The analyst will support the validation of clinical trial data to ensure accuracy and regulatory compliance. Key tasks include conducting quality checks on datasets, documenting discrepancies, and developing validation protocols and reports.
Remote Healthcare Jobs in Argentina (51)
Remote in = Argentina
Job category = Healthcare
Manage clinical laboratory studies within a Functional Service Provider (FSP) model to support clinical development. Ensure the delivery of high-quality laboratory services to accelerate the delivery of life-changing treatments to patients.
Clinical Trial Coordinator II
Thermo Fisher Scientific
·
Full Time
·
3 Days Ago
Thermo Fisher Scientific
The role involves coordinating clinical trials to support the development of life-changing therapies. The coordinator will work within a global team to enable customers to make the world healthier, cleaner, and safer.
The Senior Medical Director provides medical, clinical, and scientific advisory expertise for oncology and hematology trials, focusing on medical monitoring and strategic input. Responsibilities include overseeing patient safety, reviewing protocols, and supporting business development activities for complex multi-region studies.
The role involves coordinating the setup and monitoring of clinical trials while maintaining accurate study documentation and status reports. It also requires managing stakeholder relationships and ensuring strict compliance with regulatory requirements and patient safety protocols.
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Medical Director/Senior Medical Director Rheumatology (Client dedicated)
Thermo Fisher Scientific
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Full Time
·
6 Days Ago
Thermo Fisher Scientific
Provide medical oversight for clinical trials to ensure compliance with SOPs, GCP, and regulatory requirements. Perform medical review of safety data, including serious adverse events and periodic safety reports across the product life-cycle.
The MSL acts as a scientific liaison between the company and the medical community, providing disease state and product information to healthcare professionals. They are responsible for building relationships with Key Opinion Leaders and collaborating with internal teams to implement scientific strategies.
The role involves designing and analyzing clinical trials and interpreting complex medical data to advance innovative treatments. The liaison is responsible for cultivating relationships and recruiting appropriate sites to participate in trials.
The role involves reviewing structured clinical patient data to ensure medical plausibility, protocol adherence, and overall completeness for clinical trials. Responsibilities include identifying data anomalies, reviewing inclusion/exclusion criteria, and verifying adverse events and laboratory results.
Field Clinical Representative - Argentina Talent Pool
Boston Scientific
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Full Time
·
1 Week Ago
Boston Scientific
Provide real-time technical and clinical support during medical procedures using Boston Scientific devices. Deliver training to healthcare professionals and collaborate with internal teams to ensure safe product adoption.
Medical Monitor Associate, Dermatology & Rheumatology, Argentina
Indero
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Full Time
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1 Week Ago
Indero
Provide medical, scientific, and administrative support to the medical monitoring team for clinical trials in dermatology and rheumatology. Responsibilities include reviewing safety data, coding adverse events, and supporting protocol development and business development activities.
Clinical Operations Manager FSP 92 APPLICANTS
Thermo Fisher Scientific
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Full Time
·
1 Week Ago
Thermo Fisher Scientific
Oversee the daily line management, coaching, and professional development of clinical administration staff. Ensure operational excellence through effective resourcing, training, and adherence to SOPs and performance metrics.
The Medical Advisor serves as a medical expert providing medical monitoring and consultative support for clinical trials and contracted projects. They are responsible for reviewing study documents, ensuring patient safety, and maintaining strong relationships with sponsors and clients.
Lead the end-to-end management of paid media accounts with a focus on Paid Search strategy and KPI achievement. Partner with internal teams and clients to optimize campaigns, generate insights, and drive revenue growth.
Clinical Team Manager (CTM) – HemOnc 25 APPLICANTS
Thermo Fisher Scientific
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Full Time
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1 Week Ago
Thermo Fisher Scientific
The Clinical Trial Manager is responsible for achieving final clinical deliverables and ensuring clean data within contractual timelines and budgets. They manage operational and quality aspects of studies, including the development of monitoring plans and coordination with clinical teams.
Clinical Trial Assistant (Site contracts experience) - Buenos Aires
Syneos Health
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Full Time
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2 Weeks Ago
Syneos Health
The role involves assisting clinical monitoring staff with site management, maintaining project files, and tracking clinical and regulatory documents. It also includes coordinating site supplies, managing correspondence, and preparing meeting minutes.
