Last updated: 2025-05-22

18 Biopharmaceutical Leadership jobs in Remote - Hungary.

Hiring now: Sr Clinical Data Mgrprinc @ Precision , Srprincipal Clinical Data @ Precision , Proj Data Mgr Medical Wri @ Syneos Hea, Site Payment Lead Ii @ Parexel, Regulatory Affairs Mgr Or @ Iqvia, Sr Feasibility Associatef @ Precisionm, Sr Clinical Data Mgrprinc @ Pfm.Explore more at at kaamvaam.com

🔥 Skills

Data Management (6) clinical research (5) programming (5) CDISC standards (5) Clinical Trials (4) EDC vendor (4) scripting (4) Quality Control (3) Project Management (3) data management (3)

📍 Locations

Hungary (18)

Precision Medicine Group

Skills & Focus: Data Management, Clinical Trials, Database Development, Quality Control, Data Entry Guidelines, Clinical Study Protocol, Documentation, Training, Reporting, Data Analysis
Experience: Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company
Skills & Focus: clinical databases, EDC vendor, Data Management, Project Management, scripting, Object Oriented Programming, clinical research, programming, CDISC standards, database management
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 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.

Syneos Health

Skills & Focus: Data Management, Clinical Data, Project Management, Database Management, SOPs, Regulations, Clinical Trials, Data Review, SAS, Veeva Vault
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success, translating clinical, medical, and …
Experience: Clinical data management experience or an equivalent combination of education and experience.

Precision Medicine Group

Skills & Focus: Data Management, Clinical Trials, Database Development, Quality Control, Data Entry, Clinical Research, Project Management, Medical Coding, EDC, SOPs
Experience: Must have worked as a Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company

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
Skills & Focus: clinical database management, clinical data management, EDC, data management, clinical research, programming, scripting, CDISC standards, drug development, object-oriented programming
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.
Skills & Focus: clinical trials, Oncology, project management, client relationship, cross-functional team, GCP/ICH guidelines, data management, safety, medical monitoring, biostatistics
About the Company: Precision for Medicine's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading ope…
Experience: 5 to 7 years industry experience and at least 3 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.
Type: Full-time
Benefits: Supportive and collaborative environment which promotes work life balance and encourages team development.

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…

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: 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: Regulatory Affairs, CMC, Pharmaceutical, Biologics, Quality Control, Submission Strategies, Market Expansions, Risk Management, Collaboration, Technical Documentation
About the Company: Parexel is a global biopharmaceutical services company that provides expertise in regulatory affairs, clinical research, and other related fields to help bring…
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote
Benefits: Flexible work arrangements, supportive and inclusive environment, opportunities for career growth.
Skills & Focus: Clinical Trials, Clinical Research, CRA, Functional Service Provider, Data Management, Biostatistics, Statistical Programming, Project Leadership, Regulatory, Sales

Precisionmedicinegroup

Skills & Focus: feasibility analysis, site identification, clinical protocols, study assumptions, client information, feasibility site outreach, post-award feasibility, patient advocacy groups, enrollment modeling, clinical trial
Experience: 5 years

Pfm

Skills & Focus: clinical, data, management, database, protocol, CRF, UAT, bioinformatics, regulatory, healthcare

Parexel

Skills & Focus: Pharmacovigilance, Qualified Person, Local Qualified Person, Freelancer, Clinical Research, Pharmaceuticals, Regulatory Compliance, Safety Solutions, Medical Devices, Biotechnology
About the Company: Parexel is a global clinical research organization that provides comprehensive services to the pharmaceutical, biotechnology, and medical device industries.
Type: Freelancer

Pfm

Skills & Focus: feasibility analysis, clinical protocols, site identification, study assumptions, client information, study plans, feasibility site outreach, patient advocacy groups, site data analysis, enrollment modeling
Experience: 5 years
Skills & Focus: feasibility analysis, site identification, clinical trials, pre-award, post-award, site outreach, feasibility projects, biotech, pharma, biopharmaceutical
Experience: 5 years