לוח משרות דרושים בוגרי מדעי החיים

We are seeking an highly skilled Sensory Consumer Insights Specialist to join our team.
The specialist will report to our sensory dept manager.
The ideal candidate will be responsible for coordinating and running experiments, assisting in the preparation of experiment protocols, creating internal and external presentations, and cultivating consumer and sensory product knowledge.
This role requires a blend of scientific expertise, analytical skills, and a deep understanding of consumer behavior.
Roles and Responsibilities:
* Collaborating with the Sensory dept manager to accomplish the sensory group missions.
* Coordinate and execute sensory experiments to gather consumer insights, ensuring the smooth running of sensory panels and the collection of actionable data.
* Assist in the development and refinement of experiment protocols.
* Build and maintain a comprehensive understanding of consumer preferences, behaviors, and trends.
* Collaborate effectively with cross-functional teams.
* Communicate research findings and recommendations in a clear and concise manner.
* Analyze and interpret data from sensory evaluations to derive actionable insights, utilizing statistical analysis software and strong analytical skills.
* Assist in preparing internal and external presentations.
* creating actionable insights from experiments, data and literature research
* Support sensory team goals and activities, as needed, Including preparation of sensory panels, sourcing candidates, etc.

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.

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.