Manager, GRS, Advertising, Labeling, & Promotion

How will your role help us transform hope into reality

As GRS Manager of Advertising Labeling & Promotion you will review and submit compliant advertising materials for our commercial portfolio. Responsibilities include ensuring content meets promotional regulations (US and Ex-US) completing FDA 2253 submissions and adhering to FDA and company policies.

What will you do

• Serves as a regulatory advertising and promotion reviewer on cross-functional Promotional Review Boards (US PRB / MRB and iPRB / iMRB) for promotional regulatory review of the companys commercial programs.
• Independently develops solutions to promotional issues by utilizing scientific and regulatory knowledge to support business objectives and initiatives while effectively managing business risks.
• Identifies and provides input on development and improvement of policies processes and standards for promotional materials and related activities.
• Monitors and keeps organization up to date on regulatory promotional environment (e.g. the issuance of new regulations / guidance relevant enforcement action andgeneral awareness of industry practices including those of competitors).
• Build a strong relationship with internal customers including Commercial Corporate Affairs Legal and Medical.
• Ensure timely and accurate submission of US promotional materials.
• Participate in discussions of product labeling submissions as needed.
• Works to ensure that changes and updates in prescribing information are reflected in current promotional and advertising materials.
• Perform other responsibilities as assigned.

What minimum qualifications do we require

What additional qualifications will make you a stronger candidate

Why Blueprint

At Blueprint Medicines patients are our purpose. Their needs ignite our innovation fuel our urgency and inspire us to go further - faster. We bet on bold people who want to grow push boundaries and lead meaningful change. Here youll do the most impactful work of your career - because our commitment to changing lives isnt just what we do its who we are.

Patients are waiting. Are you ready to make the leap

Compensation and Benefits

The base salary hiring range for this position will be $$ 165000.

This position is also eligible for the following :

To apply just scroll down and click on the Apply Now link.

Equal Employment Opportunity

At Blueprint Medicines we foster an environment of fair treatment and full participation for all of our employees as we navigate complex challenges in pursuing our mission to improve the lives of patients. We celebrate our unique differences and varied career and life experiences so that we can sustain our diverse culture and ensure everyone feels accepted. We are committed to non-discrimination equal employment opportunity as well as an inclusive recruitment process. We consider all qualified applicants based on merit and without regard to race color sex gender identity sexual orientation age religion national origin ancestry ethnicity disability veteran status genetic information or any other characteristic protected under applicable federal or state law.

We will make reasonable accommodations absent undue hardship for qualified individuals with known disabilities. If you are an individual with a disability in need of an accommodation with the application or recruiting process please reach out to . We are also an E-Verify Employer. For more information please see our EEO Policy Statement the E-Verify Participation Poster the Right to Work Poster and / or the EEO Know Your Rights Poster.

Blueprint Medicines is a global fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solving important medical problems in two core focus areas : allergy / inflammation and oncology / hematology. Our approach begins by targeting the root causes of disease using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a proven track record of success with two approved medicines including bringing our medicine to patients with systemic mastocytosis (SM) in the U.S. and Europe. Leveraging our established research development and commercial capability and infrastructure we now aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases including SM and chronic urticaria breast cancer and other solid tumors.

Required Experience :

Manager

Key Skills

Sales Experience,Digital Marketing,Marketing,Google AdWords,Google Ads,Account Management,Adobe Audience Manager,Agency Management,Social Media Advertising,DoubleClick,DoubleClick for Publishers,Lead Generation

Employment Type : Full Time

Experience : years

Vacancy : 1