ASSOCIATE SCIENTIFIC DIRECTOR HEMATOLOGY
Chicago, IL 60025
LOCATION: CHICAGO, IL
COMPANY: TOP BIOPHARMA COMPANY
COMPENSATION: $150K-$200K BASE + BONUS + STOCKS + PENSION + AMAZING BENEFITS
CONTACT: KEN KUPERSMITH- [email protected]
***SERIOUS INQUIRIES ONLY: IF YOU APPLY AND DO NOT MEET THE BELOW REQUIREMENTS YOU WILL NOT BE CONTACTED OR CONSIDERED***
* AT LEAST 5 YEARS EXPERIENCE IN PHARMA INDUSTRY
* STRONG HEMATOLOGY THERAPEUTIC AREA UNDERSTANDING
* DOCTORATE REQUIRED (MD, PHD, PHARMD, ETC.)
Provides specialist medical and scientific strategic and operational input into core medical affairs activities such as:
1.Health-care professional and provider interactions (Payers, Patients, Prescribers, and Providers)
2.Generation of clinical and scientific data (enhancing therapeutic benefit and value)
3.Educational initiatives (medical education, data, guidelines, and value proposition)
4.Safeguarding patient safety (risk minimization activities and safety surveillance activities)
5.Works closely with sales, marketing and commercial teams to provide strategic medical input into core brand (product) strategies, and to support medical and marketing activities (promotional material generation and product launches) and market access.
1.With oversight, contributes to the development of brand strategies.
2.Contributes to the development of and leads the execution of the Medical Education / Advisory Board & KOL Engagement Plan generation in line with TA plan including Conference planning and execution.
3.Generates clinical and scientific data (DOF) as needed to support external communication (RRTI).
4.Responsible to manage budget for assigned projects.
5.Aligns Medical education and scientific initiatives with Sci Comm Platform. Informs Investigator Initiated Study (IIS) strategy and can act as Docent for IISs.
6.Actively contributes to the development of a TA KOL Engagement Plan.
7.Contributes to the generation of Medical Information (MI) communication content and supports training on Medical Information (MI) materials.
8.Participation in design and execution of clinical trial safety, product safety and risk management plans. Track RMP implementation.
9.Medical Review (MR) Training on label, clinical data and disease state.
1.Advanced Degree PhD, PharmD, MD, PA, NP highly preferred.
2.Residency or additional post doctorate experience highly preferred.
3.Typically 8 years' experience in the pharmaceutical industry or equivalent; substantial understanding of relevant therapeutic area, Hematology, required.
4.Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in the design of protocols preferred.
5.May have performed protocol design in the academic environment and/or acted as an assistant PI.
6.Interactions normally require the ability to gain cooperation of others, conduct presentations of technical information concerning specific projects and schedules, etc.
7.Ability to interact externally and internally to support global business strategy.
8.Represents at external meetings including investigator meetings, scientific association meetings, etc.