Last updated: 2025-05-10

12 Clinical Data And Biostatistics jobs in Beijing.

Hiring now: Centralized Monitor @ Iqvia, Medical Scientist @ Syneos Hea, Site Activation Partner I @ Parexel, Medical Science Liaison @ Amgen, Sr Ma @ Pfizer, Sr Site Mgr @ Johnson Jo.Explore more at jobswithgpt.com.

šŸ”„ Skills

project management (6) Data Management (3) clinical research (2) communication (2) team collaboration (2) clinical drug development (2) communication skills (2) Clinical Trials (2) clinical trials (2) monitoring (1)

šŸ“ Locations

Beijing (12)

Iqvia

Skills & Focus: clinical research, monitoring, analytics, data review, patient information, quality control, documentation, clinical operation, communication, site performance
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: Minimum of 2 years of relevant work experience 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.

Syneos Health

Skills & Focus: Medical Management Plan, Medical Data Review Plan, Eligibility Review Plan, medical data analysis, data visualization, protocol deviation review, project management, ICH guidelines, Good Clinical Practices, team collaboration
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Degree in life sciences (MSc, PharmD, PhD, DMD, MD) or equivalent with relevant scientific experience and/or training discipline.

Iqvia

Skills & Focus: statistical methodologies, research projects, statistical analyses, analysis plans, statistical reports, data, healthcare, clinical research, life sciences, custom studies
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…
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: Data Management, CRF, database design, validation definition, mentorship, employee engagement, clinical drug development, 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: 7 years of relevant work experience including people management
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: Data Management, clinical drug development, project management, staff management, problem solving, financial management, communication skills, leadership skills, strategic planning, customer focus
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: 10 years of relevant work experience including substantial people 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.

Parexel

Skills & Focus: Clinical Trials, Functional Service Provider, Site Activation, Clinical Feasibility, Clinical Research, Project Leader, Biostatistics, Statistical Programming, Data Management

Syneos Health

Skills & Focus: medical plans, medical review, data analysis, project management, clinical operations, data management, drug safety, pharmacovigilance, safety review, medical data queries
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Type: Full-time

Amgen

Skills & Focus: Medical Science Liaison, osteoporosis, clinical knowledge, scientific exchange, healthcare professionals, clinical trials, investigator meetings, education programs, project management, strategic thinking
About the Company: Amgen is a biotechnology company that discovers, develops, manufactures, and delivers innovative human therapeutics.
Experience: Minimum of 2 years of relevant professional experience
Type: Full-time
Skills & Focus: therapeutic areas, OL insights, collaborative relationships, scientific information, field strategy, clinical trials, project management, drug commercialization, communication skills, relationship building
About the Company: Amgen is a biotechnology company focused on the research, development, manufacturing, and delivery of innovative human therapeutics.
Experience: 1-2 years of Medical Science Liaison experience preferred
Type: Full time

Pfizer

Senior MA Beijing
Skills & Focus: Antimicrobial, Clinical Trials, Quality Improvement, Infectious Diseases, Project Management, Data Analysis, Healthcare Policy, Product Lifecycle Management, Medical Affairs, Clinical Practice
Experience: Minimum of 2 years of experience in the pharmaceuticals.
Type: Full time

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