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לפני 19 שעות
Location: Merkaz
Job Type: Full Time
If youre passionate about driving growth and delivering breakthrough innovation to patients, we invite you to be part of our journey.
Reporting to Head of Business Development, the Director, Search & Evaluation Business Development is a mission‑critical leadership role that directly shapes long‑term growth and strategic direction, while advancing our core purpose of improving and saving patients lives worldwide. The position plays a foundational role in building future pipeline by identifying high‑impact opportunities that expand global access to the most advanced therapies.
In this role, you will proactively identify best‑in‑class assets, lead rigorous scientific and clinical evaluations, and drive cross‑functional diligence to enable high‑quality, strategic partnering decisions. You will operate at the intersection of science, strategy, and execution, working in close partnership with Medical, Regulatory, and senior leadership to support disciplined growth and long‑term value creation.
Responsibilities:
Proactively screen, source, and prioritize best‑in‑class late‑stage assets from Phase 2 through marketed products across rare and severe diseases, leveraging multiple platforms, databases, and industry sources.
Build and manage a robust and high‑quality pipeline of partnership opportunities aligned with long‑term growth strategy.
Lead rigorous scientific and clinical evaluations by assessing clinical data versus current standard of care, mechanism of action differentiation, regulatory pathways, and competitive landscape.
Develop clear and data‑driven Target Product Profiles (TPPs) to support scientific, clinical, and strategic positioning.
Conduct comprehensive research, including literature review and data synthesis, to deeply understand disease biology, unmet need, and therapeutic value.
Engage directly with Key Opinion Leaders, clinical investigators, and external experts to validate assumptions and strengthen scientific and clinical assessments.
Drive cross‑functional diligence by partnering closely with function leads, Medical and Regulatory, Commercial, Legal, Finance, and other relevant stakeholders.
Support transaction strategy and execution by providing scientific and clinical input into transaction strategies, diligence materials, and contractual discussions.
Prepare clear, concise, and decision‑ready materials, including evaluation summaries, one‑pagers, presentations, and business cases for senior leadership and governance forums.
Continuously refine and strengthen Search and Evaluation processes, criteria, and scientific convergence frameworks to improve rigor, consistency, and speed of decision‑making.
Act as a trusted thought partner to leadership by surfacing insights, risks, and recommendations that directly influence portfolio strategy and growth trajectory.
Represent externally in partnering discussions, scientific meetings, and industry conferences to strengthen visibility and network.
דרישות:
An advanced degree in Life Sciences (PhD or MD) is required; an MBA or additional business training is a strong advantage.
At least eight years of relevant experience in Search and Evaluation, Business Development, Licensing, Corporate Development, venture capital, or related partnering roles within pharma or biotech.
Proven experience evaluating late‑stage assets from Phase 2 through marketed products, preferably in rare and severe diseases.
Strong understanding of drug development, clinical data interpretation, regulatory pathways, and competitive dynamics.
Demonstrated experience developing Target Product Profiles and comparing clinical data to existing standards of care.
Proven ability to lead cross‑functional diligence teams and work closely with Business Development deal leads throughout the transaction lifecycle.
Strong scientific credibility with the ability to engage המשרה מיועדת לנשים ולגברים כאחד.
 
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Location: Hod Hasharon
Job Type: Full Time
The Medical Manager in the field of Gyneco-Oncology, holds primary responsibility within the country for the development and execution of the Medical Affairs strategic plans and, is expected to spend up to 50% of their time in external engagements.

Key responsibilities include cross-functional strategy collaboration and execution, building trust with the medical/scientific community, facilitating peer-to-peer medical and scientific exchange, and providing asset issue resolution support.

