Clinical Trial Assistant Ii
hace 3 semanas
Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential Functions- Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.- Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.- Prepare site regulatory documents, reviewing for completeness and accuracy.- Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.- Review and provide feedback to management on site performance metrics.- Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.- Inform team members of completion of regulatory and contractual documents for individual sites.- Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.- Provide local expertise to SAMs and project team during initial and on-going project timeline planning.- Perform quality control of documents provided by sites.- May have direct contact with sponsors on specific initiatives.**Qualifications**:- 2 years experience in global clinical trial.- Preparing site specific ICF and any other relevant forms according to local SOP.- Previous experience with eTMF, Veeva vault of similar system.
-
Clinical Trial Educator
hace 3 semanas
Desde casa, México IQVIA A tiempo completoThe Clinical Trial Educator (CTE) will provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers. The Clinical Trial Educator will provide in-service presentations with the goal to increase patient enrollment. The CTE works in partnership with CRAs and other field-based medical teams...
-
Clinical Trial Manager
hace 4 días
Desde casa, México ICON A tiempo completoWe are currently seeking a Manager, CTM (Clinical Trial Management) to join our diverse and dynamic team. As the Manager of CTM at ICON, you will play a pivotal role in overseeing the planning and execution of clinical trials, ensuring that they are conducted efficiently and in compliance with regulatory standards. Your leadership will be crucial in driving...
-
Clinical Trial Liaison
hace 2 semanas
Desde casa, México ICON A tiempo completoICON 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...
-
Clinical Trial Educator 1- Mexico
hace 4 semanas
Desde casa, México IQVIA A tiempo completo**Job Overview**The Clinical Trial Educator (CTE) will provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers. The Clinical Trial Educator will provide in-service presentations with the goal to increase patient enrollment. The CTE works in partnership with CRAs and other field-based...
-
Clinical Study Team Assistant I, Fsp
hace 1 semana
Desde casa, México Parexel A tiempo completo**Clinical Study Team Assistant I (CSTA I)****Position Purpose**:The Clinical Study Team Assistant I (CSTA I) is an essential part of the Core Study Team and is responsible for supporting key clinical trial tasks for assigned studies to ensure compliance with ICH-GCP, SOPs, and regulatory regulations. The role collaborates with global study team members and...
-
Clinical Study Team Assistant I, Fsp
hace 1 semana
Desde casa, México Parexel A tiempo completo**Clinical Study Team Assistant I (CSTA I)** **Position Purpose**: The Clinical Study Team Assistant I (CSTA I) is an essential part of the Core Study Team and is responsible for supporting key clinical trial tasks for assigned studies to ensure compliance with ICH-GCP, SOPs, and regulatory regulations. The role collaborates with global study team members...
-
Clinical Study Team Assistant I
hace 7 días
Desde casa, México Parexel A tiempo completoParexel is looking for multiple Clinical Study Team Assistant I in Mexico, Argentina or Brazil! The Clinical Study Team Assistant I (CSTA I) is an essential part of the study team and is responsible for supporting key clinical trial tasks for assigned studies to ensure compliance with timelines, Good Clinical Practice (GCP), and client Standard Operating...
-
Clinical Study Team Assistant I
hace 5 días
Desde casa, México Parexel A tiempo completoParexel is looking for multiple Clinical Study Team Assistant I in Mexico, Argentina or Brazil!The Clinical Study Team Assistant I (CSTA I) is an essential part of the study team and is responsible for supporting key clinical trial tasks for assigned studies to ensure compliance with timelines, Good Clinical Practice (GCP), and client Standard Operating...
-
Sr. or Clinical Trial Manager, Oncology, Mexico
hace 2 semanas
Desde casa, México IQVIA A tiempo completo**IQVIA Biotech is committed and dedicated to the small biotech & biopharma companies we support.** **Opportunities available for an experienced Clinical Trial Manager II or Senior Clinical Trial Manager.** **Previous clinical trial management and CRO experience preferred.** **Therapeutic **requirements/preference**: any of the following...
-
Clinical Trial Manager
hace 3 semanas
Desde casa, México ICON A tiempo completo**Clinical Trial Manager****JR ****Site: Mexico City and São Paulo - Brazil**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 fulfil our mission to advance and improve patients’ lives.Our ‘Own It’ culture is driven by four key values that bring us together as...
