Empleos de clinical research associate cra en Xico

**Join Our Team as a Clinical Research Associate (CRA)! ** The Clinical Research Associate (CRA) plays a critical role to ensure performance and compliance for our company Protocols. Under the guidance of the Country Research Manager(CRM) / Line Manager (LM), you will be responsible for ensures country regulations, our company policies and protocol procedures fulfill in timely manner throughout...

**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 the Sponsor's standards. The Sr. CRA...

A world-leading healthcare organization based in Mexico is seeking a Senior Clinical Research Associate (CRA) to manage clinical trial activities and ensure compliance with protocols and regulations. The ideal candidate should have an advanced degree in life sciences, extensive experience in clinical research, and excellent skills in monitoring and data integrity. ICON offers a competitive salary...

**Who we are** We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright...

Site relationship management role to ensure sustainable trial execution at Site. Performs on-site and remote monitoring activities related to initiation, conduct and timely completion of Phase I-IV GDD trials within the country in adherence with monitoring procedures and processes in accordance with ICH/GCP, local regulations and SOPs. Proactive site performance management (recruitment & quality)...

Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services...

**Company Description** PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on...

**JR******** **Remote Clinical Research Associate** **Site: Reginal Mexico** 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 fulfill 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:...

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. Award winning and innovative, we'll give you access to...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90...

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout...

Parexel is looking for multiple **CRAs** with 1+ year of experience in Mexico! The **Clinical Research Associate**will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with the Study Monitoring Plan and will be performed virtually for the majority of activities to supplement on-site...

A leading clinical research organization is seeking a Clinical Research Associate II in Mexico City. In this role, you will conduct and monitor clinical trials while ensuring protocol compliance and maintaining data integrity. The ideal candidate holds a Bachelor's degree in a scientific field and has at least 2 years of experience in clinical research. This position requires strong...

A leading clinical research organization in Mexico is seeking a Clinical Research Associate II to facilitate the execution of clinical trials, ensuring compliance and data integrity. Candidates should possess a Bachelor's degree, at least 2 years of experience, and a solid understanding of trial processes. The role requires strong communication and organizational skills, as well as a willingness...

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, MSD policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout...

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, MSD policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager...

A leading healthcare intelligence firm in Mexico, Ciudad de México, is looking for a Clinical Research Associate II to manage and analyze clinical trials, ensure compliance, and work collaboratively with site staff. The ideal candidate should have a Bachelor's degree in a related field and at least 2 years of experience in clinical research. This position requires strong organizational and...

Main Point of Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT). - Experience on project management (minimum 6 months) - Knolewdge on regulatory and importation local enviroment - Responsible for project management of the assigned studies: pro-actively plans, drives andtracks execution and performance of deliverables/timelines/results to meet...

Knowledge in Project Management and site management. - Strong organizational skills with demonstrated success required. - Requires ability to make decisions independently and oversee important activities relevant to clinical research activities according to predetermined global policies and commitments with the support, oversight and supervision of the TA Head or CRD - Requires strong...

**Job Description**: Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. **Knowledge in Project Management and site management**: - Strong organizational skills with...