536 Clinical Trials jobs in Vietnam
Pharmaceutical Research Scientist - Clinical Trials
530000 Hoa Sơn
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Our client is a leading pharmaceutical company seeking a highly motivated Pharmaceutical Research Scientist to contribute to their innovative drug development pipeline. This role offers a hybrid work arrangement, combining remote flexibility with essential on-site laboratory work. You will be instrumental in the design, execution, and analysis of preclinical and clinical studies, focusing on the efficacy and safety of novel therapeutic agents. This position requires a deep understanding of pharmacology, molecular biology, and regulatory requirements within the pharmaceutical industry.
Key Responsibilities:
The ideal candidate will possess a strong scientific background with proven experience in pharmaceutical research and development. Excellent analytical, problem-solving, and communication skills are essential. You should be adept at interpreting complex data and translating scientific findings into actionable insights. The ability to thrive in a hybrid work environment, balancing independent remote work with collaborative on-site laboratory activities, is crucial.
Qualifications:
Key Responsibilities:
- Design and conduct in vitro and in vivo experiments to evaluate drug candidates.
- Analyze experimental data using advanced statistical methods and scientific software.
- Prepare detailed study protocols, research reports, and regulatory submission documents.
- Collaborate with cross-functional teams, including clinicians, chemists, and regulatory affairs specialists.
- Manage timelines and resources for research projects, ensuring timely completion.
- Contribute to the development of new research methodologies and technologies.
- Stay abreast of the latest scientific literature, industry trends, and regulatory guidelines.
- Present research findings at internal meetings and external scientific conferences.
- Ensure all research activities comply with ethical standards, GLP, and GMP regulations.
- Mentor junior research staff and provide technical guidance.
The ideal candidate will possess a strong scientific background with proven experience in pharmaceutical research and development. Excellent analytical, problem-solving, and communication skills are essential. You should be adept at interpreting complex data and translating scientific findings into actionable insights. The ability to thrive in a hybrid work environment, balancing independent remote work with collaborative on-site laboratory activities, is crucial.
Qualifications:
- Ph.D. in Pharmacology, Molecular Biology, Biochemistry, or a related life science discipline.
- Minimum of 5 years of post-doctoral or industry research experience in pharmaceutical R&D.
- Proven track record of designing and executing complex biological assays.
- Expertise in data analysis and interpretation using scientific software (e.g., GraphPad Prism, R).
- In-depth knowledge of drug discovery and development processes.
- Experience with regulatory requirements (e.g., FDA, EMA) for drug development is highly desirable.
- Excellent written and verbal communication skills.
- Strong organizational skills and the ability to manage multiple projects simultaneously.
- Experience working in a GLP/GMP regulated environment.
- Ability to work effectively both independently and as part of a team in a hybrid setting.
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0
Remote Pharmaceutical Research Scientist - Clinical Trials
440000 Hoang Hoa
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Our client, a leading innovator in the pharmaceutical sector, is actively recruiting a highly skilled and motivated Remote Pharmaceutical Research Scientist to contribute to critical clinical trial research. This is a fully remote position, offering the flexibility to work from anywhere while collaborating with a globally distributed team of scientists, researchers, and clinicians. In this role, you will be instrumental in the design, execution, and analysis of preclinical and clinical studies. Your responsibilities will include developing research protocols, identifying suitable patient populations, monitoring study progress, and analyzing complex biological data sets. You will play a key role in evaluating drug efficacy and safety, interpreting experimental results, and contributing to the preparation of regulatory submissions and scientific publications. The ideal candidate will possess a strong academic background in a relevant scientific field, such as pharmacology, biochemistry, or a related discipline, with a Master's degree or Ph.D. A proven track record of successful research in pharmaceutical development or clinical research, with hands-on experience in laboratory techniques and data analysis software (e.g., R, Python, SAS), is essential. You must demonstrate exceptional critical thinking, problem-solving abilities, and a meticulous approach to scientific methodology. Effective written and verbal communication skills are vital for collaborating with diverse teams and presenting findings. This is a unique opportunity to make a significant impact on the development of life-saving therapies from the comfort of your home. Join our remote team and advance your career in pharmaceutical research, contributing to groundbreaking advancements from **Thanh Hoa, Thanh Hoa, VN**.
