Clinical Research Manager

hace 4 semanas


Ciudad de México, Ciudad de México MEX Labcorp Clinical Development, S. de R.L. de C.V. A tiempo completo

Job Summary

MEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly skilled Clinical Research Manager to lead our global clinical trials efforts. As a key member of our team, you will be responsible for managing clinical trials from feasibility to close-out, ensuring compliance with regulatory requirements and company standards.

Key Responsibilities

  • Manage clinical trials from feasibility to close-out, ensuring compliance with regulatory requirements and company standards.
  • Develop and implement clinical trial plans, including study protocols, informed consent forms, and case report forms.
  • Collaborate with cross-functional teams, including clinical operations, medical affairs, and regulatory affairs, to ensure seamless trial execution.
  • Ensure timely and accurate reporting of trial data, including adverse event reporting and study close-out.
  • Develop and maintain relationships with investigators, site staff, and other stakeholders to ensure successful trial execution.
  • Ensure compliance with company policies and procedures, as well as regulatory requirements, including GCP and ICH guidelines.
  • Participate in the development and implementation of clinical trial budgets and resource allocation plans.
  • Provide training and support to site staff and other stakeholders as needed.

Requirements

  • Bachelor's degree in a life science or related field.
  • Minimum 5 years of experience in clinical research, including experience in managing clinical trials.
  • Strong knowledge of clinical trial regulations, including GCP and ICH guidelines.
  • Excellent communication and project management skills.
  • Ability to work in a fast-paced environment and prioritize multiple tasks and projects.

What We Offer

MEX Labcorp Clinical Development, S. de R.L. de C.V. offers a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and experienced clinical research professional looking for a new challenge, please submit your application today.



  • Ciudad de México, Ciudad de México MEX Labcorp Clinical Development, S. de R.L. de C.V. A tiempo completo

    About the RoleMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly motivated and experienced Clinical Research Manager to join our team. As a key member of our clinical operations team, you will be responsible for managing clinical trials from feasibility to close-out, ensuring timely and efficient execution of studies.Key...


  • Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completo

    About the RoleWe are seeking a skilled Clinical Research Specialist to join our team at Worldwide Clinical Trials. As a Clinical Research Specialist, you will be responsible for all aspects of assigned projects, including clinical assessment, training development, and data review.Key ResponsibilitiesAssist in the review of eCOA/ePRO specifications and engage...


  • Ciudad de México, Ciudad de México MEX Labcorp Clinical Development, S. de R.L. de C.V. A tiempo completo

    Job SummaryMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly skilled Clinical Research Manager to lead clinical trials and drive business growth. As a key member of our clinical operations team, you will be responsible for project management, protocol execution, and ensuring compliance with regulatory requirements.Key...


  • Ciudad de México, Ciudad de México Thermo Fisher Scientific A tiempo completo

    Clinical Research Associate Job DescriptionPurpose:Clinical Research Associate (CRA) Job SummaryWe are seeking a highly motivated and detail-oriented Clinical Research Associate (CRA) to join our team. The CRA will be responsible for monitoring and coordinating clinical trials, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP)...


  • Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completo

    Worldwide Clinical Trials (Worldwide) is a leading global contract research organization that works in partnership with biotechnology and pharmaceutical companies to create customized solutions for advancing new medications.We are seeking a highly skilled Clinical Assessment Specialist to join our team. As a key member of the Clinical Assessment Technologies...


  • Ciudad de México, Ciudad de México Icon Plc A tiempo completo

    Job Title: Clinical Research AssociateAs a Clinical Research Associate at ICON Plc, you will be part of a dynamic team that is dedicated to delivering high-quality clinical research services to our clients. We are seeking a highly motivated and experienced individual to join our team as a Clinical Research Associate.Job Summary:The Clinical Research...


  • Ciudad de México, Ciudad de México Allucent A tiempo completo

    We are seeking a highly skilled Clinical Research Coordinator to join our team at Allucent, a leading biopharmaceutical company dedicated to helping small-medium companies navigate the complex world of clinical trials.The successful candidate will be responsible for providing administrative support to our clinical study teams, ensuring that clinical trials...


