Title: Scientist.Location: 4300 Hacienda Drive, Pleasanton, CA, 94588.Contract Duration: 12+ months.Pay Rate: $30.00/ Hr to $45.00/ Hr on W2 (Rates will be confirmed based on the education and experience)Description:<ul><li>Works under general supervision to conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding. Makes recommendations to resolve problems encountered during experimental procedures. Assumes responsibility for the accuracy, quality, and timeliness of experimental results. Summarizes experimental results and reviews conclusions with supervisor/project leader. Communicates results of experiments in the form of reports and presentations. Keeps supervisor/project leader informed of project status, particularly of significant findings and results in critical problem areas. Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA).</li><li>Analyzes experimental data using various data analysis software and/or applying quantitative methods. Forms conclusions and provides/documents process improvements. Uses technical writing skills to produce reports and documents. May present findings at internal meetings.</li><li>Assumes accountability for own electronic notebook documentation, ensuring experimental methods and results are recorded timely, accurately, and consistently, and according to established formats.</li><li>Participates in routine lab maintenance, lab safety, ISO, and QSR implementation.</li><li>May troubleshoot issues related to instrumentation.</li><li>Receives general instructions; plans and executes own work.</li><li>Keeps informed of trends and developments in area of scientific responsibility.</li><li>May establish and work with individuals or teams outside of immediate functional area or RMD.</li><li>Knows and effectively uses the broad concepts of a particular field or specialization to resolve problems of limited scope and complexity.</li><li>Capable of providing analysis to a variety of data types with the aid of statistical or general-purpose programming.</li></ul>Other Duties:<ul><li>The essential job functions and major contributions listed above are not intended to be an exhaustive list of all responsibilities, duties, and skills. Incumbents may be required to perform other duties as required.</li></ul>Skills:<ul><li>Sci I/II: Minimum (required): Ph.D./Master’s/Bachelor’s in life sciences, chemical sciences, or related scientific field. Masters Degree with no experience for Sci II fields. Typically 0 to 3 years of relevant industry experience. Preferred: More than 1 year of relevant industry experience.</li><li>Senior Scientist: Minimum (required): Ph.D./Master’s/Bachelor’s in life sciences, chemical sciences, or related scientific field with 0/2/5+ years relevant experience. Preferred: More than 1 year of relevant industry experience.</li></ul>Other Qualifications:<ul><li>Ability to design and execute relevant laboratory experimentation and determine next steps within the context of overall project goals and direction.</li><li>Subject to OSHA Blood Borne Pathogen Standard. Routinely handle blood, blood products, body fluids or other potentially infectious materials. Subject to respiratory protection standard. Work with potential hazardous chemicals.</li><li>Work with potential radiological hazards. Work with potential biological hazards. Wear personal protective equipment, such as eye, foot, lab coat, gowning coveralls. Wear respirator dust mask cartridge/ air purifying supplied air. Wear hearing protective devices. Confined space work.</li></ul>
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Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: <ul><li>Career development with an international company where you can grow the career you dream of. </li><li>Free medical coverage for employees* via the Health Investment Plan (HIP) PPO </li><li>An excellent retirement savings plan with high employer contribution </li><li>Tuition reimbursement, the <a >Freedom 2 Save </a> student debt program and <a >FreeU </a> education benefit - an affordable and convenient path to getting a bachelor’s degree. </li><li>A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. </li><li>A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. </li> </ul>The Opportunity This position works out of our Pleasanton, CA location in the Heart Failure division. In Abbott’s Heart Failure (HF) business, we’re developing solutions to diagnose, monitor and manage heart failure, allowing people to restore their health and live full lives. The Senior Clinical Research Scientist is a member of the Global Clinical Affairs team who provides scientific expertise throughout the development and implementation of clinical evaluations, risk management and/or clinical studies. The scientist interacts with various study support groups and cross-functional teams in order to assist in clinical and data science, clinical strategy, the development of plans and reports, and project deliverables. The scientist is also responsible for interacting with regulatory agencies as needed, and using their scientific and medical knowledge in order to provide directives to the team as well as study sites as directed by their manager. What You’ll Work On <ul><li>Writes clinical evaluation plans and reports, study protocols, protocol amendments, informed consents, study reports, risk master lists, and scientific papers for publication by evaluating scientific literature, analyzing scientific data and staying abreast of current clinical practice. </li><li>Examine data sets and determine the best end-to-end analysis plan to address key scientific questions. </li><li>Analyzes data (including defining populations, creating model logic, drawing insights, refining analyses and determining outcomes). </li><li>Present analysis results in a cohesive manner. </li><li>Interprets results in preparation for product applications by evaluating clinical and scientific and risk data and literature, and staying abreast of current clinical practice. </li><li>Presents scientific data by communicating accurate, succinct summaries of clinical results at industry gatherings, investigational meetings, and regulatory agency meetings. </li><li>Facilitates communication between Sales and Marketing, R&D, Clinical R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs or Clinical Science, Risk Management, Clinical Project Management, external CROs or Medical Writers, Training, Senior Management and investigational sites as directed by your manager. </li><li>Participates in the development of clinical strategy and trial design by conducting meetings with the appropriate departments and individuals to obtain feedback/direction. </li><li>Creates, manages, or participates in clinical study or clinical evaluation timelines and budgets by utilizing the appropriate project management tools, selecting providers or external medical writers, managing vendor contracts as requested, and ensuring expenditures are within budgetary guidelines. </li><li>Facilitates regulatory submissions and communications by communicating with Regulatory Affairs during the submission process. </li><li>Participates in and supports audits. </li><li>Interfaces with management on significant matters, often requiring the coordination of activity across organizational units, physicians, and external CROs and medical