Early Research & Development Scientist Job at Revel IT (Tucson)

Scientist II/Sr. Scientist I, Analytical Research and Development

We are seeking a Scientist II/ Senior Scientist I with hands‑on experience in ph...

Location

United States , Cambridge

Salary:

130000.00 - 180000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Degree in a relevant discipline (biochemistry, biotechnology, biological sciences, bioengineering, or related fields)
Minimum PhD with 2+ years or BS/MS with 10-15 years industry experience
Must have hands-on experience on analytical method development, optimization, qualification, and testing at GMP or non-GMP environments, supporting clinical phase programs
Experience with analysis of RNAs, proteins, protein conjugates, lipids, and lipid nanoparticles (LNPs) is highly desirable
Extensive experience with at least one or several of the analytical techniques is required: HPLC (RP, IPRP, SEC, IEX), capillary gel electrophoresis, ELISA
Experience with qPCR, DNA and RNA extraction, western blotting, UV spectrophotometry, DLS, MALS, mass spectrometry, and compendial testing will be a plus
Experience with analytical CMC development, method transfer, and QC technical support is highly desirable
A good understanding of ICH Q2 and Q14, with working knowledge on analytical Quality by Design concept
Familiarity with data analysis software such as Openlab, Chromeleon, and statistical software such as JMP
Team player with excellent oral and written communication skills

Job Responsibility

Lead early through late phase method development, optimization, and transfer for lot release, stability, and characterization of drug substances, critical materials, and drug products
Establish technical leadership as subject matter expert in multiple analytical techniques during method development and transfer and provide technical troubleshooting support when needed
Work with cross-functional groups including Research & Development, Quality Control, and Process Development teams to participate in various aspects of method development, transfer, characterization, comparability, and investigation
Coordinate routine sample testing including requests from Research and Development groups and Process Development teams
Author and review SOPs, technical reports, and assist in the preparation of CMC regulatory submissions
Analyze, track, and trend data to monitor analytical assays and ensure consistency in assay performance
Maintaining detailed documentation of experiments in ELN system
Adapting to a fast-paced, dynamic research environment
Mentor and train junior scientists
Living Beam Therapeutics core values

Fulltime

Clinical Scientist Director – Early Development, Oncology

In this vital role, the Clinical Scientist Director will support early phase cli...

Location

Portugal , Lisbon

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 4 years of life sciences/healthcare experience
Master’s degree and 7 years of life sciences/healthcare experience
Bachelor’s degree and 9 years of life sciences/healthcare experience
5 years of pharmaceutical clinical drug development experience
Industry or academic experience in early-phase drug development within Oncology
Strong communication & presentation skills in English
Experience with designing, monitoring, and implementing clinical trials for Oncology and interpreting test results in compliance with Good Clinical Practice standards and regulatory requirements
Understanding of conducting study data readout activities, including data cleaning, database lock, data extract, producing outputs of data
Experience drafting high level submission documents for regulatory submissions including authoring clinical regulatory responses for health regulatory interactions
Serving as a contributing author to scientific publications and data presentations at scientific conferences

Job Responsibility

Serve as a clinical and scientific subject-matter expert for the assigned therapeutic area and disease indication, with a strong focus on protocol execution and data integrity
Contribute to medical monitoring activities and support ongoing assessment of subject-level clinical data to identify trends, risks, and emerging issues
Present information internally and externally, anticipating and actively managing problems across a broad spectrum of cross-functional teams
Provide guidance and assistance in the identification and management of collaborators, consultants, and/or Clinical Research Organizations (CROs) in completion of key projects
Work cross functionally to ensure clinical strategy is translated into the development of the study concept document, study protocol and related documents
Ensure integrity of protocols and/or components of clinical plans and for the delivery of final protocol and its governance approval
Provide clinical input into & implementation of clinical trial(s), their delivery, clinical data review, interpretation of results
Review and analyze clinical trial data to ensure accuracy, completeness and adherence to protocol and regulatory requirements
Conduct thorough data quality assessments in the context of a data monitoring plan to maintain high standards of data accuracy and integrity throughout the trial lifecycle

What we offer

Vast opportunities to learn, develop, and move up and across our global organization
Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act
Generous AMGEN Total Rewards Plan comprising healthcare, finance, wealth, and career benefits
Flexible work arrangements

Senior Project Manager, Research & Development

The hiring organisation is a pioneering Danish biotech company at the forefront ...

