לוח משרות דרושים בוגרי מדעי החיים משרה מלאה

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.

We are seeking an Experienced Clinical Research Associate (CRA).
Position Overview:
Performs and coordinates different aspects of the clinical monitoring and site management process.
Conducts remote or on-site visits to assess protocol and regulatory compliance and handles required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.).
Acts as a site processes specialist, ensuring that the trial is conducted according to the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensures audit readiness.
Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix.

We are looking for an experienced Research associate with deep research skills to join our team.
Responsibilities:
Plans, conducts and communicate laboratory research studies focusing on target, biomarker and drug discovery
Join a multidisciplinary team of professionals in biology, chemistry, software, AI, and clinical fields.

Required Analyst
Job Description:
A clinical-stage drug discovery and development company in the field of cancer immunotherapy. In line with our business model to enter into collaborations for their internally discovered, novel therapeutic candidates at various stages in research and development, the company is seeking an Analyst in support of its partnering efforts.
Reporting to the SVP Strategic Collaborations, the Analyst will lead competitive intelligence (CI) and business analysis activities to support BD and corporate objectives. She/he will be responsible for supporting aspects of competitive analysis and other activities relating to partnering efforts.
Constantly monitor the pharma and biotech space and gather competitive intelligence from various sources including company portfolios, preclinical and clinical activities, scientific data, partnerships, deal structures and terms, and other relevant intelligence
Perform analyses and provide insights into competitive landscapes, industry trends and perspectives, market developments, product developments and positioning, as well as other intelligence in support of our BD&L and R&D efforts
Provide regular updates to our management and functions
Develop Target Product Profiles for our development candidates in close collaboration with R&D teams, and build forecast models based on epidemiological data as well as customer/patient segmentation, pricing and access assumptions
Identify potential collaboration partners for various pipeline opportunities
Work closely with our R&D community and drive the preparation of materials surrounding the companys pipeline programs for internal presentation to management and also to potential partners
Contribute to the creation of valuation models and financial valuation of business development opportunities against partnering scenarios.