writers. </li><li>Participates in the development of other technical contributors by supporting training and providing feedback and guidance. </li><li>Conducts team meetings, drafting and sending routine correspondence and presenting regular updates to senior staff. </li><li>May participate in a project team, root cause analysis, preventive or corrective actions, and effectiveness monitoring. </li><li>Acts as a mentor to less-experienced staff and may provide work direction or supervise other technical employees. </li><li>Exercises judgment independently. </li><li>Plans and organizes project assignments of substantial variety and complexity. </li> </ul>Required Qualifications <ul><li>Bachelors degree in science or engineering, or related discipline. </li><li>Minimum 5 years related work experience or an equivalent combination of education and work experience. </li> </ul>Preferred Qualifications <ul><li>Advanced Degree (PhD, MD, etc.) + 2 years relevant work experience. </li><li>Strong independent data analysis and programming skills (R, SPSS, SAS, MatLab, etc.). </li><li>Strong Data Communication and Figure Creation Experience. </li><li>Understanding of statistical principles. </li> </ul><a >Apply Now </a> * Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: <a > </a> Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at <a > </a>, on Facebook at <a > </a> and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $83,600.00 – $167,200.00. In specific locations, the pay range may vary from the range posted. #J-18808-Ljbffr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. <h3>JOB DESCRIPTION: </h3>Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: <ul><li>Career development with an international company where you can grow the career you dream of. </li><li>Free medical coverage for employees* via the Health Investment Plan (HIP) PPO </li><li>An excellent retirement savings plan with high employer contribution </li><li>Tuition reimbursement, the <a >Freedom 2 Save </a> student debt program and <a >FreeU </a> education benefit - an affordable and convenient path to getting a bachelor’s degree. </li><li>A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. </li><li>A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. </li> </ul>The Opportunity This position works out of our Pleasanton, CA location in the Heart Failure division. In Abbott’s Heart Failure (HF) business, we’re developing solutions to diagnose, monitor and manage heart failure, allowing people to restore their health and live full lives. The Senior Clinical Research Scientist is a member of the Global Clinical Affairs team who provides scientific expertise throughout the development and implementation of clinical evaluations, risk management and /or clinical studies. The scientist interacts with various study support groups and cross-functional teams in order to assist in clinical and data science, clinical strategy, the development of plans and reports, and project deliverables. The scientist is also responsible for interating with regulatory agencies as needed, and using their scientific and medical knowledge in order to provide directives to the team as well as study sites as directed by their manager. What You’ll Work On <ul><li>Writes clinical evaluation plans and reports, study protocols, protocol amendments, informed consents, study reports, risk master lists, and scientific papers for publication by evaluating scientific literature, analyzing scientific data and staying abreast of current clinical practice. </li><li>Examine data sets and determine the best end-to-end analysis plan to address key scientific questions </li><li>Analyzes data (including defining populations, creating model logic, drawing insights, refining analyses and determining outcomes </li><li>Present analysis results in a cohesive manner </li><li>Interprets results in preparation for product applications by evaluating clinical and scientific and risk data and literature, and staying abreast of current clinical practice. </li><li>Presents scientific data by communicating accurate, succinct summaries of clinical results at industry gatherings, investigational meetings, and regulatory agency meetings. </li><li>Facilitates communication between Sales and Marketing, R&D, Clinical R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs or Clinical Science, Risk Management, Clinical Project Management, external CROs or Medical Writers, Training, Senior Management and investigational sites as directed by your manager. </li><li>Participates in the development of clinical strategy and trial design by conducting meetings with the appropriate departments and individuals to obtain feedback/direction. </li><li>Creates, manages, or participates in clinical study or clinical evaluation timelines and budgets by utilizing the appropriate project management tools, selecting providers or external medical writers, managing vendor contracts as requested, and ensuring expenditures are within budgetary guidelines. </li><li>Facilitates regulatory submissions and communications by communicating with Regulatory Affairs during the submission process. </li><li>Participates in and supports audits. </li><li>Interfaces with management on significant matters, often requiring the coordination of activity across organizational units, physicians, and external CROs and medical writers. </li><li>Participates in the development of other technical contributors by supporting training and providing feedback and guidance. </li><li>Conducts team meetings, drafting and sending routine correspondence and presenting regular updates to senior staff. </li><li>May participate in a project team, root cause analysis, preventive or corrective actions, and effectiveness monitoring. </li><li>Acts as a mentor to less-experienced staff and may provide work direction or supervise other technical employees. </li><li>Exercises judgment independently. </li><li>Plans and organizes project assignments of substantial variety and complexity. </li> </ul>Required Qualifications <ul><li>Bachelors degree in science or engineering, or related discipline </li><li>Minimum 5 years related work experience or an equivalent combination of education and work experience </li> </ul>Preferred Qualifications <ul><li>Advanced Degree (PhD, MD, etc) + 2 years relevant work experience </li><li>Strong independent data analysis and programming skills (R, SPSS, SAS, MatLab, etc.) </li><li>Strong Data Communication and Figure Creation Experience </li><li>Understanding of statistical principles </li> </ul><a >Apply Now </a> * Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: <a > </a> Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at <a > </a>, on Facebook at <a > </a> and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $83,600.00 – $167,200.00In specific locations, the pay range may vary from the range posted. <h3>JOB FAMILY: </h3>Manufacturing<h3>DIVISION: </h3>HF Heart Failure<h3>LOCATION: </h3>United States > Pleasanton : 6101 Stoneridge Dr<h3>ADDITIONAL LOCATIONS: </h3>United States > Massachusetts > Burlington : 168 Middlesex Turnpike<h3>WORK SHIFT: </h3>Standard<h3>TRAVEL: </h3>Yes, 5 % of the Time<h3>MEDICAL SURVEILLANCE: </h3>No<h3>SIGNIFICANT WORK ACTIVITIES: </h3>Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: is the Law link - Espanol:

