Last updated: 2025-05-22

18 Biopharmaceutical Leadership jobs in Remote - Slovak Republic.

Hiring now: Clinical Proj Mgr Sr Clin @ Precision , Site Care Partnersr Cra F @ Parexel, Srprincipal Clinical Data @ Precision , Tactical And Operational @ Iqvia, Sr Feasibility Associatef @ Precisionm, Sr Clinical Data Mgrprinc @ Pfm.Explore more at at kaamvaam.com

šŸ”„ Skills

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

šŸ“ Locations

Slovak Republic (18)

Precision For Medicine

Skills & Focus: clinical trials, oncology, project management, CRO, clinical development, GCP/ICH guidelines, budget management, team leadership, client relationship, cross-functional collaboration
About the Company: Precision for Medicine is a full-service Contract Research Organization (CRO) focused on improving the health and lives of patients around the world, especiall…
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

Parexel

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

Precision Medicine Group

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.

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.

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, 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.
Skills & Focus: Regulatory Affairs, Russian market, Technical writing, Post-approval, Stakeholders, Regulatory submissions, Health Authority, Lifecycle management, Project management, Regulatory procedures
About the Company: IQVIAā„¢ is The Human Data Science Companyā„¢, 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: Pharmacovigilance, QPPV, freelance, clinical trials, post-market, safety reporting, risk management, GVP, GCP, regulations
About the Company: Parexel is in the business of improving the world’s health. They provide a suite of biopharmaceutical services that help clients across the globe transform sci…
Experience: Minimum of at least 7 years' demonstrated experience in managing or implementing PV systems, including quality assurance experience.
Type: Freelance
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

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

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.

Pfm

Skills & Focus: feasibility analysis, site identification, clinical trials, pre-award, post-award, site outreach, feasibility projects, biotech, pharma, biopharmaceutical
Experience: 5 years