12 Biopharmaceutical Leadership jobs in Shenzhen.

Hiring now: Scientific Advisor @ Johnson Jo, Clinical Trials Asst Cta @ Iqvia, Clinical Research Associa @ Parexel, Endoluminal Market Develo @ Intuitive , Head Of Medical Affairs @ Novo Nordi, Regulatory Affairs Associ @ Amgen, Sr Exec @ Vita Green, Sr Clinical Ops Spec @ Syneos Hea.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Research (5) market insights (3) collaboration (3) stakeholder management (3) pharmaceutical industry (3) stakeholders (2) regulatory compliance (2) Clinical Trials (2) Monitoring (2) Data Management (2)

📍 Locations

Hong Kong (11) Mong Kok (1)

Johnson & Johnson

Skills & Focus: clinical resource, clinical trials, medical science literature, subject matter expert, coaches, techniques, processes, medical developments, complex information, stakeholders
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: Experienced Scientist
Type: Full-time

Iqvia

Skills & Focus: Clinical Research, Trial Master File, administrative activities, regulatory compliance, clinical documents, clinical data, Microsoft Office, Good Clinical Practice, time management, 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: 3 years administrative support experience
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs.

Parexel

Skills & Focus: Clinical Research, Clinical Trials, CRA, Monitoring, Biostatistics, Regulatory, Data Management, Patient Care, Project Leadership, Team Collaboration

Intuitive Surgical

Skills & Focus: market development, pulmonology, biopsy, stakeholders, physicians, interventional radiology, market insights, ROI, collaboration, product portfolio
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 5+ years of experience in the medical device industry

Novo Nordisk

Skills & Focus: medical communication, scientific strategy, medical education, stakeholder management, market insights, leadership, healthcare professionals, collaboration, regulatory changes, pharmaceutical industry
About the Company: Novo Nordisk is a global healthcare company with over 95 years of innovation and leadership in diabetes care. We are also a major player in areas such as hemop…
Experience: Minimum 12 years of relevant work experience, especially Medical Affairs related experiences in the pharmaceutical industry.
Skills & Focus: medical communication, scientific communication, medical education, stakeholder management, leadership, market insights, pharmaceutical industry, healthcare professionals, strategic communications, team development
About the Company: At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the w…
Experience: Minimum 12 years' of relevant work experience, especially Medical Affairs related experiences in pharmaceutical industry. Minimum 5 years' of work experience in managerial level.

Amgen

Skills & Focus: regulatory submissions, local regulatory requirements, promotional materials, safety communications, regulatory information, collaboration, lifecycle management, Healthcare Compliance, process improvements, vendor relationships
About the Company: Amgen is one of the world’s leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of…
Experience: Regulatory experience in the applicable country(ies).
Type: Contract
Benefits: Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits.

Iqvia

Skills & Focus: Clinical Research, Monitoring, Site Management, GCP, ICH guidelines, Protocol, Patient recruitment, Regulatory submissions, Data integrity, 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…
Experience: Requires at least 1 year of on-site monitoring 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 Research, FSP, Clinical Trials, Clinical Research Associate, Oncology, Functional Service Provider, Remote, Registered Nurse, Data Managers, Project Leadership
About the Company: Parexel is a Clinical Research Organization (CRO) contracted by pharmaceutical, biological, or medical device manufacturers to manage clinical research studies…

Vita Green

Skills & Focus: New Product Development, pharmaceutical industry, project management, cross-functional projects, stakeholder management, regulatory compliance, timelines, risks, continuous improvement, innovation
About the Company: Vita Green stands at the forefront of the health supplements industry, committed to enhancing well-being through innovative research and cutting-edge solutions…
Experience: 3–5 years
Benefits: Flexible working schedule that promotes work-life harmony; Opportunities for professional growth and development; Exclu…

Syneos Health

Skills & Focus: Clinical Operations, Regulatory Submission, Study Support, Project Deliverables, Compliance, Site Management, Clinical Research, Medical Terminology, Communication, Data Management
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Experience in clinical research/pharma/biotech or related field considered in lieu of degree.