25 Clinical Operations Management jobs in Warsaw.

Hiring now: Clinical Trial Payments S @ Parexel, Site Activation Coordinat @ Iqvia, Sr Site Contracts Spec @ Syneos Hea, Sr Mgr Trial Delivery Lea @ Johnson Jo, Milestone One Site Coordi @ Psicro, Medical Monitor @ Psi, Local Study Associate Dir @ Astrazenec, Site Mgr @ Care Acces, Pharmacovigilance Medical @ Ergomed, Clinical Startup Spec Cdc @ Novo Nordi.Explore more at jobswithgpt.com.

🔥 Skills

clinical trials (6) project management (5) communication (5) Clinical Trials (4) documentation (4) GCP (4) interpersonal skills (3) medical writing (3) site management (3) Project Management (3)

📍 Locations

Warsaw (25)

Parexel

Skills & Focus: Clinical Trials, Finance, Payments, Contracts, Financial Correspondence, Maintenance of Financial File, Administrative Support, Excel, Word, Communication
Experience: Desirable: financial, legal, or similar.

Iqvia

Skills & Focus: site activation, clinical trials, healthcare, documentation, compliance, regulatory, project management, communication, interpersonal skills, 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 industri…
Experience: Minimum 2 years’ work experience; 1+ years in healthcare or similar
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: contracts, clinical trials, budget negotiation, project management, clinical development, clinical operations, legal issues, customer focus, vendor management, SOPs
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Moderate contracts management experience
Type: Hybrid

Iqvia

Skills & Focus: medical writing, clinical study reports, GCP, documentation, project management, communication, regulatory knowledge, stakeholder engagement, team collaboration, statistical methods
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: Typically requires at least 5 years of highly 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.
Skills & Focus: clinical research, monitoring, site management, study protocol, regulatory submissions, data query resolution, communication, training, documentation, recruitment
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: Experience in on-site monitoring of clinical trials
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 Research, Site Management, Regulatory Compliance, Good Clinical Practice, Data Integrity, Clinical Monitoring, Patient Safety, Project Management, Training, Audit Readiness
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
Benefits: career development, supportive management, technical training, peer recognition, total rewards

Johnson & Johnson

Skills & Focus: clinical trial delivery, operational oversight, cross-functional team, budget management, timelines, quality, risk management, Health Authority inspections, process improvement, employee engagement
About the Company: Johnson & Johnson is a global leader in healthcare innovation committed to building a world where complex diseases are prevented, treated, and cured.
Experience: Minimum of 8 years in Pharmaceutical, Healthcare or related industries.
Type: Hybrid
Skills & Focus: clinical trials, vendor management, risk reviews, trial management, training, project planning, communication, analytical skills, team leadership, milestone tracking
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: Minimum of 4 years clinical trial experience in Pharmaceutical or Healthcare; Minimum of 2-3 years’ experience supporting multiple aspects of a global clinical trial.
Type: Hybrid
Skills & Focus: Oncology, Regulatory Medical Writing, Clinical Documents, Project Management, People Management, Cross-functional Team, Process Improvements, Medical Writing, Scientific Strategy, Training
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience is required.
Type: Fully Remote

Parexel

Skills & Focus: Clinical Study Administrator, trial administration, site administration, document management, budgeting, regulatory compliance, ICH-GCP guidelines, organizational skills, communication, interpersonal skills
About the Company: Parexel FSP offers you the security of a long-term position and many opportunities for career progression. They focus on clinical research and provide a range …
Experience: Minimum 2 years of previous administrative experience in the medical/life science field.
Type: Hybrid

Johnson & Johnson

Skills & Focus: Clinical Trial, Project Management, Regulatory Compliance, Site Management, Investigator Meeting, Logistical Support, Pharmaceutical Development, Training, Data Management, Safety Updates
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: Must be graduating no more than 12 months prior to the target start date of July 2025.
Type: Hybrid

