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Scientific Director, US Medical Affairs Oncology- CLL

3 months ago


Mettawa, United States AbbVie, Inc Full time

Company Description

AbbVie'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 Description

Provides specialist medical/scientific strategic and operational input into core medical affairs activities such as: health-care professional/provider interactions (Payers, Patients, Prescribers, and Providers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, data, guidelines and value proposition); safeguarding patient safety (risk minimization activities / safety surveillance activities).

Responsibilities:

* Provide scientific and technical support for assigned products; deliver scientific presentations; develops and maintains professional and credible relationships with, key opinion leaders; actively participate in relevant Brand Teams and helps develop medical affairs strategies for assigned products; develop innovative research concepts for clinical data generation; provide relevant scientific and technical training.
* In cooperation with affiliate medical departments, Marketing, RA, Clinical and other functional areas, provides leadership, oversight and support for assigned products/projects. Drives medical affairs activities and generation and dissemination of data supporting overall product scientific and business strategy.
* Keeps abreast of professional information and technology through conferences and/or medical literature and acts as a therapeutic area resource. Drive Medical Affairs strategies and be a key internal contact/subject matter expert.
* May develop of scientifically accurate marketing materials, medical education programs, advisories, and symposia.
* May assist with the scientific review, development, execution and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.
* May oversee the work of Assistant/Associate Scientific Directors
* May lead cross functional teams in development and execution of strategic initiatives requiring integration of multiple subprojects within the therapeutic area or Medical Affairs function.
* Provides guidance to cross-functional team members to aid in the development of promotional materials.
* Provides timely and accurate reviews of promotional strategies and tactics in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs
*

Significant Work Activities -Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day),Keyboard use (greater or equal to 50% of the workday)

Qualifications

Qualifications:

* Advanced Degree PhD or PharmD.
* Typically, 8-10 of experience in the pharmaceutical industry or equivalent; substantial understanding of relevant therapeutic area required.
* 5-7 years of experience in Medical Affairs highly preferred.
* Minimum of 4 years of clinical trials direct management experience in the pharmaceutical industry or academia or equivalent is preferred.
* Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
* Ability to run a clinical or real-world study independently with little supervision.
* Proven leadership skills in a cross-functional global team environment
* Must possess excellent oral and written English communication skills .
*

Additional Information

Applicable only to applicants