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Sr Scientific Communication Specialist

Position Description  This position is in the Aortic & Peripheral Vascular (APV) Business Unit, which is one of the fastest growing businesses in the entire Medtronic portfolio. The APV product portfolio contains life-saving technologies for the abdominal and thoracic aorta and innovative endovascular treatments for the peripheral vasculature (arteries and veins) that significantly improve the quality of life for patients.  The Sr Scientific Communication Specialist is responsible for the tactical execution that supports the evidence dissemination needs of the APV Medical Affairs Department.  These tactics include medical writing of scientific manuscripts/abstracts, development of podium/ poster presentations, and development of other scientific materials which communicate clinical trial-related evidence to the physician community. This position is also the owner of the APV manuscript development process and literature search activities (utilizing the Medtronic Knowledge Center).  The ideal candidate will possess advanced scientific knowledge and a demonstrated medical writing skill set.  The position will be based in/near Santa Rosa, CA or Plymouth, MN, but working remote can be considered for the right candidate.  The position will require occasional travel; volume will be dependent on candidate’s location. Position Responsibilities  • Collaborate with APV Scientific Communication Managers to support development of clinical evidence dissemination strategy. • Develop the tactical plans tied to the evidence dissemination strategy with focus on podium and publication needs of assigned therapeutic areas and/or products within Medtronic.  Evidence dissemination tactical plans should be aligned with clinical strategy and Medtronic business objectives. • Execute on tactical plan to meet pre-specified timelines and budgetary guidelines.   • Prepare documents that support publication needs of assigned therapeutic areas or products.  Write, edit, or review scientifically complex documents including abstracts, manuscripts and podium presentations.  Ensure all Medtronic APV sponsored publications and scientific presentations meet ethical publication guidelines (ICMJE), as well as Medtronic’s internal publication standards and compliance policies. • Drive use of and improve the manuscript development process and tools for APV.  Ensure all required documentation is in place for each project. • Design literature searches using relevant key words, execute literature searches in collaboration with the Medtronic Knowledge Center, analyze results and write literature summaries as needed (related to manuscript or scientific communication activities). • Develop and maintain an accessible repository for relevant Medtronic and competitive literature, including journal articles, abstracts, and presentations as requested by the Scientific Communication Managers. • Manage external medical writing vendors to obtain high quality, impactful scientific deliverables for contracted projects. • Develop, track and report on metrics related to APV medical writing services to Scientific Communication Managers, Director of Scientific Communications and key business partners. • Support activities of the Scientific Communications team at medical device congresses, as assigned.  This may include attending publication planning meetings with investigators in Medtronic clinical trials, executing Medtronic-sponsored symposia, and covering relevant scientific sessions. • Follow the Medtronic Code of Conduct, the Scientific Communication Department Operating Procedures, and the ICMJE, GPP3, and ADVAMED guidelines. IN ORDER TO BE CONSIDERED FOR THIS POSITION, THE FOLLOWING BASIC QUALIFICATIONS MUST BE EVIDENT ON YOUR RESUME Basic Qualifications  • Master of Science with 3+ years of Scientific writing experience or Bachelor of Science with 5+ years of Scientific writing experience  Desired/Preferred Qualifications  • PhD or PharmD with 2+ years of relevant experience • Knowledge of clinical research methodology, tools, processes and regulations • Ability to critically analyze and interpret scientific data • Demonstrated project management skills • Highly proficient in the use of Microsoft Office Suite software, Adobe software, and EndNote Reference software • Adept in performing literature searches in Pubmed and other relevant platforms • Expertise in literature identification and

Santa Rosa
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Senior Scientific Communications - Publications

