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If you want to be part of a leading CRO and transform scientific discoveries into new treatments, then we challenge you to live up to your potential by joining us at SCRA, home-based, Isreal.We are looking for hard-working, talented, high-caliber people. We know that employee satisfaction leads to customer satisfaction, which is the ultimate driver of long-term success.As the company that conducts vital clinical studies for sponsors, including the world's leading biotechs and top 50 pharmaceutical companies, we offer you enormous security and long-term prospects.Our CRAs work from their home office base, supporting studies within their country or region. Manageable sites, manageable protocols is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.The most significant aspect of this position is that You will be dedicated to a single client You will be responsible for all site management and supervisory activities in the assigned oncology studies. You will work with industry leaders and subject matter experts. You will have the opportunity to mentor junior CRAs. You will work with world-class technology. You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.Our people and their passion are very important to us as they are the key to our success. That's why we provide you with an open and friendly working environment where we empower people and provide them with opportunities to develop their careers in the long term. In addition, you will have the opportunity to develop within your role and take on more responsibility or develop your skill set within other related our company's departments.

Are you ready to lead and inspire? As a Local Study Associate Director (LSAD), you will lead Local Study Teams (LSTs) at the country level to deliver clinical studies within agreed resources, budget, and timelines. You will ensure compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations. In addition to leading LSTs, you may perform site monitoring as needed to support the flexible capacity model. Your role will be crucial in identifying sites, performing site qualifications, setting up, initiating, monitoring, closing, and archiving documentation.

Accountabilities
Overall responsibility for study commitments within the country and timely delivery of data to required quality.
Lead Local Study Team consisting of CRA(s), CSA(s) for assigned study/studies.
Optimize the performance of Local Study Team(s) ensuring compliance with AZ Procedural Documents, ICH-GCP, and local regulations.
Ensure high-quality clinical and operational feasibility assessments of potential studies.
Coordinate site selection by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits.
Ensure timely submission of application/documents to EC/IRB and Regulatory Authority.
Prepare and maintain accurate study budgets in AZ clinical studies financial system.
Prepare local Master CSA (including site budget) and amendments as needed.
Prepare country level Master Informed Consent Form (MICF) and subsequent site level ICFs.
Collect and verify trial essential documents prior to study start.
Plan and coordinate local drug activities.
Set up and maintain the study in CTMS at study country level.
Oversee monitoring activities from site activation through to study closure.
Review monitoring visit reports and advise monitors on study-related matters.
Perform co-monitoring, Accompanied Site Visits/training visits with study CRAs.
Identify risks and facilitate resolution of complex study problems.
Organize regular Local Study Team meetings.
Maintain good personal relationships with all Local Study Team members, sites staff, and global stakeholders.
Report study progress/update to the Global Study Associate Director/Global Study Team.
Contribute to patient recruitment strategy.
Develop and review risk management plan on country study level.
Communicate regularly with National Co-ordinating Investigator/National Lead Investigator on recruitment and other study matters.
Plan and lead National Investigator meetings. Assist in forecasting study timelines, resources, recruitment, budget, study materials, and drug supplies.
Ensure relevant systems are set-up, updated, and access is organized at country level.
Ensure accurate payments related to the study are performed according to local regulations and agreements.
Participate in training and coaching new members of the Local Study Team.
Ensure completeness of the eTMF and maintain it Inspection Ready.
Ensure all study documents are ready for final archiving and completion of local part of the eTMF.
Plan and lead activities associated with audits and regulatory inspections.
Provide input to process development and improvement.
Provide regular information to Line Managers at country level on study/ies and planned study milestones/key issues.
Update Line Managers about the performance of the CRAs/CSAs.
Ensure compliance with local policies and code of ethics.
Provide feedback on research-related information useful for the local market.
Collaborate with local Medical Affairs team.
Support SMM in different initiatives as agreed with SMM Line Management.

