11 Biopharmaceutical Leadership jobs in Remote - Argentine Republic.

Hiring now: Clinical Data Analyst @ Parexel, Site Activation Spec @ Syneos Hea, Sr Site Activation Coordi @ Iqvia.Explore more at jobswithgpt.com.

šŸ”„ Skills

Clinical Research (5) project management (4) Clinical Trials (4) Data Management (3) site activation (3) regulatory (3) Biostatistics (2) Project Leadership (2) Functional Service Provider (2) clinical trial (2)

šŸ“ Locations

Argentine Republic (11)

Parexel

Clinical Data Analyst Argentine Republic
Skills & Focus: Clinical Data, Data Management, Biostatistics, Clinical Research, Medical Trials, Statistical Programming, Project Leadership, Functional Service Provider, Clinical Operations, Health Improvement
About the Company: Parexel provides a range of services to the biopharmaceutical industry, specializing in clinical research.

Syneos Health

Site Activation Specialist Argentine Republic
Skills & Focus: clinical trial, site activation, submissions, project management, regulatory, document collection, budget negotiation, quality control, communication skills, problem-solving
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Bachelor's Degree, Detailed understanding of clinical trial process across Phases II-IV and ICH GCP.

Parexel

Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Site Care Partner, Biostatistics, Data Management, Regulatory Consultants, Statistical Programmers, Project Leaders, Clinical Research

Syneos Health

Sr Site Activation Manager Argentine Republic
Skills & Focus: clinical trial, site activation, project management, regulatory, patient enrollment, business development, vendor management, clinical protocols, risk management, communication
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Minimum 6 years CRO industry experience and/or a minimum 5 years’ experience working in a SSU, or clinical trial environment or an equivalent combination of education and experience.
Skills & Focus: regulatory submissions, project management, team management, client contact, budget development, regulatory advice, quality improvement, medical writing, staff management, communication skills
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Moderate experience in regulatory.
Salary: $71,820 to $139,600
Benefits: Company car or car allowance, Health benefits (Medical, Dental, Vision), Company match 401k, eligibility for Employee S…

Parexel

Sr. Power Apps Developer Argentine Republic
Skills & Focus: Power Apps, Development, IT, Remote, Clinical Trials, Clinical Research, Data Management, Project Leader, Regulatory, Programming
About the Company: Parexel is a global clinical research organization that accelerates the development of innovative therapies.
Type: Full-time

Syneos Health

Skills & Focus: Clinical Trials, Regulatory Affairs, Site Activation, Project Management, Client Meetings, Budget Management, Quality Standards, Regulatory Submissions, Team Collaboration, Risk Assessment
About the Company: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success, working towards simplifying and stre…

Parexel

Project Leadership Argentine Republic
Skills & Focus: Project Planning, Clinical Trials, Regulatory Consulting, Biopharmaceutical, Drug Development, Clinical Research, Project Leadership, Compliance, ICH Guidelines, GCP
About the Company: Parexel is a leading global biopharmaceutical services organization that provides comprehensive drug development and regulatory consulting services. They help …
Type: Remote

Iqvia

Skills & Focus: site activation, feasibility, regulatory, research, clinical, healthcare, accurate documents, project team, tracking tools, investigative sites
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Around 1-2 years of experience working with regulatory tasks in North America
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Global Central Site ID Argentine Republic
Skills & Focus: Site Identification, Clinical Research, Stakeholder Management, Quality Assurance, Clinical Trial, Project Management, Risk Assessment, Regulatory Guidelines, Customer Relationships, Team Collaboration
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 2+ years in Site ID, Feasibility activities into clinical research with a Global perspective.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Skills & Focus: clinical research, Good Clinical Practice, International Conference on Harmonization, clinical project plans, subject recruitment, site management, data integrity, project management, clinical delivery, team collaboration
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 5-7 years clinical research/monitoring experience
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs.