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

Food Scientist

The Food Scientist will provide technical expertise to new product development f...

Location

Canada , London

Salary:

Not provided

Cargill

Expiration Date

Until further notice

Requirements

Diploma/Certificate or bachelor’s degree in Food Science or equivalent experience
Experience working in a manufacturing environment
Two or more years of professional experience combined in the following areas: protein formulation development, ingredient functionality and product commercialization
Must be willing to participate in sensory evaluation of animal protein products
Minimum of two years of related work experience
Ability to travel up to 30% of the time, into US and Canada
Ability to support early or late hours or weekends as needed
Proficiency in Microsoft Office
Possess a valid, full Canadian Driver’s Licence in good standing, authorizing you to drive independently during the course of your employment
Must be legally entitled to work for Cargill in Canada

Job Responsibility

Identify product growth and new product opportunities
Participate in sensory evaluation of animal protein products with cross functional teams and with customers
Provide technical guidance and leadership on products, process development and improvement, and support for quality systems and regulatory oversight
Partner and stay connected with cross functional teams that include marketing, insights, sales, ops, food safety quality and regulatory
Provide findings and analysis with insights, research, and commercial brand to develop short- and long-term testing programs for experimental and commercial products and hybrids
Collaborate and build partnership with sales, business management and marketing partners to identify customer needs and translate these into new product development opportunities
Independently solve moderately complex issues with minimal supervision, while escalating more complex issues to appropriate staff
Other duties as assigned

What we offer

Relocation assistance and visa sponsorship will not be provided for this position

Fulltime

Global Development Product Lead

Leads multiple cross functional oncology product teams from pre-clinical candida...

Location

United States , La Jolla; Cambridge; Bothell; South San Francisco; New York City

Salary:

295900.00 - 478800.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

MD or MD-PhD with 10+ years of industry experience in oncology drug development is preferred, track record in oncology clinical research including early phase drug development
Clinical oncology experience: Board certification in oncology preferred
Significant industry leadership experience in clinical, translational or basic research in biomedical sciences or one of the disciplines related to drug development
Understanding of related disciplines (e.g., biostatistics, regulatory, pre-clinical pharmacology, pharmaceutical sciences)
Demonstrated scientific productivity (publications, abstracts, etc.)
Proven scientific writing skills and good communication skills
Proven leadership skills with ability to defend the clinical plan at governance meetings is essential
Capacity to adapt to a fast-paced and changing environment
Demonstrated history of effective leadership
including cross functional and matrixed teams, managing direct reports when applicable, and experience in seeking and maintaining alignment with cross-functional leaders

Job Responsibility

Leads multiple (~2-4) cross functional oncology product teams from pre-clinical candidate nomination (CAN) through Phase 1-2 clinical development and proof of concept (POC) stages
In close collaboration with functional experts on the product teams, drives the effective integration of an end-to-end cross functional molecule strategy and risk mitigation plan and ensures delivery of data-driven milestones through successful risk identification and mitigation
Support clinical trials and the development strategy for early development assets and lead development programs across multiple functions within Pfizer Oncology, as well as represent the program with the external clinical community
Develop clinical development plan from first in human clinical trial to proof-of-concept, including assessment of appropriate combinations, as well as evaluation of potential predictive and pharmacodynamics biomarker plans
To ensure the cross-functional components of the product plans including clinical expertise are provided to project teams, including medical monitoring of clinical trials
Substantial support of CDP development and diligence for external innovation activities
Lead key enterprise level cross-functional workstreams to accelerate R&D decision making
Lead, develop and execute strategic development for early development assets
Ensure timely execution and delivery of product milestones within budget
Communicate with executive management and governance committees to address program needs and provide recommendations

What we offer

Participation in Pfizer’s Global Performance Plan with a bonus target of 30.0% of the base salary
Eligibility to participate in our share based long term incentive program
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
Relocation assistance may be available based on business needs and/or eligibility

Fulltime

Oncology Early-Stage Clinical Scientist

You will lead and coordinate the development of multiple studies of novel biolog...

Location

United States , Cambridge; La Jolla; Bothell; Groton; New York City

Salary:

176600.00 - 282900.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

Relevant PhD or PharmD and a minimum of 5 years of experience in a similar role in industry/CRO
MS and a minimum of 7 years of experience in a similar role in industry/CRO
BA/BS and a minimum of 10 years of experience in a similar role in industry/CRO
Clinical Research experience in Phase 1 in Oncology, on the side of the sponsor leading studies
Experience in or strong understanding of Oncology Drug Development especially in Early Development
Strong knowledge of clinical procedures, ICH guidelines, GCP and familiarity with FDA, EMA, and global regulations
Strong scientific writing skills and communication skills (written and verbal)
Clinical document writing experience (e.g., protocol, ICD, IB, IND), as well as understanding complex data analysis
Track record of scientific productivity as evidenced by publications, posters, abstracts and/or presentations
Experience working with and solid understanding of related disciplines, e.g., Clinical Operations, Data Management, Safety, Biostatistics, Regulatory, Study Management, Pre-Clinical, Pharmacology, Quality Assurance