  • Ciudad de México, Ciudad de México PSI A tiempo completo

    Job Title: Lead CRAAbout the RoleWe are seeking a highly skilled and experienced Lead Clinical Research Associate to join our team at PSI. As a Lead CRA, you will play a key role in managing local Monitors, supervising clinical monitoring and site management activities to ensure the protection of trial subjects' rights, safety, and well-being, data quality,...


  • Ecatepec de Morelos, México Syneos Health Clinical A tiempo completo

    Syneos Health Clinical is seeking a highly motivated Oncology Clinical Research Associate to join our team in Mexico.The ideal candidate will have experience conducting site qualification, initiation, interim monitoring, site management and close-out visits ensuring regulatory compliance. They will also have strong communication and problem-solving skills,...


  • Ciudad de México, Ciudad de México Allucent A tiempo completo

    Job OverviewWe are seeking a highly skilled Clinical Research Coordinator to join our team at Allucent. This role will provide administrative support to our clinical study teams, ensuring the smooth conduct of international clinical studies.About the Role:This is an excellent opportunity for a motivated individual to develop their skills in clinical research...


  • Ciudad de México, Ciudad de México Psi CRO Ag A tiempo completo

    At PSI CRO Ag, we are seeking a Clinical Research Associate II to join our team of experienced professionals. This role will provide opportunities for professional growth and development in the field of clinical research. About the RoleAs a Clinical Research Associate II, you will be responsible for conducting and reporting onsite monitoring visits,...


  • Ciudad de México, Ciudad de México PSI A tiempo completo

    Job DescriptionAs a key member of the PSI team, you will play a critical role in the successful execution of clinical trials in Mexico. Your primary responsibility will be to provide direct operational support to project teams, ensuring that clinical projects start smoothly and on time from home-based location.You will oversee and coordinate the processes...


  • Ciudad de México, Ciudad de México M3 Global Research A tiempo completo

    About the RoleThis Quantitative Project Manager position is part of M3 Global Research, a leading provider of data-collection services for pharmaceutical and healthcare industries. We specialize in conducting qualitative and quantitative market research in The Nordics and Benelux regions, in addition to Austria and Switzerland.The mission of the Quantitative...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job OverviewWe are seeking an experienced Clinical Trials Project Manager to lead and oversee the execution of clinical projects and research studies in accordance with global and local regulations.Key Responsibilities:Support in ensuring compliance with contract, SOPs, GCPs, policies, and regulatory requirements.Meeting quality & timeline metrics.Effective...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job OverviewAt IQVIA, we are seeking a skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for conducting site monitoring visits to ensure that sites are conducting studies and reporting data as required by the study protocol, applicable regulations, and sponsor requirements.Key...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled and experienced Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local...


  • Ciudad de México, Ciudad de México Covance Latinoamérica A tiempo completo

    Job OverviewWe are seeking a highly motivated and organized Clinical Research Associate to join our team in Covance Latinoamérica. As a Clinical Research Associate, you will be responsible for managing clinical trials from start to finish, ensuring compliance with regulatory requirements and maintaining high-quality data.About the JobEstimated Salary:...


  • Ciudad de México, Ciudad de México Thermo Fisher Scientific A tiempo completo

    Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for performing and coordinating all aspects of the clinical monitoring and site management process.Key ResponsibilitiesConduct remote or on-site visits to assess protocol and regulatory compliance and manage...


  • Ciudad de México, Ciudad de México PSI CRO A tiempo completo

    As a Clinical Research Associate at PSI CRO, you will be responsible for conducting and reporting onsite monitoring visits, as well as being involved in study startup and feasibility research. You will also perform CRF review, source document verification, and query resolution, and be responsible for site communication and management. Additionally, you will...


  • Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completo

    **About the Role**Worldwide Clinical Trials is seeking a highly organized and detail-oriented Clinical Operations Specialist to join our team. As a Clinical Operations Specialist, you will be responsible for carrying out daily aspects of operational work related to rater selection, rater certification/qualification, rater training content, scale acquisition,...