8 Clinical Data And Biostatistics jobs in Remote - Kingdom of Sweden.

Hiring now: Clinical Data Analyst Ii @ Parexel, Clinical Research Associa @ Syneos Hea, Principal Statistical Pro @ Iqvia.Explore more at jobswithgpt.com.

šŸ”„ Skills

Clinical Trials (7) Statistical Programming (5) Biostatistics (4) Functional Service Provider (4) Data Management (3) Clinical Research (3) CDISC (3) Client Relationship (2) Regulatory (2) CRA (2)

šŸ“ Locations

Kingdom of Sweden (8)

Parexel

Clinical Data Analyst II Kingdom of Sweden
Skills & Focus: Data Management, Clinical Research, Biostatistics, Statistical Programming, Functional Service Provider, Clinical Trials, Project Leadership, Client Relationship, Regulatory, Epidemiology Analyst
About the Company: Parexel is a global clinical research organization.
Site Monitor - FSP Kingdom of Sweden
Skills & Focus: Clinical Trials, Functional Service Provider, Biostatisticians, Clinical Research Associates, Data Managers, Project Leaders, Regulatory Consultants, Statistical Programmers, FSP, Remote
About the Company: Parexel is a global clinical research organization that provides various solutions to the pharmaceutical, biotechnology, and medical device industries, focusin…
Type: Remote
Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Data Management, Biostatistics, Statistical Programming, Client Relationship, Research Associate, Epidemiology, Analyst
About the Company: Parexel is a company that specializes in providing comprehensive development services to the biopharmaceutical industry.

Syneos Health

Skills & Focus: Clinical Research, Site Management, Good Clinical Practice, Site Qualification, Monitoring, Pharmaceutical, Regulatory Compliance, Patient Safety, Data Integrity, Clinical Trials
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Bachelor's degree or RN in a related field or equivalent combination of education, training and experience

Iqvia

Skills & Focus: Statistical Programming, Life Science, SAS, CDISC, SDTM, Data Review Model, Regulatory Compliance, Clinical Trials, Data Mapping, Risk-based Monitoring
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: 10+ years’ of Statistical Programming experience within the Life Science and Pharmaceutical Industry
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: Statistical Programming, Clinical Data, SAS Software, ADaM, CDISC, Data Analysis, Regulatory Requirements, Quality Control, Collaboration, Clinical Trials
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 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software.
Type: Full time
Benefits: Home-based remote work opportunities, Great work/life balance, Career advancement opportunities.
Skills & Focus: Biostatistics, clinical development, statistical strategy, regulatory submissions, SAS, R, data analysis, clinical trials, CRO, CDISC
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: 5 years with PhD or 8 years with MS in drug development
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.