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📑 **Great opportunity if you want to join one of the greatest CROs and start your journey!** **Job Overview** Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. ...

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📑 **Senior Clinical Associate - Buenos Aires, Argentina** ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. ...

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📑 Clinical Operations CoordinatorFairtilityFairtility, as one of Nacre capital portfolio companies, combines clinical excellence, with cutting edge AI technology and strong business leadership to revolutionize reproductive care, supporting fertility clinics, health care professionals and their ...

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📑 You will be a practitioner on our telehealth platform 'Intellect', where your role is to support our clients' mental health and personal growth based on the individual needs and goals. This is delivered primarily through scheduled 60-minute video sessions on our platform.This is a freelance remote role with the flexibility t ...

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📑 Updated: April 10, 2024Location: Argentina-Latin America - ARG-Home-Based, ArgentinaJob ID:24002434-ARG975Medical Director Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern ma ...

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📑 Great opportunity if you want to join one of the greatest CROs and start your journey! Job Overview Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. <p ...

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📑 **Calling ALL experienced Clinical Leads.** The Clinical Lead provides leadership of the clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project’s overall objectives to the Sponsor’s satisfaction per contract while optimizing speed, quality and ...

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📑 **Job Overview** Leader of the Centralized Monitoring team, partner with the project and clinical lead to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction per contract, while optimizing speed, quality and cost of delivery and in accordance with IQVIA SOPs, policies and practices. <br ...

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📑 **MSL Oncology****WHAT YOU WILL DO**This role is for a field-based professional with scientific, clinical and therapeutic expertise.The Medical Science Liaison will deliver scientific insights to the organization which address the scientific needs of the therapeutic area colleagues and influence the strategic decision making ...

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📑 Clinical Project Leader Location: Buenos Aires, ArgentinaJob type: Permanent About the jobOur Team:The Local Study Manager (LSM) is part of the Clinical Study Unit (CSU) and is accountable for the strategic planning & management and performance of their assigned clinical trials from country allocation within feasibility process until study closure ...

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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. PLEASE SUBMIT ALL RESUMES ...

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📑 Site Manager - 2306158945W **Description** At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity. Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the hea ...

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📑 The Clinical Lead provides leadership of the clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project’s overall objectives to the Sponsor’s satisfaction per contract while optimizing speed, quality and cost of delivery and in accordance with our SOPs, policies and ...

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📑 We are currently seeking a Senior Regulatory Affairs Specialist to join our Regulatory Affairs department focusing on Argentinean Activities. This is a fantastic opportunity to further develop your regulatory career and expertise in clinical trial setting. In this role you will be a pivotal team member with regulatory affairs ...

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📑 You will be a practitioner on our telehealth platform 'Intellect', where your role is to support our clients' mental health and personal growth based on the individual needs and goals. This is delivered primarily through scheduled 30-minute video sessions on our platform.This is a freelance remote role with the flexibility t ...

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📑 ICON, a leading Clinical Research Organization, is seeking passionate, resilient candidates to join our team as a Clinical Trial Assistant. This opportunity offers a junior level permanent position to highly skilled individuals interested in a career in clinical research. We empower our Clinical Trial Assistants to work with a co ...

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📑 Project Manager (Argentina) Argentina CRO - Project Management Full-time The project manager has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials or its portion conducted in EU or APAC region ...

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📑 We’re looking for people who are determined to make life better for people around the world. The Trial Capabilities Associate provides clinical trial capabilities in support of clinical development. The associate is accountable to ensure the investigator sites meet requirements to enroll study participants into clinical trials and supp ...

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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 applicabl ...

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📑 Manage the process of designing and launching clinical research studies; manage activities of the Sponsor/Clinical Research Organization (CRO); lead colleagues in the design and organization of project components during Start-Up; develop and maintain best practices within the organization; Accountability and ownership for the quality of all start-u ...

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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 ...

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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 ...

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📑 **Job Description** 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 a ...

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📑 **Requirements:** + Located in Argentina + Bachelor’s degree + Advanced English Level + Minimum 6 years Clinical Research experience that includes a minimum 4 years relevant experience as a Senior CRA or Principal CRA (in a Lead CRA role), or at least 2 years as a CRA Manager or equivalent job role. ...