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1
Clinical Research Associate - Pharmaceutical Trials
950000 Long Xuyen, An Giang
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Our client, a leading pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to support their ongoing clinical trials in Long Xuyen, An Giang, VN . This role is critical in ensuring the smooth execution of clinical studies by monitoring trial sites, verifying data accuracy, and ensuring compliance with protocols and regulatory requirements. The CRA will act as the primary liaison between the sponsor and the investigational sites, building strong working relationships with investigators and site staff. Key responsibilities include site selection, initiation, monitoring, and close-out visits. You will review essential documents, ensure proper conduct of the study at the site level, and address any deviations or issues promptly. The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP), ICH guidelines, and relevant regulatory requirements. Exceptional organizational skills, attention to detail, and the ability to manage multiple priorities are essential. This is a field-based position requiring regular travel to assigned clinical trial sites. We are looking for an individual with a passion for science and a commitment to patient safety and data integrity. Your role will directly contribute to the development of new life-saving therapies. A proactive approach to problem-solving and excellent interpersonal skills are crucial for success in this demanding yet rewarding career path. You will be responsible for ensuring the quality and integrity of data collected during the trial, which forms the basis for regulatory submissions and drug approvals. Attention to detail in document review and site communication is paramount.
Responsibilities:
Qualifications:
Responsibilities:
- Conduct site feasibility, initiation, monitoring, and close-out visits according to protocol and GCP.
- Ensure study conduct in compliance with the protocol, FDA regulations, and ICH-GCP guidelines.
- Verify accuracy, completeness, and quality of data collected at clinical trial sites.
- Manage site relationships, providing support and guidance to investigators and study coordinators.
- Review essential study documents, including investigator site files (ISFs).
- Identify, document, and escalate study conduct issues and deviations.
- Ensure timely reporting of adverse events and product complaints.
- Prepare visit reports and follow up on action items in a timely manner.
- Contribute to the development of study-related documents.
- Ensure timely submission of regulatory and ethical committee documentation.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar role within the pharmaceutical industry.
- In-depth knowledge of ICH-GCP guidelines and clinical trial processes.
- Experience with electronic data capture (EDC) systems.
- Strong organizational skills and meticulous attention to detail.
- Excellent written and verbal communication skills.
- Ability to travel regularly to assigned clinical sites.
- Problem-solving skills and the ability to work independently.
- Certification as a CRA is a plus.
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2
Clinical Research Associate - Pharmaceutical Trials
06400 Hoi An
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Posted 2 days ago
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Our client, a leading pharmaceutical company, is seeking a meticulous and dedicated Clinical Research Associate (CRA) to join their team in **Buon Ma Thuot**. This role is instrumental in ensuring the successful execution of clinical trials, adhering to strict Good Clinical Practice (GCP) guidelines and regulatory requirements. As a CRA, you will be responsible for monitoring clinical trial sites, verifying the accuracy and completeness of data, and ensuring patient safety and rights are protected throughout the trial process. You will act as the primary liaison between the sponsor and the investigative sites, building strong relationships with investigators and study coordinators.
Key responsibilities include conducting site initiation visits, routine monitoring visits, and close-out visits to assess trial progress, data quality, and regulatory compliance. You will review source documents, case report forms (CRFs), and other trial-related records to ensure data integrity. Identifying and resolving any deviations from protocols or GCP is a crucial part of the role. You will also be responsible for managing essential trial documentation, including investigational product accountability and regulatory binders. The hybrid nature of this position allows for focused work at clinical sites and essential remote data review and reporting. Travel to various clinical sites within the region will be required. The ideal candidate possesses strong organizational skills, excellent attention to detail, and effective communication abilities. A background in a healthcare-related field (e.g., nursing, pharmacy, life sciences) or previous experience in clinical research is essential. Understanding of drug development processes and clinical trial methodologies is critical. You will contribute to bringing life-changing medicines to patients by ensuring the highest standards of quality and ethical conduct in our clinical trials. This is a rewarding opportunity to be at the forefront of medical advancement.
