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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
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...
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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
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