Senior Clinical Trials Specialist

hace 4 días


Buenos Aires, Buenos Aires C.F., Argentina Roca Alliances S.A A tiempo completo
About the Role

We are seeking a skilled CRA II & Senior CRA to join our team. In this role, you will work with a large-scale, fast-paced environment and be responsible for identifying, selecting, initiating and closing out investigational sites for clinical studies in phases II - IV.

Main Responsibilities:
  1. Study Setup and Monitoring: Work independently to coordinate activities, complete accurate study status reports, and maintain study documentation.
  2. Regulatory Submissions: Submission of protocol, consent documents for ethics/IRB approval, and assistance in preparing regulatory submissions as requested.
  3. Study Documentation: Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required.
  4. Sponsor Generated Queries: Balance queries efficiently and ensure study cost-effectiveness.
  5. Training and Mentoring: Depending on level of experience, you may assist in training and mentoring less expert CRAs and/or lead CRAs working on international projects.
About ICON

At ICON, our focus is to provide a comprehensive and competitive total reward package that comprises an excellent level of base pay, as well as a wide range of variable pay and recognition programs. Our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to support you and your family at all stages of your career.



  • Buenos Aires, Buenos Aires C.F., Argentina Itps A tiempo completo

    About the RoleIn this exciting opportunity, you will work as a Senior Clinical Trials Specialist, providing expertise in clinical research operations. You will be responsible for ensuring the highest quality standards in the industry and delivering exceptional customer service.Main ResponsibilitiesPreparation, conduct, and reporting of selection, initiation,...


  • Buenos Aires, Buenos Aires C.F., Argentina IQVIA A tiempo completo

    About the RoleWe are looking for a Global Clinical Trials Lead to join our team at IQVIA. The successful candidate will be responsible for managing and coordinating activities for assigned opportunities and projects.Key Responsibilities:Develop and implement country, site, or enrollment strategies in support of opportunities, including requests for...


  • Buenos Aires, Buenos Aires C.F., Argentina Iqvia A tiempo completo

    Job Description:Iqvia seeks a talented Associate Manager, Global Analytics who will be responsible for providing input into the development of study strategies and collaborating with IQVIA teams to ensure accurate and robust country, site or enrollment strategies.The successful candidate will have a strong background in data analysis and a deep understanding...


  • Buenos Aires, Buenos Aires C.F., Argentina Zs Associates A tiempo completo

    ZS Associates is a leading provider of clinical trial optimization solutions, partnering with pharmaceutical companies to improve trial efficiency and effectiveness.We're seeking an experienced Clinical Trial Optimization Specialist to join our team and contribute to delivering cutting-edge solutions that drive business growth and...


  • Buenos Aires, Buenos Aires C.F., Argentina Avature A tiempo completo

    About the Role:This Clinical Team Lead position is a critical role in our team at Avature, where you will lead clinical trials in the LATAM region. You will collaborate with cross-functional teams to ensure successful trial execution, focusing on site selection, document adaptation, and regulatory compliance.Main Accountabilities:Selecting and managing trial...


  • Buenos Aires, Buenos Aires C.F., Argentina IQVIA LLC A tiempo completo

    About the Job:IQVIA LLC is seeking a Clinical Trials Coordinator to join our team. As a key member of our team, you will be responsible for working with study documents, study teams, and other internal and external stakeholders to gather and synthesize the necessary information for setting up studies and data integrations.Responsibilities:Create clinical...


  • Buenos Aires, Buenos Aires C.F., Argentina Xepelin A tiempo completo

    Job DescriptionLilly is seeking a Clinical Research Lead to manage clinical investigators and sites participating in clinical trials. The successful candidate will be responsible for site identification, enrollment planning, issues management, and ensuring inspection readiness.Key AccountabilitiesManage site activities, including site qualification,...


  • Buenos Aires, Buenos Aires C.F., Argentina Web: A tiempo completo

    About Our CompanyWe are a global company founded in 1995, bringing together driven, dedicated and passionate individuals who work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.Job SummaryOur company seeks a Senior Clinical Research Associate to conduct monitoring tasks and work on clinical studies in...

  • Clinical Trials

    hace 12 minutos


    Buenos Aires, Buenos Aires C.F., Argentina ThermoFisher Scientific A tiempo completo

    ThermoFisher Scientific Clinical Trials - Senior PMO in Buenos Aires, ArgentinaWork Schedule: OtherEnvironmental Conditions: OfficeJob Description: Coordinating multiple complex projects from initiation through delivery, ensuring they meet scope, quality, time, and cost constraints.Key Responsibilities:Lead Projects: Manage and monitor multiple related...