Title: Scientist. Location: 4300 Hacienda Drive, Pleasanton, CA, 94588. Contract Duration: 12+ months . Pay Rate: $30.00/ Hr to $45.00/ Hr on W2 (Rates will be confirmed based on the education and experience) Description: <ul><li>Works under general supervision to conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding. Makes recommendations to resolve problems encountered during experimental procedures. Assumes responsibility for the accuracy, quality, and timeliness of experimental results. Summarizes experimental results and reviews conclusions with supervisor/project leader. Communicates results of experiments in the form of reports and presentations. Keeps supervisor/project leader informed of project status, particularly of significant findings and results in critical problem areas. Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA). </li><li>Analyzes experimental data using various data analysis software and/or applying quantitative methods. Forms conclusions and provides/documents process improvements. Uses technical writing skills to produce reports and documents. May present findings at internal meetings. </li><li>Assumes accountability for own electronic notebook documentation, ensuring experimental methods and results are recorded timely, accurately, and consistently, and according to established formats. </li><li>Participates in routine lab maintenance, lab safety, ISO, and QSR implementation. </li><li>May troubleshoot issues related to instrumentation. </li><li>Receives general instructions; plans and executes own work. </li><li>Keeps informed of trends and developments in area of scientific responsibility. </li><li>May establish and work with individuals or teams outside of immediate functional area or RMD. </li><li>Knows and effectively uses the broad concepts of a particular field or specialization to resolve problems of limited scope and complexity. </li><li>Capable of providing analysis to a variety of data types with the aid of statistical or general-purpose programming. </li> </ul>Other Duties: <ul><li>The essential job functions and major contributions listed above are not intended to be an exhaustive list of all responsibilities, duties, and skills. Incumbents may be required to perform other duties as required. </li> </ul>Skills: <ul><li>Sci I/II: Minimum (required): Ph.D./Master’s/Bachelor’s in life sciences, chemical sciences, or related scientific field. Masters Degree with no experience for Sci II fields. Typically 0 to 3 years of relevant industry experience. Preferred: More than 1 year of relevant industry experience. </li><li>Senior Scientist: Minimum (required): Ph.D./Master’s/Bachelor’s in life sciences, chemical sciences, or related scientific field with 0/2/5+ years relevant experience. Preferred: More than 1 year of relevant industry experience. </li> </ul>Other Qualifications: <ul><li>Ability to design and execute relevant laboratory experimentation and determine next steps within the context of overall project goals and direction. </li><li>Subject to OSHA Blood Borne Pathogen Standard. Routinely handle blood, blood products, body fluids or other potentially infectious materials. Subject to respiratory protection standard. Work with potential hazardous chemicals. </li><li>Work with potential radiological hazards. Work with potential biological hazards. Wear personal protective equipment, such as eye, foot, lab coat, gowning coveralls. Wear respirator dust mask cartridge/ air purifying supplied air. Wear hearing protective devices. Confined space work. </li> </ul>#J-18808-Ljbffr

