Top 240 Life technologies research & development Jobs in Middleton, Wi

Clinical Trial Associate I
Abbott Laboratories —Madison, WI
- $50,700 - $101,300 a year
- Weekends as needed
- Microsoft Outlook
- Continuous improvement
- Travel
- Health insurance
- Tuition reimbursement
7d
Psychometrician
University of Wisconsin–Madison —Madison, WI
- From $80,000 a year
- Full-time
- Remote
- Mid-level
- Analysis skills
- Continuous improvement
- Paid holidays
- Dental insurance
5d
Process Development Engineer
Scientific Protein Laboratories —Waunakee, WI
- Full-time
- Senior level
- Communication skills
- Commercial
- AD&D insurance
- Paid holidays
13d
Sample Coordinator – 1st Shift
Thermo Fisher Scientific —Middleton, WI
- $19.50 an hour
- Full-time
- Background check
- Microsoft Excel
- Mid-level
- Health insurance
- Dental insurance
Group Leader - Analytical Development
Catalent —Madison, WI
- Email
- Master's degree
- Bachelor's degree
- Continuous improvement
- Paid holidays
- Health insurance
13d
Senior Artificial Intelligence (AI) Developer
Amtelco —McFarland, WI
- Full-time
- Hybrid work
- Background check
- Azure
- Computer Science
- Health savings account
- Health insurance
Quick Apply
Assignment System Coordinator
University of Wisconsin–Madison —Madison, WI
- From $60,000 a year
- Online Application
- Management
- Writing skills
- Mid-level
- Paid holidays
- Paid time off
1d
Systems Analyst Solutions Architect
Greenheck Group —Wisconsin
- $144,462 - $178,453 a year
- Full-time
- Research
- Office
- Bachelor's degree
Manager, Quality and Compliance
Catalent —Madison, WI
- Email
- Doctoral degree
- Master's degree
- Bachelor's degree
- Paid holidays
- Health insurance
Automation Systems Technician
Ultratec, Inc. —Madison, WI
- $24 - $26 an hour
- Full-time
- Microsoft Word
- Computer literacy
- Mid-level
- Health savings account
- Health insurance
1d
Veterinary Technician- Research Animal Operations
Labcorp —Madison, WI
- Overtime
- Medication administration
- Customer service
- Surgery
- Employee stock purchase plan
- Disability insurance
12d
Field Service Technician II
TDS Telecom —Waunakee, WI
- $25.13 - $37.69 an hour
- Overtime
- Microsoft Word
- Background check
- Microsoft Excel
- Paid parental leave
- Paid holidays
Field Service Technician
TDS Telecom —Waunakee, WI
- $22.62 - $33.94 an hour
- Overtime
- Microsoft Word
- Background check
- Microsoft Outlook
- Paid parental leave
- Paid holidays
Senior Research Scientist-Field Day
University of Wisconsin–Madison —Madison, WI
- From $100,000 a year
- Full-time
- Remote
- Education
- Continuous improvement
- Doctor of Philosophy
- Dental insurance
- Paid time off
9d
Strategy Consultant
Abbott Laboratories —Madison, WI
- $61,300 - $122,700 a year
- Weekends as needed
- Microsoft Excel
- Word processing
- Computer literacy
12d
Clinical Affairs Specimen Operations Specialist
Abbott Laboratories —Madison, WI
- $61,300 - $122,700 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
LTE - Digital Learning Specialist - Doyle - 1.0 FTE - 26-27 SY
Madison Metropolitan School District —Madison, WI
- $45 an hour
- Weekends as needed
- High school
- Office
- Bachelor's degree
17h
Study Coordinator
Labcorp —Madison, WI
- Full-time
- Microsoft Word
- Mid-level
- Master's degree
- Employee stock purchase plan
- Disability insurance
Jr. Marketing Specialist
The Digital Ring —Madison, WI
- Full-time
- Remote
- Communication skills
- Entry level
Oncology Imaging Quality Control Specialist II (US Remote)
MERIT CRO, Inc. —Madison, WI
- Full-time
- Remote
- 5 years
- Computer literacy
- Mid-level
- AD&D insurance
- Paid holidays
Quick Apply

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Clinical Trial Associate I

Abbott Laboratories -
Madison, WI

Apply Now

Job Details

Full-time
$50,700 - $101,300 a year
7 days ago

Benefits

Health insurance
Tuition reimbursement
Retirement plan

Qualifications

Search engines
Microsoft Outlook
Spreadsheets
ICH guidelines
Typing
Clinical quality assurance standards

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 your 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.
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
An excellent retirement savings plan with a 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 worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Madison, WI location in the Cancer Diagnostics division. This position is responsible for assisting in the execution of clinical trials by providing quality administrative and project management support. This position will coordinate with all members of the Clinical Affairs team and internal and external stakeholders to successfully execute the clinical study plans of the company.