Position Description  This position is in the Aortic & Peripheral Vascular (APV) Business Unit, which is one of the fastest growing businesses in the entire Medtronic portfolio. The APV product portfolio contains life-saving technologies for the abdominal and thoracic aorta and innovative endovascular treatments for the peripheral vasculature (arteries and veins) that significantly improve the quality of life for patients.  The  Sr. Medical Writer is responsible for the preparation of documents that support the publication and presentation needs of assigned therapeutic areas and/or product in the Scientific Communications Group. The Scientific Communications Group is part of the APV Medical Affairs Department.  These tactics include medical writing of scientific manuscripts/abstracts, development of podium/ poster presentations, and development of other scientific materials which communicate clinical trial-related evidence to the physician community. This position is also the owner of the APV manuscript development process and literature search activities (utilizing the Medtronic Knowledge Center).  The ideal candidate will possess advanced scientific knowledge and a demonstrated medical writing skill set.  Preferably, the position will be based in/near Minneapolis, MN or Santa Rosa, CA,  but working remote can be considered for the right candidate.  The position will require occasional travel; volume will be dependent on candidate’s location. Position Responsibilities  • Partner with APV Scientific Communication Managers & Specialists to support execution of clinical evidence dissemination plans with focus on publication and podium needs of assigned therapeutic areas and/or products within Medtronic.  Evidence dissemination plan are aligned with clinical strategy and Medtronic business objectives. • Prepare documents that support publication needs of assigned therapeutic areas or products.  Write, edit, or review scientifically complex documents including abstracts, manuscripts and podium presentations.  Ensure all Medtronic APV sponsored publications and scientific presentations meet ethical publication guidelines (ICMJE), as well as Medtronic’s internal publication standards and compliance policies. • Drive use of and improve the manuscript development process and tools for APV.  Ensure all required documentation is in place for each project. • Design literature searches using relevant key words, execute literature searches in collaboration with the Medtronic Knowledge Center, analyze results and write literature summaries as needed (related to manuscript or scientific communication activities). • Develop and maintain an accessible repository for relevant Medtronic and competitive literature, including journal articles, abstracts, and presentations as requested by the Scientific Communication Managers. • Manage external medical writing vendors to obtain high quality, impactful scientific deliverables for contracted projects. • Develop, track and report on metrics related to APV medical writing services to Scientific Communication Managers, Director of Scientific Communications and key business partners. • Support activities of the Scientific Communications team at medical device congresses, as assigned.  This may include attending publication planning meetings with investigators in Medtronic clinical trials, executing Medtronic-sponsored symposia, and covering relevant scientific sessions. • Follow the Medtronic Code of Conduct, the Scientific Communication Department Operating Procedures, and the ICMJE, GPP3, and ADVAMED guidelines. IN ORDER TO BE CONSIDERED FOR THIS POSITION, THE FOLLOWING BASIC QUALIFICATIONS MUST BE EVIDENT ON YOUR RESUME Basic Qualifications  • Master of Science with 3+ years of scientific writing experience or Bachelor of Science with 5+ years of scientific writing experience  Desired/Preferred Qualifications  • PhD or PharmD with 2+ years of relevant experience • Knowledge of clinical research methodology, tools, processes and regulations • Ability to critically analyze and interpret scientific data • Demonstrated project management skills • Highly proficient in the use of Microsoft Office Suite software, Adobe software, and EndNote Reference software • Adept in performing literature searches in Pubmed and other relevant platforms • Expertise in literature identification and analysis • Understanding of statistical

Santa Rosa
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Senior Field Clinical Research Specialist