Contract Senior Clinical Research Associate
ProTrials Research, Inc.
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Full Time
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2 Weeks Ago
ProTrials Research, Inc.
The Senior CRA is responsible for monitoring clinical trials to ensure they are conducted according to protocols, SOPs, and regulatory requirements. This includes performing site visits, managing site personnel, and ensuring the integrity of clinical data and regulatory files.
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Sr. Clinical Trial Manager (CTM) - Non-Interventional Studies (NIS)
Thermo Fisher Scientific
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Full Time
·
2 Weeks Ago
Thermo Fisher Scientific
Accountable for achieving final clinical deliverables and clean data within contractual timelines and budgets. Manages all operational and quality aspects of moderate to high complexity clinical studies in compliance with ICH GCP.
Lead data management activities from study start-up to database lock, ensuring deliverables meet quality expectations, timelines, and budgets. Act as a subject matter expert for sponsors and provide guidance, mentoring, and training to junior data management staff.
Clinical Research Associate II or Senior Clinical Research Associate
ICON plc
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Full Time
·
3 Weeks Ago
ICON plc
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Responsibilities include ensuring protocol compliance, maintaining data integrity, and collaborating with investigators to facilitate study conduct.
Medical Director/ Sr. Medical Director- Cardiology
Thermo Fisher Scientific
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Full Time
·
3 Weeks Ago
Thermo Fisher Scientific
Provide medical oversight for clinical trials to ensure compliance with SOPs, regulatory requirements, and good clinical practice. Perform medical review and analysis for serious adverse events, safety reports, and other critical client deliverables.
The Biostatistician serves as a lead or support on phase 1-4 clinical trials, developing statistical analysis plans and overseeing the production of clinical study reports. They collaborate with programmers and other departments to ensure deliverables meet ICH guidelines and regulatory requirements while managing project budgets.
The Biostatistician acts as a lead or support on Phase 1-4 clinical trials, developing Statistical Analysis Plans and overseeing the production of TLFs. They collaborate across departments to ensure deliverables meet ICH guidelines and regulatory requirements while managing study budgets and timelines.
Manage personal injury cases from intake to resolution, serving as the primary contact for clients and coordinating medical records and billing. Support attorneys with case strategy, document drafting, and communication with insurance companies and third parties.
Senior Clinical Research Associate, Oncology - Argentina - Remote
Worldwide Clinical Trials
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Full Time
·
4 Weeks Ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down. Ensure compliance with regulatory requirements, informed consent, and safety reporting during study maintenance.
Responsible for overall clinical site management, including identification, start-up, monitoring, and close-out of Phase I-IV studies. Ensures patient safety, data accuracy, and compliance with ICH-GCP guidelines and regulatory requirements.
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The role involves creating and maintaining data management plans and resolving data discrepancies to ensure high data quality throughout the study lifecycle. Additionally, the coordinator collaborates with cross-functional teams and mentors junior staff on cleaning and reconciliation procedures.
Senior Clinical Research Associate (Argentina)
Precision Medicine Group
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Full Time
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5 Weeks Ago
Precision Medicine Group
The Senior CRA independently oversees all aspects of study site management, including start-up, on-site monitoring, and ongoing site management to ensure patient safety and data integrity. They also provide guidance for audit readiness, mentor junior staff, and maintain study-specific trial management tools.
Senior Clinical Research Associate (Argentina)
Precision for Medicine
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Full Time
·
5 Weeks Ago
Precision for Medicine
The Senior Clinical Research Associate independently oversees all aspects of study site management, including start-up, on-site monitoring, and ongoing site management to ensure patient safety and data integrity. They also provide guidance on audit readiness, mentor junior staff, and maintain effective relationships with investigators and study teams.
Non Interventional Studies - Sr. Clinical Lead/ Sr. Clinical Trial Manager
Thermo Fisher Scientific
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Full Time
·
5 Weeks Ago
Thermo Fisher Scientific
The Senior Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, oversee project financials, and ensure compliance with ICH GCP and regulatory standards.
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