Cra I
hace 2 semanas
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 to accelerate the development of drugs and devices that save lives and improve quality of life.Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP.The role:- Independent, proactive work to set up and monitor studies, complete reports and maintain documentation- Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions- Balancing sponsor generated queries- Taking responsibility for study cost efficiency- Preparation and review of study documentation and feasibility studies for new proposals- Potential to assist in training and mentoring fellow CRAsYou will need:- 12 months of monitoring experience as a CRA- University degree in medicine, science, or equivalent- You should also have knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data- Good social skills enabling you to deal with queries in a timely manner- You will be asked to travel at least 60% of the timeBenefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.Are you a current ICON Employee? Please click here to apply:link
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Cra I
hace 3 semanas
Ciudad de México ICON A tiempo completoICON plc is a world-leading healthcare intelligence and clinical research organization. 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.As Clinical Research Associate you will be joining the world’s largest & most comprehensive...
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Cra I
hace 3 semanas
Ciudad de México Icon plc A tiempo completoICON 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.With our patients at the centre of all that we do, we help to accelerate the development...
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Cra I
hace 5 días
Ciudad de México Fortrea A tiempo completoLabcorp Drug Development is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. Are you ready for the next step in your career? We are currently recruiting for a Clinical Research Associate I in Mexico. Role description: - Ensure the study staff who will conduct the protocol have...
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Sr Cra I
hace 3 semanas
Edo. de México Syneos Health Clinical A tiempo completo**Description****Clinical Research Associate I**Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our...
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Cra Ii
hace 7 días
Ciudad de México ICON plc A tiempo completo**Experienced CRA - Mexico City, home-based role** 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. With our patients at the centre of...
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Ihcra I
hace 4 semanas
Ciudad de México Fortrea A tiempo completo**Job Overview**:**Summary of Responsibilities**:- To serve as contact for project team and investigative sites, conduct site contacts and document contacts for assigned sites as required per study guidelines, including creating contact reports for each telephone session (outbound or inbound) with sites.- To monitor site performance and implement action...
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Sr Cra
hace 5 días
Ciudad de México PPD A tiempo completo**JOB DESCRIPTION**:PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic...
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Sr Cra
hace 2 semanas
Ciudad de México PPD A tiempo completoPPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams.Our global...
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Cra Ii
hace 5 días
Ciudad de México Fortrea A tiempo completo**Summary of Responsibilities**: - Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. - Conducts site monitoring responsibilities for clinical trials according to Fortrea’s...
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Cra Ii
hace 4 días
Ciudad de México Fortrea A tiempo completo**Summary of Responsibilities**:- Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.- Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...
