20 Clinical Data And Biostatistics jobs in Remote - Serbia.

Hiring now: Site Contract Associate I @ Parexel, Srprincipal Clinical Data @ Precision , Sr Clinical Data Mgrprinc @ Precision , Srprincipal Statistical P @ Syneos Hea, Regulatory And Start Up D @ Iqvia.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Trials (7) Data Management (6) clinical research (5) EDC vendor (5) programming (5) CDISC standards (5) Clinical Research (4) SAS (4) Statistical Programming (3) data management (3)

📍 Locations

Serbia (20)

Parexel

Skills & Focus: Clinical Trials, Contract, Associate, Remote, Biostatistics, Data Management, Project Leadership, Clinical Research, Statistical Programming, Healthcare
Skills & Focus: Clinical Programming, SQL, Data Review, Statistical Programming, Clinical Trials, Data Management, Biotechnology, Life Sciences, Software Development, eClinical Solutions
About the Company: Parexel supports clinical studies across the full range of therapeutic areas, with longstanding partnerships with a vast client base. The company undertakes vi…
Experience: Minimum of 5 years of experience in developing software in a clinical trial environment using SQL, including at least 3 years of clinical programming experience.
Type: Remote
Benefits: Provides an open and friendly work environment where we empower people and offer opportunities for career advancement.

Precision For Medicine

Skills & Focus: clinical database management, clinical research, data management, EDC vendor, programming, scripting, CDISC standards, object-oriented programming, clinical research tasks, biomarkers
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline; Medidata Rave EDC Certified Study Builder; Rave API integration experience.
Skills & Focus: Clinical Database Manager, clinical data management, EDC vendor, Medidata Rave, Rave API, programming, scripting, CDISC standards, drug development, clinical research
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline

Precision Medicine Group

Skills & Focus: Data Management, Clinical Trials, Database Development, Quality Control, CRF Specifications, Data Management Documentation, Training, Medical Coding, SOPs, Clinical Study Protocol
Experience: Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company
Type: Remote

Syneos Health

Skills & Focus: SAS, programming, statistical analysis, clinical trials, CDISC, quality standards, data listings, team collaboration, project documentation, mentoring
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.

Precision Medicine Group

Skills & Focus: clinical databases, Data Management, EDC vendor, operational training, programming, clinical research, Object Oriented Programming, scripting language, CDISC standards, database management systems
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Skills & Focus: Data Management, Clinical Trials, Database Development, Quality Control, Data Entry, Clinical Protocol, Training, Documentation, Medical Coding, SOP Development
Experience: Bachelors and/or a combination of related experience; Must have worked as a Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company

Parexel

Skills & Focus: Investigator Payment, clinical trial, payment setup, project team, risk management, budgeting, audits/inspections, payment strategy, timely payments, data analysis
About the Company: Parexel is in the business of improving the world’s health by providing a suite of biopharmaceutical services that help clients across the globe transform scie…
Type: Remote
Benefits: competitive base salary and a benefits package including holiday as well as other benefits

Syneos Health

Skills & Focus: project management, clinical trial, regulatory documents, team communication, administrative support, quality assurance, data queries, audits, Good Clinical Practice, organization
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.

Precision For Medicine

Skills & Focus: Drug Safety, Pharmacovigilance, Clinical Trials, Signal Detection, Risk Management, Safety Reporting, Safety Data Management, Adverse Events, Regulatory Compliance, Medical Review
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level usi…
Experience: minimum of 7 years in Drug Safety related activities in pharma/biotech
Type: Remote
Skills & Focus: clinical databases, EDC vendor, Data Management, Project Management, programming, scripting, Microsoft Office, clinical research, data management, leadership
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline.

Syneos Health

Skills & Focus: Clinical Research, Site Management, Regulatory Compliance, Good Clinical Practice, Data Integrity, Monitoring Activities, Project Management, Clinical Trials, Patient Safety, Data Review
About the Company: Syneos Health® 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
Type: Full-time
Benefits: Total rewards program, career development, supportive and engaged management.
Skills & Focus: Clinical Trial, Regulatory Affairs, Project Management, Submission Strategy, Risk Assessment, Stakeholder Management, Quality Assurance, Clinical Research, GxP Compliance, Technical Writing
About the Company: At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. Our work improves patients’ lives around the world.

Parexel

Skills & Focus: clinical programming, data review, SQL, eClinical Solutions, CDISC, clinical trials, biotechnology, data management, relational database, communication
About the Company: Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the t…
Experience: Minimum of 5 years of experience in developing software in a clinical trial environment using SQL, including at least 3 years of clinical programming experience.

Iqvia

Skills & Focus: clinical studies, management, leadership, training, resource allocation, quality metrics, employee relations, professional development, clinical research, 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 industrie…
Experience: Prior clinical trial experience including experience in a management/leadership capacity or equivalent combination of education, training and 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: statistical programming, clinical data, SAS, ADaM, regulatory requirements, programming activities, CDISC standards, data structure, quality control, exploratory analyses
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
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Precision Medicine Group

Skills & Focus: Clinical Database Manager, Clinical Data Management, EDC vendor, Microsoft Office, Object Oriented Programming, Rave API integration, SAS, CDISC standards, Clinical database management, Leadership skills
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…

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: Clinical Research, Trial Master File, administrative support, CRAs, clinical documentation, GCP, ICH guidelines, regulatory requirement, data flow, Case Report Forms
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: 3-4 years administrative support experience. Minimum one year clinical research 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.