12 Biopharmaceutical Leadership jobs in Remote - Hellenic Republic.

Hiring now: Site Monitor I Fsp @ Parexel, Experienced Clinical Rese @ Iqvia, Principal Biostatistician @ Syneos Hea.Explore more at jobswithgpt.com.

šŸ”„ Skills

Clinical Research (6) clinical trials (4) biostatistics (4) project management (3) Monitoring (3) regulatory submissions (3) Project Management (3) monitoring (2) ICH-GCP (2) clinical research (2)

šŸ“ Locations

Hellenic Republic (12)

Parexel

Site Monitor I - FSP Hellenic Republic
Skills & Focus: Clinical Research Associate, monitoring, ICH-GCP, protocol compliance, clinical trial, relationship building, data integrity, investigator sites, adverse event monitoring, compliance
About the Company: Parexel provides innovative solutions to the pharmaceutical, biotechnology, and medical device industries.
Experience: Minimum of 1 year experience as a clinical monitor
Type: Contingent
Site Monitor I - FSP Hellenic Republic
Skills & Focus: clinical trials, clinical research, biostatistics, project management, data management, functional service provider, remote work, biopharma, patient care, research operations
About the Company: Parexel is a global clinical research organization that provides a range of services related to clinical research and regulatory consulting.
Type: Freelance
Site Monitor I - FSP Hellenic Republic
Skills & Focus: clinical trials, clinical research, biostatistics, project management, data management, functional service provider, remote work, biopharma, patient care, research operations
About the Company: Parexel is a global clinical research organization that provides a range of services related to clinical research and regulatory consulting.
Type: Freelance

Iqvia

Skills & Focus: Clinical Research, monitoring, Good Clinical Practice, protocol, site management, regulatory submissions, data query, communication, subject recruitment, documentation
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: At least 2 years of on-site monitoring experience
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: Regulatory Affairs, Technical Writing, Project Management, Budget Management, Russian Language, Post Approval Regulatory, Lifecycle Management, Clinical Research, Regulatory Procedures, Client Relationships
About the Company: IQVIAā„¢ is The Human Data Science Companyā„¢, focused on using data and science to help healthcare clients find better solutions for their patients. Formed throug…
Experience: At least 5 years relevant experience in lifecycle management regulatory affairs for Russian market
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: Therapeutic Strategy, Nephrology, Cardiology, Endocrinology, Clinical Research, Business Development, Project Management, Market Trends, Operational Delivery, Customer Management
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: Minimum required experience in life sciences and relevant global clinical research experience (director level), including hands-on operational delivery and/or drug development experience in the applicable therapeutic area.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Syneos Health

Skills & Focus: biostatistics, clinical trials, statistical analysis, data monitoring, regulatory submissions, programming, training, project management, quality control, data safety
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Extensive experience in clinical trials or an equivalent combination of education and experience.
Type: Full-time
Benefits: Career development and progression; supportive and engaged line management; total rewards program.
Skills & Focus: Clinical Research, Site Management, ICH-GCP, Regulatory Compliance, Monitoring, Patient Safety, Clinical Data, Investigator Meetings, Training, Document Management
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Type: Full-time
Skills & Focus: Biostatistics, Clinical Trials, Statistical Analysis Plans (SAPs), Regulatory Submissions, Programming, Data Insights, Mentorship, Statistical Programming, Quality Control, Cross-functional Collaboration
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Extensive experience in clinical trials or an equivalent combination of education and experience.

Iqvia

Skills & Focus: Project Management, eCOA, Clinical Research, Client Communication, Budget Management, Monitoring, Documentation, Risk Management, Collaboration, Metrics
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: Minimum of 1 year
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.