Principal Consultant, Regulatory Advertising & Promotion

Dennis Partners; Massachusetts; On-site; USD 240,000 - 275,000; Full time

Benefits offered by this job

Comprehensive employee benefits

Quarterly bonus program

Work from home flexibility

Job summary

A niche Regulatory consulting firm is seeking a Regulatory Affairs Advertising & Promotions Principal Consultant to lead regulatory requirements for advertising and promotions in a remote setting. This role involves managing compliance for various client projects, reviewing promotional materials, and acting as a key regulatory expert. Candidates must have a Bachelor's degree and at least 7 years of experience in pharmaceutical regulatory affairs. The position offers a competitive salary, estimated at $240,000 to $275,000, plus bonuses and comprehensive benefits.

Qualifications

• Minimum of 7 years of experience in pharmaceutical regulatory affairs focusing on Advertising & Promotions.
• Experience reviewing promotional materials across various platforms including print and digital.
• Prior experience with product launches and Accelerated Approvals is essential.

Responsibilities

• Manage regulatory requirements for advertising and promotions across client projects.
• Review client team submissions for compliance with regulations.
• Act as a regulatory affairs expert within client teams.

Skills

Pharmaceutical regulatory affairs

Advertising & Promotions

Regulatory strategy

Project management

Veeva management

Education

Bachelor's degree in a scientific discipline

Advanced degree (MS, MD, PharmD, or PhD)

Job description

Our client is a niche Regulatory consulting firm which provides the highest-level Regulatory expertise to a variety of biotech and pharmaceutical clients. They are seeking a Regulatory Affairs Advertising & Promotions Principal Consultant who can provide leadership on advertising and promotional materials for various client projects. You will be responsible for the daily management of regulatory requirements for Advertising & Promotions and serve as a subject matter expert. This is a remote role where you will work closely with exciting biopharma clients and collaborate internally with a team of biopharmaceutical leaders and innovators. This company offers a competitive salary, comprehensive employee benefits, and the ability to work from home. Now is an exciting time to join this dynamic and growing organization!

Responsibilities

• Daily management of regulatory requirements for advertising and promotions for one or more client projects.
• Review and evaluate materials submitted by client teams to ensure that the content, quality, and format comply with applicable laws, regulations, and client policy.
• Act as a key regulatory affairs expert within a client regulatory team, providing expertise on regulatory strategy, process, filing, best practices, etc. in conjunction with client leadership.
• Provide strategic and operational leadership for promotional, educational, and investigative communications.
• Use extensive knowledge of country-specific regulatory requirements (US, EU and ICH) and the ability to apply knowledge both strategically and operationally to development projects and marketed product regulatory issues to support clients' corporate goals.
• Manage launch preparation of promotional material for one or more products.
• Provide support and guidance to regulatory teams on RA requirements for one or more drug products.
• Maintain knowledge of changing regulatory requirements and advise teams as appropriate.
• Represent the client regulatory affairs team in other client meetings or workstreams; provide support for ancillary projects.

Qualifications

• Bachelors in a scientific discipline required. Advanced degree (eg. MS, MD PharmD, or PhD) preferred.
• Must have a minimum of 7 years of experience in pharmaceutical regulatory affairs specializing in Advertising & Promotions.
• Must have experience reviewing promotional materials across a variety of platforms (print, TV, online, DTC, etc)
• Prior experience with product launches is required. Experience with Accelerated Approvals highly desired.
• Experience working directly with OPDP is a must. Experience with APLB is a plus, but not required.
• Prior experience with payer materials and medical affairs required.
• Experience across multiple therapeutic areas is a plus, and experience with oncology and/or rare disease areas is highly desired.
• US experience is required and global/international experience is desired.
• Must have experience working with Veeva for management of promotional materials.
• Proven project management skills to support the planning and coordination of regulatory submissions and appropriate regulatory inspections.
• Ability to work independently and innovatively in tackling operational challenges.
• Must be collaborative and work well with clients.

This is a remote position with some occasional travel for client meetings. The budgeted salary range for this position is $240,000 to $275,000 plus a quarterly bonus program and comprehensive benefits. Actual salaries may be based on a number of factors including, but not limited to, a candidate’s skill set, experience, education, and other qualifications. Posted salary ranges do not include incentive compensation or any other type of renumeration.