Novo Nordisk

Principal Scientist – Small Molecules, Biochemistry and Biophysics

Novo Nordisk

full-time

Posted on:

Location Type: Office

Location: LexingtonMassachusettsUnited States

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Salary

💰 $152,700 - $267,300 per year

Job Level

Tech Stack

About the role

  • Proposing and developing assays for hit identification strategies for new programs and to drive hit-to-lead and lead optimization projects
  • collaborating within a cross-functional project team to improve compound potency, properties, and understanding of compound mechanism of action (MoA)
  • work collaboratively through interactions across TAs within NN
  • managing a number of contract research organizations (CRO) across the globe
  • supporting the preparation of patents, reports, scientific publications, and serving as functional expert in supporting IND filings
  • Lead functional groups for the design, development, validation, and implementation of biochemical & biophysical assays for small molecule hit ID and MoA
  • Analyze, interpret, and communicate high-quality data to a multi-disciplinary project team
  • Manage global CROs and external partners on a day-to-day basis to achieve project goals
  • Develop and direct collaborations with external CROs performing assay development and transfer, library screening, and hit validation across projects
  • Has accountability for CROs timelines and data quality
  • Enhance operational efficiency and implementing best practices within Line of Business (LoB)
  • Critically evaluate project data while rigorously driving data-driven Go/No-go decisions, including the identification of resource constraints and bottlenecks
  • Communicate project plans/priorities to management
  • Effectively communicate and collaborate across global sites
  • Represent the organization through external communication of impactful scientific research in the form of presentation at external conferences and publication in scientific journals and patents
  • Contribute subject matter expertise to develop the research agenda with a clear understanding of the link between scientific project goals and overall long-term business needs
  • Propose new projects that support the strategic agenda and address gaps in technological capabilities and therapeutic areas

Requirements

  • Master’s degree with 12+ years of relevant experience, or PhD with 8+ years of relevant experience required
  • 8+ years of biochemistry and enzymology industry experience preferred
  • 3+ years of previous experience managing CROs preferred
  • 3+ years of biochemistry & biophysics work in a hybrid model preferred
  • In-depth knowledge in biochemical and biophysical assay development and validation
  • Expert in enzymology, enzyme kinetics, and current assay formats for multiple enzyme classes and protein-protein-interaction targets
  • Expert in steady-state and pre-steady state kinetics to determine enzyme and inhibitor mechanism of action
  • Broad experience in HTS assays
  • Expertise in utilizing a wide array of biochemical and biophysical technologies, including FI, FP, TR-FRET, AlphaScreen, radiometric methods, DSF, SPR, ITC, MST
  • Additional Hit finding knowledge: DEL, ASMS, and fragment-based screening beneficial
  • Experience developing and executing strategies to address key aspects of small molecule mechanism of action
  • Expert and hands-on experience with high throughput screening and hit validation techniques
  • Broad experience with automation beneficial
  • Demonstrated highly successful project execution across disease areas using in-house and/or CRO resources leading to preclinical and clinical development candidates
  • Impeccable attention to detail; Maintain detailed documentation
  • Experienced at writing IND reports and scientific papers
  • Broad experience with protein crystallography
  • Knowledge and experience using corporate database (e.g. CDD Vault/Abase, Dotmatics); Experience with data fitting software
  • Experience enhancing operational efficiency and implementing best practices within LoB
  • Track record of innovation and impact on programs documented with co-inventorship on issued patents and/or authorship of publications in peer-reviewed journals
  • Demonstrates excellent verbal and written communication skills, strong interpersonal skills with a demonstrated ability to work collaboratively on multidisciplinary teams
  • Proficient in Microsoft Office suite of products (Outlook, Excel, Word, PowerPoint)
Benefits
  • medical, dental and vision coverage
  • life insurance
  • disability insurance
  • 401(k) savings plan
  • flexible spending accounts
  • employee assistance program
  • tuition reimbursement program
  • voluntary benefits such as group legal, critical illness, identity theft protection, pet insurance and auto/home insurance
  • time off pursuant to its sick time policy
  • flexible vacation policy
  • parental leave policy
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
biochemical assay developmentbiophysical assay validationenzyme kineticshigh throughput screeninghit validation techniquesprotein-protein interactionsteady-state kineticspre-steady state kineticsdata analysisproject execution
Soft Skills
collaborationcommunicationattention to detailproject managementinterpersonal skillsinnovationproblem-solvingleadershipcritical evaluationstrategic thinking
Certifications
Master's degreePhD