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

Hiring now: Proj Mgr Iisr Pm Early Ph @ Syneos Hea, Risk Surveillance Lead Fs @ Parexel, Srprincipal Clinical Data @ Precision , Srprincipal Clinical Data @ Precision , Global Sr Trial Delivery @ Iqvia.Explore more at jobswithgpt.com.

🔥 Skills

project management (6) clinical trials (6) clinical research (5) programming (4) risk management (4) GCP (3) compliance (3) SOPs (3) data management (3) EDC vendor (3)

📍 Locations

Republic of Poland (20)

Syneos Health

Skills & Focus: project management, clinical research, GCP, budget management, compliance, team lead, client relations, documentation, risk mitigation, business development
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience. Clinical research organization (CRO) and relevant therapeutic experience preferred.

Parexel

Skills & Focus: Project Leadership, Risk Surveillance, FSP, Clinical Research, Project Plans, SOPs, ICH, GCP, Compliance, Budget
Skills & Focus: Clinical Research, FSP, Remote, CRA, Biostatisticians, Clinical Trials, Project Leaders, Data Managers, Regulatory Consultants, Statistical Programmers

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.

Parexel

Skills & Focus: Clinical Research Associate, monitoring duties, clinical trials, protocols, regulatory submissions, oncology studies, ICH GCP compliance, site management, independent monitoring, flexible work arrangements
About the Company: Parexel is a global leader in biopharmaceutical services, helping customers maximize their chances of success in clinical research and market access.
Experience: Minimum of 3 years of active independent field monitoring experience.
Type: Remote
Benefits: Premium salary, car or car allowance, paid holidays, medical care plan: Health, Dental & Vision, life assurance.

Syneos Health

Skills & Focus: Clinical Trial Management, Oncology, Pharmacovigilance, Trial Master File, Global implementation, Study oversight, Site management, Vendor management, Patient Registration, Good Clinical Practice
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Previous CTM experience gained from a CRO or Pharma company.
Type: Fully home based

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: SAS, programming, clinical trials, statistical analysis, data listings, quality standards, validation, documentation, project management, mentoring
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.

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

Iqvia

Skills & Focus: clinical trial management, study management team, project planning, risk mitigation, compliance, stakeholder management, data collection, vendor oversight, document management, training materials
About the Company: IQVIA is working to create a healthier world through diverse expertise, innovation, and powerful capabilities in the healthcare sector.
Experience: 6-8 years clinical trial management experience in the pharmaceutical industry or CRO.
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: site qualification, monitoring, regulatory compliance, Good Clinical Practice, patient safety, clinical data integrity, communication, project management, investigator meetings, audit readiness
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience

Iqvia

Skills & Focus: clinical trials, study management, Vendor Management, project management, patient outcomes, data management, healthcare intelligence, protocol development, regulatory documents, Good Clinical Practice
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: 2-5 years of experience in managing late phase clinical trials at global level
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

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

Precision For Medicine

Skills & Focus: clinical databases, EDC vendor, Data Management, Project Management, programming, scripting, Microsoft Office, clinical research, data management, leadership
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.

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.

Precision For Medicine

Drug Safety Physician Republic of Poland
Skills & Focus: pharmacovigilance, safety reporting, clinical support, risk management, signal detection, safety data management, adverse events, compliance, drug safety, clinical trials
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level usi…
Experience: Minimum of 7 years in Drug Safety related activities in pharma/biotech.
Drug Safety Physician Republic of Poland
Skills & Focus: Drug Safety, Pharmacovigilance, clinical trial, safety reporting, risk management, signal detection, safety data, case processing, FDA, EU regulations
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level usi…
Experience: Minimum of 7 years in Drug Safety related activities in pharma/biotech, with at least 3 years being in early clinical development.

Precision Medicine Group

Skills & Focus: Clinical Data Manager, Clinical trial data management, Database development, Data entry quality, CRF specifications, Quality control, SOPs, CDISC standards, Medical coding, Clinical research tasks
About the Company: Precision Medicine Group is an Equal Opportunity Employer focusing on innovative solutions in clinical development and other healthcare services.
Experience: 8+ years’ experience with strong Oncology and/or Orphan Drug therapeutic experience
Type: Full-time
Drug Safety Physician Republic of Poland
Skills & Focus: Drug Safety, Pharmacovigilance, Safety reporting, Risk management, Clinical trial, Adverse Event, Signal detection, GCP, SOPs, Regulatory requirements
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level usi…
Experience: 7 years in Drug Safety related activities in pharma/biotech

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.