Lead TA Specialty MA-PCSU

General Information

Job Advert Title Lead TA Specialty MA-PCSU Location Czech Republic Function/Business Area Medical & Clinical Employment Class Permanent

Description

Lead TA Specialty MA-PCSU
 About Astellas:

At Astellas we are making treatments that matter to people.

We are tackling the toughest health challenges putting the patient at the heart of every move we make.

Our global vision for Patient Centricity is to support the development of innovative health solutions through a deep understanding of the patient experience. At Astellas, Patient Centricity isn’t a buzzword - it’s a guiding principle for action. We believe all staff have a role to play in creating a patient-centric culture and integrating an awareness of the patient into our everyday working practices, regardless of our role, team or division.

We have developed ground-breaking, innovative medicines in immunology, oncology and urology. Our medicines are extending and saving the lives of cancer patients, making transplantation possible and improving the quality of life for those living with conditions where needs are often overlooked.

We take a patient-focused approach, that allows us to convert brilliant early science into treatments and solutions that directly improve and save patients’ lives.

From lab to clinic to patient, we focus on the most promising science, empower the best talent to pursue it, and develop life-changing solutions alongside the best partners.

The Opportunity:

As a Therapeutic Area Lead Medical Affairs – Czech Republic and Slovakia, you will be responsible for implementation of the medical strategy (Core Medical Plan) in the designated therapeutic area at the affiliate level by coordinating and executing medical / scientific activities to understand the local external environment and data gaps; to translate insights into strategies and activities and to ensure the information needs of key stakeholders are fulfilled to help ensure the safe and appropriate use of Astellas products.

Hybrid Working

At Astellas we recognise the importance of balancing your work and home life.  This role offers a remote working solution so you can optimise the most productive work environment for you to succeed and deliver.

Responsibilities:

• Provision of strategic medical and scientific expertise in support of all affiliate Medical Affairs deliverables and cross-functional activities
• Demonstration of matrix leadership by developing and maintaining integrated partnerships with key internal and external stakeholders to ensure all MA affiliate activities address local needs and advance the medical/scientific understanding of Astellas products across their lifecycle
• Understanding, alignment, and engagement with external stakeholders to advance the understanding of and science behind compounds in development, the safe and effective use of Astellas products and disease states that they treat.
• Engaging with Key External Experts in relevant TA and working closely with key internal stakeholders, including the brand teams across the affiliate to achieve business objectives for the affiliate.
• Ensuring all affiliate MA activities deliver value and are based on scientific validity, clinical importance and on time & budget
• Responsibility for 2-3 TA’s or for more than 1 product.
• high level of proficiency in interpersonal skills to engage effectively with a range of internal and external stakeholders.
• Active building of compliant and value-added bridges between internal colleagues by working to remove barriers to collaboration (i.e. strategic and tactical plans collaboration, Account Management, Omnichannel)
• Training of field representatives, participation in international and national congresses, physician meetings, and educational events for doctors

Essential Knowledge & Experience:

• Solid professional experience in Pharmaceutical industry, Medical Affairs experience is preferred.
• Strong expertise in the therapeutic area including clinical/ hospital practice, clinical development, experience in designing, executing and reporting of clinical trials can be considered.
• Foundational understanding of the drug development process as well as commercialization and strong understanding and knowledge of industry laws and regulations.
• Knowledgeable on local health care environment and health care dynamics.
• Preferable a good understanding of the dynamics of a large corporate environment; comfortable with matrix reporting lines.
• Excellent presentation skills; fully fluent in written and verbal business English.

Preferred Experience:

Doctoral degree (MD, PhD in health-related science or PharmD).

Education:

• Bachelor or Master degree in Health related Science or equivalent.

Additional Information

• This is a permanent full-time position.This position is office based in Czech Republic and 20-30% travel to Slovakia is expected in line with your role.

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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