Research Associate

Laboratory Corporation; Madison (WI); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading company in the healthcare sector seeks a Research Associate to join the Metabolism team in Madison, WI. This role entails conducting laboratory analyses, maintaining compliance with regulatory standards, and collaborating on study protocols. Candidates should possess a relevant bachelor's degree and experience in a lab setting, with opportunities for professional growth and comprehensive benefits.

Benefits

Medical, Dental, Vision Benefits

401(k) Plan

Paid Time Off (PTO)

Tuition Reimbursement

Employee Stock Purchase Plan

Qualifications

• Bachelor's degree in relevant scientific discipline required.
• Experience in a research or lab environment strongly preferred.
• Proficient in Microsoft Office and adaptable with software.

Responsibilities

• Conduct analyses using various instrumentation and methods.
• Review study protocols and maintain documentation.
• Participate in QC review and prepare results and presentations.

Skills

Analytical Skills

Attention to Detail

Problem Solving

Communication

Education

Bachelor’s degree in biology, chemistry or other relevant scientific discipline

Tools

Microsoft Office Suite

Job description

Why People choose to work at Labcorp:
At Labcorp, it is our people that make us great – it’s what our clients, our partners and, most importantly, what our employees say. Here, you will have the opportunity to collaborate with extraordinary people with diverse viewpoints. You will discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends.

We have an excellent career opportunity for a Research Associate to join our Metabolism team in Madison, WI.

Position Summary:

The Research Associate will conduct all work in compliance with appropriate company standards, GLP, GCP, GMP (where appropriate)and regulatory guidelines specified in the study plans, protocols, or work agreements governing the work in which they areinvolved.

Essential Duties:

• Set up and perform a variety of analyses using appropriate instrumentation with routine and non-routine methods
• Critically review study protocol in primary areas of work and suggest changes where appropriate
• Provides input and participates in study meetings (ie pre-initiation meeting)
• Maintains study documentation in compliance with regulatory guidelines
• Ability to recognize deviations from normal results and inform Study Director, Study Coordinator and/or management of any problems that may affect integrity of the data
• Ability to recommend modifications to routine procedures to adapt to problems in primary area
• Ability to understand the scope of a study (primary area of work) and be able to complete with no supervision
• Deliver results within the agreed timeframe, whilst recognizing changes in priorities
• Routinely support studies in non-primary areas of work
• Ability to write, review and revise standard SOPs related to primary area of work.
• Participate in QC review of selected routine data and methodology section within reports within scope of current role
• Ability to prepare results and presentations based on the work performed
• Evaluates data for experiment modification and contribute to report preparation/review
• Participate in method development and validation projects
• Maintains a clean and safe laboratory work environment and perform routine maintenance
• Performs other related duties as assigned

Education/Experience:

• Bachelor’s degree in biology, chemistry or other relevant scientific discipline
• Experience in a research or lab environment strongly preferred
• Must be proficient in Microsoft Office Suite and comfortable using or learning additional software as needed

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, pleaseclick here.

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

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