Associate Scientist II, Toxicology Study Coordinator

Allergan; Lincoln (NE); On-site; USD 65,000 - 85,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking an Associate Scientist, Toxicology Study Coordinator to join their Preclinical Safety group. In this role, you will assist in planning, conducting, and reporting toxicology studies. Candidates should have a Bachelor's degree in a scientific field with relevant experience, strong communication skills, and the ability to manage multiple projects. This position offers a comprehensive benefits package and opportunities for growth within the organization.

Benefits

Comprehensive benefits package

Paid time off

Qualifications

• 3+ years of experience or Master's Degree with 0-2 years of related experience.
• Expertise in Good Laboratory Practices preferred.

Responsibilities

• Draft study plans and report components.
• Assist in technical conduct of nonclinical studies.
• Facilitate communications among study personnel.

Skills

Excellent oral and written communication skills

Aptitude for managing multiple projects

Proven flexibility

Education

Bachelor’s Degree in scientific field

Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik Tok.

Job Description

The position ofAssociate Scientist, Toxicology Study Coordinatoris in the Preclinical Safety group and will report to a manager in Toxicology. The Associate Toxicologist aides in the planning, conduct and reporting of non-GLP and GLP toxicology studies, acting to support the Study Director and regulatory infrastructure.

Responsibilities:

• Draft study plans, amendments, and report components
• Assist in the technical conduct of nonclinical studies including protocol set-up in electronic data capture system and scheduling of study events
• Perform data review periodically through study conduct and at study completion
• Facilitate communications among study personnel
• Coordinate the archival of study data and specimens
• Support GLP infrastructure through quality control responsibilities and active participation in process improvement activities

ACCOUNTABILITY / SCOPE:

• Responsible for key tasks in the set-up and conduct of nonclinical studies
• Support the Study Director, acting as a designee for some tasks
• Study support may include data review, preparing report data tables, drafting report sections, coordinating study data archiving, and other tasks as needed
• Compile input from subject matter experts and incorporate into study plans
• Facilitate study scheduling and resource allocation
• Assist in driving assigned deliverables to timely completion
• Maintain training to meet compliance standards

Qualifications

Required:

• Bachelor’s Degree, or equivalent education, with typically 3 or more years’ experience or Master’s Degree or equivalent education with 0-2 years of related experience.
• • Degree in scientific field preferred
• Aptitude for managing multiple projects in a regulated environment
• Excellent oral and written communication skills
• Proven flexibility to deal with changing timelines, shifting work priorities, and evolving regulatory/industry requirements
• Computer skills appropriate for job task

Preferred Qualifications:

• Expertise in Good Laboratory Practices
• Previous experience in the conduct and/or reporting of nonclinical studies

Position will be filled at level commensurate with extent of education, experience, and accomplishment. Associate Scientist I or Associate Scientist II.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

• The compensation range described below is the range of possible base pay compensation that the Company believes ingood faith it will pay for this role at the time of this posting based on the job grade for this position. Individualcompensation paid within this range will depend on many factors including geographic location, and we may ultimatelypay more or less than the posted range. This range may be modified in the future.

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/visioninsurance and 401(k) to eligible employees.

• This job is eligible to participate in our short-term incentive programs.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, and determinable.The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html