  • Buenos Aires, Buenos Aires C.F., Argentina 4Peeq A tiempo completo

    About UsAt 4Peeq, we are passionate about improving patient outcomes through innovative clinical trials. We are seeking an experienced Clinical Trial Liaison Director to join our team and lead a team of Clinical Trial Ambassadors across LATAM.Main ResponsibilitiesDevelop and implement strategies to improve patient recruitment and retentionLead a team of...


  • Buenos Aires, Buenos Aires C.F., Argentina Allergan A tiempo completo

    Job Summary: We are seeking a highly skilled Clinical Research Associate II to join our team. In this role, you will be responsible for advancing AbbVie's pipeline by striving for excellence in clinical research.About the Role: As a Clinical Research Associate II, you will partner with study teams, internal stakeholders, investigators, and site staff to...


  • Buenos Aires, Buenos Aires C.F., Argentina Iqvia Llc A tiempo completo

    Role OverviewThis Senior Clinical Operations Manager position plays a critical role in the delivery of clinical trials at Iqvia Llc. As a key member of the project team, you will be responsible for ensuring the timely and successful delivery of clinical studies in accordance with regulatory requirements, customer specifications, and internal standards.Your...


  • Buenos Aires, Buenos Aires C.F., Argentina Avature A tiempo completo

    Responsibilities:The Clinical Team Lead will be responsible for leading clinical trials in the LATAM region, working closely with cross-functional teams to ensure successful trial execution. Key responsibilities include:Selecting sites, conducting and delivering trials according to the clinical trial protocol.Adapting required documents for submission and...


  • Buenos Aires, Buenos Aires C.F., Argentina Xometry A tiempo completo

    Senior Clinical Research Associate, ArgentinaBASIC FUNCTIONS: Participates in the preparation and execution of Phase I-IV clinical trials.Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close-out visits to sites.Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth...


  • Buenos Aires, Buenos Aires C.F., Argentina IQVIA A tiempo completo

    Role OverviewThis role is responsible for managing all laboratory aspects of assigned clinical trial projects for a customer or a specific program for a customer.Main TasksAct as the main point of contact for the Customer after study award and throughout the entire study lifecycle.Ensure work is conducted in line with standard operating procedures, policies...


  • Buenos Aires, Buenos Aires C.F., Argentina Innovaderm Research Inc. A tiempo completo

    We are looking for a highly skilled Global Project Management Director to lead our clinical trials at Innovaderm Research Inc.About the RoleDevelop and implement project plans, ensuring timely completion of deliverables and effective communication with stakeholders.Lead cross-functional teams, managing vendor relationships and ensuring high-quality project...


  • Buenos Aires, Buenos Aires C.F., Argentina Softwaremind A tiempo completo

    Key ResponsibilitiesDevelop and maintain ML algorithms and workflows on DatabricksAssess patient risk and screen and match patients for clinical trials based on historical health recordsCollaborate with clinical and technical teams to analyze user flows and optimize data integrationsProvide insights through complex data migration analysisUtilize AWS, Python,...


  • Buenos Aires, Buenos Aires C.F., Argentina Avature A tiempo completo

    Job Summary:We are seeking a highly skilled and experienced Clinical Team Lead to join our team at Avature. In this role, you will be responsible for leading clinical trials in the LATAM region, working closely with cross-functional teams to ensure successful trial execution.Key Responsibilities:Select sites, conduct and deliver trials according to the...


  • Buenos Aires, Buenos Aires C.F., Argentina Universal Assistance Sociedad Anonima A tiempo completo

    Job Summary: Medpace is a full-service clinical contract research organization (CRO) that accelerates the global development of safe and effective medical therapeutics. We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.We are currently seeking a full-time Sr. Contract Specialist to join...


  • Buenos Aires, Buenos Aires C.F., Argentina St Andrew's Scots School A tiempo completo

    Job Summary: We are seeking a highly skilled and experienced Senior Clinical Research Associate to join our team at St Andrew's Scots School. As a key member of our clinical research team, you will be responsible for site monitoring and site management for clinical studies according to Covance Standard Operating Procedures and Regulatory Guidelines.Main...