POSITION DESCRIPTION: Field based position responsible for clinical trial site management, case coverage and enrollment activities. POSITION RESPONSIBILITIES: Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines, and policies.  Oversee preparation of and revisions to the Clinical Investigation Plan for assigned clinical studies.  Oversee preparation of study materials and/or training (e.g., training of investigators, site staff and Medtronic field staff).  Interface with, and assure training of investigators, site staff, and Medtronic clinical staff.  Assist in site initiation (e.g. oversight of start-up document preparation, distribution, receipt, and review).  Set-up and maintain accurate study status and implant logs.  Interfaces with representatives from key functional groups (Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs, Legal, and European Clinical Groups).    Long term maintenance of study project plan.  Identify and mitigate quality risks and issues for assigned clinical studies. May Oversee PR and enrollment activities at assigned sites by managing enrollment meetings and deliverables with various marketing teams. May review and present cases for a screening committee to ensure study subjects meeting trial inclusion/exclusion.  May proctor or provide case support.  May arrange conference calls, staff meetings and training events.  Assist in compilation and review of adverse event information.  Assist in coordinating field staff activities with clinical site needs.  Oversee follow-up and resolution of site issues noted by field staff.  Assist in compilation, review and conclusion of device complaints.  Oversee study closure activities (e.g. close-out document preparation, distribution, receipt and review, audit and archive).  Assist data management group with review of clinical data/information and oversight of data correction.  Assist in preparation of annual, interim and final reports and presentations.  Assist in control of device allocation, distribution and reconciliation.  Oversee activities performed by Contract Research Organizations (e.g. CROs, core labs).  May provide work direction to Project Coordinator(s) and Clinical Research Associate(s).  May provide work direction to Clinical Monitors to ensure compliance with the Clinical Investigation Plan and appropriate regulations, guidelines and policies.  Able to refer to Standard Operating Procedures (SOPs) and study management process for guidance on everyday study tasks.  Contribute to ongoing SOP development and review.  Participate in training to enhance knowledge base. IN ORDER TO BE CONSIDERED FOR THIS POSITION, THE FOLLOWING BASIC QUALIFICATIONS MUST BE EVIDENT ON YOUR RESUME BASIC QUALIFICATIONS: • Bachelor’s degree EDUCATION REQUIRED:  • 4+ years experience directly supporting clinical research or relevant experience in medical/scientific area. Masters degree will substitute for 1 year of experience.  PhD or MD will substitute for 2 years of experience. DESIRED/PREFERRED QUALIFICATIONS   • Hospital/Clinical experience • Working knowledge of Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials. • Strong written, oral, and interpersonal communication skills including proficient knowledge of medical terminology • Computer skills (MS Office products, word processing, spreadsheets, etc.) • High attention to detail and accuracy • Ability to manage multiple tasks • Good prioritization and organizational skills • Excellent problem solving skills • Positive outlook • Flexible and dependable • Works effectively on cross-functional teams PHYSICAL JOB REQUIREMENTS:  • The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • While performing the duties of this job, the employee is regularly required to be independently mobile.  The employee is also required to interact with a computer, and communicate with peers and co-workers. • Travel can be up to 50- 75% MEDTRONIC OVERVIEW: Together, we can change healthcare worldwide.  At Medtronic, we push the limits of what technology can do to

Santa Rosa
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Desarrolla Tu Propio Negocio

Si sos emprendedor y tenes ganas de tener tu propio negocio, esta es tu oportunidad de conseguirlo.Inicia tu negocio hoy mismo con mínimos requisitos, genera ingresos extras, maneja tus tiempos, desde la comodidad de tu hogar.Recibirán capacitaciones y entrenamientos sobre finanzas, negocios y desarrollo personal para formarse como emprendedores de éxito.REQUISITOS:1)Una computadora con acceso a internet.2)Ser emprendedor/a.3)Deseos de superación personal y crecimiento económico.4)Una mínima inversión para activar tu negocio y herramientas de trabajo.Contáctame para más información.Contacto: SebastiánWhatsApp: 380 - 4617840Email: sebamolina_22@hotmail.comIMPORTANTE: SOLO PARA EMPRENDEDORES, ESTO NO ES UN TRABAJO, ES UN NEGOCIO.