Key responsibilities include conducting site initiation visits, routine monitoring visits, and close-out visits to assess trial progress, data quality, and regulatory compliance. You will review source documents, case report forms (CRFs), and other trial-related records to ensure data integrity. Identifying and resolving any deviations from protocols or GCP is a crucial part of the role. You will also be responsible for managing essential trial documentation, including investigational product accountability and regulatory binders. The hybrid nature of this position allows for focused work at clinical sites and essential remote data review and reporting. Travel to various clinical sites within the region will be required. The ideal candidate possesses strong organizational skills, excellent attention to detail, and effective communication abilities. A background in a healthcare-related field (e.g., nursing, pharmacy, life sciences) or previous experience in clinical research is essential. Understanding of drug development processes and clinical trial methodologies is critical. You will contribute to bringing life-changing medicines to patients by ensuring the highest standards of quality and ethical conduct in our clinical trials. This is a rewarding opportunity to be at the forefront of medical advancement.
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3
Clinical Research Associate - Oncology Trials
01000 Bien Hoa, Dong Nai
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Our client, a leading pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their expanding team. This role is crucial for overseeing and managing clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. You will play a pivotal role in advancing groundbreaking cancer treatments by meticulously monitoring trial sites, ensuring data accuracy, and facilitating the efficient progression of oncology studies.
Your responsibilities will include site selection, initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) guidelines and relevant regulatory standards. You will be responsible for reviewing and verifying case report forms (CRFs), source documents, and study-related data to ensure accuracy, completeness, and consistency. Building and maintaining strong relationships with investigators and site staff, providing training on study protocols and procedures, and resolving site-level issues will be key aspects of your role. You will also track patient recruitment, review safety reports, and ensure timely reporting of adverse events.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, pharmacy, or a related discipline. A minimum of 3-5 years of experience as a CRA in the pharmaceutical or biotechnology industry, with a significant focus on oncology clinical trials, is required. Comprehensive knowledge of GCP, FDA regulations, and ICH guidelines is essential. Excellent monitoring skills, strong attention to detail, and the ability to analyze and interpret clinical data are critical. Exceptional organizational, time management, and communication skills are necessary to effectively manage multiple sites and interact with diverse teams. You should be proficient in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems. This is an excellent opportunity to contribute to life-saving research within a supportive and collaborative environment, making a tangible difference in patient lives.
Your responsibilities will include site selection, initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) guidelines and relevant regulatory standards. You will be responsible for reviewing and verifying case report forms (CRFs), source documents, and study-related data to ensure accuracy, completeness, and consistency. Building and maintaining strong relationships with investigators and site staff, providing training on study protocols and procedures, and resolving site-level issues will be key aspects of your role. You will also track patient recruitment, review safety reports, and ensure timely reporting of adverse events.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, pharmacy, or a related discipline. A minimum of 3-5 years of experience as a CRA in the pharmaceutical or biotechnology industry, with a significant focus on oncology clinical trials, is required. Comprehensive knowledge of GCP, FDA regulations, and ICH guidelines is essential. Excellent monitoring skills, strong attention to detail, and the ability to analyze and interpret clinical data are critical. Exceptional organizational, time management, and communication skills are necessary to effectively manage multiple sites and interact with diverse teams. You should be proficient in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems. This is an excellent opportunity to contribute to life-saving research within a supportive and collaborative environment, making a tangible difference in patient lives.
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4
Clinical Research Associate - Oncology Trials
530000 Thuy Van
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Our client, a leading pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to support critical oncology clinical trials. This role involves a hybrid work model, offering a balance between remote work and on-site responsibilities, primarily focused within the Hue, Thua Thien–Hue, VN region. As a CRA, you will be responsible for monitoring clinical trial sites to ensure adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. Your core duties will include site initiation, routine monitoring visits (both remote and on-site), data verification, and ensuring the accuracy and completeness of trial documentation. You will act as the primary liaison between the investigational sites, the sponsor, and regulatory authorities, fostering strong working relationships. Key responsibilities include conducting source data verification, identifying and resolving discrepancies, and reporting adverse events and protocol deviations. You will also be involved in training site staff on study procedures and regulatory compliance. The ideal candidate will possess excellent organizational and time-management skills, with a strong understanding of clinical trial processes and regulatory frameworks. A bachelor's degree in a life science or related field is required, along with at least 2-3 years of direct experience as a CRA or in a similar clinical research role. Strong communication and interpersonal skills are essential for effective site interaction. This is an excellent opportunity to contribute to life-saving research and advance your career in the pharmaceutical industry. Your work will directly impact the development of new cancer treatments within the therapeutic area of oncology, based in and around Hue .
