20 Biopharmaceutical Leadership jobs in Remote - Hungary.

Hiring now: Clinical Programmer Fsp @ Parexel, Principal Biostatistician @ Syneos Hea, Srprincipal Clinical Data @ Precision , Associate Dir Coa Managem @ Iqvia, Srprincipal Clinical Data @ Precision .Explore more at jobswithgpt.com.

🔥 Skills

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

📍 Locations

Hungary (20)

Parexel

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.

Syneos Health

Skills & Focus: biostatistics, clinical trials, data analysis, Statistical Analysis Plans, SAS, training, programming, project management, regulatory submissions, quality control
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Extensive experience in clinical trials or an equivalent combination of education and experience.
Benefits: Comprehensive career development and progression, supportive and engaged line management, technical and therapeutic are…

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

Syneos Health

Skills & Focus: SAS, statistical programming, clinical trials, CDISC, programming code, data listings, quality control, documentation, mentoring, biostatistics
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success through clinical, medical affairs, a…
Experience: Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.

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

Iqvia

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 industri…
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.

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

Iqvia

Skills & Focus: Clinical Research, monitoring, Good Clinical Practice, regulatory requirements, subject recruitment, data query resolution, organizational skills, problem-solving skills, team collaboration, time 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 industrie…
Experience: 1+ years of on-site monitoring experience
Type: Full time
Benefits: Company car, mobile phone, and attractive benefits package

Syneos Health

Skills & Focus: Biostatistics, Clinical Trials, Statistical Analysis Plans, Programming, Regulatory Submissions, Project Management, Data Safety Monitoring Board, Team Collaboration, Quality Control, Statistical Design
About the Company: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medica…
Experience: Extensive experience in clinical trials or an equivalent combination of education and experience, demonstrated by the ability to lead multiple projects and programs of studies.

Parexel

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.

Syneos Health

Skills & Focus: Regulatory Affairs, Oncology, Clinical Trials, Site Start-Up, Project Management, Patient Enrollment, Project Deliverables, CRO Industry, Clinical Protocols, Risk Management
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; technical and therapeutic area training; pe…

Precision For Medicine

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: 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, 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.

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…
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