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Required Health Tech Sector Lead - Maternity leave replacement
Location: Tel-Aviv/Hybrid
Responsibilities:
The position is made up of 3 main pillars:
1.Relationship building: Manage our relationships with key players, including VCs and MNCs operating in Israel, and proactively engage with them to provide value to the sector. In this capacity the sector lead will collaborate with internal stakeholders (Press, Marketing, Global Partnerships, Product and Human Capital) to achieve projected impact.
2.Deep sector knowledge: Challenges, trends, numbers/data, key players, prominent startups, and their needs
3.Design, plan and execute sector workplan and roadmap leveraging deep knowledge of the sector and our capacities. The sector lead is required to translate sector-specific challenges into actionable projects, from ideation and design to effective execution.

We are looking for a Clinical and RA associate.
Primary function of the position:
Under the oversight of the CRA manager (CTM) the person ensures compliance of study conduct with ICH/GCP and country regulations, companys policies and procedures, quality standards and adverse event reporting requirements internally and externally.
Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
Roles and responsibilities:
Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.
Gains an in-depth understanding of the study protocol and related procedures.
Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
Performs remote and on-site monitoring & oversight activities using various tools to ensure:
Data generated at site are complete, accurate and unbiased
Subjects right, safety and well-being are protected
Conducts site visits including but not limited to initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.
Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.
Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.
Supports and/or leads audit/inspection activities as needed
Following the country strategy defined by CRD and CTM, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities
Whiling to travel abroad including US for sites oversights

Our company is a global pharma company on a mission to help patients worldwide get faster access to lifesaving, innovative, breakthrough therapies.
We operate on 4 continents in over 25 countries and are growing fast.
If you want to be part of our mission and help save patients by getting them the latest treatments, join us!
Our company seeks a Therapeutic Area Manager for the Neuro Rare Diseases Unit.
This role includes independently managing a Therapeutic Area.
Outline strategic policies for several fields and products and implement the policy.
Prepare a plan for achieving and maintaining goals.
Managing human resources.
Responsible for the budget of the Therapeutic Area, planning and monitoring it.
Working closely with overseas partners, having an in-depth understanding of the field and KOL's.
Mentoring employees for personal and career development.
Responsibilities:
- Responsible for managing the product managers and human resources within the unit.
- Mentoring team members, product managers, and product specialists.
- Career development for employees.
- Approving and monitoring business plans.
- Involved in building cooperation between marketing units.
- Maintaining strong relationships with overseas partners.
- Business meetings with overseas partners, training sessions, conferences, etc.
- Monitoring and following up on the unit's goals.
- Locate new companies/new products.
- Implement company's principles and vision.
- Report all safety data received within the working framework and pass it on to the PV dept.
- Work by company's code of ethics and guidelines set by the compliance and regulatory dept.
- Report to BUM.

Our company is a fast-growing, global leader in energy-based solutions for Aesthetics and Eye-Care.
We are based in Yokneam (with offices also in Tel-Aviv) with a strong business performance worldwide.
Our company is looking for a Clinical Director for the Aesthetics Business, which includes a broad portfolio of leading solutions in the market as well as an exciting innovation pipeline.
The Clinical Director will be responsible for pre- and post-market activities for the assigned product portfolio and will lead a team of Clinical Managers.
The Director will own all clinical aspects including: pre-clinical, clinical input to regulatory submissions and registrations, market conditioning for new solutions, post-market evidence generation and KOL development.
The individual will serve as a major pillar in building relationships with global KOLs and demonstrating the value of benefits of the solutions.
Key responsibilities:
- Own the Clinical Strategy for assigned portfolio and be a key contributor to overall Business strategy.
- Lead all R&D clinical activities for assigned portfolio including: bench-top, pre-clinical ex-vivo and in-vivo, validation, usability and more.
- Lead post-market clinical activities for evidence generation and training: clinical trials and different clinical activities (sponsored, IIT, grants) according to GCP(ISO-14155/MDR/CFR) and following company SOPs, protocol development, training development and more.
- Lead the clinical input and support for key regulatory submissions and processes: regulatory submission clinical input, clinical validations, CER, CDP, CEP and more.
- Support marketing/commercial activities from the scientific/medical point of view: review and input to marketing collateral, develop white papers, active participation in scientific meetings and more.
- Lead a team of clinical managers and oversee the relevant budget.
- Form and cultivate strong collaborative relationships with cross-functional partners in R&D, product, marketing and regional teams.

We are looking for a Clinical Affairs Manager to implement and oversee all activities related to clinical research and clinical studies in the company.
DiA Imaging Analysis provides AI-powered solutions to make ultrasound image analysis smarter and more accessible.
Its AI-based solutions help ultrasound users acquire the right image and analyze it automatically, allowing them to identify clinical abnormalities that are often difficult to find visually and enabling them to make better decisions based on accurate and objective data.
Your role:
Designing and managing the execution of clinical studies that demonstrate medical product safety and efficacy.
Ensuring that trials are conducted in full compliance to GCP.
Full responsibility on sites initiation, site personnel training and monitoring.
Working closely with the principal investigators and study coordinators.
Working with regulatory, development and marketing teams to create scientific publications, clinical marketing material and clinical background required for regulatory submissions.