18 Clinical Operations Management jobs in Remote - Slovak Republic.

Hiring now: Srprincipal Clinical Data @ Precision , Sr Clinical Data Mgr @ Precision , Clinical Trials Jobs @ Parexel, Tactical And Operational @ Iqvia, Clinical Regulatory Affai @ Syneos Hea.Explore more at jobswithgpt.com.

🔥 Skills

Data Management (6) clinical research (5) Clinical Trials (5) clinical trials (4) risk management (4) EDC vendor (3) programming (3) Functional Service Provider (3) Site Care Partner (3) Oncology (3)

📍 Locations

Slovak Republic (18)

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.

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: clinical trial management, project timeline, meeting minutes, study supplies, training records, study trackers, Microsoft Office, customer service, ICH-GCP, communication
About the Company: Precision for Medicine is a precision medicine CRO. Our uniquely integrated offering enables the science of precision medicine by combining novel clinical tria…
Experience: Minimum of 3 years of relevant experience.

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

Precision For Medicine

Drug Safety Physician Slovak Republic
Skills & Focus: pharmacovigilance, safety reporting, clinical support, risk management, signal detection, safety data management, adverse events, compliance, drug safety, clinical trials
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.

Iqvia

Skills & Focus: clinical documentation, Trial Master File, administrative support, Case Report Forms, clinical data flow, project communications, Good Clinical Practice, regulatory requirements, tracking management, clinical research
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: 2-3 years administrative support experience; minimum one year clinical research experience strongly preferred.
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

Iqvia

Study Start Up Lead Slovak Republic
Skills & Focus: site activation, clinical trials, regulatory compliance, project management, biotechnology, clinical practice guidelines, study initiation, budget planning, contract negotiation, regulatory intelligence
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: 7 years relevant 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: monitoring, site management, regulatory requirements, Good Clinical Practice, site training, project management, recruitment plan, data integrity, collaboration, 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 1 year 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.

Parexel

Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Site Care Partner

Precision Medicine Group

Drug Safety Physician Slovak Republic
Skills & Focus: Drug Safety, Pharmacovigilance, clinical trial, Serious Adverse Event, safety data analysis, risk management, FDA, EMA, GCP, safety reporting
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

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.