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 are looking to make a difference in people's lives, we invite you to join us! The position includes all aspects of quality assurance for all companies in the group. Job includes: Drafting new SOPs and updating existing SOPS and reports according to GMP and GDP regulations. Build and follow up work processes, set yearly training and conduct continuous training sessions for employees and suppliers. Document training. Conduct validation and monitor prevention and improvement activities (CAPA). Assist in preparing for inspections, executing internal auditing and partner audits as needed. Qualify suppliers, manage investigations and deviations. Risk management and support regulatory and operations divisions. Prepare specified yearly quality reports and be of assistance to manager in any way required. Quality activities are not inspections, rather supervision. The purpose is to coordinate the company's management and regulatory efforts in a specific field.

Responsibilities:

* Ensure that the quality assurance system is implemented in a way that the approved activities can be managed.
* Ensure precision and quality where listed and approve inspected documents.
* Supervising that employee training is implemented and maintained.
* Handle changes and deviations according to managers' requirements. Implement preventative and correction measures when necessary.
* Ensure implementation of periodic management survey.
* Ensure implementation of risk management.
* Ensure that suppliers and partners are approved and qualified.
* Approve every activity performed by sub-contractor that may indicate the quality of the
* products.
* Implement and ensure that internal inspections are carried out regularly and according to a set plan and ensure that corrective actions are set up after inspections.
* Keep account of all assignments carried out for person/company.
* File all relevant documentation.
* Carry out any task requested by superior.
* The role includes leading, coordinating and performing, validation and calibration activities in the warehouse areas and distribution-- vehicles. Occasionally, early work hours are require

were passionate about simplifying healthcare by automating the accurate interpretation of clinical language.
Our interdisciplinary team has developed innovative technology that understands clinical language, offering a groundbreaking way to analyze and decode medical records into clear, concise, and actionable information. This ensures that clinical and administrative teams can dedicate more time to patient care.

the future is bright. Our engine currently processes over six million charts annually across more than 300 emergency departments and urgent care settings in the U.S. Backed by top-tier VCs, we are growing rapidly, with offices in NYC and Tel Aviv.

Role and Responsibilities:
looking for a Medical Developer to join our growing R&D group, reporting to our Chief Architect. The ideal candidate will play a key role in developing new sub-engines for emerging projects and clients. This role involves maintaining and improving product quality, upholding high coding standards, and driving customer satisfaction.

Success in this role requires strong project management experience, analytical and problem-solving skills, cross-team collaboration, and a flexible, solution-oriented mindset in a dynamic environment.

As a Medical Developer, you will:
Analyze and understand clients business objectives and needs, designing Clinical Language Understanding engine accordingly.
Lead new specialty projects, guiding technical development, identifying and recommending improvements, and proactively resolving alerts and escalated issues.
Collaborate with multidisciplinary teams, including customer success, R&D (software engineers, linguists, medical doctors, product managers, data analysts, and medical coders).

We seek a highly motivated and experienced Senior Researcher to join our dynamic team. This role is pivotal in advancing our companys collaboration with leading academic institutions and healthcare organizations globally and helping our company deliver cutting-edge insights that support business growth and B2B opportunities. The ideal candidate will contribute to the entire research lifecyclefrom study design to publication.
Responsibilities
Research Collaboration:
Work closely with universities, academic institutions, and research teams worldwide to design, execute, and manage collaborative studies focused on metabolic health and performance.
Study Design & Execution:
Develop robust study designs tailored to explore metabolic health, fitness optimization, and related areas. Oversee the execution of studies, ensuring alignment with scientific standards and ethical guidelines.
Data Analysis & Insight Generation:
Analyze study and retrospective data to extract actionable insights that advance metabolic research and support our company's product development, marketing, and B2B initiatives.
Publication & Thought Leadership:
Lead the drafting and submission of high-quality manuscripts to peer-reviewed journals.
Innovation & Product Integration:
Collaborate with cross-functional teams to translate research findings into innovative product features, user education materials, and growth strategies.
Strategic Input:
Provide strategic insights to enhance our companys position as a metabolic health research leader. Identify new research opportunities that align with business goals.
Why Join us?
Be part of a company that is redefining metabolic health through groundbreaking research and technology.
Collaborate with top-tier universities and institutions worldwide.
Work in a fast-paced, innovative environment that values curiosity, creativity, and impact.
Contribute to insights that drive global health and wellness improvements.