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Ofertas sugeridas de otras empresas

• Tusclasesparticulares

  

  Teletrabajo - Profesor/a Particular - Sin Experiencia

  hace 14 horas

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  No se requiere experiencia previa como profesor. Posibilidad de teletrabajo / trabajo desde casa.

• Artivion

  

  Clinical Research Associate Iii

  hace 18 horas

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  It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Bring your strengths and let us grow together. We are hiring a Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) Your Strength Minimum of 4 years of advanced experience in clinical research monitoring In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.G., ISO 14155, GCP, MDR, EU, FDA) Ability to independently manage 10–15 study sites from start-up through close-out Excellent communication skills for site interaction, training, and issue resolution Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members Hands-on experience with monitoring systems, source data verification, and compliance tracking Strong organizational skills with the ability to manage multiple priorities in a dynamic environment Willingness to travel regularly for site visits and investigator meetings across France and Spain Based in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring) Fluent communication in English and Spanish (Catalan is preferred, French optional) Your Contribution Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements Act as the primary contact for investigational sites, ensuring compliance and providing ongoing support Build and maintain strong relationships with investigators, study coordinators, and site personnel Identify study risks, recommend solutions, and ensure timely resolution of site-related issues Perform source data verification and data review to ensure patient safety, protocol compliance, and data integrity Conduct site training, initiation visits, and support audit and inspection readiness Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams Support investigator meetings, coordinator meetings, and deliver presentations or training sessions when required Mentor junior CRAs and contribute to process improvements and best practices Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts Our Strength A mission-driven company focused on saving lives International and collaborative MedTech environment Hybrid working model with flexibility Opportunities for growth and professional development Innovative products and meaningful clinical impact Contact Apply now and join the Artivion team. We look forward to receiving your application documents in English through our online application system. Brian Russo T: JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. Lotzenäcker 23, 72379 Hechingen

• Cactus Communications

  

  Guest Lecturer / Workshop Trainer

  hace 18 horas

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  Researcher Training is a client-facing function that imparts training to researchers, universities, and corporate clients through live in-person sessions and online webinars. Asegúrese de que toda la información de su solicitud está actualizada y en orden antes de inscribirse en esta oportunidad. We have a global pool of trainers who conduct these events for our research base around the world. Training topics include manuscript writing, journal selection, submission package, grant writing, science communication, graphical abstracts, case report writing, thesis writing, AI for research, etc. The training session formats: In-person workshops (CACTUS will cover travel and other domestic expenses) Online webinars As an Academic Publication Trainer and Consultant, you will work closely with the training team and be involved in delivering high-quality training programs to researchers from various disciplines which may on occasions include reviewing manuscripts of researchers and offering on-site, one-on-one guidance for how to improve them further. Some requests also include preparing training materials, while others could involve live sessions on a social channel. Essential duties and responsibilities Delivering high-quality training. Preparing and customizing training content as per request. Understanding in adequate detail the author services Editage, CACTUS offers. Collaborate with the training team on designing the outline of training programs on the basis of client requirements, modifying training content and approach on the basis of feedback shared by Editage or the client. Occasionally reviewing research manuscripts written by workshop participants either before or during sessions and sharing personalized feedback and tips with participants on how to improve the language, flow, structure, and other aspects of content presentation. Knowledge and skills: PhD in the field of Physical Sciences. Excellent oral and written communication skills in Spanish(Native). Experience in publishing research articles in international high-impact-factor journals. In-depth knowledge of processes and trends in the academic publishing industry. xsgfvud High level of ownership and ability to work with tight deadlines.

• C1 English Pro

  

  Profesor/A De Inglés - Remoto

  hace 14 horas

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  En el puesto de Profesor/a de inglés en C1 English Pro, te encargarás de impartir clases de inglés online a estudiantes de diferentes niveles, con enfoque en la mejora de la expresión oral, comprensión auditiva, lectura y escritura.

