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Featured Employers
Analyst, Regulatory Affairs- Regulatory Policy and Intelligence
Company: AbbVie
Location: Rockville, MD
Employment Type: Full Time
Date Posted: 02/06/2026
Job Categories: Advertising/Marketing/Public Relations, Biotechnology and Pharmaceutical, Engineering, Finance/Economics, Government and Policy, Information Technology, Sales, Science, Quality Control
Job Description
Analyst, Regulatory Affairs- Regulatory Policy and Intelligence

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 Analyst, Regulatory Policy and Intelligence (RPI) support the US RPI function by conducting research on regulatory intelligence questions and topics within assigned areas and regions. Responsibilities include analyzing and utilizing relevant regulatory approval databases, as well as preparing and delivering regulatory intelligence summaries both orally and in writing.

The Analyst should be comfortable working in a dynamic environment and proactively contributing new ideas and process improvements that enhance assigned projects.

The Analyst also serves as the office manager for the Rockville MD location and should be comfortable assisting with general office duties. This includes oversight of rental and service agreements, office maintenance, office equipment, coordination with real estate affiliates, suite and building safety and security, parking support, IT upgrades and support, coordinating logistics for office visitors, and management of on-site deliveries, including after-hours as needed.

Analyst Responsibilities:

  • Review and evaluate regulatory intelligence for assigned regions and topics, partnering with RPI policy topic and/or regional leads to provide context and assessment.
  • Analyze regulatory trends in key areas of interest to AbbVie and provide insights to inform strategic decisions, leveraging Excel for data analysis and visualization.
  • Conduct research to address regulatory policy and procedure questions received from business colleagues.
  • Prepare supporting materials for regulatory policy topics, including presentations and summaries using PowerPoint for clear and impactful communication.
  • Assist with regulatory policy and intelligence activities as needed, such as attending and documenting FDA virtual meetings.
  • Co-manage and edit regulatory policy newsletters and other general communications, in partnership with RPI analysts in EU and Intercon regions.
  • Support RPI staff by organizing routine meetings, developing agendas, preparing background materials, and drafting meeting summaries. Coordinate functional area goals and projects, including partnering with other functions to develop communications and presentations.
  • Co-manage global departmental databases and SharePoint sites, ensuring accurate content management and leveraging information to provide recommendations to senior RPI staff. Responsibility shared with RPI analysts in EU and Intercon regions.

  • Office Manager Responsibilities:
  • Facilities: stock office and kitchen supplies; research, order, setup, clean up catering; equipment maintenance, repair, and inventory.
  • Expenses: as necessary, prepare reports for RPI Directors and Senior Director.
  • Key point of contact with landlord and AbbVie Real Estate for suite projects, including (but not limited to): security, real estate, accounting, painting, and carpet refreshes.
  • Key RPI liaison contact to AbbVie product teams and individuals that use the office when visiting the area. Provide logistical support to AbbVie product teams and visiting colleagues using the Rockville office for FDA-related meetings or local engagements. This includes organizing transportation to FDA, arranging catering, and offering general assistance.

Significant Work Activities:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required


Qualifications

  • Bachelors degree required, Regulatory certifications a plus
  • 6+ years of industry experience
  • Experience with Internet searching, Word, PowerPoint, and Excel. Demonstrated competency in conducting primary research and distilling large amounts of information into concise executive summaries.
  • Excellent communicator in written and verbal forms & excellent organizational skills
  • Note: Higher education may compensate for years of experience and vice versa

Preferred Experience:

  • Regulatory intelligence gathering and analysis
  • Good understanding of regulatory environment including regulatory pathways

Additional Information

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

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

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

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

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

Contact Information
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