Location

Denmark

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

Minimum of 5 years of practical project management experience from a biotech or pharmaceutical company, ideally in an R&D environment
Strong scientific background and hands-on understanding of microbiology and bacteriology
Documented experience leading complex, agile projects with a high degree of uncertainty
Ability to operate in cutting-edge research where outcomes are not always predictable and project plans must evolve quickly
Natural authority, professional weight and interpersonal maturity to gain respect from senior specialists
Strong listening skills combined with the ability to stand firm when project progress requires decisions, prioritisation or escalation
Ability to translate technical complexity into practical project actions and create alignment across different scientific and operational groups
A diplomatic and constructive style, with the ability to manage different personalities with both confidence and empathy
Experience with CRISPR, bacteriophages or antimicrobial resistance is advantageous, but not a requirement

Job Responsibility

Lead and drive the day-to-day progress of two or more research projects within microbiology, bacteriology and synthetic biology
Act as the central hub for project coordination, creating transparency and ensuring clear communication across the team and with adjacent functions such as process development and production
Maintain and continuously revise project plans based on new data, experimental results and changing scientific priorities
Manage shifting timelines, milestones and dependencies in a research environment where uncertainty is part of the work
Identify project blockers early, especially tight deadlines and resource constraints, and escalate or resolve them proactively
Facilitate effective problem-solving among highly specialised scientists and ensure constructive collaboration, particularly under pressure
Apply a mature project management toolbox pragmatically, introducing the right level of structure and process without slowing innovation
Challenge technical assumptions and discussions in a qualified manner by understanding the scientific details well enough to ask the right questions
Ensure a strong flow of information to leadership, including preparation of material and, when relevant, presentations for board meetings and external stakeholders
Help professionalise project leadership practices in the research organisation through leading by doing

Senior Scientist – Research Computational Biology Platforms

The ARIA Computational Biology team is seeking a talented and creative computati...

Location

United States , South San Francisco; Boston; Thousand Oaks

Salary:

146404.00 - 198076.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

PhD in computational biology, bioinformatics, data science, or a related discipline [and relevant post-doc where applicable]
Master’s degree in computational biology, bioinformatics, data science, or a related discipline and 3 years of relevant research experience
Bachelor’s degree in computational biology, bioinformatics, data science, or a related discipline and 5 years of relevant research experience
Strong programming expertise in Python and R, with proficiency in Linux/Unix environments, cloud computing, HPC, and collaborative development practices (e.g., Git)
Experience developing complex computational tools and visualizations that translate biological insights into actionable strategies
Experience developing and deploying computational tools and pipelines, including use of workflow management systems (e.g., Nextflow), CI/CD practices, and interactive visualization tools (e.g., Shiny/Streamlit)
Strong background in molecular and systems biology
Demonstrated expertise in the analysis and interpretation of single-cell omics data
Experience leveraging and fine-tuning transcriptional foundation models, large language models (LLMs), and biomedical knowledge graphs to advance research objectives
Familiarity with high-value public data resources (e.g., DepMap, Human Cell Atlas, TCGA, GTEx, and Tahoe-100M) used to complement and enhance analyses of internal datasets

Job Responsibility

Developing and applying methods and platforms to discover, prioritize, and validate targets across a broad range of diseases and therapeutic modalities
Designing and building a Precision Targeting Engine that integrates internal and high-value public data into an automated, scalable framework with custom expression analytics across diverse data types and disease areas
Contributing to the design and evolution of Amgen’s preclinical omics data ecosystem in partnership with the Research Informatics team
Evaluating and integrating emerging AI/ML technologies (e.g., biological foundation models), and developing custom research agents to accelerate early pipeline efforts
Partnering with data science and information systems teams to embed tools and analyses developed within ARIA Computational Biology into integrated R&D platforms
Training and mentoring other scientists in the use of advanced research tools and platforms

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Research Scientist Intern, MSL Infra Kernels & Optimizations

Meta’s Meta SuperIntelligence Labs (MSL) Infra Kernels & Optimizations (K&O) tea...

Location

United Kingdom , London

Salary:

Not provided

Research Scientist in Quantum Photonic Integrated Circuits

With over two decades of research, innovation and development, Toshiba is at the...