• TutorABC

  

  Bilingual English Teacher - Remote Role T - Remote

  hace 14 horas

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  Why Join Us Remote teaching structure Self-managed scheduling Access to professional development opportunities Supportive global educator network Dedicated online teaching portal Core Requirements · Bachelor’s Degree or higher · Recognized English teaching certification (TESOL / TEFL /

• MDx CRO

  

  Clinical Research Specialist | MedTech

  hace 2 días

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  Clinical Research and Regulatory Specialist | MedTech Puede obtener más detalles sobre la naturaleza de esta vacante y lo que se espera de los solicitantes leyendo la información a continuación. Location: Spain (Remote) Employment type: Full-time Role Summary We are looking for a motivated junior professional who wants to develop their career in the MedTech and IVD sector. As a Clinical Research and Regulatory Specialist , you will support clinical research activities, scientific and medical writing, and the creation of documentation essential to product validation and regulatory pathways. You will work closely with senior experts and multidisciplinary teams, gaining hands-on experience with clinical investigations, performance studies (ISO 14155 and ISO 20916), technical documentation, and clinical evidence development. Ideal for candidates with 0.5–2 years of experience in MedTech, IVD, clinical research or R&D — or strong scientific backgrounds eager to enter the industry. Responsibilities You will: • Support the preparation and execution of Clinical Investigations and Performance Studies, • Assist in developing study documentation (protocols, CRFs, ICFs), • Collaborate with study sites and internal teams following ISO 14155 and ISO 20916 standards, • Handle study documentation and communication with investigators, • Assist with monitoring‐support activities and data‐related tasks, • Contribute to scientific and medical writing, including study summaries and evidence-based content, • Support literature reviews, background research, and documentation preparation, • Assist in drafting components of clinical evidence documentation under supervision, • Help coordinate project activities, timelines, and communication You will receive structured onboarding, mentoring, and progressive responsibility. You are not expected to know everything on day one — you will learn with us. Requirements (Must‐Have) • Based in Spain or eligible for a Spanish employment contract, • 0.5–2 years of experience in MedTech, IVD, clinical research, or R&D, • Strong interest in MedTech, IVDs, clinical research, and scientific development, • Bachelor's degree in Life Sciences, • Enrolment in or completion of a Master's degree in Life Sciences, • Knowledge of GCP and clinical/lab standards, • Advanced English (C1–C2), especially for scientific writing, • Motivation to grow in a dynamic and international environment, • Availability for remote work with occasional in‐person activities Nice to Have • Exposure to ISO 14155 or ISO 20916, • R&D experience, • Regulatory exposure, • Academic research experience or authorship in scientific literature Why Join MDx CRO At MDx CRO, you will join a dynamic and rapidly growing company recognised across the MedTech and IVD industry. We offer: • Structured onboarding and continuous training, • Close mentorship from senior specialists, • Exposure to real clinical and scientific projects, • Growth opportunities as your skills develop About MDx CRO MDx CRO is a leading Contract Research Organisation specialising in in vitro diagnostics (IVDs) and medical devices. We provide regulatory consulting, clinical research, and quality assurance services, helping clients bring safe and effective products to market in full compliance with global regulatory standards. xqysrnh We operate on five core principles: Make it POSSIBLE Make it WIN-WIN Keep IMPROVING Keep GROWING Keep it DIVERSE Our Vision To democratise access to world-class regulatory and clinical strategies, ensuring safer and more effective medical technologies for all. Our Mission We pioneer emerging technologies and navigate uncharted territories to redefine the future of the medical sector. Grow with Us If you want to accelerate your development in the MedTech and IVD sector within a supportive and expert‐driven environment, we would love to hear from you.

• Universidad Nebrija

  

  Profesor/a Ayudante Doctor/a de Enfermería

  hace 5 días

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  La Facultad de Ciencias de la Vida y la Naturaleza de la Universidad Antonio de Nebrija precisa incorporar a su claustro docente varios/as Profesores/as Ayudantes Doctores/as de Enfermería para impartir docencia en distintas áreas de especialización durante el próximo curso académico.

• domestiko.com

  

  Trabajadores y educadores sociales (Ayuda a la dependencia)

  hace 11 días

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  ¿Buscas trabajo en ayuda a la dependencia? Este mes de septiembre surgen nuevas oportunidades para trabajadores y educadores sociales en Lugo. ¡Inscríbete gratis hoy mismo!