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Senior Manager/Associate Director, Medical Communications Ad Promo
100 Park Ave Florham Park, NJ 07932 US
Job Description
Target PR Range: 30-40/hr
*Depending one experience
Function Overview: The Senior Manager/Associate Director, Medical Communications Ad Promo, represents the Medical function in the Material Review Process to guarantee medical, clinical, and scientific data accuracy, relevance, objectivity, balance and alignment with product label. Functions as the lead medical reviewer and sign-off for all promotional materials in designated area(s) of responsibility. Provides proactive guidance as needed for brand concepts and campaigns. Engages Commercial business partners early in the development of promotional materials to enhance efficiency and maintains ongoing communication. Attends, advises, and approves in collaboration /steering committee meetings as the lead Medical Reviewer for promotional review.
Key Responsibilities:
1. Provides medical expertise and expert review including discussing and collaborating with appropriate review colleagues from other functions. Reviews promotional materials within the area of scientific expertise to ensure that the materials represent a balanced view of all available product information, all claims are scientifically accurate, the most current and appropriate evidence has been used and the item is in line with the licensed indications and product safety. Advises and gives guidance on the rigor of data in relation to scientific standards for promotional claims
2. Serves as a medical/scientific expert to advise commercial colleagues and provide proactive guidance on brand concepts/campaigns and proper product/disease state claims development, etc. in collaboration with other business partners
3. Maintains current and comprehensive knowledge of aesthetics medical information, techniques, appropriate medical approaches, competitive landscape, and patient outcomes.
4. Provides strategic input, negotiates/resolves most decisions with business partners and collaborates effectively across functions.
5. Supports departmental and business strategies. Has accountability for the sound representation of the medical position within and external to and demonstrates adherence to medical guidance and standards.
6. Attends, advises, and approves in review meetings as the lead Medical Reviewer for designated product areas.
7. Maintains on-going communication with therapeutic area peers in Medical Affairs and Regulatory peers to ensure alignment
Qualifications:
MINIMUM REQUIREMENTS
Education and Experience:
• Advanced health science education or equivalent combination of education and experience required. (PhD, PharmD, or MD preferred)
• 2-5 years experience in clinical practice, academic research, pharmaceuticals, regulatory/scientific, or medical science liaison (MSL) environment
• Previous experience as Regulatory or Medical reviewer for promotional materials (ideally greater than 1 year).
• Medical affairs or medical communications experience preferred
• Strong knowledge of the IFPMA code (and any other applicable code depending on the region)
Essential Skills and Abilities:
• Ability to learn and convey medical information effectively.
• Works individually (reviewing materials electronically) and collaboratively with other review team members
• Strong communication skills, both oral and written, with proven ability to effectively present to audiences of varying levels
• Proven ability to manage multiple projects and product responsibilities
• Strong analytical and organizational skills
*CO/NYC candidates might not be considered
Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
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