Responsibilities and Primary Activities

Strategic and Tactical Leadership

Consolidates actionable medical insights to inform company strategies
Translates Global Medical Goals and Strategies into tactics and solutions that support optimal scientific exchange aimed at helping improve patient outcomes and enhancing access
Supports execution of and quickly adapts tactical plans to local business realities
Follows up on Investigator-Initiated Study (IIS) proposals aligned with Our Company ISS Program areas of interest
Collaborates with our research laboratories/Global Clinical Trial Operations (GCTO) personnel to identify potential investigators for our clinical development programs
In collaboration with colleagues, facilitates the delivery of data generation activities (phases I-IV), including the identification of suitable research projects, research centers, investigators, and innovative methods to generate data
Provides non-promotional, balanced, and reliable scientific information following company standards and local regulations


Medical and Scientific Leadership

Brings the local scientific and healthcare environment perspective to the Regional Medical Affairs team
Communicates scientific and business needs appropriately and effectively across internal and external stakeholders
Builds trust with the external scientific community via peer-to-peer scientific exchange, research, and educational collaborations, as well as interactions with scientific societies, health organizations, publications, etc.
Provides therapeutic/functional training to assigned teams and affiliate functions
Develops and executes country medical educational programs and symposia
Leads country advisory boards and expert input forums
Participates in and contributes to professional organizations and academic/regulatory working teams


Regulatory and Market Access Support

Collaborates and leads resolution of regulatory, public relations, compliance, and other asset issues
Supports the resolution of asset safety or quality issues (i.e., contributes content and strategy in regulatory responses and interactions, risk management planning, and implementation)
Provides access support as needed (e.g., health technology assessment, pre-license patient access, reimbursement dossier)
Requirements:
MD, PhD, or PharmD
A minimum of 2-3 years of clinical and/or research experience in a relevant disease area- preferred
Excellent interpersonal, communication, networking, and presentation skills
Experience with local pharmaceutical industry guidelines, regulatory/reimbursement framework, and clinical research guidelines
Strong prioritization skills and ability to understand how decisions fit into the broader context of corporate strategies
Demonstrated ability to develop a network of scientific leaders and other key stakeholders (e.g., public groups, government officials, medical professional organizations)
Proven ability to effectively communicate information at country management level
Ability to effectively collaborate across functions in a matrix environment
This position is open to all candidates.
 
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26/07/2026
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time and English Speakers
We are looking for a highly skilled and motivated Senior Academic Editor to lead and support the preparation, writing, and submission of peer-reviewed scientific publications related to our Healths clinical, technological, and regulatory activities.

This is a cross-functional role that requires excellent academic writing skills in English, strong collaboration across departments (Clinical, R&D, Product, Regulatory), and the ability to communicate complex scientific data in a clear and compelling way.

The ideal candidate has a background in life sciences, biomedical engineering, or clinical research, and a proven track record in academic publishing-preferably in the fields of medical devices, SaMD, AI in healthcare, or digital health.

Responsibilities:

Write, edit, and manage scientific manuscripts, abstracts, posters, and white papers for submission to peer-reviewed journals and scientific conferences.

Collaborate with internal teams (Clinical, R&D, Data Science, Regulatory) to gather and validate data for publication.

Conduct literature reviews and maintain up-to-date knowledge of relevant clinical and scientific developments.

Manage the end-to-end publication process, including journal selection, formatting, submission, and peer-review response.

Support clinical and regulatory documentation when relevant, such as clinical evaluations, study reports, or white papers.

Maintain a pipeline of upcoming publications and coordinate timelines with key stakeholders.

Ensure all scientific materials align with AEYE Healths strategic positioning and messaging.
Requirements:
English - native language a must.

2+ years of hands-on experience in academic or scientific writing, preferably in a medical, clinical, or biotech environment.

Proven publication of more than 10 academic papers.

Demonstrated experience publishing in peer-reviewed journals, as lead or contributing author.

Strong understanding of clinical research methodologies, data interpretation, and ethical publishing standards.

Ability to work independently and manage multiple writing projects simultaneously.

Excellent attention to detail, with strong editing and proofreading skills.

Academic background in life sciences, biomedical engineering, clinical research, or related field.

