Clinical Scientist- Fsp
hace 15 horas
**PXL FSP is seeking a Clinical Scientist for a remote role in Latin America** Job Purpose: The Clinical Scientist (CS) assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies (e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management). Key Accountabilities: May include but not limited to the following: Clinical Trial Operational Delivery - May support a single study or multiple studies - May lead a study with limited scope (e.g., Survival Follow-up) - Liaises with cross-functional lines as appropriate - May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives Compliance with Parexel Standards - Complies with required training curriculum - Completes timesheets accurately as required - Submits expense reports as required - Updates CV as required - Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements **Skills**: - Demonstrated oral and written communication skills - MS Office Suite Experience Required - including Word, Excel, and Power Point - Proficient in written and spoken English - Proficient in local language (as applicable) - Willingness to travel as required for key company meetings Knowledge and Experience: - Pharmaceutical experience beneficial but not required - Therapeutic Area (TA) specific experience beneficial - 2 years medical monitoring experience preferred Education: - Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience - If no degree in Life Sciences, must have significant experience in clinical development (>5 years) LI-REMOTE
-
Global Clinical Lead
hace 3 semanas
Buenos Aires, Argentina ACTIF A tiempo completoA global biopharmaceutical solutions organization is seeking a Global Clinical Lead/CTM in RWE. The role involves leading observational studies, collaborating with multinational teams, and ensuring consistent execution across therapeutic areas. The ideal candidate will have a strong background in epidemiology, clinical research, and project management....
-
Regulatory & Start Up Specialist, Fsp
hace 2 semanas
Buenos Aires, Argentina Blue Collar Scholars A tiempo completoWe are looking for a Regulatory & Start Up Specialist to join our FSP team in a Home Based role! What You’ll Do Perform 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...
-
Client Relationship Director, Fsp Sales
hace 2 días
Buenos Aires, Argentina Parexel A tiempo completo**The Client Relationship Director, FSP Sales** will work closely with Commercial Operations, SBU Delivery, Solutions Consultants, and Clients and Partners. - Responsible for identifying, targeting, and securing new business across Parexel’s FSP services, primarily clinical operations, through professional, consultative, proactive sales activities directed...
-
Senior Clinical Research Associate I
hace 7 días
Buenos Aires, Argentina Parexel A tiempo completo**Parexel FSP is looking for multiple Sr CRAs in Argentina!** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP),...
-
Senior Cra-fsp-global Cro
hace 2 semanas
Buenos Aires, Argentina NonStop Consulting A tiempo completoEstoy trabajando con una de las mejores CRO a nível mundial para buscar a un Senior CRA para su modelo FSP (sponsor dedicated). Hay muchas oportunidades de promocion interna ya que los managers siempre estan intentando promocionar a los empleados, ademas cualquiera que sea la progresion que quieras, sea a Project Manager o a otro tipo de puesto sera...
-
Clinical Research Associate II
hace 1 semana
Buenos Aires, Argentina ICON A tiempo completoClinical Research Associate II - Buenos Aires (FSP - Sponsor Dedicated) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a...
-
Lead Clinical Data Manager
hace 4 semanas
Buenos Aires, Argentina Red Bull A tiempo completoParexel FSP is looking for a Lead Clinical Data Manager with Early Development experience to join the Argentina team. Description of Role & Responsibilities Under the direction of the applicable management, the Lead Clinical Data Manager (LCDM) is responsible for executing end-to-end data management activities pertaining to clinical trials, including but not...
-
Clinical Operations Manager FSP 360
hace 7 días
Buenos Aires, Buenos Aires C.F., Argentina サイネオス・ヘルス A tiempo completoUpdated: November 12, 2025Location: Buenos Aires, B, ArgentinaJob ID: Not ready to apply?Join our Talent NetworkDescriptionClinical Operations Manager FSP 360Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into...
-
Lead Clinical Data Manager
hace 2 días
Buenos Aires, Argentina Parexel A tiempo completoParexel FSP is looking for a Lead Clinical Data Manager with Early Development experience to join the Argentina team. **Description of Role & Responsibilities** Under the direction of the applicable management, the Lead Clinical Data Manager (LCDM) is responsible for executing end-to-end data management activities pertaining to clinical trials, including...
-
Clinical Trials Assistant
hace 6 días
Buenos Aires, Argentina IQVIA A tiempo completo**_Although this role is home-based, it's a requirement to go to the client's office once a week, located in Belgrano, Buenos Aires._** Job 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...