20 Clinical Operations Management jobs in Beijing.

Hiring now: Cra1 Adpbeijingshanghai @ Iqvia, Dir Cpp Group Lead China @ Johnson Jo, Clin Ops Spec @ Syneos Hea, Sr Study Mgr @ Pfizer, Clinical Feasibility Lead @ Parexel, Regulatory Writing Sr Mgr @ Amgen, Clinical Operation Proj M @ Alcon.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Research (6) clinical research (5) Clinical Trials (5) GCP (5) clinical trials (4) Compliance (4) project management (4) Data Management (4) monitoring (3) communication (3)

📍 Locations

Beijing (20)

Iqvia

Skills & Focus: clinical research, site management, monitoring, Good Clinical Practice, protocol adherence, regulatory submissions, subject recruitment, data management, communication, documentation
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.

Johnson & Johnson

Skills & Focus: Clinical Pharmacology, Pharmacokinetics, Drug Development, Regulatory Requirements, Leadership, Team Development, R&D Strategy, Innovation, Performance Management, Clinical Trials
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: PhD in Pharmaceutical Sciences, or related field plus a minimum of 10 years’ experience in clinical development; or M.S. in Pharmaceutical Sciences plus 14 years’ experience.
Type: Full-time

Iqvia

Skills & Focus: management, clinical research, staff development, quality metrics, training, clinical trials, regulatory requirements, leadership, 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 industrie…
Experience: Prior clinical trial experience including experience in a management/leadership capacity or equivalent combination of education, training and 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, Trial Master File, Compliance, Documentation, CRAs, Clinical Trial Supplies, Case Report Forms, Mentoring, GCP, 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 industrie…
Experience: 5 administrative support experience. Minimum two years clinical research experience strongly preferred.
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 Operations, Site Management, Trial Master File, Clinical Research, Compliance, Database Management, Team Coordination, Communication, Interpersonal Skills, 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…
Experience: High School diploma or equivalent
Benefits: We are passionate about developing our people, through career development and progression; supportive and engaged line …
Sr CRA I Beijing
Skills & Focus: site qualification, monitoring, GCP compliance, subject safety, data integrity, investigational product, project management, clinical trial, auditing, patient recruitment
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Skills & Focus: Project Administration, Trial Master File Management, Vendor Management, Financial Reporting, Risk Mitigation, Customer Proposal Development, Team Training, Stakeholder Communication, Data Analysis, Clinical Research
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Prior experience in a contract research organization (CRO), pharmaceutical, or biotechnology company preferred.
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…

Pfizer

Skills & Focus: study management, clinical trials, site monitoring, feasibility, protocol design, subject enrollment, risk assessment, budget phasing, drug supply management, GCP
Experience: At least 5 years in clinical practices
Type: Full time

Iqvia

Skills & Focus: clinical research, planning services, business development, enrollment strategies, feasibility, stakeholders, data analysis, communication skills, GCP, FDA regulations
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
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Parexel

Skills & Focus: feasibility, clinical trials, site identification, strategic thinking, analytical skills, communication, leadership, problem-solving, teamwork, project management
About the Company: Parexel provides leading biopharmaceutical services and is dedicated to providing high-quality services to its clients, focusing on aspects like innovation and…
Experience: Relevant clinical research experience in management of international clinical trials.
Type: Full-time
Benefits: Flexible work arrangements, opportunities for career advancement, and a focus on employee well-being.

Johnson & Johnson

Skills & Focus: Site Management, Clinical Trial, Monitoring, Compliance, Recruitment, Data Integrity, Adverse Events, Training, Regulatory, Stakeholder Management
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: A minimum of 2 years of clinical trial monitoring experience is preferred.
Type: Full-time

Amgen

Skills & Focus: Regulatory writing, clinical study reports, regulatory submission documents, clinical development, cross-functional teams, global regulatory standards, project management, scientific writing, team collaboration, medical writing
About the Company: Amgen is a leading biotechnology company focused on developing innovative human therapeutics.
Experience: Doctor degree and 3-5 years of Writing Regulatory or scientific submission/documents experience OR Master’s degree and 8-10 years of Writing Regulatory or scientific submission/documents experience >10 years industry working experience
Type: Full time

Parexel

Skills & Focus: Clinical Trials, Clinical Operations Leader, Functional Service Provider, Oncology, Study Start-up, Site Care Partner, Biometrics, Project Leadership, Clinical Feasibility, Data Management

Pfizer

Skills & Focus: Clinical Trial, Project Management, Budget Management, GCP, Operational Risk Management, Study Management, Cross-functional Teams, Compliance, Quality Metrics, Health Assessment
Experience: 8+ years relevant experience
Type: Full time

Parexel

Skills & Focus: Clinical Trials, Feasibility, Clinical Research, FSP, CRA, Project Leader, Biostatistics, Data Management, Regulatory, Statistical Programming
About the Company: Parexel is a global company dedicated to providing insights that will help deliver safe and effective new therapies to market.
Skills & Focus: Clinical Research, Project Management, Regulatory Compliance, Data Management, Clinical Trials, Statistical Analysis, Biostatistics, Collaboration, Patient Recruitment, Research Methodology
About the Company: Parexel is a global biopharmaceutical services organization that helps clients accelerate the development of new treatments. They are dedicated to building suc…
Type: Full-time

Johnson & Johnson

Skills & Focus: clinical trial, site management, monitoring, regulations, SOP, GCP, training, data entry, risk-based monitoring, patient recruitment
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 2 years of clinical trial monitoring experience preferred.
Type: Fully Onsite

Alcon

Skills & Focus: clinical trials, clinical research, project management, clinical operation, timelines, budgets, clinical study, resources, team leadership, communication skills
About the Company: Alcon is a global leader in eye care, innovating boldly to help people see brilliantly. They foster an inclusive culture and are dedicated to making an impact …
Experience: A minimum of 5 years experience in the field of clinical research of which 1 year must have been in a project lead role.
Benefits: Alcon offers competitive performance-based compensation, flexible benefits, commercial insurance for health, medical, r…

Johnson & Johnson

Skills & Focus: clinical trial agreements, negotiation, ancillary agreements, clinical research, contract management, budget development, customer focus, compliance, collaborative team, problem solving
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: 3 years
Type: Hybrid