Knowledge of regulatory and clinical frameworks (e.g., MDR, FDA, GCP) - an advantage.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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לפני 19 שעות
חברה חסויה
Location:
Job Type: Full Time
we are looking for a Corporate Development Manager
We are seeking a driven and analytical Corporate Development Manager, valuation and financial modelling, to lead transaction valuation, financial modelling and deal analysis. Reporting directly to Head of Corporate Development, you will be a key member of the Business Development & Corporate Strategy division, evaluating and structuring strategic transactions that drive the company's long-term growth.
This role offers significant exposure to senior leadership and provides a unique opportunity to influence high-impact business decisions through rigorous analysis and strategic thinking.
(*Please note, the internal title for this role is Manager, Corporate Development, Business Development & Corporate Strategy)
Responsibilities
Build integrated financial models for strategic transactions, covering P&L, cash flow, valuation.
Assess transaction economics, evaluate deal structures, and identify key risks and value drivers.
Support the underlying patient and market-based sales forecasts, incorporating epidemiology, patient journeys, pricing, market access, launch timing, market penetration, and competitive dynamics across multiple geographies.
Present transaction analyses, recommendations, and potential outcomes to senior management and executive leadership.
Partner with Corporate Strategy and cross-functional stakeholders to support Long-Range Plan, Board of Directors materials, investment cases, and strategic financial assessments.
Conduct post-deal reviews to evaluate performance, capture insights, and incorporate key learnings into future business development activities.
Support negotiations and contribute to the structuring of strategic transactions.
Requirements:
3-7 years of relevant experience in investment banking, management consulting, Big Four Transaction Services/Deals, corporate development, business development, FP&A or a related field.
Advanced Excel skills is a must, with hands-on professional experience building complex financial models. Proficiency in advanced functions and techniques.
Deep expertise in financial analysis, valuation methodologies, and deal structuring, including DCF, NPV, IRR, risk-adjusted modeling, scenario analysis, and transaction economics.
Bachelor's degree in finance, economics, accounting, business, or another relevant discipline.; MBA, CFA, or other advanced degree is an advantage.
Highly motivated, entrepreneurial, hands-on, and comfortable operating in a dynamic, high-growth environment.
Excellent communication and presentation skills, with the ability to influence senior stakeholders.
Strong collaboration skills and a demonstrated ability to build trust and alignment across functions and organizational levels.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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Location: Petah Tikva
Job Type: Full Time
Medison is a rapidly growing global pharmaceutical company with a strong international footprint, operating across 4 continents and more than 24 countries. Our mission is to expand access to highly innovative therapies for patients suffering primarily from cancer and rare diseases across global markets. If you are motivated by impact, complexity, and building scalable global capabilities, we invite you to join our mission. We are seeking a highly skilled, experienced, and strategic New Partner and Product Integration (NPPI) Lead to drive end?to?end excellence in onboarding, planning, and operational integration of new strategic partners into Medison’s global ecosystem. This role will lead and coordinate all cross-functional activities - including Supply Chain, Regulatory Affairs, Pharmacovigilance, Quality Assurance, Finance, Legal, Medical, and Commercial - ensuring alignment with the Medison Partner Integration Playbook. The primary objective is to enable rapid, seamless integration of new partners while ensuring all activities remain on track for timely, launch-ready product delivery. This role is critical to ensuring readiness, alignment, coordination and flawless execution across functions and geographies when introducing new partners, assets, or collaborations. The NPPI Lead will design, lead, and continuously enhance Medison’s global New Partner and Product Integration Playbook and framework, acting as the central PMO and orchestration point across global, and regional teams. The role partners closely with the Global Brand & Alliance Lead while owning structured planning, risk mitigation, governance, and performance tracking from deal signing through full operational handover. This is a global role requiring strong PMO expertise, cross?functional leadership, strong business acumen and operational rigor in complex, fast?moving environments. The position reports to the Global Head of Commercial Operations. Location is flexible, preferably in Central Eastern Europe. Regular international travel is expected.