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Project Coordinator III

POSITION DESCRIPTION: Provides project and administrative support for the Coronary and Structural Heart Clinical organization. POSITION RESPONSIBILITIES: • Independently maintains systems to monitor project status and metrics through the use of specialized software applications and is able to extract data and generate reports requiring little assistance. • Creates spreadsheets and presentations independently.   • Develops tracking documents with assistance. • Applies adequate level of knowledge and experience in company operations to assist in the development, implementation and administration of project guidelines and procedures. • Contribute to ongoing departmental and project-specific process improvement efforts. • Manages filing of study and departmental documents. • Coordinates projects and meetings with cross-functional teams. • Manages issues and requests from staff, including providing technical support. Technical support may include system or process training and documentation of training. • May be involved in planning and preparation of communications. • Document meeting minutes as needed. • Assist with onboarding of new study team members. • Conducts special projects as directed. IN ORDER TO BE CONSIDERED FOR THIS POSITION, THE FOLLOWING BASIC QUALIFICATIONS MUST BE EVIDENT ON YOUR RESUME BASIC QUALIFICATIONS: EDUCATION REQUIRED   • High School Diploma or GED YEARS OF EXPERIENCE  • At least four (4) years experience in administrative support, or clinical research experience. DESIRED QUALIFICATIONS:  • Certification or advanced skills in administrative and project management work preferred • Capable of clearly and effectively communicating verbally and in writing • Excellent interpersonal skills • Experience working in a team/matrix environment  • Ability to handle and prioritize multiple projects simultaneously  • Ability to work in a fast paced environment • Ability to adapt to shifting priorities and competing demands • Ability to utilize tact, persuasion, judgment and/or negotiation to accomplish objectives. • Good attention to detail and accuracy • Good organizational skills • Good problem solving skills/able to develop solutions to problems (medium level complexity). • Very proficient in word processing, spreadsheets, presentations and databases applications (e.g., Microsoft Office Suite and Adobe Acrobat Professional) • Experience with clinical trial management and document management systems preferred  • Ability to work independently or with little direction/self motivated. PHYSICAL JOB REQUIREMENTS:  • The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. MEDTRONIC OVERVIEW: Together, we can change healthcare worldwide.  At Medtronic, we push the limits of what technology can do to help alleviate pain, restore health and extend life.  We challenge ourselves and each other to make tomorrow better than yesterday.  It is what makes this an exciting and rewarding place to be. We can accelerate and advance our ability to create meaningful innovations – but we will only succeed with the right people on our team.  Let’s work together to address universal healthcare needs and improve patients’ lives.  Help us shape the future. It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status or any other characteristic protected by federal, state or local law.  In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities. This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the

Santa Rosa
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Trabaja Desde Tu Hogar

Excelente oportunidad de crecimiento personal y económico, no necesitas título ni experiencia previa. Ideal para personas que quieran generar ingresos extras y tengan deseos de superarse todos los días.Te brindamos todas las herramientas para que puedas comenzar con tu negocio, desde la comodidad de tu hogar, sin jefes ni horarios.Si sos emprendedor/a, si tenes metas y sueños por cumplir en tu vida, te invito a que te sumes a nuestro equipo de trabajo que crece día a día con nuevos socios en todo el país.No pierdas tiempo contáctate conmigo para más información.Contacto: SebastiánWhatsApp: 380-4617840Mail: sebamolina_22@hotmail.com

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Negocio Por Internet

Cansado de buscar trabajo? El dinero no te alcanza? Emprende tu propio negocio con mínimos requisitos en tan solo 24 horas. Empresa con más de 8 años de trayectoria en Argentina busca personas que quieran ser dueños de su propio negocio. Recibirás capacitaciones y entrenamientos para que puedas lograr tus resultados.Requisitos1-Una computadora con acceso a internet.2-Ser emprendedor/ra, y querer crecer económicamente.3-2 horas por día para dedicarle a tu negocio.4-Una mínima inversión para activar tu negocio y herramientas de trabajo. Si contas con estos requisitos podes formar parte de esta gran empresa y ser dueño de tus tiempos. NO TRABAJES PARA NADIE, TRABAJA PARA TI, SUMATE A NUESTRO EQUIPO DE EMPRENDEDORES. ANIMATE A CAMBIAR TU VIDA.Contacto: SebastiánWhatsapp: 380-4617840Email: sebamolina_22@hotmail.comIMPORTANTE: ESTO NO ES UN EMPLEO ES UN NEGOCIO.

