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Associate I, Clinical Pharmacology Scientific Support & Reporting

AbbVie

North Chicago, ILJob$66K/yrSeen 2w agoSeen in employer's feed today

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At a glance

Compensation
$66K/yr
Location
North Chicago, IL
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Associate I will build all necessary data and information to prepare internal scientific reports and documents for clinical trials, assisting with ongoing blinded efficacy and safety reviews while ensuring high quality and attention to detail.

Skills & qualifications

RequiredNice to have

Skills

Scientific ReportingData AnalysisLiterature SearchOral CommunicationWritten CommunicationComputer ProficiencyProcess Improvement

Qualifications

Bachelor's in ScienceMaster's in Pharmacology or Related FieldAssociate's Degree or RN2+ Years Pharmaceutical Industry Experience6+ Years Pharmaceutical Industry Experience

Benefits

Paid Time Off
Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

Company Description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, (https://www.linkedin.com/company/abbvie/) Facebook, Instagram (https://www.instagram.com/abbvie/) , X (https://twitter.com/abbvie) and YouTube. (https://www.youtube.com/user/AbbVie)

Job Description

To build all necessary data/information needed to prepare internal documents/scientific reports related to clinical trials by assisting with ongoing blinded efficacy and safety reviews.

Responsibilities

  • Prepare scientific reports and presentations related to clinical trials using available software and templates.

  • Assists in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols.

  • Comply with procedures set forth in relevant IQS documents and Study protocols

  • Comply with the directives issued by the management regarding clinical studies.

  • Commit to producing work of the highest quality

  • Pay close attention to detail

  • Perform literature and competitive intelligence searches

  • Apply experience to analyze clinical study data, using available software to assist with ongoing blinded/un-blinded pharmacokinetic analysis

  • Responsible for receiving and completing assignments and tasks from functional Scientific Staff or Therapeutic Area MD within a given time period with supervision.

Qualifications

  • Bachelor’s degree, in Science, related to Field with +2 years’ experience in pharmaceutical industry. Or Masters degree in pharmacology or related field.

  • Associates degree/RN with 6+ years of experience in pharmaceutical industry may be additionally considered.

  • Must possess good oral and written communication skills

  • Ability to use computer to generate reports, analyze data, and create presentations

  • Previous experience may be narrowly-focused or limited.

  • Ability to identify opportunities and participate in process improvement initiatives.

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 in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay 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/vision insurance and 401(k) to eligible employees.

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

Note: No amount of pay is considered to be wages 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 benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may 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, visit https://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

Salary: $65,500

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