Responsibilities:
New Partner and Product Integration Strategy & Framework Development
* Develop, refine, and implement a standardized global New Partner and Product Integration (NPPI) framework, including governance, detailed playbooks, templates, and activity trackers, to ensure consistent and high-quality partner onboarding across all regions.
* Design end?to?end NPPI roadmaps and integrated plans, covering commercial, medical, regulatory, supply, quality, IT/data, and financial readiness.
* Build structured timeline planning, dependency mapping, and milestone tracking tools to ensure alignment between Medison and partner organizations.
* Define and monitor clear KPIs, dashboards, and success metrics to track NPI progress, readiness, risks, and value realization across countries and functions. PMO Leadership & Cross?Functional Coordination
* Act as the central PMO lead for all New Partner Integrations, ensuring disciplined planning, execution, and governance across multiple concurrent initiatives.
* Lead the global NPPI Steering Committees and Working Groups, aligning Commercial, Medical, Market Access, Regulatory, Supply Chain, Quality, Alliance Management, Finance, IT, and Legal teams.
* In close collaboration with the relevant global functional lead, engage regional or local teams as needed to address specific issues, ensuring they are resolved efficiently and promptly.
* Partner closely with Global Launch Excellence and Global Brand & Alliance Lead to translate deal terms into clear, executable operational plans, including aligned systems and processes, supporting the delivery of integrated global go-to-market, launch, and brand plans with defined ownership and milestones.
* Proactively identify interdependencies, resource constraints, and critical path items, driving timely decision?making and issue resolution. Partner & Product Integration and Rea
Requirements:
This position is open to all candidates.
 
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3 ימים
Location: Ramat Gan
Job Type: Full Time
We are looking for a clinician with a background in medical psychology to join our multidisciplinary team as Therapeutics Program Manager. The ideal candidate will demonstrate the ability to translate psychological interventions into protocols that fit a digitized format, with a product-oriented mindset, strong English writing skills and a commitment to integrative, holistic, and patient-centered approaches to chronic disease management.

What Youll Do
Clinical Protocol & Framework Development - Develop, research, and refine psychological therapeutic protocols and care frameworks grounded in evidence-based, integrative, and holistic approaches. Transform these into concise, actionable treatment pathways.
‍Digital Translation of Therapeutic Content - Create psychological therapeutic protocols that can integrate into digital therapeutics and product features. Collaborate with product, design, and engineering teams to ensure clinical accuracy and usability in digital implementations.
‍Clinical Content Creation - Write and edit high-quality clinical materials, care protocols, and white papers. Review and synthesize clinical literature with scientific rigor and clarity.
‍Expert Collaboration - Engage in discussions with physicians, therapists, scientists, and other clinical domain experts. Capture essential insights and integrate them into well-structured, clinically meaningful content.
‍Research & Literature Analysis - Conduct literature reviews on therapeutic modalities, chronic disease management, integrative care, and rehabilitation sciences. Assess emerging evidence and incorporate validated insights into therapeutic frameworks.
‍Holistic & Integrative Perspective - Maintain a systems-level, whole-person viewpoint blending conventional clinical practice with complementary and lifestyle-based interventions. Stay informed about developments across integrative medicine and digital health.
Requirements:
Medical psychology or similar background required
Experience working with CBT, ACT and mindfulness
Experience in integrating technology into treatment.
Direct experience working with patients with chronic conditions in clinical settings. Preference for experience in the fields of neurology, womens health, and oncology.
Strong academic writing and research abilities, with experience producing structured, evidence-informed material.
Experience in developing or contributing to clinical protocols, care pathways, or therapeutic programs is strongly preferred.
Exceptional ability to synthesize complex information and distill it into clear, organized, accurate content.Deep interest in holistic, integrative, whole-person care approaches.
Excellent communication skills and comfort collaborating with cross-disciplinary team members.
High-level proficiency in both written and spoken English
This position is open to all candidates.
 