Job Responsibility

Partner closely with the Global Development Lead (GDL) in the execution of the clinical development strategy and plan for the assigned molecule(s)/indication(s)
Responsible for scientific leadership and execution of clinical studies and delivering on innovative clinical study designs, high quality trial execution, safety assessment and interpretation of clinical study results
Support execution for all FIH programs through proof-of concept
Set the clinical data review strategy, ensure quality data and conduct review of emerging clinical data and trends
review and query data
present and discusse relevant data to appropriate teams, governance bodies, and other internal and external stakeholders
Conduct data review, analysis and interpretation of clinical trials data together with the GDL, Clinical Safety, and Biostatistics
Serve as technical resource for clinical issues raised by internal and external collaborators, investigators, consultants and contractors
Support and assist in the development of publications, abstracts, and presentations
May sit on project teams to support clinical development implementation and contribution to key development milestones, e.g. start-up and delivery of ESoE and PoC trials

What we offer

Eligibility for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary
Eligibility to participate in our share based long term incentive program
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
Relocation assistance may be available based on business needs and/or eligibility

Fulltime

Scientist II, In Vivo, Enzymatic and Metabolic Therapeutic Area

The Scientist will join the Enzymatic and Metabolic In Vivo team to design and e...

Location

United States , Petaluma, CA

Salary:

116000.00 - 159500.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

PhD in a related subject area with demonstrated in vivo research experience in metabolic disease
Postdoctoral or industry (2-5 years preferred) experience in genetic metabolic diseases
Extensive hands-on experience with rodent in vivo work in the metabolic field
Demonstrated experience in metabolic biology/disease research in academia or industry (preferred) including publication record
Strong analytical, problem-solving, and decision-making skills
Strong understanding of genetically engineered models, breeding, and management and Gene therapy modalities
Excellent oral and written communication skills
Passion for contributing your scientific skills to develop therapies for patients in need
Must be able to utilize computer databases for analysis, data entry, and point of care observations
Must be able to work under time constraints with minimal direction of day-to-day responsibilities, including collaboratively working with multidisciplinary teams

Job Responsibility

Conduct research on genetic metabolic diseases
Contribute to novel therapeutic programs based on innovative, ground-breaking discoveries that could lead to new, high-impact opportunities for patients
Perform research and publish findings in high-impact journals and present research at major conferences
Effectively partner with other scientists and the Research and Early Development team to develop and execute on the program's strategic plan
Present program data at a range of internal forums, including project team meetings, Research Department Seminars and Research leadership governance forums
Write, review and contribute to study synopses, protocols, study reports and regulatory documents
Collaborate with various BioMarin functions, CROs, university or analytical laboratories, business partners, as necessary to ensure appropriate/timely progression of projects
Participate in multi-disciplinary drug development teams and may lead sub-teams
Execute hands-on responsibilities including but not limited to animal handling and restraint (rodents), administration via various routes of administration, including intravenous (tail-vein), in-life animal health monitoring and measurements, clinical observations, sample collection and processing, and accurate data collection
Provide daily care and monitoring of mice or rats, including health checks and documentation

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

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

Medical Director, Hematology

Lead the science that shapes tomorrow's hematology breakthroughs. Proclinical is...

Location

United States , Boston

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Medical degree (MD or equivalent), ideally with Hematology/Oncology fellowship training
Strong interest in developing innovative therapies and impacting patient populations
Experience in clinical research or drug development, spanning Phases I through IV, is preferred
Medical and scientific expertise in hematology or oncology is advantageous
Excellent collaboration and communication skills to work effectively with diverse teams and stakeholders

Job Responsibility

Lead clinical deliverables for a designated section of a clinical program with minimal supervision
Manage operational aspects and ensure successful execution of the clinical program in partnership with global line functions, Clinical Scientists, and Clinical Operations teams
Support and occasionally lead interactions with external collaborators, including regulatory authorities, key opinion leaders, advisory boards, and patient advocacy groups
Collaborate with internal teams such as Research, Early Clinical Development, Medical Affairs, Marketing, and HEOR
Contribute to Global Clinical Development training programs, author or review clinical SOPs, and participate in taskforces or panels to shape clinical development strategies

Ux Research Manager, Monetization

Monetization is looking for a Research Manager with skills in user experience re...

Location

United States , Bellevue

Salary:

193000.00 - 266000.00 USD / Year

New

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

Early Research & Development Scientist

Revel IT

Location:
United States , Tucson

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 21, 2026

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