy for clinical programs, ensuring alignment with clinical objectives, regulatory expectations, and translational hypotheses.
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Design and oversee development, qualification, and validation of biomarker assays at CROs and external laboratory partners.
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Provide scientific oversight for assay selection, fit-for-purpose validation, and performance monitoring.
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Contribute to clinical protocol development, statistical analysis plans, and regulatory documents (e.g., INDs, briefing books).
Assay Development & Validation
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Direct development and validation/qualification of blood-based and other fluid biomarker assays (e.g., protein, enzymatic, molecular assays).
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Ensure assays are developed under appropriate regulatory frameworks (GLP/GCLP/CLIA as applicable).
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Evaluate assay performance characteristics including sensitivity, specificity, precision, robustness, and stability.
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Troubleshoot assay performance issues and implement corrective actions.
Clinical Study Execution
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Partner closely with clinical operations and sample management teams to ensure seamless biomarker sample collection, handling, and analysis.
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Collaborate with peers responsible for immunogenicity and PK assays to ensure integrated PK/PD and biomarker analysis.
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Oversee data generation timelines, budgets, and vendor performance.
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Lead scientific review and interpretation of biomarker data to support internal decision-making.
Cross-Functional Collaboration
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Work closely with Clinical Development, Regulatory, Biostatistics, CMC, and Research teams.
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Contribute to cross-program biomarker governance and best practices.
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Represent the Biomarkers group in cross-functional team meetings and external vendor discussions.
Data Analysis & Interpretation
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Perform and/or oversee robust statistical and scientific analysis of biomarker data.
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Integrate biomarker findings with clinical endpoints and PK data.
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Prepare high-quality summaries and presentations for internal governance and external regulatory interactions.
Qualifications Education & Experience
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PhD in Immunology, Molecular Biology, Biochemistry, Translational Medicine, or related discipline with 4+ years of industry experience; or
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MS with 8+ years of relevant industry experience.
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Demonstrated experience supporting clinical-stage programs.
Technical Expertise
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Strong experience in assay development and fit-for-purpose validation (protein, enzymatic, or molecular assays).
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Hands-on experience managing assay development at CROs and external laboratories.
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Deep understanding of GCLP/GLP principles and regulatory expectations for clinical biomarker assays.
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Experience with blood-based biomarker assays required.
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Familiarity with PK/PD concepts and translational biomarker strategy strongly preferred.
Scientific & Analytical Skills
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Strong data analysis skills and ability to interpret complex biomarker datasets.
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Experience contributing to regulatory submissions (INDs, briefing documents, clinical study reports) preferred.
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Ability to critically evaluate assay performance and scientific rigor.
Leadership & Operational Skills
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Demonstrated ability to manage external vendors and timelines.
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Strong time and resource management skills.
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Ability to operate independently while thriving in a collaborative, cross-functional environment.
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Excellent written and verbal communication skills.
Preferred Qualifications
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Experience in rare disease programs.
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Experience with genetic medicine or gene editing platforms.
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Experience supporting first-in-human studies.
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Exposure to multiplexed, LC/MS-based, or advanced molecular biomarker platforms.
The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity).
Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company-wide recharge breaks.
Our commitment to employee well-being reflects our belief that when we care for our people, we strengthen our ability to put patients first and make meaningful impact together.
U.S. Pay Range**$145,000—$177,000 USD**
Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.
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Prime Medicineについて

Prime Medicine
Series BBiotechnology company.
51-200
従業員数
Cambridge
本社所在地
レビュー
10件のレビュー
3.8
10件のレビュー
ワークライフバランス
3.2
報酬
3.5
企業文化
4.1
キャリア
2.8
経営陣
2.3
65%
知人への推奨率
良い点
Supportive and collaborative team
Good benefits and compensation
Cutting-edge research and technology
改善点
Poor management and lack of direction
Limited career advancement opportunities
High workload and stress
給与レンジ
17件のデータ
Director
Director · DIR. OF BUSINESS DEVLP, HEAD OF ALLIANCES & CORP. INITIATIVE
2件のレポート
$273,000
年収総額
基本給
$210,000
ストック
-
ボーナス
-
$273,000
$273,000
面接レビュー
レビュー62件
難易度
3.7
/ 5
期間
14-28週間
内定率
30%
体験
ポジティブ 69%
普通 21%
ネガティブ 10%
面接プロセス
1
Phone Screen
2
Technical Interview
3
System Design
4
Behavioral
5
Team Fit
よくある質問
Tell me about a challenging project
System design question
Coding problem
Why this company
最新情報
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