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חברה חסויה
Location: Ramat Gan
Job Type: Full Time
Required SMB Account Manager - Benefits
What youll be doing:
As an SMB Account Manager, youll be joining the growing Benefits team. As part of this team, youll play a crucial role in scaling a solution that is redefining how we serve our SMB & corporate partners.
This role focuses on managing a portfolio of SMB clients, from onboarding to long-term support, while driving excellent service and business growth.
Day-to-day in this role youll:
Manage a portfolio of SMB clients - building strong relationships at senior levels and ensuring mutual success.
Lead and manage company launches end-to-end - including planning and executing launch events, delivering employee and manager training sessions, and providing close guidance throughout the implementation process.
Own the full client lifecycle - from identifying opportunities and pitching solutions, to providing long-term strategic support.
Collaborate cross-functionally with Product, Marketing, Support, and Operations to tailor solutions to client needs and ensure delivery excellence.
Analyze account performance and market trends to identify areas for optimization and growth.
Represent us at industry events and client meetings, positioning us as a partner of choice in the B2B space.
Drive initiatives to improve client satisfaction, retention, and revenue growth - working closely with our internal Support and Operations teams to ensure a smooth, high-quality client experience at every touchpoint.
Requirements:
Background in account management, business development, or partnerships with B2B partners - 2-4 years
Demonstrates strong commercial acumen and an understanding of business dynamics, especially in B2B or partnership settings.
Brings strong relationship-building skills, with the ability to influence senior stakeholders internally and externally.
Is data-driven and skilled at transforming insights into actionable business decisions.
Is an independent self-starter, able to prioritize, make decisions, and drive initiatives with ownership and accountability.
Thrives in a dynamic, fast-paced environment, and enjoys building things from the ground up.
Is fluent in both Hebrew and English (spoken and written).
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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5 ימים
Location: Tel Aviv-Yafo
Job Type: Full Time
We're looking for problem-solving, opportunity-finding teammates with a sense of urgency, who believe in the scale of our ambition and thrive on a path not fully paved - people who want to grow their careers alongside a team of experts across energy, manufacturing, data center construction, and cloud services.
If you want to do the most meaningful work of your career, help our customers and partners advance their AI strategies, and be part of a high-performing team that believes in each other, come build with us at our company.
About This Role:
As the Business Development, Strategic Initiatives, you will serve as the "Demand-Side Translator" and the critical bridge between the worlds most advanced AI labs and our companys internal Product, Engineering, and Capacity (DIG) teams. You aren't just closing deals; you are architecting the evolution of our cloud platform. By owning strategic relationships with industry leaders, you will integrate complex architectural needs-from networking requirements to storage I/O constraints-directly into our product roadmap and capacity planning. Your work ensures that Crusoes infrastructure is built with surgical precision to meet the demands of the next generation of AI.
The ideal candidate is a "rare hybrid" who possesses elite commercial acumen and a deep technical foundation in cloud infrastructure. You are the ultimate midfielder, capable of discussing K8s and KV caching with engineers in the morning and negotiating $200M+ TCV compute contracts with C-suite executives in the afternoon. You understand the full vertical chain, from how a utility deposit in Texas impacts silicon supply to how a GPU allocation influences the final product delivered to the customer. This is a full-time position dedicated to aligning the future of computing with the future of the climate.
What Youll Be Working On:
Strategic Deal Orchestration: Lead and close nine-figure, multi-year compute and managed inference deals with the worlds top AI developers to drive massive-scale revenue growth.
Customer-Driven Roadmap Integration: Translate the highly technical requirements of "whale" clients into actionable directives for our companys Product and Engineering leadership to ensure our platform stays ahead of market needs.
Cross-Functional Synchronization: Partner closely with the Data Center Infrastructure (DIG) and Energy teams to map customer model architecture impacts directly to power procurement and site planning.
GTM Strategy & Commercialization: Drive the go-to-market motion for complex new offerings, including Managed Inference, Managed K8s, and Bare Metal clusters, ensuring Sales and Marketing are equipped to win.
Stakeholder Management: Act as a technical authority and lead negotiator, influencing C-level executives both internally and externally to align long-term infrastructure investments with customer demand.
Process Improvement & Risk Mitigation: Identify potential bottlenecks in the silicon supply chain or power allocation early, developing strategies to mitigate risks before they impact customer delivery.
Requirements:
Extensive Cloud Deal Experience: A proven track record of structuring and closing complex, massive-scale cloud consumption deals exceeding $100M in Total Contract Value (TCV).
Technical Authority: Practical, deep-seated knowledge of AI workloads, distributed computing frameworks (Slurm, Kubernetes), high-performance networking (RDMA/InfiniBand/RoCE), and storage architectures.
Professional Experience: At least 5+ years of high-level experience in Product Management, Business Development, or Strategic Partnerships within the technology sector.
Hyperscaler Background: Previous leadership experience at a major hyperscaler (AWS, GCP, Azure), a leading AI startup, or a top-tier cloud infrastructure provider.
This position is open to all candidates.
 