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📑 Job Description Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. Hybrid position in Buenos Aires, Argentina Only CVs in English will be accepted. You will be respo ...

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📑 When our values align, there's no limit to what we can achieve. Join Parexel’s team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do. Job Title Project Specialist At Parexel, we are a leading Clinical ...

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📑 **CRA 2 - Homebased** Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on perfo ...

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📑 Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. ...

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📑 Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific ...

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📑 **Job Description** We are currently seeking a Senior Regulatory Affairs Specialist to join our Regulatory Affairs department focusing on Argentinean Activities. This is a fantastic opportunity to further develop your regulatory career and expertise in clinical trial setting. In this role you will be a pivotal ...

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📑 Job DescriptionOnly CVs in English will be consideredIn this position, you will be responsible for coordinating activities of project teams ensuring milestones are met and ensuring consistency of Clinical Operations processes across regions. This function holds project managerial responsibilities under supervision.&# ...

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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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📑 Updated: March 11, 2024Location: Argentina-Latin America - ARG-Home-Based, ArgentinaJob ID:23007145-ARG975Senior Regulatory Intelligence AssociateSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcom ...

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📑 According to the specific role, coordinates, oversees and completes functions on assigned trial(s) activities as detailed on the task matrix. Ensures allocated tasks are performed on time, within budget and to a high[1]quality standard. Proactively communicates any risks to project leads. Provides system support (, Act ...

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📑 **Job Overview** A Central Monitor is a key skilled and clinically experienced team member of IQVIA Central Monitoring Department. Provides remote project support and assistance across multiple projects, sites and teams and reviews the structured clinical data output with access to medical charts. **Essential F ...

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📑 **Job Description** 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 an ...

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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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📑 **Job Description** Supports supply chain for moderate complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements. May act as a representative and project lead for the department on less complex projects. • Develops study specific plans for each assig ...

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📑 PPD, part of Thermo Fisher Scientific centralized monitoring group delivers a new approach to risk surveillance and centralized statistical monitoring, combining the power of statistical and analytical tools with expertise from operationally experienced staff to monitor and manage clinical study data. Centralized monitoring staff expl ...

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📑 JOB DESCRIPTION We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to ...

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📑 JOB DESCRIPTION We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the t ...

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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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📑 Calling ALL experienced Clinical Leads. The Clinical Lead provides leadership of the clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project’s overall objectives to the Sponsor’s satisfaction per contract while optimizing speed, quality and co ...

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📑 Job Overview Leader of the Centralized Monitoring team, partner with the project and clinical lead to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction per contract, while optimizing speed, quality and cost of delivery and in accordance with IQVIA SOPs, policies and practices. Es ...

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📑 **Job Description** Summarized Purpose: Supports supply chain for moderate complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements. May act as a representative and project lead for the department on less comple ...

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📑 Teladoc Health is a global, whole person care company made up of a diverse community of people dedicated to transforming the healthcare experience. As an employee, you’re empowered to show up every day as your most authentic self and be a part of something bigger – thriving both personally and professionally. Together, let’s empower people ever ...

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📑 The Clinical & Ancillary Supplies Services (CASS) Senior Specialist: Coordinate and oversee aspects of logistics related to Clinical and Ancillary Supplies services. Support these services to both internal and external clients. Responsible for the set-up and coordination of project activities related to clinical and ...

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📑 **Job Description** Provides complete oversight of supply chain for complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements. Acts as a representative for the department on all assigned projects. • Develops study specific plans for each assigned pro ...

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📑 **Job Overview** Responsible for providing input into the generation of the study strategies and collaborating with other involved IQVIA teams. Perform, manage and co-ordinate activities for assigned opportunities and projects. Perform data mining and analysis, formulate recommendations and present to internal and potentially external stak ...

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📑 **Join our team as a Senior Data Team Lead, IQVIA Biotech!** Senior Data Team Lead position is to manage all data management (DM) tasks to include more complex and/or larger studies and/or a program of studies from start-up through database closure and archival producing high-quality databases for analysis and potential regulator ...

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