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5
Remote Clinical Research Associate (CRA) - Oncology Trials
900000 Can Tho , Can Tho
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Our client is seeking a dedicated and experienced Remote Clinical Research Associate (CRA) to join their dynamic clinical operations team, focusing on groundbreaking oncology trials. This is a fully remote position, allowing you to contribute to life-saving research from the comfort of your home. As a CRA, you will play a crucial role in ensuring the quality and integrity of clinical trial data by monitoring study sites, verifying compliance with protocols, and adhering to regulatory guidelines. You will be responsible for all aspects of site management and monitoring, from initiation to close-out.
Key responsibilities include conducting pre-study, initiation, interim, and close-out visits to clinical sites, ensuring adherence to Good Clinical Practice (GCP) and all applicable regulations. You will also verify the accuracy and completeness of source data and other trial-related information, prepare and present monitoring visit reports, and train and support site staff. The ideal candidate possesses a strong understanding of clinical trial processes, regulatory requirements (e.g., ICH-GCP), and has extensive experience in monitoring oncology studies. Excellent organizational, communication, and interpersonal skills are essential for effective collaboration with investigative sites and internal teams.
We are looking for a meticulous individual with a keen eye for detail and a commitment to scientific rigor. Experience with electronic data capture (EDC) systems and various clinical trial management systems (CTMS) is highly desirable. If you are passionate about advancing cancer research, possess a proactive approach to problem-solving, and excel in a remote work environment, we encourage you to apply. This is an excellent opportunity to make a tangible impact on patient lives and advance your career in clinical research, working from anywhere.
Key responsibilities include conducting pre-study, initiation, interim, and close-out visits to clinical sites, ensuring adherence to Good Clinical Practice (GCP) and all applicable regulations. You will also verify the accuracy and completeness of source data and other trial-related information, prepare and present monitoring visit reports, and train and support site staff. The ideal candidate possesses a strong understanding of clinical trial processes, regulatory requirements (e.g., ICH-GCP), and has extensive experience in monitoring oncology studies. Excellent organizational, communication, and interpersonal skills are essential for effective collaboration with investigative sites and internal teams.
We are looking for a meticulous individual with a keen eye for detail and a commitment to scientific rigor. Experience with electronic data capture (EDC) systems and various clinical trial management systems (CTMS) is highly desirable. If you are passionate about advancing cancer research, possess a proactive approach to problem-solving, and excel in a remote work environment, we encourage you to apply. This is an excellent opportunity to make a tangible impact on patient lives and advance your career in clinical research, working from anywhere.
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6
Senior Research Scientist - Oncology Drug Development
200000 Phuong Son
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Our client, a leading biopharmaceutical company, is seeking a highly skilled and dedicated Senior Research Scientist to join their pioneering Oncology Drug Development team. This is a fully remote position, offering an exceptional opportunity to contribute to the discovery and advancement of innovative cancer therapies from the comfort of your home. You will be responsible for designing, executing, and interpreting complex experiments in areas such as molecular biology, cell biology, and pharmacology to identify and validate novel drug targets and develop promising therapeutic candidates. Your role will involve in-depth analysis of preclinical data, including in vitro and in vivo study results, to assess drug efficacy, safety, and mechanism of action.
You will collaborate closely with a multidisciplinary team of scientists, clinicians, and project managers, both internally and externally, to advance drug candidates through the development pipeline. This includes contributing to the preparation of regulatory documents, research publications, and patent applications. The ideal candidate will possess a deep understanding of cancer biology and the current landscape of oncology drug development. You will be expected to stay abreast of the latest scientific literature and technological advancements in the field. Strong problem-solving skills, critical thinking, and the ability to independently troubleshoot experimental challenges are essential. Experience in managing research projects, mentoring junior scientists, and working effectively in a remote, collaborative environment is highly valued.
Qualifications:
This is a critical role for advancing our client's mission to develop life-saving treatments for cancer patients worldwide.
