Medical Promotional Review - Plainsboro Township, United States - Integration International Inc.

Integration International Inc. Plainsboro Township, United States

2 weeks ago

Integration International Inc. background

Description

Description:

Must haves:

No specific "must haves" outside of what is listed in the job description: PharmD/MD/DO/NP with a minimum of two years of relevant professional experience (e.g. academic, clinical or industry experience); post-doctoral fellowship may be substituted for professional experience, as appropriate.

Interview Process:

In addition to an interview process with a few interviewers, the process will likely include a 20-minute medical presentation with 10 minutes for Q&A where the candidate will present their summary, analysis, and interpretation of a pre-selected peer-reviewed journal article.
Additional interview details such as specific journal article and interview panel are to be determined.

Essential functions:

Provide critical review of promotional pieces to ensure medical accuracy, validity and appropriateness of content in accordance with approved labeling, scientific data and relevant laws, regulations and NNI policies to support the safe and effective use of products by patients and the medical community.
Determine appropriateness of data and references used to support promotional claims and marketing messages and provide proactive recommendations and/or guidance for alternative data/references/language where needed.
Align and collaborate with key cross-functional stakeholders including other PRB reviewers and commercial team members on issues or concerns related to promotional materials or claims.
Engage with commercial business partners early in the development of promotional materials to enhance efficiency, when applicable
Work with the Medical Director for the assigned product(s)/therapeutic area(s) to increase efficiency, medical alignment, and mitigate risk of promotional claims.
Review, provide comments and document verdicts for all assigned promotional materials within PRB workflow system based on assigned deadlines.
Participate in PRB meetings as assigned.
Remain current with medical literature and data in assigned therapeutic area(s)
Participate in relevant internal and external meetings and trainings on new guidance/regulations, new scientific information and marketing strategy.

Qualifications:

PharmD / MD/ DO / NP with a minimum of two years of relevant professional experience (e.g. academic, clinical or industry experience); post-doctoral fellowship may be substituted for professional experience, as appropriate.
Thorough understanding of the US pharmaceutical industry and healthcare landscape, promotional review process and relevant guidance and compliance requirements
Detail-oriented with demonstrated editorial skills.
Strong organization and prioritization skills
Ability to work on cross-functional teams.
Ability to critically analyze and apply scientific data in a customer-focused manner.
Strong verbal and written communication skills
Effective negotiation skills and ability to influence others.

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