Top 865 Abbott Laboratories Jobs

Scientist, Clinical Research
Abbott Laboratories —Sylmar, CA
- $114,000 - $228,000 a year
- Full-time
- 8 years
- Bachelor's degree
- Contracts
- Health insurance
- Tuition reimbursement
Onsite EMT ( Occupational Health)
ABBOTT —Baltimore, MD
- $26 - $28 an hour
- Part-time
- CPR Certification
- Construction site
- Customer service
- Paid training
Quick Apply
2d
Operations Manager
Abbott Laboratories —Scottsdale, AZ
- $129,300 - $258,700 a year
- Full-time
- Assembly
- Senior level
- Associate's degree
Scientist II – Oligonucleotide Process Development, Manufacturing Development and Scale-Up
Abbott Laboratories —San Diego, CA
- $85,600 - $156,000 a year
- Full-time
- Computer literacy
- Bachelor of Science
- Mid-level
- Health insurance
- Tuition reimbursement
1d
Quality Engineer II
Abbott Laboratories —Alameda, CA
- $90,000 - $180,000 a year
- Full-time
- 5 years
- Mid-level
- Continuous improvement
- Health insurance
- Tuition reimbursement
Quality Engineer
Abbott Laboratories —Houston, TX
- $61,300 - $122,700 a year
- Full-time
- Up to 50% travel
- Mid-level
- Travel
- Health insurance
- Tuition reimbursement
Senior Field Clinical Specialist - REMOTE
Abbott Laboratories —Abbott Park, IL
- $78,000 - $156,000 a year
- Full-time
- Remote
- 7 years
- Travel
- Organizational skills
- Health insurance
- Tuition reimbursement
Specialist, Clinical Planning and Performance
Abbott Laboratories —Maple Grove, MN
- $61,300 - $122,700 a year
- Full-time
- Mid-level
- Office
- Master's degree
- Health insurance
- Dental insurance
Medical Science Liaison, Abbott Point of Care (APOC) (Medical Affairs Team- Southeast Territory)
Abbott Laboratories —Abbott Park, IL
- $113,300 - $226,700 a year
- Full-time
- Mid-level
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
- Tuition reimbursement
Senior Field Clinical Specialist
Abbott Laboratories —Abbott Park, IL
- $78,000 - $156,000 a year
- Full-time
- Remote
- 7 years
- Travel
- Organizational skills
- Health insurance
- Tuition reimbursement
Manager, Quality Assurance
Abbott Laboratories —Atlanta, GA
- $99,300 - $198,700 a year
- Full-time
- Analysis skills
- Bachelor's degree
- Mentoring
- Health insurance
Senior Specialist, Benefits
Abbott Laboratories —Abbott Park, IL
- $78,000 - $156,000 a year
- Full-time
- Research
- Office
- Bachelor's degree
- Health insurance
- Tuition reimbursement
Associate Scientist Research and Development
Abbott Laboratories —Abbott Park, IL
- $50,700 - $101,300 a year
- Full-time
- Computer literacy
- Master's degree
- Bachelor's degree
- Health insurance
- Tuition reimbursement
5d
Senior Project Manager, Clinical Risk Evaluation
Abbott Laboratories —Plano, TX
- $78,000 - $156,000 a year
- Full-time
- 6 years
- Office
- Master's degree
- Health insurance
- Tuition reimbursement
Method Development Scientist
Abbott Laboratories —Santa Rosa, CA
- $90,000 - $180,000 a year
- Full-time
- Bachelor's degree
- Doctor of Philosophy
- Senior level
- Health insurance
- Tuition reimbursement
6d
Senior R&D Clinical Engineer
Abbott Laboratories —Menlo Park, CA
- $90,000 - $180,000 a year
- Full-time
- 6 years
- Doctoral degree
- Bachelor of Science
- Health insurance
- Dental insurance
Director, Biocompatibility
Abbott Laboratories —Santa Clara, CA
- $172,000 - $344,000 a year
- Full-time
- 5 years
- Bachelor's degree
- Continuous improvement
- Health insurance
- Tuition reimbursement
Associate Quality Engineer
Abbott Laboratories —Houston, TX
- $50,700 - $101,300 a year
- Full-time
- Mid-level
- Master's degree
- Experience equivalent to degree accepted
- Health insurance
- Tuition reimbursement
Engineering Lead
Abbott Laboratories —Buffalo Grove, IL
- $86,700 - $173,300 a year
- Full-time
- Analysis skills
- Travel
- Senior level
- Health insurance
- Tuition reimbursement
Quality Systems Analyst
Abbott Laboratories —Temecula, CA
- $61,300 - $122,700 a year
- Full-time
- Mid-level
- Master's degree
- Project management
- Health insurance
- Dental insurance
6d

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Scientist, Clinical Research

