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📑 **Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) te ...

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📑 Are you a freelance translator with a passion for life sciences content? Join us on an exciting journey and become a member of our growing global community of linguists. The IQVIA Translation Services team is looking for freelance translators from English into Hebrew. You will work with a truly global industry leader to deliver content in our targe ...

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📑 Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. **RESPONSIBILITIES** + Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex + Ability to administratively and te ...

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📑 Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs **RESPONSIBILITIES** + Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Ove ...

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📑 The Internal Translator is responsible for linguistically and culturally interpreting the written material in a way that maintains or duplicates the structure and style of the original text while keeping the ideas and facts of the original material accurate. They possess fluency in two or more languages and skills that allow for them to re ...

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📑 **Job Overview** Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. **Essential Functions** • Perform site monitoring visits (selection, initiat ...

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📑 **Job Overview** Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. **Essential Functions** • Perform site monitoring visits (selection, initiat ...

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📑 The Internal Translator is responsible for linguistically and culturally interpreting the written material in a way that maintains or duplicates the structure and style of the original text while keeping the ideas and facts of the original material accurate. They possess fluency in two or more languages and skills that allow for them to r ...

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📑 **Job Overview** Provides administrative and/or technical support. **Essential Functions** • Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors’ studies, as well as reconcile the total GPS Sponsor balance to the Corporate Sponsor Balance on a monthly basis per S ...

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📑 Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scie ...

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📑 Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a ...

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📑 Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, initiation, ...

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📑 Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, initiation, ...

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📑 Job Overview Provides administrative and/or technical support. Essential Functions • Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors’ studies, as well as reconcile the total GPS Sponsor balance to the Corporate Sponsor Balance on a monthly basis per SSAE16 ...

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📑 a global medical device comany is looking for an experienced clinical project manager to to join our clinical team and take part in planning clinical trials. Duties and Responsibilities:Serve as a liaison between the company and the study site, investigators, study coordinators, and staff membersCoordinate activities to s ...

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📑 As a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. <br ...

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📑 **Job title:** Clinical Affairs Manager 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 solu ...

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📑 Description: *2YR OR 3YR SIGN-ON BONUSES AVAILABLE* Job Responsibilities: Medical Laboratory Scientists perform a full range of simplex-to-complex patient testing and laboratory services that will provide specialized expertise in one or more of the following laboratory disciplines: Hematolo ...

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📑 BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: ...

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📑 **Job Description** At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career g ...

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📑 : Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as ap ...

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📑 Are you an experienced regulatory affairs writer looking for a new challenge? We have just the opportunity for you! Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This role offers a stimulating work environment at the forefront of medical research, along with ample opportunit ...

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📑 Clinical Support Specialist - 2306153206W **Description** Johnson & Johnson is currently seeking a Clinical Support Specialist to join our Johnson Med-Tech team located in Israel. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex disease ...

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📑 **Job Description** At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual caree ...

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📑 **Job Description** At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career g ...

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📑 Are you ready to lead and manage a Start-Up team? Do you have experience in executing clinical trials and ensuring compliance with regulations? If so, we have an exciting opportunity for you to join our team as a Start-Up Tea ...

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📑 Requisition Number7110Employment Type:Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our comp ...

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📑 Director, Clinical Biomarker Lead Date: Apr 18, 2024 Location: Netanya, Israel, 1 Company: Teva Pharmaceuticals Job Id: 52697 **Who we are** Together, we’re on a mission to make good health more affordable and accessible, to he ...

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📑 a global medical device company is looking for CTAThe Clinical Trial Assistant in gather and the preparation of document for clinical trial applications for the submission and approval from the competent authority and ethical committees. The Clinical Trial Assistant is responsible for the correct filing and archiving of clinical trial doc ...

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📑 a gloabal medical device company is looking for in house CRAProvide support in the clinical trial operations and execution Provide general administrative support to the clinical team. Provide oversight on clinical documentation filling Main responsibilities shall include (but not be limited to):Assist the cli ...

