Job Details

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 at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) .

Job Description

Purpose

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 ( e.g., Phase 1 Clinical Study Reports and Protocols) and presentations related to clinical trials using available software and templates.

• 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.

This position is required to sit on-site 3 days / week*

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