Last updated: 2025-05-22

28 Biopharmaceutical Leadership jobs in Remote - Republic of Poland.

Hiring now: Supply Logistics Proj Mgr @ Parexel, Srprincipal Clinical Data @ Precision , Srprincipal Clinical Data @ Precision , Sr Clinical Data Mgrprinc @ Precisionm, Site Management Associate @ Syneos Hea, Medical Science Liaison @ Biomarin, Consultant Veeva Safety M @ Veeva Syst, Sr Feasibility Associatef @ Pfm, Tactical And Operational @ Iqvia, Medical Science Liaison @ Biomarin P.Explore more at at kaamvaam.com

🔥 Skills

clinical research (7) programming (6) clinical trials (6) Data Management (5) CDISC standards (5) EDC vendor (4) scripting (4) data management (4) regulatory compliance (4) feasibility analysis (4)

📍 Locations

Republic of Poland (28)

Parexel

Skills & Focus: Supply Chain Management, Project Management, Clinical Logistics, Biopharmaceutical, Regulatory Consulting, Laboratory Logistics, Clinical Research, Remote Work, Job Opportunities, Network of Talent
About the Company: Parexel is a global biopharmaceutical services organization that specializes in conducting clinical research and regulatory consulting.

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.
Clinical Scientist Republic of Poland
Skills & Focus: Clinical Scientist, oncology standards, data quality, clinical trials, electronic data capture, data management, clinical operations, CSA, UAT, GCP/ICH
About the Company: Precision Medicine Group is an Equal Opportunity Employer.
Experience: At least two (2) years in clinical operations and/or data management or related discipline.
Type: Remote

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

Parexel

Skills & Focus: SAS, programming, clinical trials, data analysis, regulatory compliance, statistics, Hematology, Oncology, data entry, quality
About the Company: Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the t…
Experience: 1-2 years of industry experience (CRO/Pharma/Biotech) is required.
Type: Full-time
Benefits: We offer competitive financial packages, training, and development. Expect exciting professional challenges but with a …

Precision For Medicine

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.

Precisionmedicinegroup

Skills & Focus: clinical, data, management, database, protocol, CRF, EDC, quality, training, oversight

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…

Syneos Health

Skills & Focus: site management, clinical trials, Good Clinical Practice, data collection, regulatory compliance, subject recruitment, monitoring activities, investigator meetings, clinical tracking, communication skills
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Previous site management (in-house, on-site, Study Coordinator) or equivalent experience.
Benefits: career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…

Precision Medicine Group

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

Biomarin

Medical Science Liaison Republic of Poland
Skills & Focus: Medical Science Liaison, scientific engagement, healthcare professionals, Key Opinion Leaders, Patient Advocacy Groups, clinical management, drug administration training, evidence generation, medical strategic planning, cross-functional team collaboration
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: MSc minimum, coupled with significant medical/clinical/academic credentials typically often consisting of but not limited to a doctorate degree (MD, PhD, PharmD, etc.) in the life sciences.
Type: Field Based

Parexel

Site Payment Lead II Republic of Poland
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
Skills & Focus: Medical Director, Dermatology, Clinical Research, Medical Sciences, Remote, Biopharma, Patient Care, Regulatory Compliance, Team Leadership, Data Management

Veeva Systems

Skills & Focus: Drug Safety, Pharmacovigilance, consulting, customer facing, solution design, communication, collaboration, SaaS solutions, configuration, post-implementation support
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Type: Full-time
Benefits: Private medical insurance, Health & wellness programs, 1% charitable giving program, Mentorship programs

Pfm

Skills & Focus: feasibility analysis, clinical protocols, site identification, pre-award projects, post-award projects, feasibility analysis, site outreach, study strategy, biotech, pharma
Experience: 5 years+

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.

Biomarin Pharmaceutical Inc.

Medical Science Liaison Republic of Poland
Skills & Focus: Medical Science Liaison, scientific engagement, Key Opinion Leaders, Health Care Professionals, strategic medical plans, evidence generation, Patient Advocacy Groups, post-marketing studies, clinical management, genetic discoveries
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…

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.

Pfizer

Skills & Focus: Risk Management, pharmacovigilance, drug safety, RMP, regulatory requirements, risk mitigation, clinical research, safety regulations, project management, pharma
Experience: Minimum 5 years of broad and progressive pharma experience in medical, clinical or pharmacovigilance but with a clear focus on drug safety risk management
Salary: $112,700.00 to $187,800.00
Type: Full-time
Benefits: Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

Pfm

Skills & Focus: clinical trial, data management, database development, regulatory directives, CRF specifications, database build, UAT, quality control, medical coding, SOPs

Johnson & Johnson

Skills & Focus: regulatory strategies, acquisition, divestitures, regulatory compliance, global health authority, asset transfer, project management, regulatory risk, cross-functional collaboration, regulatory intelligence
About the Company: Johnson & Johnson is a healthcare company focused on innovative medicines and MedTech solutions.
Experience: 8-10+ years
Type: Full-time

Biomarin Pharmaceutical Inc.

Medical Science Liaison Republic of Poland
Skills & Focus: Medical Science Liaison, scientific engagement, Key Opinion Leaders, Patient Advocacy Groups, scientific information, evidence generation, clinical management, healthcare systems, medical strategic planning, drug education
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: MSc minimum, coupled with significant medical/clinical/academic credentials typically often consisting of but not limited to a doctorate degree (MD, PhD, PharmD, etc.) in the life sciences. Industry experience.

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

Iqvia

Study Start Up Lead Republic of Poland
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