Title: Scientist.Location: 4300 Hacienda Drive, Pleasanton, CA, 94588.Contract Duration: 12+ months.Pay Rate: $30.00/ Hr to $45.00/ Hr on W2 (Rates will be confirmed based on the education and experience) Description:<ul><li>Works under general supervision, to conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding. Makes recommendations to resolve problems encountered during experimental procedures. Assumes responsibility for the accuracy, quality, and timeliness of experimental results. Summarizes experimental results, and reviews conclusions with supervisor/project leader. Communicates results of experiments in the form of reports and presentations. Keeps supervisor/ project leader informed of project status, particularly of significant findings and results in critical problem areas. Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA).</li><li>Analyzes experimental data using various data analysis software and/or applying quantitative methods. Forms conclusions, and provides/documents process improvements. Uses technical writing skills to produce reports and documents. May present findings at internal meeting.</li><li>Assumes accountability for own electronic notebook documentation, ensuring experimental methods and results are recorded timely, accurately and consistently, and according to established formats.</li><li>Participates in routine lab maintenance, lab safety, ISO, and QSR implementation.</li><li>May troubleshoot issues related to instrumentation.</li><li>Receives general instructions; plans and executes own work.</li><li>Keeps informed of trends and developments in area of scientific responsibility.</li><li>May establish and work with individuals or teams outside of immediate functional area or RMD.</li><li>Knows and effectively uses the broad concepts of a particular filed or specialization to resolve problems of limited scope and complexity.</li><li>Capable of providing analysis to a variety of data types with the aid of statistical or general purpose programming.</li></ul> Other Duties:<ul><li>The essential job functions and major contributions listed above are not intended to be an exhaustive list of all responsibilities, duties and skills. Incumbents may be required to perform other duties as required.</li><li>Job Level Criteria: Job Level Criteria defines additional responsibilities for this job, which includes such things as Strategic Focus, Leadership Responsibility and Impact of Work on the organization.</li><li>To obtain appropriate Job Level Criteria, please go to the HR Intranet site under Job Descriptions and Levels.</li><li>Position Specific Qualifications (Training Requirements): Position specific job qualifications are maintained in the RMS Learning Solution within SAP. Managers and employees can contact their department’s Learning Solutions.</li><li>Support Administrator (LSSA) to get a complete list of qualifications for a specific position.</li></ul> Skills:<ul><li>Sci I/II: Minimum (required): Ph.D./Master’s/Bachelor’s in life sciences, chemical sciences, or related scientific. Masters Degree with no experience for Sci II fields. Typically 0 to 3 years of relevant industry experience. Preferred: More than 1 year of relevant industry experience. </li><li>Senior Scientist: Minimum (required): Ph.D./Master’s/Bachelor’s in life sciences, chemical sciences, or related scientific field with 0/2/5+ years relevant experience. Preferred: More than 1 year of relevant industry experience.</li></ul> Other Qualifications:<ul><li>Ability to design and execute relevant laboratory experimentation and determine next steps within the context of overall project goals and direction.</li><li>Subject to OSHA Blood Borne Pathogen Standard Routinely handle blood, blood products, body fluids or other potentially infectious materials Subject to respiratory protection standard Work with potential hazardous chemicals.</li><li>Work with potential radiological hazards Work with potential biological hazards Wear personal protective equipment, such as eye, foot, lab coat, gowning coveralls Wear respirator dust mask cartridge/ air purifying supplied air Wear hearing protective devices Confined space work.</li></ul>

