Msl Oncology

A career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

**The Role**:Responsible for ensuring the Company´s compliance with pharmaceutical regulations and laws as well as providing expertise on drug safety and medical topics. Provides medical advice to ensure accuracy of data to support existing or new product promotion. Develops medical product information and stays informed on scientific trends and competition. Manages relationships with target opinion leaders and trains local teams in medical topics.
- Impacts the results of the team or even influences a range of customer, operational, project or service activities of closely related teams with own contributions. Explains complex or even difficult/critical information to others in straightforward situations and interacts across business areas. May even advance discussions and build consensus across the business and with external parties regarding own technical area.
- Performs a range of routine or even non-routine assignments to solve problems of low to moderate complexity that require solid understanding and experience in own job field. Analyzes factual information and solutions to make independent judgement, recommendations and decisions. May also use best practices to improve products or services.
- Accountable for the quality of work. Works independently and receives a moderate to low level of guidance and direction within clear or even broad guidelines.
- Act as Local Medical Affairs TA expert in one or more Tas.
- Co-leading Local TA, Launch and Brand Strategies and lead the Medical Affairs Tactics.
- Lead Medical Affairs activities in assigned territory along defined local Medical Launch / Brand strategies.
- Responsible for assigning, tracking and monitoring relevant KPIs and metrics for Medical affairs
- Consolidate and communicate trends, market insights, and unmet needs identified in the field Operations.
- Develop Medical material, review marketing material, trainings. Ensure scientific and clinical accuracy for specific product or brand.
- Comply to relevant training and SOPs. Maintains up-to-date GxP knowledge by following internal and external trainings.
- Conduct Local internal scientific training and ensure continuous Medical education of existing teams and new employees working in the Local TA.
- Review and communicate insights collected by Medical colleagues.
- Develop Medical KTL scientific interaction plans. Positively impact external perceptions and knowledge regarding company and company products.
- Maintain and demonstrate comprehensive and in-depth scientific TA knowledge when performing assigned tactics.
- Ensure operational excellence by sharing best practices.
- Map treatment landscape and medical environment for indications/ programs in the Therapeutic Area.
- Responsible for the planning and tracking of the (TA-specific) medical budget.
- Lead/ support (depending on nature of study) Medical studies, assist to coordinate Local clinical projects and contribute to site selection for clinical projects. Lead Local publication process, publication dissemination and alignment with Local, Regional and Global publication plan.
- Support communications for ISS between investigators and internal stakeholders.
- Coordinate with ClinDev and ClinOps in providing field support for research studies and assist in the selection of clinical study sites
- May lead presentation and discussion on local Studies at internal study review committee meetings.
- Assimilate, process and share medical information with stakeholders

**Who you are**:Academic Background:

- University degree (Bachelor's) required, preferably in scientific field of relevance to position. Secondary / advanced scientific degree (e.g., MSc, PharmD, PhD, DO, MD) required. Scientific and / or clinical training.
- Fluency in English.

**Experience**:

- Clinical or clinical research experience specific to therapeutic area preferred, advanced degree advantageous.
- Substantial professional, clinical or research experience in a scientific or related field required (minimum of 5 years).
- Previous MSL, Medical Advisor or related