18 Biopharmaceutical Leadership jobs in Remote - Slovak Republic.

Hiring now: Qualified Person For Phar @ Parexel, Srprincipal Clinical Data @ Precision , Associate Dir Coa Managem @ Iqvia, Sr Clinical Data Mgr @ Precision , Clinical Regulatory Affai @ Syneos Hea.Explore more at jobswithgpt.com.

🔥 Skills

Data Management (7) Clinical Trials (6) clinical research (5) EDC vendor (5) programming (4) CDISC standards (4) Functional Service Provider (3) Biostatistics (3) data management (3) scripting (3)

📍 Locations

Slovak Republic (18)

Parexel

Skills & Focus: Qualified Person, Pharmacovigilance, Freelancer, Clinical Trials, Functional Service Provider, Clinical Operations, Data Management, Medical Writing, Regulatory Affairs, Biostatistics
About the Company: Parexel is a global leader in providing innovative solutions to accelerate the drug development process for the biopharmaceutical industry.
Type: Freelancer

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.

Iqvia

Skills & Focus: COA Management, Patient Centered Solutions, Clinical Trials, Consulting, Health Technology Assessments, Product Lifecycle Management, Market Access, Research, Stakeholder Engagement, Financial 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 industri…
Experience: 8-10 years total work experience with 5+ years in the pharmaceutical/medical device 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.

Precision For Medicine

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: Clinical Trial, Data Management, Database Development, Quality Control, Medical Coding, CDISC Standards, Data Entry Guidelines, Regulatory Directives, Clinical Research, Data Management Documentation
About the Company: Precision Medicine Group is focused on providing comprehensive support in clinical trials and healthcare services.
Experience: 8+ years’ experience in a clinical, scientific or healthcare discipline
Type: Full-time
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

Precision For Medicine

Skills & Focus: Principal Clinical Scientist, clinical trials, data cleaning, data management, oncology, medical terminology, electronic data capture, leadership experience, cross-functional, clinical data review
About the Company: Precision for Medicine is a company focused on applying innovative solutions to clinical trials and data management in the medical field.
Experience: Minimum of 8 years of clinical research experience, including 1 year of leadership experience
Type: Remote

Iqvia

Skills & Focus: FSP, Real-World Evidence, business development, operational oversight, collaboration, Epidemiology, Data Science, Psychometrics, Health Economics, cross-functional
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: 10+ years
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Parexel

Clinical Trials Jobs Slovak Republic
Skills & Focus: Clinical Trials, Functional Service Provider, Site Care Partner, CRA, Biostatistics, Data Management, Project Leader, Oncology, Regulatory Consultants, Senior Clinical Research Associate

Precision For Medicine

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.

Iqvia

Skills & Focus: clinical trials, project management, study management, clinical research, customer satisfaction, risk management, collaboration, financial success, communication, problem solving
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 of prior relevant experience including > 1 year project management 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.

Parexel

Skills & Focus: contracting, budget negotiation, site management, clinical trials, investigational sites, clinical study agreements, risk management, collaboration, communication skills, clinical development
Experience: 5+ years of experience in clinical development operations or clinical trial outsourcing OR Juris Doctorate or equivalent and 2+ years of experience in clinical development operations or clinical trial outsourcing

Iqvia

Skills & Focus: Regulatory Affairs, Russian market, Technical writing, Post-approval, Stakeholders, Regulatory submissions, Health Authority, Lifecycle management, Project management, Regulatory procedures
About the Company: IQVIA™ is The Human Data Science Company™, 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.

Parexel

Skills & Focus: Clinical Trials, Functional Service Provider, Site Care Partner, Biostatistics, Clinical Research, Regulatory Consulting, Data Management, Project Leader, Statistical Programming, Quality Management
About the Company: Parexel is a leading global biopharmaceutical services organization that provides comprehensive drug development and regulatory consulting services. The compan…
Type: Full-time

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…

Syneos Health

Skills & Focus: Clinical Regulatory Affairs, Oncology, Clinical Trial Management, Project Management, Site Start-Up, Patient Enrollment, Regulatory Activities, Clinical Trial Agreements, Budget Management, Quality Deliverables
About the Company: Syneos Health® 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.
Benefits: Career development and progression; supportive and engaged line management.
Skills & Focus: Clinical Regulatory Affairs, Oncology, Site Start-Up, Project Management, Clinical Trials, Regulatory Pathway, Patient Enrollment, Risk Management, Budget Management, Quality Standards
About the Company: Syneos Health® 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.