Senior Clinical Research Associate

hace 6 días


Ciudad de México PSI CRO A tiempo completo

**Company Description**PSI is a leading Contract Research Organization with more than 27 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.We 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 Mexico**You will**:- Conduct and report all types of onsite monitoring visits- Be involved in study startup (if applicable)- Perform CRF review, source document verification and query resolution- Be responsible for site communication and management- Be a point of contact for in-house support services and vendors- Communicate with internal project teams regarding study progress- Participate in feasibility research- Support regulatory team in preparing documents for study submissions**Qualifications**- College/University degree in Life Sciences or an equivalent combination of education, training & experience- Independent on-site monitoring experience in Mexico- Experience in all types of monitoring visits in Phase II and/or III- Availability to travel- Experience in Oncology or Infectious Diseases is a plus- Full working proficiency in English and Spanish- PC skills to be able to work with MS Word, Excel and PowerPoint- Ability to plan, deal with different tasks and work in a dynamic team environment- Communication, collaboration, and problem-solving skills**Additional Information**Become a full-fledged clinical research professional with the support of a knowledgeable and professional team. You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.



  • Ciudad de México ICON Plc A tiempo completo

    Senior Clinical Associate - Mexico - Hybrid or Homebased ICON 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 We are currently seeking a Senior...


  • México FHI Clinical Inc A tiempo completo

    **Summary of the Position**:The Senior Contract Clinical Research Associate III (Snr. CRA III) monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), study protocols and applicable regulatory requirements. Reviews study documents as required and prepares site visit reports....


  • Ciudad de México Medpace, Inc. A tiempo completo

    Job Summary: The Clinical Research Associate at Medpace is offering the unique opportunity to have an **exciting career** in the research of drug and medical device development. For those with **medical and/or health/life science interest and background** who want to explore the research field, **travel throughout Brazil**, and be part of a team bringing...

  • Senior Clinical Associate

    hace 2 semanas


    Ciudad de 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...


  • Ciudad de México MSD A tiempo completo

    The role is accountable for performance and compliance for assigned protocols and sites in a country under the oversight of the Clinical Research Associate 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...

  • Senior Clinical Associate

    hace 4 semanas


    Ciudad de 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...


  • Ciudad de México, CDMX PSI CRO A tiempo completo

    **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. Only CV's in English will be considered We are looking...


  • Ciudad de México PSI CRO A tiempo completo

    **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...


  • Ciudad de México MSD A tiempo completo

    With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. - Performs clinical study site management/monitoring...


  • Ciudad de México MSD A tiempo completo

    **Job Description**: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, policies and procedures, quality standards and adverse event reporting requirements internally and externally.Acts...