Location

United Kingdom , Cambridge

Salary:

Not provided

Toshiba EMEA

Expiration Date

Until further notice

Requirements

PhD in Physics, Photonics, Electronic Engineering, or a closely related field
Research experience with relevant technology such as: Photonic integration, hybrid integration, design, simulations, modelling and measurements of photonic chips
Quantum communications, quantum key distribution, quantum networks
High-speed coherent optical communications
Experience with RF test and measurements
Competence in Python, Matlab, Labview or similar languages
Ability to work both independently and collaboratively in multi-disciplinary team
Excellent technical presentation skills, both written and oral
Proactive with strong organisational skills and strong communication stills

Job Responsibility

Devise and implement new concepts for photonic chips for quantum communications
Conceptualize new experiments and new protocols for quantum communications
Measure, characterize, validate and optimize the performance of photonic chips and demonstrate their capabilities with large-scale deployment
Understand the framework of security analysis for quantum key distribution and quantum random number generation
Work within a multi-disciplinary team to develop innovative approaches for packaging and system integration of quantum photonic chips, including optical and electrical interconnect, electronic control, high-speed signal processing, software and firmware
Develop system control, automation, synchronisation, simulation, and data analysis
Develop and operate research-grade systems
Analyse experimental data and communicate findings through scientific publications, internal reviews, and international conferences
Collaborate with industrial partners and academic groups across the UK, Europe, and Japan
Mentor PhD students and early career staff researchers

What we offer

Generous Benefits Package

Senior Scientist, Early Formulation Science and Drug Delivery, Drug Product Design

This position will be reporting into the Early Formulation Science and Drug Deli...

Location

United States , La Jolla

Salary:

90900.00 - 151500.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

Recent PhD with 0-3 year post-doctoral experience, MS with 7+ years experience, or BS with 8+ years experience in Chemistry, Chemical Engineering, Physical Chemistry, Physics, Physical Organic Chemistry, Pharmaceutics, or Pharmaceutical Sciences
Experience working independently and collaboratively in a laboratory environment

Job Responsibility

Evaluate the physicochemical properties of potential small molecule drug candidates to inform a drug product formulation strategy and developability risk assessment
Design and develop fit for purpose and diagnostic traditional and enabled formulations for preclinical studies
Design, execute, and interpret the results of polymorph and salt screens for potential drug candidates related to stability, manufacturability, and bio-performance
Apply first principles understanding of thermodynamics and kinetic processes to dissolution and precipitation of drugs in biorelevant conditions and physical and chemical stability in the solid state
Work in cross-disciplinary teams and partner with subject matter experts in Medicinal Chemistry, Pharmacokinetics & Drug Metabolism, and Clinical Pharmacology departments to influence candidate selection and progression
Develop strategic collaborations with academic and industrial researchers for addressing gaps in fundamental or applied science related to the pharmaceutical sciences
Conduct novel research and present significant findings via internal and external presentations or publications

What we offer

401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
paid vacation, holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage
participation in Pfizer’s Global Performance Plan with a bonus target of 12.5% of the base salary
eligibility to participate in our share based long term incentive program
Relocation support available

Fulltime

Research Scientist II

Microsoft is a company where passionate innovators come to collaborate, envision...

Location

India , Hyderabad

Salary:

Not provided

Microsoft Corporation

Expiration Date

Until further notice

Requirements

Master's Degree in relevant field AND 1+ year(s) related research experience
Bachelor's Degree in relevant field AND 2+ years related research experience
OR equivalent experience
Proven ability to communicate complex technical concepts to diverse stakeholders
Ability to meet Microsoft, customer and/or government security screening requirements
Microsoft Cloud Background Check
Doctorate in relevant field OR Master's Degree in relevant field AND 3+ years related research experience OR Bachelor's Degree in relevant field AND 5+ years related research experience OR equivalent experience
Experience publishing academic papers as a lead author or essential contributor
Experience participating in a top conference in relevant research domain
Strong track record in cross-functional product development and delivering measurable impact through data-driven iteration

Job Responsibility

Build and expand collaborative partnerships across product, engineering, and research groups inside and outside Microsoft
Provide growing expertise that accelerates technology transfer, strengthens data security practices, and advances internal tools, benchmarking efforts, patent filings, and whitepaper development
Contribute to cutting-edge research by collaborating with peers and engineering teams to advance existing projects, develop new ideas, and publish high-quality papers
Coauthor or lead publications for top-tier conferences and journals with impact on par with postdoctoral research output
Drive research projects to completion, delivering novel algorithms, prototypes, theories, datasets, tools, or insights that meaningfully advance one or more open research problems
Uphold Microsoft’s commitments to security, ethics, and privacy by incorporating responsible research practices into data collection, experimentation, and system design
Support the development of trustworthy, robust, privacy-preserving, and ethically aligned technologies
Help define clear research problems and goals, contributing to the formulation of compelling problem statements and feasible research plans with measurable impact
Develop deep understanding of the state of the art, tracking new methods, tools, and breakthroughs in the research community
Contribute domain expertise in multiple specialized techniques to guide project planning, scoping, and execution

Fulltime

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