Associate Director of Regulatory Affairs, Advertising & Promotion *** NJ ** Exciting Portfolio including ATMP’s *** Varied TA’s

Reference: TM190522C

Expiry Date: 23-08-2022

Categories Biotech, Regulatory Affairs

Salary: On Application

Job Type: Full Time

Location:
Somerset County
United States

Apply for position

Job Description

If you are interested a new role with scope to have an impact, for an organization with a strong portfolio and a friendly and engaging Advertising & Promotional team… this could be the role for you…!

My client is Blue-chip organization with a great pipeline, relaxed creative culture and an innovative approach to drug development and product launches and their Regulatory Advertising and Promotional team is strong, established….. and fun!  This is a group who are spoilt for choice with over 50 indications in development across 4 key therapeutic areas and includes all major modalities including ATMP’s. So the roles and projects in Ad Promo are always varied and broad-based, and can include new products, blockbuster products and niche products across all modes of communication, from journal and TV ads to social media post and internal facing communication.

So, we are looking for someone special, who wants to join a special team in a special environment. We are looking for someone experienced in Regulatory Affairs Advertising and Promotion who enjoys being challenged to come up with new solutions and options, who enjoys working closely with the commercial teams, not just focusing on compliance, but working with the teams to develop ideas and concepts in sometimes highly competitive market segments.

In exchange for your ideas, passion, and creativity, you will have several exciting project options to work on including participating and leading multiple successful launches, serving as liaison with FDA, communicating with the OPDP division for a variety of topics, and operating as the internal expert on several key areas and issues.

The ideal candidate will be dedicated, team focused and an established Regulatory Lead, with strong communication skills that has served on multiple Review Committees (RCs) and worked with numerous brands on competitively positioning assigned products appropriately while maintaining compliance with applicable FDA regulations and company policies for the advertising and promotion of prescription drugs and biologics. You will also have participated and lead multiple successful launches and have a strong track record of liaising with the FDA.

In return, you will receive a very competitive package, including a high base salary, good bonus ratio (paid every year), and a lucrative stock plan - my client will also ensure they cover any loss of bonus or vesting stock (for the next 2 years), so you leave nothing on the table when you join!

“There is no doubt, this this is really great role, for indications with huge potential….!”

 

To Apply!

If you are interested this role or are open to something new in the Regulatory CMC space, please contact me, Theo Moore on Theo@AdvTalent.com or call US 908 348 6714 - We are available 8.30am to 6pm EST or can happily take a call over the weekend until 1pm EST. I will support you throughout the interview and on-boarding experience.

LinkedIn Profile: https://uk.linkedin.com/in/theo-moore-b33696a

GDPR & Data Protection: Your information is safeguarded for GDPR, and you will have the right to edit, amend or delete and ’’be forgotten’’ at any time after your initial registration.