21 Clinical Operations Management jobs in Seoul.

Hiring now: Sr Clinical Data Analyst @ Parexel, Clinical Research Associa @ Iqvia, Sr Clinical Research Asso @ Psi, Local Trial Mgr @ Amgen, Clinical Research Associa @ Astrazenec, Clinical Trial Mgr Ii @ Syneos Hea, Mktg Surveillance Associa @ Novo Nordi.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Research (7) Clinical Trials (6) monitoring (6) project management (6) clinical trials (6) regulatory compliance (6) ICH-GCP (5) CRA (4) Data Management (3) Functional Service Provider (3)

📍 Locations

Seoul (21)

Parexel

Skills & Focus: Clinical Trials, Data Management, Biostatistics, Clinical Research, FSP, CRA, Functional Service Provider, Oncology, Statistical Programming, Epidemiology
About the Company: Parexel helps clients accelerate the development and commercialization of innovative new therapies with expertise in regulatory consulting, clinical trials, an…
Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Site Care Partner, Data Managers, Project Leaders, Biostatisticians, Regulatory Consultants, Statistical Programmers, Emerging Talent
Skills & Focus: Clinical Research, Clinical Trials, CRA, Monitoring Operations, Technology, Work-life balance, Career path, Flexibility, Local law enforcement, Employee well-being

Iqvia

Skills & Focus: clinical research, monitoring, site selection, project management, communication, regulatory submissions, data query resolution, recruitment, training, oncology
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: At least 1-2 years of on-site monitoring experience
Type: Full time
Benefits: Various benefits including Employee Assistance Program, support for various activities, special leave, and insurance pa…

Parexel

Skills & Focus: Clinical Research, CRA, Remote, FSP, Biostatistics, Statistical Programming, Clinical Trials, Data Management, Project Leadership, Functional Service Provider
About the Company: Parexel is a global biopharmaceutical services organization that provides a range of services to assist clients in the development of new therapies and in brin…
Type: Full-time

Psi

Skills & Focus: Clinical Research, Site Selection, Monitoring, Regulatory Submission, Patient Enrollment, Query Resolution, Investigator Training, Document Verification, Safety Information, Project Timelines
Type: Office-based/Hybrid

Amgen

Skills & Focus: clinical trials, project management, country strategy, regulatory knowledge, stakeholder collaboration, study execution, site relationships, monitoring, budget management, enrollment
About the Company: Global biotechnology company headquartered in Thousand Oaks, California. Amgen focuses on developing innovative therapies for patients with serious illnesses.
Type: Full time

Iqvia

Skills & Focus: Clinical Trials, Clinical Research Associates, Trial Master File, administrative activities, clinical documents, Compliance, performance tracking, documentation, archiving, communication
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: 1 year
Type: Full time
Skills & Focus: Clinical Trial Manager, clinical delivery, project management, regulatory requirements, clinical quality, stakeholder management, project finances, risk mitigation, collaboration, 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 industrie…
Experience: Requires at least 2 years of Project Management experience, including Clinical Lead experience. Requires at least 6 years of CRA experience with global 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.

Astrazeneca

Skills & Focus: clinical research, monitoring, oncology, investigators, site qualification, ICH-GCP, regulatory authorities, data management, adverse events, compliance
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, focused on innovation and creativity.
Experience: 1 year or more of oncology clinical trial monitoring experience preferred

Syneos Health

Skills & Focus: Clinical Trial Management, Site Management, Patient Safety, Protocol Compliance, Data Integrity, Risk Management, Clinical Monitoring, Stakeholder Communication, Training Coordination, Regulatory Compliance
About the Company: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They focus on simplifying and stream…
Experience: Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience

Psi

Skills & Focus: medical monitoring, clinical development, clinical studies, data safety monitoring, regulatory compliance, pharmacovigilance, risk management, clinical protocols, study participants, safety monitoring
About the Company: PSI's Medical Monitoring team

Iqvia

Skills & Focus: Clinical Research, Site Management, Monitoring Plan Compliance, Study Monitoring, Data Management, Good Clinical Practice, Clinical Trials, Study Coordination, Regulatory Requirements, Project Execution
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…
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Novo Nordisk

Skills & Focus: pharmaceutical, post marketing surveillance, project management, ICH-GCP, PMS, PASS, compliance, clinical trials, project timelines, safety reporting
About the Company: Novo Nordisk is a global healthcare company with a strong commitment to life-changing innovations in diabetes care.
Experience: At least 3 years of working experience in clinical trials, PMS/PASS, CRA is preferred

Syneos Health

Skills & Focus: site qualification, site management, monitoring, GCP, regulatory compliance, clinical data, patient safety, investigational product, documentation, 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

Psi

CRA II Seoul
Skills & Focus: Clinical Research, Monitoring Visits, Study Startup, CRF Review, Source Document Verification, Query Resolution, Site Budgets, Contract Negotiations, Trial Progress, Regulatory Support
Type: Hybrid

Syneos Health

Skills & Focus: Clinical Research, GCP, site management, monitoring, data integrity, investigator meetings, audit readiness, regulatory compliance, clinical trials, patient safety
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
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…

Astrazeneca

Skills & Focus: clinical trials, study management, site monitoring, ICH-GCP, regulatory submissions, risk management, team leadership, project management, financial management, patient recruitment
About the Company: AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines.
Experience: Minimum 7 years of experience in Development Operations (CRA, SrCRA + at least 1 year study management experience)
Type: Full-time

Syneos Health

Skills & Focus: site qualification, site monitoring, regulatory compliance, ICH-GCP, informed consent, data capture, audit readiness, clinical trial management, pharmacovigilance, remote monitoring
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
Type: Hybrid
Benefits: Total rewards program including career development and progression

Astrazeneca

Skills & Focus: clinical trials, quality management, ICH-GCP, regulatory compliance, site management, monitoring, audits, risk management, negotiation, problem solving
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies. We are committed to helping patients by delivering life-chan…
Experience: At least 5 years of proven relevant experience.

Novo Nordisk

Skills & Focus: post marketing surveillance, clinical trials, project management, regulatory compliance, therapeutic expertise, project timelines, vendor management, safety reporting, communication, audit support
About the Company: We are a proud life-science company, committed to ensuring people can lead a life independent of chronic disease.
Experience: At least 3 years of working experience in clinical trials, PMS/PASS, CRA is preferred