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Negocio Por Internet

Cansado de buscar trabajo? El dinero no te alcanza? Emprende tu propio negocio con mínimos requisitos en tan solo 24 horas. Empresa con más de 8 años de trayectoria en Argentina busca personas que quieran ser dueños de su propio negocio. Recibirás capacitaciones y entrenamientos para que puedas lograr tus resultados.Requisitos1-Una computadora con acceso a internet.2-Ser emprendedor/ra, y querer crecer económicamente.3-2 horas por día para dedicarle a tu negocio.4-Una mínima inversión para activar tu negocio y herramientas de trabajo. Si contas con estos requisitos podes formar parte de esta gran empresa y ser dueño de tus tiempos. NO TRABAJES PARA NADIE, TRABAJA PARA TI, SUMATE A NUESTRO EQUIPO DE EMPRENDEDORES. ANIMATE A CAMBIAR TU VIDA.Contacto: SebastiánWhatsapp: 380-4617840Email: sebamolina_22@hotmail.comIMPORTANTE: ESTO NO ES UN EMPLEO ES UN NEGOCIO.

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Asesores De Ventas Para Garbarino En Santa Rosa, La Pampa

Orientamos la búsqueda a hombres entre 20 y 30 años, con marcado perfil comercial para Sucursales de GARBARINO en la Ciudad de Santa Rosa, La Pampa. La función a desempeñar es integral orientada hacia el cliente, incluyendo la venta, cobro y entrega del producto al mismo. Se valorará que la persona cuente con experiencia comprobable en comercialización de productos tangibles y/o intangibles, como así también marcada orientación al cliente. Es indispensable contar con disponibilidad full time para horarios rotativos. Es excluyente contar con excelentes referencias laborales y Secundario Completo (se solicitará título). Se ofrece: Muy buen nivel de remuneración. Excelentes condiciones de contratación, con amplias y concretas posibilidades de desarrollo.

Santa Rosa
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La Pampa Buscamos Personas Que Quieran Ganar Dinero Por Internet Desde Su Casa

ATENCION LA PAMPA !!!!BUSCAMOS 10 PERSONAS EMPRENDEDORAS QUE QUIERAN GANAR DINERO POR INTERNET DESDE SU CASA EN SUS TIEMPOS LIBRES"ESTO NO ES UN EMPLEO" - "ESTO ES UN NEGOCIO"Y DEBES HACER UNA MÍNIMA INVERSIÓN DE DINERO POR ÚNICA VEZ PARA TENER TU PROPIO "NEGOCIO" Y HABILITAR TUS HERRAMIENTAS Y CAPACITACIÓN.PODRAS TRIPLICAR TU SUELDO TRABAJANDO 3 HORAS POR DIA EN TU NEGOCIO GANANDO DINERO DE 2 FUENTES DE INGRESOS AL 50 % Y 100%.RECIBIRAS HERRAMIENTAS Y CAPACITACION EN AUDIOS VIDEOS Y ONLINE DESDE TU CASA PARA APRENDER A TRABAJAR Y TENER RESULTADOS INMEDIATOS.REQUISITOS:1. COMPUTADORA CON ACCESO A INTERNET2. 3 O 4 HORAS LIBRES POR DIA PARA DEDICARLE A TU NEGOCIO3. SER EMPRENDEDOR/RA Y QUERER CAMBIAR TU VIDA ECONOMICA4. MINIMA INVERSION PARA HABILITAR TU NEGOCIOSI CONTAS CON ESTOS REQUISITOS PODES SER PARTE DE ESTA GRAN EMPRESA INTERNACIONAL Y COMENZAR A TRABAJAR Y GANAR DINERO YA !!!YO TE AYUDO Y VAMOS A TRABAJAR JUNTOS - CONTACTAME -infojre@yahoo.com - JORGE

Santa Rosa
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