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Global Medical Development Manager (d/f/m)

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

Slovenia

Offer summary

Qualifications:

MD degree in medicine, Minimum 2 years of Product Development experience, Fluency in English, Knowledge of Microsoft Office.

Key responsabilities:

Identify medical development implications
Engage in product-specific analysis
Provide medical expert assessments
Contribute to clinical study design

Novartis XLarge http://www.novartis.com

10001 Employees

See all jobs

Job description

Job Description Summary

The future is ours to shape.

Job Description

Sandoz, of which Lek is also a part, is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Generic and Biosimilar medicines.

Now as an independently listed company, Sandoz aims to increase its strategic focus, operate with greater agility, set clearer business objectives, enhance shareholder returns, and strengthen its culture for us, the Sandoz and Lek associates. This is an exciting time in our history, and by creating a new and ambitious path, it will provide a unique opportunity for us all, both professionally and personally.

Join us as a Founder of our ‘new’ Sandoz and Lek! 

As a Global Medical Development Manager (d/f/m) you will be a part of the Sandoz Global Development organization, which is responsible for development & delivery of high quality Biosimilar and Small molecule products. We are looking for experienced, curious, and inspiring associates to join the team and support development of complex generic pharmaceuticals.

Your key responsibilities:

Your responsibilities include, but not limited to:

Identifying the medical development implications of preclinical findings, drug formulation information, regulations and any other relevant medical information.
Engaging in product or indication specific analysis of existing data sources to develop medical insights in optimization of the formulation, medical device and medical therapy, improved clinical outcomes, enhanced value proposition, and new insights into disease pathophysiology with the aim to increase the probability of success of the product development.
Providing medical expert assessment to support selection of new product opportunities pursued by Global Portfolio Management and Business Development and Licensing (BD&L).
Providing medical input to product development teams and patent department during product development phase according to milestone guidance and have an ability to cover several Therapeutic Areas.
Active collaboration with cross-functional partners, collaboration with external experts as indicated by project/product requirements, other functions within Product Development.
Providing input to clinical study design and owning the preparation of scientific documents.
Performing Medical Monitoring for clinical studies in patients according to applicable requirements.
Medical writing for registration purpose, medical interpretation of study results for clinical endpoint or safety studies and preparation of Medical Development Product Pack for handover to Medical Affairs.

What you will bring to the role:

University diploma in medicine (MD degree).
Minimum 2 years’ Product Development experience in the pharmaceutical industry (preferably generic drug development) in local or global roles.
Excellent in English, both written and spoken.
Knowledge of Microsoft Office.
At least 50% presence on-site (in Slovenia).

We are looking for responsible, objective-driven candidates who value collaboration, teamwork and are open to new challenges and expanding their knowledge and expertise.

You’ll receive:

Employment at the most reputable employer in Slovenia offers Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical, mental and social well-being (Energized for Life), Unlimited learning and development opportunities. 

We offer permanent contract with 6 months of probation period. You are kindly invited to submit your application in English language, including CV, by 22 January 2025.

Why Sandoz?

Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!

With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.

Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!

The future is ours to shape!

Commitment to Diversity & Inclusion:

Sandoz is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. 

Join our Sandoz Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Sandoz and our career opportunities, join the Network here: https://talentnetwork.novartis.com/sandoztalentpool

#Sandoz

Skills Desired