We are looking for a Medical writer and Regulatory Affairs associate.
Roles and Responsibilities:
Work with clinical teams and clients to understand the nature of the scientific work that they will be covering.
Assess data or products using medical expertise, and quickly develop expertise in new areas as needed for their writing.
Help to write studies for submissions to the FDA. The writing is also used in publications or medical journals, or for internal company use.
Comprehensive writing of clinical study reports, study protocols, annual reports, investigator brochures, risk/benefit analysis and integrated summaries from raw data.
Prepare abstracts, scientific exhibits, posters and verbal presentations.
Help with develop and write pharmaceutical training materials, eLearning content, video scripts, magazine articles, and presentations to be used by a variety of audiences.
Conduct comprehensive literature searches to enhance background understanding, and evaluate and analyze the information which will be written about.
Provide responses to regulatory agencies regarding product information or issues.
Maintain current knowledge of relevant regulations, including proposed and final rules. Help in manage activities such as audits, regulatory agency inspections etc.
Participate in the development or implementation of clinical trial protocols. Preparation and submission of regulatory agency applications, reports, or correspondence.
Provide regulatory guidance to departments or development project teams regarding design, development, evaluation, or marketing of products.
Primary function of the position
Clinical scientific knowledge and writing skills to effectively and clearly communicate medical science information in writing. Generally, focus on either scientific medical writing, which includes clinical studies, and regulatory documents, scientific articles or marketing medical writing. Experience in regulatory aspects (RA), help to lead regulatory strategy and provide ongoing regulatory input.

Medison offers hope to patients suffering from rare and severe diseases by forming partnerships with emerging biotech companies to accelerate access to highly innovative therapies in international markets. As the creator and leader of the global partnership category in the pharma industry, we strive to be Always Ahead and work relentlessly to bring therapy to patients in need, no matter where they live. Our values are at the core of every action we take, and we are committed to going above and beyond for the benefit of the patients we serve. We are a dynamic, fast-paced company operating in over 25 countries on 5 continents. We are looking for out-of-the-box thinkers, people who are passionate, caring, agile, and adaptive, to join us on our mission. If you want to make a difference in people's lives, we invite you to join us! The product manager will be responsible for fully managing the commercial aspects of the product- strategy, budgeting, and business plan, including its execution, and checking if it meets its target. Working closely with overseas partners, having an in-depth understanding of the field, and KOL's. The role combines working in the field, implementing and monitoring unique projects, and working at the office. It also combines managing the field force.

Responsibilities:

* Full ownership of the products, leading them to sales targets
* Collect in-field,cross-functional, and market analysis data and synthesize insights and stakeholders’ behavior and drivers
* Work with a cross-functional team to build a strategic business cross-functional plan based on strategic objectives and define KPIs
* Build a tactical plan including innovative tactics and omni-channel plan to meet strategic objectives
* Execute tactical plan according to KPIs, objectives, and timeline, and monitor it.
* Prepare & execute a budget plan.
* Build and manage a territory plan and monitor it.
* Management of field force, including KPIs setting, planning and monitoring field work, employees development, and recruitment to handle complex field projects.
* Project Management: Identifying and driving critical projects that generate exponential growth
* Develop marketing material for in-field use in collaboration with the partner and according to local regulatory requirements.
* Working with the medical manager to analyze scientific data and present to stakeholders
* Troubleshoot and objection handling.
* Work in accordance with the company code of ethics and guidelines laid down by the regulatory department.
* Work with the internal team to find solutions to get things done in a simplified way.
* Business meetings with overseas partners, training sessions, conferences, etc
* Participation in conferences in Israel and abroad according to strategic priorities.

we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at our cpmpany enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the way its about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.Our ValuesWe Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer careWe Make It Happen: We act with urgency, commit to quality, and bring fun to our hard workWe Are Stronger Together: We collaborate openly, seek to understand, and celebrate our winsWe Care Deeply: We embrace our differences, do the right thing, and encourage each otherThe PositionWe are looking for a Bioinformatics Scientist, experienced in high-throughput DNA data analysis and with a strong interest in genomics and algorithm development. The successful candidate will provide support for analysis of large and complex genomics data sets related to cancer and will empower, through the specific domain knowledge and experience, the various aspects related to the research and development of our tools and products.An essential role of this position is to engineer, in collaboration with R&D and production team members, high-quality tools for genomic sequence data analysis while adhering to our state of the art software engineering methodologies. The bioinformatician will create novel tools, customize existing and third-party tools to implement new or improve existing applications of our products.The successful candidate will be an essential team player in the effort for significant optimization of our growing genomic data analytic platform. This entails working cross-functionally with data scientists, clinical analysts, software engineers, and business analysts to ensure our genomic data becomes a powerful asset and value growth driver. Specifically, the candidate will participate in the design and prototyping of processing pipelines and algorithms for analysis of the genetic data to improve clinical performance and to optimize the entire system to shorten the processing times and costs. The ideal candidate will have the ability to see the big picture, understand user needs and requirements, and identify the opportunities for applying solutions from bioinformatics, algorithms, and data science domains.This is a remote position based out of our Israel office. ResponsibilitiesAnalyze next-generation high-throughput DNA sequencing data ranging from single research experiments to very large data setsDevelop tools and automated analysis pipelines for bioinformatics analyses, diagnostic tests, including variant detection and quality control Design new algorithms, methods and tools for DNA sequencing data analysis and propose improvements to the existing research infrastructure Produce high quality written documentation including study plans and reports Produce correct conclusions based on rigorous mathematical analysis and principles of statistics and probability Collaborate effectively with R&D, production, and clinical teams to build efficient workflows Be the "go to" person for bioinformatics and related issues Ensure internal processes and metrics are aligned to create the highest product quality and competitive advantage Develop Python software infrastructure to support algorithm testing and simulation studies Produce clear, concise and correct technical documentation including research reports and algorithm specifications

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

you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life
The Regulatory Affairs Post-Market Specialist leads and executes key post-market activities to ensure compliance with the Israeli Ministry of Health (AMAR) and requirements. This includes managing adverse event (vigilance) reporting, coordinating Field Safety Corrective Actions (FSCAs), and serving as a regulatory contact for post-market issues in Israel. The role involves close collaboration with cross-functional and global teams to maintain the highest standards of quality and patient safety.