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📑 At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions.< ...

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📑 Are you ready to lead and manage a Start-Up team? Do you have experience in executing clinical trials and ensuring compliance with regulations? If so, we have an exciting opportunity for you to join our team as a Start-Up Team Manager at Novo Nordisk Israel. Read on to learn more and apply today for a life-changing career. The Po ...

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📑 Description: We invite you to become a vital member of the Willis-Knighton Med Surg Nursing Team where we are committed to collaboration and the delivery of exceptional care. With a 1:5 nurse-to-patient ration, our unit maintains a positive and friendly work culture where professionals are valued and respected. The unit b ...

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📑 Description: We invite you to become a vital member of the Willis-Knighton Med Surg Nursing Team where we are committed to collaboration and the delivery of exceptional care. With a 1:5 nurse-to-patient ratio, our unit maintains a positive and friendly work culture where the professionals are valued and respected. The uni ...

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📑 Thriveworks is currently seeking Licensed Clinicians to provide telehealth sessions in Illinois. Thriveworks is a clinician-founded national private practice group with locations in 48 states. Our mission is to help people live happy, successful lives, and we believe that client accessibility, integrity, and quality care are what is mos ...

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📑 Are you ready to lead and manage a Start-Up team? Do you have experience in executing clinical trials and ensuring compliance with regulations? If so, we have an exciting opportunity for you to join our team as a Start-Up Team Manager at Novo Nordisk Israel. Read on to learn more and apply today for a life-changing career. The Position As a Start-U ...

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📑 Reference OTRRBA210224A Products Advanced Wound Care Dressings, Absorbents, Skin Protectants, Peak Flow Meters, Gloves, & Surgical Tapes Customers TVNs, Procurement, Nursing Homes, Lymphedema Specialists, Practice Nurses, Pharmacists, District Nurses and a range of Key Opinion Leaders Location South East, South West Package £55k-£65k Basic + £16.5k ...

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📑 At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a s ...

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📑 a global biotech company is looking for CMC Managerresult-oriented and team-building capabilities with credentialed scientific background and experience in leading manufacturing operations and drug product development.Specifically - comprehensive experience in small proteins/peptides drug manufacturing in Escherichia coli expression syste ...

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📑 United States (US) Here at Avanos Medical, we passionately believe in three things: Making a difference in our products, services and offers, never ceasing to fight for groundbreaking solutions in everything we do; Making a difference in how we work and collaborate, constantly nurturing our nimble culture of innovation;</li ...

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📑 **Job Description** PPD, part of Thermo Fisher Scientific, is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. At PPD, we are passionate, deliberate, and driven by our purpose- to improve health! We are vital links between an idea f ...

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📑 Medical device sales representative - 2406177019W **Description** Johnson & Johnson is currently seeking a Medical Device Sales Representative to join our Johnson Med-Tech team located in Israel. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where ...

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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...

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📑 a global medical device device company is looking for CRAResponsibilitiesConducts site monitoring visits and follow-up to identify significant problems and issues and to ensure that all clinical aspects of studies are being carried out in accordance with state and federal regulations, guidelines and policies (MOH, CRF, GDPR ISO).subm ...

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📑 *Position is 100% remote, Part- time (24 hours per week) - 12-14 patient facing hours, 10-12 administrative hours. 2 Evenings required per week, along with day time hours (Mon-Fri). Benefits Eligible! Seeking therapists licensed with a Psychology Interjurisdictional Compact (PSYPACT) License and willing ...

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📑 ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help t ...

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📑 Requisition Number7110Employment Type:Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our comp ...

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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...

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📑 **Job Description Summary** Radiation Therapy (RT) is a key strategic pillar for GE HealthCare’s Oncology Care pathways Therapy Guidance strategy. As Clinical Applications leader, you will be on the Global Oncology Care Pathways Team in GE HealthCare. The role will provide global clinical expertise and leadership on shaping our multi-modal ...

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📑 At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid*/remote). As a Sr. CRA at Allucent, you ...

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