Title:  Scientist.
Location:  4300 Hacienda Drive, Pleasanton, CA, 94588.
Contract Duration:  12+ months .
Pay Rate:  $30.00/ Hr to $45.00/ Hr on W2 (Rates will be confirmed based on the education and experience)
Description:
Works under general supervision to conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding. Makes recommendations to resolve problems encountered during experimental procedures. Assumes responsibility for the accuracy, quality, and timeliness of experimental results. Summarizes experimental results and reviews conclusions with supervisor/project leader. Communicates results of experiments in the form of reports and presentations. Keeps supervisor/project leader informed of project status, particularly of significant findings and results in critical problem areas. Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA).
Analyzes experimental data using various data analysis software and/or applying quantitative methods. Forms conclusions and provides/documents process improvements. Uses technical writing skills to produce reports and documents. May present findings at internal meetings.
Assumes accountability for own electronic notebook documentation, ensuring experimental methods and results are recorded timely, accurately, and consistently, and according to established formats.
Participates in routine lab maintenance, lab safety, ISO, and QSR implementation.
May troubleshoot issues related to instrumentation.
Receives general instructions; plans and executes own work.
Keeps informed of trends and developments in area of scientific responsibility.
May establish and work with individuals or teams outside of immediate functional area or RMD.
Knows and effectively uses the broad concepts of a particular field or specialization to resolve problems of limited scope and complexity.
Capable of providing analysis to a variety of data types with the aid of statistical or general-purpose programming.
Other Duties:
The essential job functions and major contributions listed above are not intended to be an exhaustive list of all responsibilities, duties, and skills. Incumbents may be required to perform other duties as required.
Skills:
Sci I/II: Minimum (required): Ph.D./Master’s/Bachelor’s in life sciences, chemical sciences, or related scientific field. Masters Degree with no experience for Sci II fields. Typically 0 to 3 years of relevant industry experience. Preferred: More than 1 year of relevant industry experience.
Senior Scientist: Minimum (required): Ph.D./Master’s/Bachelor’s in life sciences, chemical sciences, or related scientific field with 0/2/5+ years relevant experience. Preferred: More than 1 year of relevant industry experience.
Other Qualifications:
Ability to design and execute relevant laboratory experimentation and determine next steps within the context of overall project goals and direction.
Subject to OSHA Blood Borne Pathogen Standard. Routinely handle blood, blood products, body fluids or other potentially infectious materials. Subject to respiratory protection standard. Work with potential hazardous chemicals.
Work with potential radiological hazards. Work with potential biological hazards. Wear personal protective equipment, such as eye, foot, lab coat, gowning coveralls. Wear respirator dust mask cartridge/ air purifying supplied air. Wear hearing protective devices. Confined space work.

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Research Scientist Jobs in Pleasanton, CA

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Research Scientist
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Research Scientist Jobs in Pleasanton, CA

Research ScientistDecember 11, 2024

Sr Clinical Research ScientistDecember 10, 2024

Sr Clinical Research ScientistDecember 9, 2024

Research ScientistDecember 9, 2024

Research ScientistDecember 7, 2024

Research ScientistDecember 2, 2024