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AbbVie Evidence generation Lead in Prague, Czech Republic

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

Evidence generation Lead is responsible for keeping oversight of evidence generation activities across all therapeutic areas. This role supervises the affiliate real-world evidence (RWE)/real-world data (RWD), and has direct impact and shapes the RWE/RWD generation strategy (incl. financial planning) for Czechia and Slovakia.

As a subject matter expert in research methodologies, this Lead identifies and co-creates with the affiliate RWE/RWD group, as well as with brand teams/medical affairs/market access employees on scientifically robust and innovative research initiatives.

Main Responsibilities:

  • To act as country representative at the evidence-generation internal and external focused activities and networks;

  • To facilitate the implementation of a strong culture of strategic evidence generation and portfolio mindset, supporting early integrated evidence planning and execution;

  • To lead and oversee cross-functional activities involving the Medical Department related to financial planning, evidence solutions, medical excellence, in accordance with Global/Area and Local processes and policies in place;

  • To define strategy and guide implementation of the Digital Transformation and Customer Focused Communication of Medical Department;

  • To drive and execute our evidence generation plans and evidence gap assessment work;

  • To identify innovative solutions and training needs to improve agility and operational excellence.

Qualifications

Qualifications:

  • Master’s degree in a scientific discipline or higher;

  • At least 5 years of experience in pharmaceutical industry, CRO or academic research with demonstrated experience in a range of evidence generation methodologies including clinical research, real-world data or registry research, and the ability to understand brand strategies and brand development plans;

  • Knowledge of health care environment, patient needs, market access, and reimbursement issues; solid knowledge and experience in drug development and commercialization processes; sound and current knowledge of the regulatory environment; significant experience in overseeing or conducting clinical trials; solid understanding and experience in trial design and research methodology and understanding of the need to balance safety and efficacy concerns;

  • Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity;

  • Strong planning incl. financial planning and organizational skills, and the ability to get things done;

  • Excellent written and spoken communication and presentation skills in Czech/ Slovak and English languages are must;

  • Dynamic, Innovative, curious and strategic thinker as well as sound judgment;

  • Ability to work independently and in a team-oriented environment.

Additional Information

AbbVie 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.

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