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

The mission of Scientific Support is to be a trusted partner and an integral part of Clinical Pharmacology at AbbVie. Scientific Support is dedicated to supporting the successful construction and submission of trial protocols, clinical study reports, and other documents required to progress drug development programs to subsequent Phases and regulatory submissions. As an Associate II of Clinical Pharmacology Scientific Support & Reporting, your role is to build all necessary data and information needed to prepare internal documents/scientific reports related to clinical trials - keeping multiple reports moving forward simultaneously! You will also be responsible for:

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

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

• Complying with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical studies.

• Applying experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded/un-blinded PK, safety and efficacy reviews.

• Receiving and completing tasks and assignments from function or Therapeutic Area MD or Scientific Staff within timeline with minimal supervision.

• Performing literature and competitive intelligence searches

• Ensuring scientific integrity of all processes by applying current electronic document conventions and processes consistently and accurately.

• Integrating clinical trial data across studies, identifying issues impacting projects and providing the relevant information to internal peers and therapeutic area management.

• Managing appropriate and effective use of resources to complete tasks and meet required timelines.

• Maximizing individual, function/therapeutic area and team productivity; and mentoring function/therapeutic area personnel.

Qualifications

You are qualified for this position if you hold a Bachelors/Master’s degree in a Science related to Field and have +5 years’ experience in the pharmaceutical industry, or have an associates degree/RN with 9+ years' of experience in the pharmaceutical industry.

Qualified applicants must also:

• Have a good understanding of basic clinical study principles

• Possess good oral and written communication skills

• Be proficient in using computer to analyze clinical study data, generate reports and create presentations

• Experience supporting clinical research, drug development and/or function/therapeutic area operations

• Have a proven record of successful project management.

• Be detail oriented and able to identify and participate in opportunities for process improvement

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: $82,500 - $157,500