ProPharma Group

Medical Promotional Review Consultant

ProPharma Group$100K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5+ years of experience in pharmaceutical/biotech industry, preferably in medical affairs
  • Proven project management skills within the pharmaceutical sector
  • Strong grasp of FDA regulations regarding advertising and promotion
  • Ability to interpret clinical data and support claims consistent with FDA approval
  • Proficient in Microsoft Office, Adobe Acrobat, and electronic review systems like Veeva Vault

Responsibilities

  • Provide scientifically sound marketing solutions for promotional materials
  • Review independent scientific and medical materials for assigned projects
  • Lead Medical role during Promotion Review Committee meetings
  • Offer guidance on medical and scientific support for promotional materials
  • Participate in cross-functional team discussions for promotion review
  • Communicate insights from review meetings to the broader Medical team
  • Stay updated with clinical data and FDA guidelines to ensure compliance

Benefits

  • Flexible remote work options with encouragement for hybrid collaboration
  • Opportunities for professional development at industry meetings
Full Job Description
The Medical Promotional Review Consultant is responsible for:
  • Providing compliant, medically accurate and scientifically sound solutions while providing marketing with competitive solutions for consumer, healthcare provider and managed care promotional and non-promotional materials.
  • Review of independent scientific/ medical/clinical materials for Established
    brand and Derivative materials for assigned projects.
  • Acting as lead for Medical role during Promotion Review Committee (PRC)
    meetings and overseeing the medical advertising promotional review
    process.
  • Providing guidance on the Medical /scientific support for PRC and if need
    be, elevating the risk to their manager/line manager within the client.
  • Provide detailed review of promotional, disease awareness and medical.
  • Participate in cross functional team meetings and prioritization discussions for the assigned promotion review team.
  • Communicate information provided during promotion review meetings to the broader Medical team when appropriate and elevating risk items to management.
  • Partner with job owners and other stakeholders in the execution and creation of tactics related to label changes for assigned brands.
  • Stay up to date with relevant clinical data, publications, and treatment guidelines published by medical associations.
  • Monitor US regulatory promotional environment by staying up-to-date on FDA regulations and guidance's, reviewing untitled and warning letters issued to pharmaceutical companies published by OPDP, APLB, Center for Devices and Radiological Health (CDRH), Federal Trade Commission (FTC), National Advertising Division (NAD) or other governing bodies.
  • As appropriate, attendance at major FDLI, DIA, and other industry/FDA meetings.
  • Only materials for scientific and medical accuracy


Necessary Skills and Abilities:
  • Strong ability to work independently, with flexibility and a strong ability to connect and collaborate with clients and team members while working remotely.
  • Proven ability to provide strategic direction and innovate, forward thinking medical guidance and analyze and interpret efficacy and safety data.
  • Working knowledge of FDA and Pharmaceutical regulatory and compliance guidelines on advertising and promotion.
  • Deep understanding scientific data from clinical trials, review articles, medical textbooks, etc. and how this data supports claims made consistent with the FDA approval label. Understanding of pharmaceutical advertising/creative review and approval process.
  • Proficiency in computer applications and configuration, including Microsoft Office, Adobe Acrobat
  • Proficiency in Veeva Vault Promo Mats or other electronic review platforms.


Educational Requirements:
  • A Bachelor's degree is required, focus in Medical, Science, Marketing, Business or Communications; a PharmD is highly preferred.


Experience Requirements:
  • 5+ years of related experience in the pharmaceutical/biotech industry is required. May consider related experience from healthcare advertising agency.
  • Functional experience in pharmaceutical industry medical affairs is required.
  • Strong project management experience is required, in pharmaceutical industry is preferred.


#LI-KP1

#LI-REMOTE

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

About ProPharma Group

ProPharma Group is a pharmaceutical consulting company that provides regulatory compliance, pharmacovigilance, and medical information services to clients in the healthcare industry. The company was founded in 2001 and is headquartered in Shawnee Mission, Kansas. ProPharma Group offers a range of services, including clinical trial support, quality assurance, and validation services. The company has worked with clients in a variety of industries, including pharmaceuticals, biotechnology, and medical devices.
Learn more about ProPharma Group
Size
500 employees
Industry
Net Income
$5 million
Founded
2001
5 Year Trend
+30%
Revenue
$50 million

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