What You’ll Work On

Include, but are not limited to, the following:

Collect essential documents and review for completeness and compliance with Standard Operating Procedures, the protocols, and appropriate regulations; review Trial Master File (TMF) inventory for missing and expiring documents.
Interact with clinical study sites to support study start-up, execution, and close-out activities.
Create and maintain study related trackers, including but not limited to, enrollment, study supplies, receipt of samples, and site information.
Coordinate the ordering, tracking, and accountability of clinical supplies, including investigational product materials, equipment, and special-order items as requested.
Review for completeness and route legal documents for execution. File all versions in document management database.
Draft study documents (study trackers, templates, presentations, etc.) as requested.
Support case report form (CRF) development, participate in user acceptance testing (UAT) for electronic data systems and review related data management documents, as applicable.
Represent Exact Sciences as a customer advocate/liaison both internally and externally.
Coordinate study start-up, execution, and close-out activities, or Investigator Meetings, as requested.
Responsible for completing assigned tasks to support study timelines and metrics with minimal ongoing direction.
Identify and report problems, investigate alternatives, and make recommendations for resolution and process improvements.
Responsible for organizing cross-functional project meetings. Distribute agendas, take and distribute meeting minutes.
Provide follow-up support and data collection for Research and Development teams to advance project objectives.
Initiate purchase requests liaise with Accounts Payable and vendors as needed.
Provide support to Clinical Trial Manager for clinical study budget review, tracking, and maintenance.
Must be able to work both independently and collaboratively as part of the clinical study team to meet study objectives and timelines.
Author and provide input to Clinical Affairs business processes.
Maintain a working understanding of current SOPs, work instructions, applicable regulations, and guidance documents, such as FDA Code of Federal Regulations (CFR) and International Council on Harmonisation (ICH), Guideline for Good Clinical Practices (GCP).
Maintain applicable clinical study data in Clinical Trial Management System.
Ability to organize, present, and convey problems or issues.
Strong verbal and written communication skills.
Effective presentation skills.
Ability to interface and work effectively within team and department with changing priorities.
Ability to frequently and accurately communicate with co-workers, customers, and vendors, via the telephone or by email.
Ability to exercise judgment and determine appropriate action to a variety of problems of varying complexity.
Ability to manage multiple deadlines.
Analytical, problem solving and decision-making skills.
Excellent attention to detail and organizational skills.
Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
Support and comply with the company’s Quality Management System policies and procedures.
Maintain regular and reliable attendance.
Ability to act with an inclusion mindset and model these behaviors for the organization.
Ability to work designated schedule.
Ability to work nights and/or weekends.
Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.
Ability to travel 5% of working time away from work location, may include overnight/weekend travel.

Required Qualifications

Bachelor’s degree in the life sciences or related field; or Associates degree in the life sciences or related field and 2 years of relevant experience in lieu of Bachelor’s degree.
General knowledge of applicable clinical research principles and requirements, including GCP and ICH guidelines.
Proficient in using basic software applications including Microsoft Office (Word - generate documents and tables, Excel - create and modify spreadsheets, create complex formulas, etc., Email – preferably Outlook) and various search engines for conducting Internet searches.
Demonstrated ability to perform the essential duties of the position with or without accommodation.
Authorization to work in the United States without sponsorship.

Preferred Qualifications

1+ year of experience in a clinical research setting (Clinical Trial Assistant, Study Coordinator, or similar).
Experience in a healthcare, clinical, or science related field.

Apply Now

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.

The base pay for this position is $50,700.00 – $101,300.00. In specific locations, the pay range may vary from the range posted.

Apply Now

Refine Your Search

life technologies research & development jobs in middleton, wi

Clinical Trial Associate I

Psychometrician

Process Development Engineer

Sample Coordinator – 1st Shift

Group Leader - Analytical Development

Senior Artificial Intelligence (AI) Developer

Assignment System Coordinator

Systems Analyst Solutions Architect

Manager, Quality and Compliance

Automation Systems Technician

Veterinary Technician- Research Animal Operations

Field Service Technician II

Field Service Technician

Senior Research Scientist-Field Day

Strategy Consultant

Clinical Affairs Specimen Operations Specialist

LTE - Digital Learning Specialist - Doyle - 1.0 FTE - 26-27 SY

Study Coordinator

Jr. Marketing Specialist

Oncology Imaging Quality Control Specialist II (US Remote)

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