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חברה חסויה
Location: Work At Home
Job Type: Full Time
we are looking for a CTC/Sr CTC - FSP - EMEA.
As part of our global team, youll have the opportunity to provide administrative and technical support to the Project Team. As a Senior Clinical Trial Coordinator, you'll coordinate and facilitate project activities and may serve as a study lead, acting as a cross-functional liaison for the project team. You will act as a buddy during the onboarding phase and provide training to new staff as needed. Additionally, you will support departmental and cross-functional initiatives for process improvements and enhancements.
What Youll Do:
According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate.
Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers including but not limited to: study team lists, tracking of project specific training requirements, system access management for organization/vendor/clients, and tracking of project level activity plans in appropriate system. Ensures (e)TMF is up to date by following file review schedules and documents findings in appropriate system.
Provides system support (i.e. GoBalto & eTMF).
Supports RBM activities.
Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members.
Supports scheduling and organization of client and/or internal meetings with completion of related meeting minutes.
Reviews and tracks local regulatory documents.
Transmits documents to client and centralized IRB/IEC.
Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.
Maintains vendor trackers.
Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites.
Assists with study-specific translation materials and translation QC upon request.
May attend Kick off meeting and take notes when required.
דרישות:
High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
Bachelor's degree preferred.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
Ability to work in a team or independently as required
Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Strong customer focus
Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines
Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout
Excellent English language and grammar skills and proficient local language skills as needed
Good presentation skills
Excellent computer skills, proficient in המשרה מיועדת לנשים ולגברים כאחד.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8758390
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סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
3 ימים
חברה חסויה
Location: Ramat Gan
Job Type: Full Time
We are looking for a Therapeutics Program Manager to join our multidisciplinary team. This role is ideal for someone with a strong clinical background or deep experience working within clinical, therapeutic, or healthcare environments, whether from medicine, rehabilitation or allied health. The ideal candidate will demonstrate the ability to translate therapeutic interventions into protocols that fit a digitized format, with a product-oriented mindset, strong English writing skills and a commitment to integrative, holistic, and patient-centered approaches to chronic disease management.
Work Environment
This full-time role is based in our office in Ramat Gan, offering the opportunity to collaborate closely with our dynamic team in person.

