דרושים » רפואה ופארמה » Obesity Medical Science Liaison

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.

As the Israel CDC Therapeutic Area Head, you will manage and lead the clinical research Therapeutic Area team and ensure that all clinical trial activities are carried out in compliance with all policies, procedures and local requirements.
You will also have the following responsibilities:
Ensure Clinical Therapeutic Area team set-up as per procedures and local regulatory requirements, unit processes & systems, resources and conduct of clinical trials in the CDC.
Drive implementation and execution of CDC trial delivery strategies and make sure risk plans are in place when needed in close cooperation with the CDC director.
Ensure performance management of the Clinical Therapeutic Area team, while guaranteeing the Clinical Research Unit goals are met.
Develop and maintain partnerships and effectively communicate with internal stakeholders, as well as external such as investigators, vendors, clients, KOLs, Ethics Committees and Health Authorities.
Inform internal stakeholders about trial/project related issues and the local therapeutic business scenario covering any current and/or potential changes in local trial related regulation.

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.