Responsibilities may include the following and other duties may be assigned:
Lead the execution and follow-up of Field Safety Corrective Actions (FSCAs) including coordination with internal teams, customers, and submission to the Ministry of Health (MOH)
Manage the adverse event (vigilance) reporting process to the Israeli MOH, ensuring timely and accurate submissions in accordance with local regulatory timelines and guidelines
Collaborate closely with internal stakeholders including global post market teams to ensure consistent and compliant execution of post-market activities
Serve as a regulatory contact for the Israeli MOH on all post-market issues, including adverse events, recalls, field actions, and periodic updates
Stay up to date with changes in AMAR regulations, MOH guidelines, and industry standards, and communicate potential impacts to management and relevant teams
Participate in the local recall committee or crisis response team in the event of product safety issues requiring urgent action
Provide training to local teams on vigilance reporting, complaint handling, and FSCA procedures to ensure consistent and compliant practices

Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.
Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.

​Medical​
Our Sales teams help to deliver purpose by building shared success with our customers, making access to the highest quality hygiene, wellness, and nourishment possible in-stores and online.
Within Sales, we're focused on achieving outperformance across all of our channels, operating in highly competitive categories. This focus results in a dynamic, fast paced environment where cross functional teams are encouraged to collaborate to achieve success.
We have around 10,000 sales people across the world, within market roles and ranging in areas like Field Sales, Key Accounts, Trade Marketing and Category Development.

About the role
Working with Pediatricians, GP and pharmaceutical in sick fund clinics. Youll take ownership for your own area of the business. Managing your own territory. Youll build trust and relationships. Youll educate doctors, medical and pharmaceutical specialists to understand the benefits of our products. Ultimately helping to improve the lives of millions of patients.

Your responsibilities
Responsibility for a defined customer line in the Southern region
Responsibility for detailing meeting targets
Concern and treatment of the availability and visibility of products on the shelf.
What we offer
With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way.

We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with pay for performance philosophy.

Equality
We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you.
All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.

Required Organic Researcher 1
We enjoy food so much that sometimes we forget how complicated it is to produce. It sometimes takes months of hard work and efforts to grow the vegetables in our salad. Even the milk that we consume comes from a cow that eats 7 tons of grain in a single year.
More than 90% of our food comes from what framers grow. Imagine if almost half of the worlds growing populations' food would disappear. That's exactly what would happen if farmers would not be able to protect their crops from weeds, insects, and diseases. For decades, We have been helping framers to do just that.
We are one of the worlds largest crop protection companies. Being a part of the Syngenta group, a leading agricultural innovation group, we make our best efforts to meet the worlds future food challenges. Our global distribution expands to more than 100 countries in which we deliver what farmers need to be able to produce the highest quality products.
An expert company in crop protection. We consonantly invest in research and development, daring to innovate and create new solutions to protect the worlds best foods.
Today, we operate five global R&D research centers in four countries: two in Israel (MCW and Agan), China, India and Brazil. The R&D centers include organic chemistry, analytical chemistry, formulations, and pilot units.
We offer a highly rewarding career opportunity for a strongly motivated and professional candidate to join our Organic Chemistry R&D Department as a Researcher at Makhteshim in Neot Hovav.
In our Organic Chemistry R&D Department, you will take an influencing part in the development of new and innovative chemical processes, troubleshooting of various chemical production challenges, improvement of existing chemical procedures and handle diverse interactions with various interfaces inside and outside.
Areas of Responsibility
Experimental work in a synthetic organic lab.
Conducting and analyzing literature reviews.
Planning, performing, and analyzing experimental work at the laboratory level.
Preparation of summaries and conclusions of experiments.
Cooperation with internal units such as analytical, pilot and manufacturing departments.
Support the product development cycle from early development to manufacturing launch and beyond.

We are offering you to take a vital role in our research team that is responsible for constantly driving forward our ability to detect accessibility issues, enhancing the intelligence of our platform to provide customers with insights and usability enhancements that allow them to work more efficiently, and building innovative new products

To achieve those ends the team employs classic algorithms, data analysis, machine learning and generative AI.

You will be joining a team of highly professional and innovative engineers and scientists that are driven by passion for the domain and the mission of the company. We value scientific and engineering excellence, are committed to creating high impact products that reach our customers and work in collaboration with each other in an egoless environment.

Your Impact:
Research, design and implement new detection algorithms for web accessibility issues and improve existing ones.
Ensure all research is well documented and reproducible.
Build and enhance tools that enable data collection, labeling and analysis at scale for research purposes.
Integrate new models and algorithms into existing products.
Build interfaces for projects in the POC phase to enable demonstration and the collection of feedback from internal users and select design partners.

Were based in Tel Aviv, 5 minutes from Hashalom train station, and Yehudit light train station, and we have our own parking lot. We work in a hybrid mode, with flexible working hours.