Last updated: 2025-05-03

13 Business Development And Sales jobs in Remote - Slovak Republic.

Hiring now: Mgr Clinical Science Anal @ Precision , Regulatory Mgr Sr Regulat @ Precision , Clinical Regulatory Affai @ Syneos Hea, Contract Negotiator Fsp E @ Iqvia.Explore more at jobswithgpt.com. at kaamvaam.com

šŸ”„ Skills

project management (5) clinical trials (4) Project Management (4) clinical research (3) compliance (3) Regulatory submissions (3) Compliance (3) management (2) data quality (2) training (2)

šŸ“ Locations

Slovak Republic (13)

Precision Medicine Group

Skills & Focus: clinical research, management, data quality, team leadership, resource allocation, performance reviews, compliance, training, business development, project management
Experience: Minimum of 8 years of clinical research experience

Precision For Medicine

Skills & Focus: regulatory strategy, clinical trials, regulatory submissions, regulatory guidance, project management, Regulatory Authorities, clinical development, regulatory compliance, ICH GCP, drug development
About the Company: Precision for Medicine specializes in providing regulatory strategy and development guidance for clinical trials, ensuring compliance with applicable regulatio…
Experience: 5 years Regulatory experience required for the Manager level and 7 years Regulatory experience required for the Senior Manager Regulatory level
Skills & Focus: clinical research, management, development, data quality, clinical trials, supervisory experience, compliance, training, project management, communication
About the Company: Precision for Medicine is a leading provider of integrated services to the biopharmaceutical industry for the design and implementation of clinical trials.
Experience: Minimum of 8 years of clinical research experience.

Precision Medicine Group

Skills & Focus: Clinical Science, Analytics, Insights, Clinical Trials, Management, Career Development, Team Leadership, Project Management, Data Quality, Mentorship
About the Company: Precision for Medicine is focused on supporting and delivering high-quality clinical research and development for life sciences companies.
Experience: Minimum of 8 years of clinical research experience.
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 HealthĀ® 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.

Precision For Medicine

Skills & Focus: Regulatory strategy, Clinical trials, Regulatory submissions, Compliance, Project management, Regulatory Authorities, Drug development, Clinical Research Organisation, ICH, Quality initiatives
Experience: 5 to 7 years Regulatory experience

Precision Medicine Group

Skills & Focus: evidence synthesis, systematic literature reviews, health technology assessment, project management, client communications, deliverable creation, pharmaceutical industry, mentorship, qualitative evidence, business development
Experience: 4-6 years’ professional experience

Precision For Medicine

Skills & Focus: Regulatory strategy, Clinical trials, Regulatory submissions, Orphan designations, Clinical development, Regulatory guidance, Regulatory Affairs, Drug development, Clinical Research, Compliance
About the Company: Precision for Medicine is a precision medicine Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medici…
Experience: 5 years for Manager level and 7 years for Senior Manager level

Iqvia

Skills & Focus: contract negotiation, clinical research, contract management, budget templates, proposal development, clinical trials, investigator grants, compliance, financial contracting, team collaboration
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 to 5 years relevant sponsor or clinical research organization clinical site contracting 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.

Syneos Health

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 HealthĀ® 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.

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: 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.

Precision Medicine Group

Skills & Focus: Clinical Science Analytics, Team Management, Oncology Clinical Trials, Performance Reviews, Employee Development, Compliance, Project Management, Training, Data Quality, Cross-functional Collaboration
About the Company: Precision for Medicine is a leading provider of specialized services for the life sciences including clinical research, regulatory, and commercial solutions.
Experience: Minimum of 8 years of clinical research experience or proven competencies for this position.
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.