Psicro

Skills & Focus: clinical trial, monitoring visits, patient enrollment, GCP, data entry, adverse events, protocol deviations, regulatory documents, contract negotiations, study audits

Parexel

Skills & Focus: Clinical Trials, Project Leadership, Financial Coordination, Clinical Research, Project Plans, SOP Compliance, Risk Prevention, Pharmaceuticals, Patient Safety, Biopharma
About the Company: Parexel is a global biopharmaceutical services organization that provides a wide range of solutions to help its clients develop and launch new drugs. With a fo…
Type: Hybrid

Syneos Health

Skills & Focus: clinical trial management, site management oversight, monitoring deliverables, data integrity, risk assessment, compliance, patient recruitment, budget management, Good Clinical Practice, communication skills
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Demonstrated ability to lead and align teams in the achievement of project milestones
Type: Hybrid
Benefits: We are passionate about developing our people, through career development and progression; supportive and engaged line …
Skills & Focus: clinical trials, site activation, regulatory affairs, project management, submissions, budget negotiation, quality control, team collaboration, training materials, problem solving
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Type: Hybrid

Parexel

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

Iqvia

Skills & Focus: site management, feasibility assessments, site start-up, Regulatory Authority, Ethics Committee, essential document collection, study-specific meetings, interpersonal skills, local healthcare systems, planning and organizational skills
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: At least 5 years of relevant experience in the biopharmaceutical/CRO industry.
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Psi

Skills & Focus: Medical, Clinical Trials, GCP, Safety, Data Review, Pharmacovigilance, FDA Compliance, Clinical Development, Risk Mitigation, Study Protocol
About the Company: Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and wel…

Astrazeneca

Skills & Focus: study commitments, data quality, site selection, risk management, project management, ICH-GCP, team management, clinical trials, budget management, regulatory submissions
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, focused on helping patients by delivering life-changing medi…
Experience: Minimum 3 years of experience in Development Operations (CRA, SrCRA) or other related fields; at least 1 year of experience in team management or project management.
Type: Fixed-term

Care Access

Skills & Focus: clinical research, site management, GCP, staff training, patient enrollment, site SOPs, communication skills, organizational skills, problem solving, regulatory compliance
About the Company: Care Access is a unique, multi-specialty network of research sites which operates as one connected team of physician investigators, nurse coordinators, and ope…
Experience: 2+ years proven experience in the management of a clinical research site/clinic/hospital department conducting clinical trials
Type: Full-time
Benefits: PTO/vacation days, sick days, holidays, LuxMed, PPK Plan, Life Insurance, Health & Wellness Allowance, Bonus system bas…

Ergomed

Skills & Focus: pharmacovigilance, medical writing, PSURs, PBRERs, PADERs, ACOs, DSURs, RMPs, quality documentation, aggregate reports

Novo Nordisk

Skills & Focus: Clinical Trials, Start-Up Specialist, Management, Stakeholders, Regulations, Submissions, Protocols, Quality Data, Team-oriented, Proactive
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy …
Experience: At least one year of experience with EU CTR submissions

Biogen

Skills & Focus: clinical development, local operational expertise, clinical trial, investigator engagement, QSDO, CRO, site selection, performance KPIs, cross functional coordination, therapeutic area knowledge
About the Company: Biogen is a biotechnology company that specializes in the discovery, development, and delivery of innovative therapies for neurological and neurodegenerative d…
Type: Full-time

Astrazeneca

Skills & Focus: clinical data sharing, anonymization, regulatory submission, data risk management, clinical document sharing, attention to detail, SAS programming, medical writing, quality, continuous improvement
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies dedicated to delivering life-changing medicines.
Type: Hybrid

Novo Nordisk

Skills & Focus: clinical trials, start-up activities, EU CTR, regulations, ICH-GCP, data management, documentation, stakeholders, submission process, team-oriented
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases.
Experience: at least one year of experience with EU CTR submissions