ASSISTANT/ASSOCIATE DIRECTOR, SCIENTIFIC MEDICAL AFFAIRS, ONCOLOGY (REMOTE)
Company: AbbVie
Location: Libertyville
Posted on: October 9, 2024
Job Description:
Company DescriptionAbbVie's mission is to discover and deliver
innovative medicines and solutions that solve serious health issues
today and address the medical challenges of tomorrow. We strive to
have a remarkable impact on people's lives across several key
therapeutic areas - immunology, oncology, neuroscience, and eye
care - and products and services in our Allergan Aesthetics
portfolio. For more information about AbbVie, please visit us at
www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram,
YouTube and LinkedIn.Job DescriptionPosition in Medical Affairs has
a key role within the designated Therapeutic Area. This leader
supports the development and execution of the therapeutic area
medical and scientific strategy, specifically as it pertains to the
specific asset or indication by providing scientific, strategic and
operational input into core medical affairs activities including
thought leader engagement plans and field provider interactions;
generation and dissemination of clinical and scientific data;
provider and payer educational initiatives; promotional material
generation and works closely with cross-functional teams to provide
strategic medical input. This leader ensures tactical execution is
relevant to the market- physicians, patients and
payors.Responsibilities:
- With oversight, contributes to the development of the
Hematology Oncology therapeutic area strategy.
- Contributes to the development of and leads the execution of
the medical education tactics, advisory boards, and thought leader
engagement plan in line with the indication or asset's strategic
plan.
- Leads conference planning and execution. Represents AbbVie at
external meetings including investigator meetings, scientific
association meetings, etc.
- May be responsible for Medical Review (MR) training for on
label, clinical data and disease state.
- Responsible for managing budget for assigned projects including
consulting and vendor management.
- Supports clinical and scientific data generation including
alignment of the Investigator Initiated Study (IIS) strategy as
needed to support external communication
- Provides subject matter expertise for commercial teams
including competitive assessments and regular scientific literature
reviews.
- Aligns medical education and scientific initiatives with the
Scientific Communication Platform.
- Contributes to the generation of Medical Information (MI)
communication content and supports training on MI materials.
- Contributes to all launch readiness
reviews/planning.Qualifications
- Scientific Bachelor's Degree in the sciences. Advanced Degree
PhD, PharmD, PA or NP preferred. Residency or additional post
doctorate experience preferred.
- 3+ years of clinical, scientific/research, or industry related
experience or equivalent required demonstrating strong leadership
competencies and proven team-building skills with ability to lead
in a global matrixed environment. Substantial understanding of
relevant therapeutic area required.
- Good understanding of legal and regulatory guidelines (e.g.
knowledge of OPDP promotional regulations, CDER/CBER regulations as
they relate to drug approvals).
- Good understanding of Good Clinical Practices, ICH guidelines,
PhRMA code, FDA CFR, ISO, clinical research ethics, HIPAA and
patient privacy laws, EU Directive and other applicable local
regulations
- Good understanding of Medical Affairs principles, study design
and publications.
- Knowledge of clinical trial methodology, regulatory
requirements governing clinical trials and experience in the design
of protocols preferred.
- Interactions normally require the ability to gain cooperation
of others, conduct presentations of technical information
concerning specific projects and schedules, etc.
- Ability to interact externally and internally to support global
business strategy. Ability to work effectively with different cross
functional groups and have strong interpersonal and communication
skills.
- Able to coordinate appropriate scientific and medical
activities with internal stakeholders (i.e. commercial, clinical
operations, discovery, statistics, regulatory, etc.) as they relate
to on-going medical affairs projects.
- Ability to work effectively in a team/matrix environment.
Ability to influence others without direct reporting
relationshipsPreferred:
- Expertise in the therapeutic area of Hematology
Oncology.Additional InformationApplicable only to applicants
applying to a position in any location with pay disclosure
requirements under state or local law: ------
- The compensation range described below is the range of possible
base pay compensation that the Company believes in good faith it
will pay for this role at the time of this posting based on the job
grade for this position. Individual compensation paid within this
range will depend on many factors including geographic location,
and we may ultimately pay more or less than the posted range. This
range may be modified in the future.---
- We offer a comprehensive package of benefits including paid
time off (vacation, holidays, sick), medical/dental/vision
insurance and 401(k) to eligible employees.---
- This job is eligible to participate in our short-term incentive
programs. ---
- This job is eligible to participate in our long-term incentive
programs------Note: No amount of pay is considered to be wages or
compensation until such amount is earned, vested, and determinable.
The amount and availability of any bonus, commission, incentive,
benefits, or any other form of compensation and benefits that are
allocable to a particular employee remains in the Company's sole
and absolute discretion unless and until paid and may be modified
at the Company's sole and absolute discretion, consistent with
applicable law.AbbVie is an equal opportunity employer and is
committed to operating with integrity, driving innovation,
transforming lives, serving our community and embracing diversity
and inclusion. It is AbbVie's policy to employ qualified persons of
the greatest ability without discrimination against any employee or
applicant for employment because of race, color, religion, national
origin, age, sex (including pregnancy), physical or mental
disability, medical condition, genetic information, gender identity
or expression, sexual orientation, marital status, status as a
protected veteran, or any other legally protected group status.US &
Puerto Rico only - to learn more, visit
https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS
& Puerto Rico applicants seeking a reasonable accommodation, click
here to learn
more:https://www.abbvie.com/join-us/reasonable-accommodations.html
Keywords: AbbVie, Glenview , ASSISTANT/ASSOCIATE DIRECTOR, SCIENTIFIC MEDICAL AFFAIRS, ONCOLOGY (REMOTE), Executive , Libertyville, Illinois
Didn't find what you're looking for? Search again!
Loading more jobs...