Last updated: 2025-05-22

23 Clinical Operations Management jobs in Remote - Republic of Poland.

Hiring now: Supply Logistics Proj Mgr @ Parexel, Sr Feasibility Associatef @ Precision , Srprincipal Clinical Data @ Precision , Sr Feasibility Associatef @ Precisionm, Site Management Associate @ Syneos Hea, Sr Feasibility Associatef @ Pfm, Tactical And Operational @ Iqvia.Explore more at at kaamvaam.com

šŸ”„ Skills

feasibility analysis (6) clinical research (6) site identification (5) clinical protocols (5) Data Management (5) Project Management (4) data analysis (4) programming (4) CDISC standards (4) Clinical Trials (4)

šŸ“ Locations

Republic of Poland (23)

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 For Medicine

Skills & Focus: feasibility analysis, pre-award, post-award, site identification, clinical protocols, enrollment modeling, data analysis, patient advocacy, RFPs, team collaboration
About the Company: Precision for Medicine is not your typical CRO. At Precision for Medicine, we have brought together new technologies, expertise and operational scale to help t…
Experience: A minimum of 5 years of related experience
Type: Remote

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.

Precisionmedicinegroup

Skills & Focus: feasibility analysis, site identification, clinical protocols, study assumptions, feasibility site outreach, feasibility projects, global trials, project analysis, data analysis, study strategy
Experience: 5 years

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 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 HealthĀ® 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

Parexel

Skills & Focus: Finance, Reconciliation, Remote, Clinical Trials, Biopharmaceutical, Data Management, Regulatory Affairs, Operations, Statistical Programming, Project Management
About the Company: Parexel is a global biopharmaceutical services organization dedicated to the development of innovative technologies and support for clinical trials.
Type: Full-time

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

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: Clinical Trials, CRA, Oncology, FSP, Project Leadership, Clinical Research, Monitor, Biostatistics, Regulatory, Clinical Operations

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.
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.

Pfm

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

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
Skills & Focus: feasibility analysis, site identification, clinical protocols, study assumptions, epidemiology analysis, study delivery, study feasibility, site outreach, post-award feasibility, data analysis
Experience: At least 5 years

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.