14 Clinical Data And Biostatistics jobs in Remote - Kingdom of Belgium.

Hiring now: Site Contract Associate I @ Parexel, Clinical Research Associa @ Iqvia, Experienced Clinical Rese @ Syneos Hea, Clinical Research Associa @ Precision .Explore more at jobswithgpt.com.

šŸ”„ Skills

monitoring (5) regulatory submissions (5) Good Clinical Practice (4) project management (4) Clinical Trials (3) Biostatistics (3) Data Management (3) Clinical Research (2) Statistical Programming (2) Clinical Research Associate (2)

šŸ“ Locations

Kingdom of Belgium (14)
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Parexel

Site Contract Associate II Kingdom of Belgium
Skills & Focus: Clinical Trials, Contract, Associate, Remote, Biostatistics, Data Management, Project Leadership, Clinical Research, Statistical Programming, Healthcare

Iqvia

Clinical Research Associate FSP Belgium Kingdom of Belgium
Skills & Focus: Clinical Research Associate, site selection, monitoring, Good Clinical Practice, subject recruitment, regulatory submissions, data query resolutions, collaborating, organizational skills, communication skills
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrieā€¦
Experience: Experience in Pharma Industry, and/or Clinical Trials environment
Type: Full time
Benefits: Company car, mobile phone and attractive benefits packaging.

Parexel

Site Care Partner (Lead CRA) Kingdom of Belgium
Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Site Care Partner, Biostatisticians, Data Managers, Project Leaders, Regulatory Consultants, Statistical Programmers, Emerging Talent Opportunities
About the Company: Parexel is a global biopharmaceutical services organization that offers solutions to expedite the development of safe and effective medical products.

Iqvia

Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated Kingdom of Belgium
Skills & Focus: clinical trials, study management, Vendor Management, project management, patient outcomes, data management, healthcare intelligence, protocol development, regulatory documents, Good Clinical Practice
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industriā€¦
Experience: 2-5 years of experience in managing late phase clinical trials at global level
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

Experienced Clinical Research Associate (CRA) Kingdom of Belgium
Skills & Focus: Clinical Research Associate, monitoring, Good Clinical Practice, Site Management, site qualification, informed consent, data integrity, clinical trial, regulatory compliance, patient safety
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medicā€¦
Experience: Previous monitoring experience in Belgium
Type: Full-time
Sr. R Programmer (TEAL Module Development - R/RShiny) Kingdom of Belgium
Skills & Focus: SAS, programming, clinical trial, quality standards, project management, documentation, datasets, communication skills, team collaboration, mentoring
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medā€¦
Experience: Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.

Parexel

Client Relationship Director Kingdom of Belgium
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.
Site Care Partner (Lead CRA) Kingdom of Belgium
Skills & Focus: Clinical Research, Site Management, Recruitment, Patient Safety, Study Activation, Stakeholder Collaboration, Data Management, Quality Assurance, Site Oversight, Project Management

Syneos Health

Principal/Sr Regulatory Medical Writer Kingdom of Belgium
Skills & Focus: medical writing, clinical study protocols, IND submissions, FDA regulations, ICH guidelines, peer reviewer, clinical development, project management, review documents, data management
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medicā€¦
Experience: Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree (Social Sciences, English or Communications, preferred) with relevant scientific and/or medical knowledge and expertise.
Type: Full-time
Benefits: Professional development, supportive management, and rewards programs.
Clinical Research Associate Kingdom of Belgium
Skills & Focus: site qualification, site initiation, monitoring, regulatory compliance, GCP, informed consent, data integrity, clinical study, project management, audit readiness
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medicā€¦
Experience: Previous monitoring experience in Belgium
Benefits: Career development, supportive and engaged line management, technical and therapeutic area training, peer recognition aā€¦

Precision For Medicine

Clinical Research Associate (CRA) Kingdom of Belgium
Skills & Focus: clinical studies, monitoring, investigative sites, SOPs, ICH-GCP, onsite monitoring, regulatory submissions, protocol, oncology experience, domestic travel
About the Company: Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help thā€¦
Experience: At least 2 years independent on site monitoring experience within the CRO or Pharmaceutical industry
Type: Full-time
Clinical Research Associate (CRA) Kingdom of Belgium
Skills & Focus: clinical studies, protocol expertise, site monitoring, investigator meeting, regulatory submissions, ICH-GCP, oncology experience, travel commitment, quality outcomes, risk mitigation
About the Company: Precision for Medicine is not your typical CRO. We have brought together new technologies, expertise and operational scale to help the life sciences improve thā€¦
Experience: At least 2 years independent site monitoring experience within the CRO or Pharmaceutical industry
Type: Full-time

Iqvia

Senior Clinical Research Associate FSP Belgium Kingdom of Belgium
Skills & Focus: site selection, monitoring, Good Clinical Practice, regulatory submissions, subject recruitment plan, data query resolutions, collaboration, problem-solving skills, time management, flexibility to travel
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrieā€¦
Experience: Experience in Pharma Industry, and/or Clinical Trials environment
Type: Full time
Benefits: Company car, mobile phone and attractive benefits packaging
Principal Biostatistician (FSP - Permanent Homebased) Kingdom of Belgium
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 industriā€¦
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.