Senior Cra
hace 4 semanas
**Senior CRA****Remote role**At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.That’s our vision. We’re driven by it. And we need talented people who share it.If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.**Overview**: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 CRAs**You will need**:- 24 months+ of monitoring experience in Oncology Trials as as a CRA- English advanced- College degree in medicine, science, or equivalent- Previous monitoring experience in medium-sized studies, including study start-up and close-out- Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data- Excellent written and verbal communication- Ability to work to tight deadlines- Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license**Benefits of Working in ICON**:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.ICON 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.LI-DG1LI-Remote
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Senior Cra
hace 2 días
Desde casa, México ICON A tiempo completo**Senior CRA** **Remote role** At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization:...
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Senior or Clinical Trial Manager
hace 2 semanas
Desde casa, México IQVIA A tiempo completo**IQVIA Biotech is seeking Senior and/or Clinical Trial Manager(s), with expereince in the following therapeutic areas**:Oncology/Hematology/CAR** T/Cell & Gene Therapy.** Please provide English version CV's/resumes. **MINIMUM REQUIRMENTS** - BS/BA (or equivalent) in one of the life sciences plus a minimum of 4 years direct experience in clinical studies -...
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Senior Clinical Research Associate
hace 4 semanas
Desde casa, México IQVIA A tiempo completo**BASIC FUNCTIONS**:Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works...
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Senior or Clinical Trial Manager
hace 2 semanas
Desde casa, México IQVIA A tiempo completo**IQVIA Biotech is seeking Senior and/or Clinical Trial Manager(s), with expereince in the following therapeutic areas**:Oncology/Hematology/CAR** T/Cell & Gene Therapy.**Please provide English version CV's/resumes.**MINIMUM REQUIRMENTS**- BS/BA (or equivalent) in one of the life sciences plus a minimum of 4 years direct experience in clinical studies- At...
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Sr. or Clinical Trial Manager, Oncology, Mexico
hace 2 días
Desde casa, México IQVIA A tiempo completo**IQVIA Biotech is committed and dedicated to the small biotech & biopharma companies we support.** **Opportunities available for an experienced Clinical Trial Manager II or Senior Clinical Trial Manager.** **Previous clinical trial management and CRO experience preferred.** **Therapeutic **requirements/preference**: any of the following...
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Sr. or Clinical Trial Manager, Oncology, Mexico
hace 4 semanas
Desde casa, México IQVIA A tiempo completo**IQVIA Biotech is committed and dedicated to the small biotech & biopharma companies we support.****Opportunities available for an experienced Clinical Trial Manager II or Senior Clinical Trial Manager.****Previous clinical trial management and CRO experience preferred.****Therapeutic **requirements/preference**: any of the following...
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Senior Clinical Research Associate I
hace 3 semanas
Desde casa, México Parexel A tiempo completo**Parexel FSP is looking for multiple Sr CRAs in Mexico!**The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and...
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Senior Clinical Research Associate
hace 2 semanas
Desde casa, México Parexel A tiempo completoEverything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction. As a CRA...
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Senior Clinical Research Associate
hace 2 semanas
Desde casa, México Parexel A tiempo completoEverything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction.As a CRA at...
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Clinical Research Associate Ii
hace 2 semanas
Desde casa, México Parexel A tiempo completo**More about you** On your first day we’ll expect you to have: - Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. - Ability to perform all clinical monitoring activities independently. - Bachelor’s or equivalent degree in biological science, pharmacy or other health...