Medical Content Lead, Sandoz, Sweden

315226BR
Aug 02, 2021
Sweden

Job Description

Sandoz provides patient access to 7 biosimilar brands and more than 400 small molecule medicines in the Nordics today!

Your responsibilities include, but not limited to:
• Support country medical affairs strategy in line with the global strategy, country insights and market conditions, and secure implementation of planned Medical Affairs activities within the designated therapy area(s).
• Coordinate scientific meeting, and other medical / scientific exchange and engagement activities which could bring additional value to the relevant therapy area; and support customer-facing medical activities and events, and ensure timely execution of planned medical affairs activities in an efficient and compliant way.
• Ensure medical enquiries are responded to in a high quality, timely manner, and in accordance with applicable standards; establish standard response documents as appropriate, for frequently asked questions.
• Coordinate review and approval of medical materials and locally developed promotional materials; ensure medical materials provided from global or region for stakeholder engagement and events are tailored to local needs, and reviewed/approved per local/P3 guidelines.
• Ensure medical insights are provided to cross functional groups, including, but not restricted to: Pharmacovigilance, Regulatory affairs, Market Access, QA, Commercial teams, Brand team and others.
• Responsible for risk identification and assessment, mitigation planning as well as implementation and monitoring of appropriate internal controls within the area of responsibilities, capability to manage 500 plus items per year within medical compliance review process for non/promotional materials excellent administration skills supporting medical affairs projects scientific overview knowledge on strategic Areas as Oncology, Neurology Rheumatology, Gastroenterology experience in engagement with external experts, clinicians, pharmacists.

Diversity & Inclusion / EEO

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

Minimum Requirements

What you’ll bring to the role:
• Fluent in English & one Scandinavian language (preferably Swedish); good command of Finnish would be an advantage
• 3-4 years relevant experience
Relevant experience in medical compliance review of promotional material
• Project management of a cross-functional team to drive pre-launch phase activities, including budget/resource allocation
• Great teammate and efficient collaborator; able to build positive relationships
• Concise communication & presentation skills; knows how to summarize and communicate the key points and business case to others.

You’ll receive:
Competitive salary, annual bonus, pension scheme, health insurance, flexible working arrangements, subsidized dining facilities, employee recognition scheme.

Why consider Sandoz?

Our number 1 priority is to pioneer patient access to better healthcare. We are a company of firsts. 1st to develop an oral penicillin antibiotic. 1st to develop and launch biosimilars and we never stop asking: how can we continue to pioneer access in an ever-more digital and global world?
The answers come when curious, courageous and collaborative people are empowered to ask new questions, make bold decisions and take smart risks.
Sandoz, a Novartis division, is a leader in generic and biosimilar medicines
.
Join us and help us reimagine medicine.

Sandoz stands up for equal opportunities and for the integration of persons with disabilities. Hiring decisions are only based on the qualification for the position, regardless of gender, ethnicity, religion, sexual orientation, age and disability
SANDOZ
COMMERCIAL OPS EUROPE SZ
Sweden
Stockholm
Research & Development
Full Time
Regular
No
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315226BR

Medical Content Lead, Sandoz, Sweden

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