Clinical Research Associate

hace 1 semana

Desde casa, México ICON A tiempo completo

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 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.

**What will you be doing?**

The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

This role will be dedicated to one sponsor & local sites.

**What do you need to have?**

Education: Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required

**Skills**:

- Read, write and speak fluent English; fluent in host country language required.
- 1+ years of clinical monitoring experience required
- Knowledge of ICH and local regulatory authority regulations regarding drug
- Clinical research experience
- Knowledge of ICH and local regulatory authority regulations regarding drug
- Experience in monitoring all trial components (PSSV to COV)
- Ability to travel as needed (greater than 50%)

**Benefits 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.

  • Senior Clinical Research Associate

    hace 4 semanas

    Desde casa, México Parexel A tiempo completo

    Everything 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...

  • Senior Clinical Research Associate

    hace 9 horas

    Desde casa, México Parexel A tiempo completo

    Everything 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...

  • Clinical Research Associate

    hace 7 días

    Desde casa, México Parexel A tiempo completo

    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...

  • Senior Clinical Research Associate

    hace 4 días

    Desde casa, México IQVIA A tiempo completo

    Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

  • Remote Clinical Research Associate

    hace 7 días

    Desde casa, México ICON A tiempo completo

    **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: Accountability &...

  • Senior Clinical Research Associate I

    hace 1 semana

    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...

  • Clinical Trials Assistant, Cfsp

    hace 4 semanas

    Desde casa, México IQVIA A tiempo completo

    **Job Overview** Perform daily administrative activities in collaboration with Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams to ensure the accurate delivery of the Trial Master File (TMF).**Essential Functions**- Assist CRAs and RSU teams with updating and maintaining clinical documents and systems (e.g., TMF) to track site...

  • Clinical Trials Assistant, Cfsp

    hace 10 horas

    Desde casa, México IQVIA A tiempo completo

    **Job Overview** Perform daily administrative activities in collaboration with Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams to ensure the accurate delivery of the Trial Master File (TMF). **Essential Functions** - Assist CRAs and RSU teams with updating and maintaining clinical documents and systems (e.g., TMF) to track site...

  • Manager, Clinical Operations

    hace 4 días

    Desde casa, México IQVIA A tiempo completo

    **Unleash Your Potential**: It takes curiosity and intellectual courage to accomplish great things. It takes brave minds to bring powerful ideas to reality and transform healthcare. We are a diverse, global team that shares a passion for collaboration and solving complex problems. Together, we help customers drive healthcare forward. Join IQVIA and see...

  • Manager, Clinical Operations

    hace 2 semanas

    Desde casa, México ICON A tiempo completo

    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...