Cra I

hace 5 días

Ciudad de México Fortrea A tiempo completo

Labcorp Drug Development is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. Are you ready for the next step in your career? We are currently recruiting for a Clinical Research Associate I in Mexico. Role description: - Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study - Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements - Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review - Ensure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Covance travel policy - Travel, including air travel, may be required and is an essential function of the job. - Manage small projects under direction of a Project Manager/Director as assigned - Serve as lead monitor for a protocol or project, and may assist in establishing monitoring plans and trip report review as assigned - Review progress of projects and initiate appropriate actions to achieve target objectives - Organize and make presentations at Investigator Meetings - Act as contact for clinical trial supplies and other suppliers (vendors) as assigned - Responsible for all aspects of registry management as prescribed in the project plans - Conduct, report and follow-up on Quality Control Visits (CQC) when requested - Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assigned. Requirements: - A minimum of 2 years of experience in a related role (e.g. site management, in-house CRA, study coordinator, research nurse, etc) - Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries - Thorough understanding of the drug development process - Fluent in local office language and in English, both written and verbalFortrea is proud to be an Equal Opportunity Employer:As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.For more information about how we collect and store your personal data, please see ourPrivacy Statement.

  • Cra I

    hace 3 semanas

    Ciudad de México ICON A tiempo completo

    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.As Clinical Research Associate you will be joining the world’s largest & most comprehensive...

  • Cra I

    hace 3 semanas

    Ciudad de México Icon plc 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...

  • Cra I

    hace 2 semanas

    Ciudad de México Icon plc A tiempo completo

    ICON plc is a world-leading healthcare intelligence and clinical research organization. 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 center of all that we do, we help to accelerate the development...

  • Sr Cra I

    hace 3 semanas

    Edo. de México Syneos Health Clinical A tiempo completo

    **Description****Clinical Research Associate I**Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our...

  • Cra Ii

    hace 6 días

    Ciudad de México ICON plc A tiempo completo

    **Experienced CRA - Mexico City, home-based role** 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...

  • Ihcra I

    hace 4 semanas

    Ciudad de México Fortrea A tiempo completo

    **Job Overview**:**Summary of Responsibilities**:- To serve as contact for project team and investigative sites, conduct site contacts and document contacts for assigned sites as required per study guidelines, including creating contact reports for each telephone session (outbound or inbound) with sites.- To monitor site performance and implement action...

  • Sr Cra

    hace 2 semanas

    Ciudad de México PPD A tiempo completo

    PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams.Our global...

  • Sr Cra

    hace 5 días

    Ciudad de México PPD A tiempo completo

    **JOB DESCRIPTION**:PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic...

  • Cra Ii

    hace 5 días

    Ciudad de México Fortrea A tiempo completo

    **Summary of Responsibilities**: - Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. - Conducts site monitoring responsibilities for clinical trials according to Fortrea’s...

  • Cra Ii

    hace 3 días

    Ciudad de México Fortrea A tiempo completo

    **Summary of Responsibilities**:- Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.- Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...