Senior Clinical Research Associate

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-timeJob Overview Provides high quality, timely development and on-time input to client solutions for the pharmaceutical...

Job Description SummaryLocation: Mexico CityAbout the role:We are seeking a Clinical Research Associate who will supply, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of...

Covance is growing again in Mexico This is an exciting opportunity to join one of the fastest growing parts of our business • Act as contact for project team and study sites.• Perform CRF review, query generation and resolution against established data review guidelines, under direct supervision on Covance or client data management systems, as assigned...

Covance is growing again in Mexico This is an exciting opportunity to join one of the fastest growing parts of our business • Act as contact for project team and study sites. • Perform CRF review, query generation and resolution against established data review guidelines, under direct supervision on Covance or client data management systems, as assigned...

Clinical Research AssociateCategory:Clinical DevelopmentLocation:Ciudad de México, Ciudad de México, MX- Are you ready for a life-changing career at Novo Nordisk Mexico? Join us.- Working at Novo Nordisk is never just a job, it is an opportunity to have a life-changing career - you grow professionally, and you impact the lives of our patients for better....

Requisition Number7914**Employment Type:Regular**Who we areWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company's scientific heritage,...

Job Description The role is accountable for performance and compliance for assigned protocols and sites in acountry. Under the oversight of the CRA manager the person ensures compliance of study conduct withICH/GCP and country regulations, our company policies and procedures, quality standards andadverse event reporting requirements internally and...

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 organizations.With our patients at the Centre of all that we do, we help to accelerate the development...

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do.A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals.We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.If you...

Job DescriptionWe are looking for an experienced CRA ready to train and coordinate junior CRAs on site. Here you will have the opportunity to develop yourself as a trainer, mentor and leader. We are committed to develop our employees in their careers by providing tailored courses and mentoring.Only CVs in English will be consideredHome-based position in...

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...

Job DescriptionThe 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...

Job DescriptionThe 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...

Job DescriptionThe 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...

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 all that we do, we help to accelerate the development...

Job DescriptionOur Clinical Research and Pharmacovigilance team strives to advance global healthcare through groundbreaking research and innovation. By conducting clinical trials and surveillance, we guarantee the safety and effectiveness of our current and upcoming products, producing cutting-edge, secure, and effective medications.Essential Knowledge in...

Job DescriptionOur Clinical Research and Pharmacovigilance team strives to advance global healthcare through groundbreaking research and innovation. By conducting clinical trials and surveillance, we guarantee the safety and effectiveness of our current and upcoming products, producing cutting-edge, secure, and effective medications.Essential Knowledge in...

Job DescriptionThe 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 company policies and procedures, quality standards and adverse event reporting requirements internally and...

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.Primary Activities: Main Point of Contact (POC) for...

Requisition Number7564**Employment Type:Regular**Who we areWorldwide, a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company's scientific heritage, our dedicated therapeutic...