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Required MSL- Severe Asthma biologics
Job ID R-197316
Introduction to role:
Join a global leader pushing the boundaries of science to deliver life-saving breakthrough medicines.
As a Medical Science Liaison (MSL), you will play a pivotal role in shaping the optimal performance of our brands. You will be responsible for building scientific partnerships with Key External Experts (KEE) and other healthcare professionals, providing high-quality, up-to-date scientific and medical information. This role is field-based and requires robust scientific and medical expertise, strong communication skills, and a business acumen attitude.
Accountabilities:
As an MSL, you will conduct scientific exchange and collect customer insights, interact with other MSLs from different countries or TAs, gain input from and co-create projects with KEE, manage scientific partnerships with KEE, deliver key medical input into the brand strategy, and ensure compliance with all external regulations & internal policies. You will also educate sales representatives, support clinical operations as needed, and work in collaboration with the Marketing and Market Access Departments.

looking for an Obesity Medical Scientific Liaison for the center-south region. In this role, you will be responsible for delivering high level medical and scientific expertise to internal and external stakeholders, within the obesity therapeutic area. You will be responsible for internal insight generation, scientific communications, and regional medical activities. In addition, you will work most of the time in the central and southern region of Israel with an 80 percent work rate in the field.
Your main accountabilities will be:
Development of professional relationships with external key opinion leaders and other stakeholders.
Leading scientific dialogue with key opinion leaders, including scientific presentations and personal meetings.
Identification of healthcare professional influencers within the obesity therapeutic area.
Drive internal and external scientific updates.
Drive local, regional, and international medical meetings and activities.
Generate insights from the field and participate in internal medical strategic planning.

As a Start-Up Team Manager, you will be responsible for executing the Start-Up team activities in clinical trials performed in Israel, ensuring compliance with local regulations, ICH-GCP, procedures and protocol requirements.
In addition, you will have the following responsibilities:
Manage and lead the Start-Up team, set and monitor performance targets and KPIs for the team and functional area in close cooperation with Israels Clinical Development Center (CDC) Director and with the Therapeutic Area (TA) Heads.
Ensure preparation and submission of local Clinical Trial Application to Health Authorities and Ethics Committees (ECs) to obtain all necessary regulatory approvals within defined timelines.
Deliver reliable, high-quality data and ensure study participants protection to activate sites prior to FPFV (First Patient First Visit) in the country.
Manage the lifecycle of clinical trial agreements/contracts, including sub-contractors, across trials.
Execute regulatory submissions of Clinical Trial Applications (CTA) and ongoing submissions and obtaining approvals.