Abbott Laboratories -
Sylmar, CA

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Job Details

Full-time
$114,000 - $228,000 a year

Benefits

Health insurance
Tuition reimbursement
Retirement plan

Qualifications

Project reporting
Technical writing for researchers
Clinical program budget management
Medical writing
Vendor selection
Managing healthcare project budgets
Resource allocation (project management tasks)
Informed consent
Clinical trial risk management
Project communication management
Scientific research papers
Research project design
8 years
Newsletter content drafting
Schedule management
Collaboration with product development teams
Bachelor's degree
Scientific protocols
Clinical program data analysis
Project management experience in healthcare
Informed consent procedures implementation
Clinical data report preparation
Contracts
Vendor contract management
Newsletters (communication methods)
Implementing research protocols
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
Managing projects
IRB compliance

Full Job Description

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 115,000 colleagues serve people in more than 160 countries.

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:

Career development with an international company where you can grow the career you dream of.
Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
An excellent retirement savings plan with high employer contribution
Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
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.
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.

The Opportunity

We are seeking an experienced, high caliber Clinical Research Scientist in Sylmar, CA who provides scientific expertise throughout the development and implementation of clinical studies, clinical evaluations, or risk management. Writes / manages clinical trial protocols, protocol amendments, clinical study project timelines, clinical evaluations (planning and reports), risk master lists, clinical trial registrations and results postings, and scientific publications. Interacts with various study support groups and cross-functional teams in order to assist in clinical strategy, the development of study or clinical evaluation plans, and project or report deliverables. Interacts with regulatory agencies as needed, and will use their scientific and medical knowledge in order to provide directives to staff as well as study sites as appropriate.

Job Duties:

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, and/or Senior Management and investigational sites as directed by your manager.
Conducts team meetings, drafting and sending routine correspondence (e.g., newsletters) and by presenting regular updates to senior staff.
Participates in site selection process by conducting meetings with appropriate departments and individuals to review and revise draft site list as necessary, and by communicating the final site list to team members.
Creates, manages, or participates in clinical study or clinical evaluation timelines, and budgets by utilizing the appropriate project management tools, selecting providers, managing vendor contracts as requested, and ensuring expenditures are within budgetary guidelines.
Allocates resources by utilizing the appropriate project management tools.; 5. Facilitates regulatory submissions and communications by communicating with Regulatory Affairs during the submission process.
Participates in the development of clinical strategy and trial design by conducting meetings with the appropriate departments and individuals to obtain feedback/direction.
Writes study protocols, protocol amendments, informed consents, clinical evaluation plans and reports, risk master lists, and scientific papers for publication by evaluating scientific literature and publications, analyzing scientific data and staying abreast of current clinical practice.
Interprets Phase I to IV clinical study results in preparation for new product applications by evaluating scientific literature and publications, analyzing scientific and risk data and staying abreast of current clinical practice.
Presents scientific data by communicating accurate, succinct summaries of clinical study work at industry gatherings, investigational meetings and regulatory agency meetings.
Provides accurate progress reports on clinical projects by writing assigned clinical portions of reports for submission to regulatory agencies, Institutional Review Boards, Medical Ethics Committees, etc.
Participates in and supports audits.

Qualifications:

Education:

Bachelors Degree (± 16 years) In related field or an equivalent combination of education and work experience

Experience/Background

Minimum 8 years Related work experience with a complete understanding of specified functional area.
Comprehensive knowledge of a particular technological field.
Uses in-depth knowledge of business unit functions and cross group dependencies/ relationships.
Is recognized as an expert in work group and across functions.
Will perform this job in a quality system environment.
Failure to adequately perform tasks can result in noncompliance with governmental regulations.
Works on complex problems where analysis of situations or data requires an in-depth evaluation of various factors.
Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results.
Has broad knowledge of various technical alternatives and their potential impact on the business.

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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: www.abbottbenefits.com

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 www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.

The base pay for this position is $114,000.00 – $228,000.00. In specific locations, the pay range may vary from the range posted.

Apply Now

Refine Your Search

Abbott Laboratories jobs

Scientist, Clinical Research

Onsite EMT ( Occupational Health)

Operations Manager

Scientist II – Oligonucleotide Process Development, Manufacturing Development and Scale-Up

Quality Engineer II

Quality Engineer

Senior Field Clinical Specialist - REMOTE

Specialist, Clinical Planning and Performance

Medical Science Liaison, Abbott Point of Care (APOC) (Medical Affairs Team- Southeast Territory)

Senior Field Clinical Specialist

Manager, Quality Assurance

Senior Specialist, Benefits

Associate Scientist Research and Development

Senior Project Manager, Clinical Risk Evaluation

Method Development Scientist

Senior R&D Clinical Engineer

Director, Biocompatibility

Associate Quality Engineer

Engineering Lead

Quality Systems Analyst

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