Empleos actuales relacionados con Clinical Research Associate Ii - Bogota - Labcorp
-
Clinical Research Associate
hace 7 días
Bogota, Colombia MSD A tiempo completo**Job Description**: We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” and that great medicines can make a significant impact to our world. And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations...
-
Clinical Research Associate
hace 2 horas
Bogota, Colombia 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, company policies and procedures, quality standards and adverse event reporting requirements internally and...
-
Senior Clinical Research Associate
hace 2 semanas
Bogota, Colombia Novo Nordisk A tiempo completoSenior Clinical Research Associate **Category**:Clinical Development**Location**:Bogota, Cundinamarca, CO- **The Position** - The Senior CRA will manage and execute the entire Novo Nordisk clinical trials process in compliance with internal SOPs including GCP-ICH and Colombia regulatory framework.**Activities and Responsibilities** - Clinical Trials...
-
Clinical Research Associate
hace 2 semanas
Bogota, Colombia MSD A tiempo completoThe 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 International Conference on Harmonisation Good Clinical Practice and country regulations, our company policies and procedures, quality...
-
Senior Clinical Research Associate
hace 2 semanas
Bogota, Colombia MSD A tiempo completoThe role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as...
-
Clinical Research Manager
hace 2 semanas
Bogota, Colombia MSD A tiempo completo**Job Description**: This role is primarily accountable for the end-to-end performance and project management for assigned protocols in compliance with country regulations, policies and procedures, quality standards and adverse event reporting requirements internally and externally. The Clinical Research Manager could be responsible for a particular study...
-
Clinical Research Associate
hace 1 semana
Bogota, Colombia AstraZeneca A tiempo completo¿Tienes experiência y pasión por estudios clínicos? ¿Te gustaría aplicar tu experiência para impactar en una empresa que sigue la ciencia y convierte las ideas en medicamentos que cambian la vida? ¡Entonces AstraZeneca podría ser la empresa indicada para ti!_ En el Clúster Andino tenemos una gran oportunidad dentro del área de estudios clinicos...
-
Clinical Trial Assistant
hace 6 días
Bogota, Colombia IQVIA A tiempo completoJob Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...
-
Remote Clinical Research Associate
hace 2 semanas
Bogota, Colombia ICON plc A tiempo completoAt 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 fulfill our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery,...
-
Clinical Trial Manager Ii
hace 6 días
Bogota, Colombia Icon plc A tiempo completoClinical Trial Manager II JR090304 Site: Peru / Brazil / Chile / Colombia / Mexico 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...
Clinical Research Associate Ii
hace 2 semanas
1) The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. 2) Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned 3) Responsible for all aspects of site management as prescribed in the project plans 4) General On-Site Monitoring Responsibilities 5) Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study 6) Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements 7) Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review 8) Monitor data for missing or implausible data 9) 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 10) Ensure audit readiness at the site level 11) Travel, including air travel, may be required and is an essential function of the job. 12) Prepare accurate and timely trip reports 13) Responsible for all aspects of registry management as prescribed in the project plans 14) Undertake feasibility work when requested 15) Participate in and follow up on Quality Control Visits (QC) when requested 16) 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 17) Might be requested to work in a client facing environment 18) Track and follow up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAE 19) Independently perform CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management 20) Assist with training, of new employees, e.g. co-monitoring 21) Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned 22) Perform other duties as assigned by management
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
For more information about how we collect and store your personal data, please see our Privacy Statement.