Key Responsibilities
Clinical Protocol & Framework Development
Develop, research, and refine therapeutic protocols and care frameworks grounded in evidence-based, integrative, and holistic approaches.
Transform complex, multidisciplinary clinical discussions into concise, actionable treatment pathways.
Digital Translation of Therapeutic Content
Create therapeutic protocols that can integrate into digital therapeutics and product features.
Collaborate with product, design, and engineering teams to ensure clinical accuracy and usability in digital implementations.
Clinical Content Creation
Write and edit high-quality clinical materials, care protocols, and white papers.
Review and synthesize clinical literature with scientific rigor and clarity.
Expert Collaboration
Engage in discussions with physicians, therapists, scientists, and other clinical domain experts.
Capture essential insights and translate them into well-structured, clinically meaningful content.
Research & Literature Analysis
Conduct literature reviews on therapeutic modalities, chronic disease management, integrative care, and rehabilitation sciences.
Assess emerging evidence and incorporate validated insights into therapeutic frameworks.
Holistic & Integrative Perspective
Maintain a systems-level, whole-person viewpoint blending conventional clinical practice with complementary and lifestyle-based interventions.
Stay informed about developments across integrative medicine and digital health.
Requirements:
Clinical background required (e.g. in physical therapy, occupational therapy, speech and language therapy, MD or similar clinical professional).
Experience in integrating technology into treatment.
Direct experience working with patients in clinical or therapeutic settings.
Strong academic writing and research abilities, with experience producing structured, evidence-informed material.
Experience in developing or contributing to clinical protocols, care pathways, or therapeutic programs is strongly preferred.
Exceptional ability to synthesize complex information and distill it into clear, organized, accurate content.
Deep interest in holistic, integrative, whole-person care approaches.
Excellent communication skills and comfort collaborating with cross-disciplinary team members.
High-level proficiency in both written and spoken English
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8800870
סגור
שירות זה פתוח ללקוחות VIP בלבד
סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
5 ימים
Location: Tel Aviv-Yafo
Job Type: Full Time
We're looking for problem-solving, opportunity-finding teammates with a sense of urgency, who believe in the scale of our ambition and thrive on a path not fully paved - people who want to grow their careers alongside a team of experts across energy, manufacturing, data center construction, and cloud services.
If you want to do the most meaningful work of your career, help our customers and partners advance their AI strategies, and be part of a high-performing team that believes in each other, come build with us at our company.
About This Role:
As Business Development, Technical Partner, you will serve as the end-to-end dealmaker at the intersection of datacenter construction, infrastructure finance, and AI compute demand. This is not a traditional sales role - you are the single owner of complex, multi-stakeholder opportunities spanning site selection, build financing, and capacity commercialization. By building deep relationships with datacenter developers, colocation operators, financial partners, and government stakeholders, you will architect deals that directly shape our company's physical infrastructure footprint and long-term commercial trajectory.
The ideal candidate combines hands-on knowledge of how datacenters are built and financed - power procurement, shell construction, critical systems fit-out - with the financial structuring fluency of a leading investment bank or infrastructure-focused private equity firm. You understand the full development lifecycle, from greenfield site evaluation through energization, and know how to structure the commercial and financial frameworks that make large-scale builds viable.
What You'll Be Working On:
Datacenter Development & Co-location Sourcing: Lead the identification, evaluation, and negotiation of datacenter opportunities - both ground-up builds and colocation arrangements. Assess sites across key technical dimensions: power availability and utility interconnection timelines, critical load capacity, cooling infrastructure, fiber access, and physical security. Own key deal metrics including all-in cost per MW, construction schedules, and long-term capacity optionality.
Financial Structuring & Deal Architecture: Structure complex agreements with datacenter developers and colocation partners, including backstop mechanisms, capacity reservation frameworks, and construction-phase financing arrangements.
Business Development & Customer Relationships: Build and own a portfolio of enterprise customer relationships across the AI developer ecosystem. Translate customer compute requirements - cluster scale, networking topology, power density per rack - into site-level specifications that inform development decisions. Partner closely with Account Executives to drive opportunities from origination through close.
Government & Regulatory Relationships: Cultivate and maintain strategic relationships with Israeli government stakeholders.
Requirements:
Datacenter Development Expertise: Direct experience with the technical and commercial dimensions of datacenter builds - including site due diligence, power procurement, utility negotiations, critical systems design (UPS, cooling, generators), and construction milestone management. Ability to evaluate a site's feasibility and model its economics from first principles.
Financial Orientation & Structuring Experience: A background at a leading investment bank, infrastructure-focused private equity firm, or project finance institution. Demonstrated ability to structure and negotiate complex financial arrangements, including capacity backstops, long-term offtake agreements, construction financing, and sale-leaseback structures.
Government & Public Sector Fluency: Established relationships or demonstrated experience engaging with Israeli government institutions, defense-adjacent agencies, or regional regulatory bodies. Comfort navigating formal procurement frameworks and policy environments.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8797840
סגור
שירות זה פתוח ללקוחות VIP בלבד