Last updated: 2025-05-03
10 Clinical Data And Biostatistics jobs in Remote - Argentine Republic.
Hiring now: Site Care Partnersr Cra F @ Parexel, Sr Clinical Research Asso @ Syneos Hea, Clinical Proj Mgr @ Alimentiv, Coordinating Cra Ccra @ Iqvia.Explore more at jobswithgpt.com. at jobswithgpt.com
š„ Skills
Clinical Research (5)
Clinical Trials (4)
Data Management (4)
Functional Service Provider (2)
Regulatory Compliance (2)
Project Management (2)
Risk Management (2)
Training (2)
CRA (1)
Site Care Partner (1)
š Locations
Argentine Republic (10)
Syneos Health
Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medicā¦
Sr Clinical Research Associate I - Sponsor dedicated
Argentine Republic
- Skills: Clinical Research, Site Management, Monitoring, GCP, Regulatory Compliance, Data Review, Patient Recruitment, Biopharmaceutical, Pharmacovigilance, Investigator Meetings
- Experience: Bachelorās degree or RN in a related field or equivalent combination of education, training and experience
Alimentiv
Clinical Project Manager
Argentine Republic
- Skills: Clinical Research, Project Management, Clinical Study Delivery, Risk Management, Regulatory Compliance, Cross-functional Team, Patient Safety, Data Management, Stakeholder Training, Sponsor Liaison
- Experience: 1-3 years
- Type: Full-time, Permanent
Syneos Health
Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medicā¦
Data Ops Technical Specialist
Argentine Republic
- Skills: Data Management, Technical Processes, Specifications, User Test Plans, Clinical Development, Regulatory Requirements, Training, Audits, Proposal Process, Team Collaboration
IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industriā¦
Coordinating CRA (CCRA)
Argentine Republic
- Skills: monitoring, site management, clinical research, Good Clinical Practice, regulatory requirements, communication, problem-solving, database maintenance, performance management, team coordination
- Experience: at least 3 years of on-site monitoring experience
- Type: Full time