Cra 2
hace 2 semanas
**Join IQVIA as a Clinical Research Associate 2 (CRA 2)****Location**: Mexico City, Guadalajara or Monterrey**About the role**:At IQVIA, we’re reshaping the future of healthcare through innovation and data-driven insights. As a Clinical Research Associate (CRA), you’ll be at the forefront of clinical excellence—ensuring that investigational sites conduct studies with precision, integrity, and compliance. This is more than monitoring; it’s about making a real impact on global health.**Key Responsibilities**:- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.- Collaborate and liaise with study team members for project execution support as appropriate.- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.**Basic Qualifications**:We’re looking for passionate professionals who thrive in a fast-paced, purpose-driven environment.- Bachelor's Degree in scientific discipline or health care preferred.- Requires at least 1 year and a half of on-site monitoring experience.- Requires experience in all on-site monitoring visits.- Fluent conversational English**Others requirements**:- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).- Good therapeutic and protocol knowledge as provided in company training.- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).- Organizational and problem-solving skills.- Effective time and financial management skills.- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.**Ready to make your mark in clinical research?
-
Cra 2
hace 3 días
Ciudad de México IQVIA A tiempo completo**Join IQVIA as a Clinical Research Associate 2 (CRA 2)****Location**:Mexico City**About the role**:At IQVIA, we’re reshaping the future of healthcare through innovation and data-driven insights. As a Clinical Research Associate (CRA), you’ll be at the forefront of clinical excellence—ensuring that investigational sites conduct studies with precision,...
-
Cra Ii
hace 1 semana
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 2
hace 5 días
Ciudad de México Novasyte A tiempo completoJob 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...
-
Cra I
hace 2 semanas
Ciudad de México Fortrea A tiempo completoLabcorp 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...
-
Cfsp Cra 2
hace 5 días
Ciudad de México Novasyte A tiempo completoJob 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...
-
Clinical Research Associate
hace 4 semanas
Ciudad de México AstraZeneca A tiempo completo**Location** Mexico City, Mexico City, Mexico**Job ID** R- **Date posted** 23/06/2025**CRA**Location: CDMXThe Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/...
-
Cra Ii
hace 3 días
Colonia Lomas de Chapultepec, México Labcorp A tiempo completoThe Clinical Research Associate II (CRA II) is responsible and accountable for site monitoring and site management. Has responsibility for clinical studies according to Company, and/or Sponsor Standard Operating Procedures, and local regulatory guidelines. Assures the implementation of project plans, as assigned. Act in the project role of a Local Project...
-
Cra Ii
hace 5 días
Ciudad de México Icon plc A tiempo completo**Overview**: - We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and...
-
Associate Clinical Research Associate
hace 7 días
Ciudad de México MSD A tiempo completoWith 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...
-
Ihcra I
hace 5 días
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...
