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Medical Reviewer

AbbVie

Save Job
AbbVie

Medical Reviewer

Onsite Dublin, Ireland Full Time
Posted 11 hours ago
Save Job
powertofly approved What AbbVie Has to Offer:

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

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.


Job Description

AbbVies Commercial affiliate in Citywest, Dublin have an exciting vacancy for a Medical Reviewer to join our team  on an initial 12 Month FTC basis.

The Medical Reviewer is responsible for ensuring the accuracy and compliance of promotional and non-promotional materials, and other medical content. This role requires a thorough understanding of assigned therapeutic area, regulatory guidelines, and local and global policies to effectively review and approve materials for compliance with applicable regulations and company standards.

 

Responsibilities will include:

Promotional Material Review and Certification: Review and certification of promotional and non-promotional materials ensuring material is technically, medically, and scientifically accurate, and complies with SI 541, IPHA Code of Practice and applicable AbbVie policies.

Develop and maintain up-to-date knowledge of respective therapy, strategic direction and treatment landscape

Collaboration: Collaborate with cross-functional teams. Support marketing and medical teams with advice on promotional and non-promotional activities with respect to local and global policies and code of practice compliance

Documentation & Reporting: Prepare detailed reports and documentation when required, of reviewed materials and maintain records of deviations in accordance with company policies. Update standard operating procedures within areas of scope on a required basis.

Bridging Programs- Responsible for the documentation and compliance of AbbVie Bridging programs. Work with Medical Affairs to ensure appropriate approvals and documentation are in place for the Bridging Program. Responsible for tracking product distribution with external wholesalers and Hospital Pharmacists as per AbbVie Procedures.

 


Qualifications

 

  • Degree with a scientific background
  • Excellent attention to detail and the ability to interpret complex clinical data and terminology.
  • Problem solving skills and the ability to think strategically
  • Strong written and verbal communication skills.
  • Ability to work effectively in a team environment and manage multiple projects simultaneously.

 


Additional Information

Key Stakeholders

 

  • Medical affairs team
  • Brand teams
  • Regulatory Affairs
  • PV

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

Company Details
AbbVie
 Chicago, IL, United States
Work at AbbVie

Together, we break through We believe the paths we take to achieving our breakthroughs matter. At AbbVie, every one of our 50,000 employees is a... Read more

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