14 Biopharmaceutical Leadership jobs in Bangkok.

Hiring now: Regulatory Affairs Associ @ Parexel, Medical Advisor Oncology @ Amgen, Milestone One Site Coordi @ Psicro, Regulatory Affairs Spec @ Boston Sci, Professional Education Le @ Johnson Jo, Sr Clinical Research Asso @ Iqvia, Rare Disease Mgr @ Astrazenec, Medical Monitor @ Psi.Explore more at jobswithgpt.com.

🔥 Skills

Regulatory Affairs (5) Clinical Research (5) Clinical Trials (3) Consulting (3) Project Management (2) Compliance (2) Documentation (2) Biostatistics (2) Statistical Programming (2) Data Management (2)

📍 Locations

Bangkok (14)

Parexel

Skills & Focus: Regulatory Affairs, Clinical Research, Project Management, Compliance, FDA, Documentation, Drug Development, Submission, GxP, Life Sciences
About the Company: Parexel is a global biopharmaceutical services organization that provides integrated solutions to help clients develop and deliver innovative drugs and therapi…
Type: Full-time
CRA - FSP Bangkok
Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Biostatistics, Statistical Programming, Data Management, Consulting, Regulatory Affairs, Project Leader, Clinical Research
Skills & Focus: Clinical Research, Regulatory Affairs, Biostatistics, Consulting, Statistical Programming, Data Management, Clinical Operations, Patient Engagement, Regulatory Affairs Associate, Clinical Trials
About the Company: Parexel is a leading global clinical research organization that provides comprehensive drug development and regulatory consulting services. Focused on improvin…
Type: Full-time
Benefits: Flexible Work Arrangement, Global Inclusion Benefits & Support

Amgen

Skills & Focus: medical strategies, oncology, hematology, value proposition, stakeholder engagement, medical evidence, healthcare ecosystem, external collaborations, lifecycle management, scientific communication
About the Company: Amgen is one of the world’s leading independent biotechnology companies, pioneering biotechnology breakthroughs for over 4 decades to bring state-of-the-art me…
Experience: Doctorate degree & 3 years of directly related experience or Bachelor’s degree & 6 years of directly related experience
Type: Full-time

Psicro

Skills & Focus: ICH-GCP, protocol requirements, monitoring visits, patient enrollment, data entry, adverse events, regulatory documents, contract negotiations, study procedures, audits

Parexel

Skills & Focus: Regulatory Affairs, Biologics, Consulting, Clinical Trials, Remote, Medical Device, Publishing, Senior Associate, Technical, Drug & Device
About the Company: Parexel is a global clinical research organization that provides expertise in regulatory affairs, medical writing, and clinical trials management.
Type: Remote

Boston Scientific

Skills & Focus: Regulatory Affairs, Compliance, Medical Device, Pharmacy, Advertising, Legal, Healthcare, Marketing, Quality training, Interpersonal skills
About the Company: As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Ou…
Experience: 1-2 years in medical device submission (CSDT submission) will be an advantage
Type: Hybrid

Amgen

Skills & Focus: Product Manager, Cardiovascular, Brand strategies, Marketing plans, Cross-Function Collaboration, Budgeting, Forecasting, Promotional activities, Patient needs, Pharmaceutical industry
About the Company: Amgen is one of the world’s leading independent biotechnology companies, pioneering biotechnology breakthroughs to bring state-of-the-art medicines from labora…
Experience: Minimum 5 years of working experience, with a minimum of 2 years in Product Management/Marketing role in the pharmaceutical industry.
Type: Full time
Benefits: In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with lo…

Johnson & Johnson

Skills & Focus: Professional Medical Education, Surgery, MedTech, Medical Affairs, Leadership, Stakeholder management, Cross-functional, Customer engagement, Market development, Healthcare solutions
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: 8-10 years of relevant business experience in Professional education, Marketing, General Management, or a related field, preferably medical device.
Type: Full-time

Iqvia

Skills & Focus: clinical research, monitoring, GCP, ICH, site management, data reporting, study protocol, subject recruitment, regulatory requirements, 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…
Experience: Prior on-site monitoring experience; or equivalent combination of education, training and experience.
Type: Full time

Astrazeneca

Skills & Focus: rare disease, stakeholder management, cross-functional collaboration, market access, patient experience, pharmaceutical products, strategy development, business sustainability, sales management, Neurology
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies focused on delivering life-changing medicines.
Experience: Minimum 4 years of sales management/marketing/key account experience in the pharmaceutical industry.

Iqvia

Skills & Focus: Site Activation, Clinical Research, Feasibility, Regulatory Submission, GCP/ICH Guidelines, Documentation, Project Management, Interpersonal Skills, Negotiating Skills, Independent Work
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 - 2 years’ clinical research or other relevant experience; or equivalent combination of education, training, and experience.
Type: Contract
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, administrative support, clinical documents, performance tracking, project timelines, clinical team, Case Report Forms (CRFs), Good Clinical Practice (GCP), International Conference on Harmonization (ICH)
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 so you can thrive at work and at home.

Psi

Skills & Focus: medical matters, clinical development plans, clinical studies, data safety monitoring, regulatory compliance, Pharmacovigilance, risk mitigation, GCP guidelines, clinical documents, study team compliance
About the Company: As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science an…