You will collaborate closely with a multidisciplinary team of scientists, clinicians, and project managers, both internally and externally, to advance drug candidates through the development pipeline. This includes contributing to the preparation of regulatory documents, research publications, and patent applications. The ideal candidate will possess a deep understanding of cancer biology and the current landscape of oncology drug development. You will be expected to stay abreast of the latest scientific literature and technological advancements in the field. Strong problem-solving skills, critical thinking, and the ability to independently troubleshoot experimental challenges are essential. Experience in managing research projects, mentoring junior scientists, and working effectively in a remote, collaborative environment is highly valued.
Qualifications:
- Ph.D. in Molecular Biology, Cell Biology, Pharmacology, Cancer Biology, or a related field.
- Minimum of 5 years of postdoctoral or industry research experience in oncology drug discovery and development.
- Proven expertise in designing and executing preclinical studies relevant to cancer therapeutics.
- Strong knowledge of cancer biology, signaling pathways, and drug discovery methodologies.
- Experience with various molecular and cellular biology techniques (e.g., Western blotting, PCR, flow cytometry, cell-based assays).
- Demonstrated ability to analyze and interpret complex biological data and draw meaningful conclusions.
- Excellent scientific writing and presentation skills.
- Experience in managing research projects and mentoring junior staff.
- Proficiency in bioinformatics tools and databases is a plus.
- Ability to thrive in a fully remote, collaborative scientific setting.
This is a critical role for advancing our client's mission to develop life-saving treatments for cancer patients worldwide.
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7
Pharmaceutical Research Scientist
53000 Thuy Van
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Our client, a leading pharmaceutical company, is seeking a highly skilled and dedicated Pharmaceutical Research Scientist to join their innovative, fully remote research and development team. This role is critical for advancing drug discovery and development efforts. You will be responsible for designing and conducting complex experiments, analyzing data, and contributing to the formulation of new pharmaceutical products. Your expertise will be applied in areas such as molecular biology, pharmacology, or medicinal chemistry, depending on your specialization. You will be expected to stay abreast of the latest scientific advancements and research methodologies in the field.
The ideal candidate will possess a Ph.D. or Master's degree in Pharmacy, Chemistry, Biology, or a related life science discipline, with significant post-graduate research experience. Proven experience in laboratory techniques, experimental design, and data interpretation is essential. Strong analytical skills and the ability to troubleshoot complex scientific challenges are required. Excellent written and verbal communication skills are crucial for preparing research reports, presenting findings to scientific colleagues, and contributing to publications and patent applications. Proficiency in scientific literature databases and data analysis software is necessary. This fully remote position allows you to contribute your scientific acumen from your home laboratory or office. You will collaborate with a team of world-class scientists, contributing to the development of life-changing medications. This is an exceptional opportunity to make a profound impact on global health through cutting-edge pharmaceutical research.
The ideal candidate will possess a Ph.D. or Master's degree in Pharmacy, Chemistry, Biology, or a related life science discipline, with significant post-graduate research experience. Proven experience in laboratory techniques, experimental design, and data interpretation is essential. Strong analytical skills and the ability to troubleshoot complex scientific challenges are required. Excellent written and verbal communication skills are crucial for preparing research reports, presenting findings to scientific colleagues, and contributing to publications and patent applications. Proficiency in scientific literature databases and data analysis software is necessary. This fully remote position allows you to contribute your scientific acumen from your home laboratory or office. You will collaborate with a team of world-class scientists, contributing to the development of life-changing medications. This is an exceptional opportunity to make a profound impact on global health through cutting-edge pharmaceutical research.
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8
Pharmaceutical Research Scientist
450000 Nam Dinh , Nam Dinh
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Our client is looking for an innovative and dedicated Pharmaceutical Research Scientist to contribute to groundbreaking research and development in Nam Dinh, Nam Dinh, VN . This role is critical in advancing our understanding of therapeutic targets and developing novel drug candidates. You will be responsible for designing and executing experiments, analyzing complex data, and interpreting results to inform the drug discovery process. Key responsibilities include conducting literature reviews, developing new research methodologies, and collaborating with cross-functional teams of scientists and clinicians. You will also be involved in manuscript preparation, presenting findings at scientific conferences, and ensuring compliance with all relevant regulatory and safety guidelines. The ideal candidate will possess a Ph.D. or Master's degree in pharmacology, medicinal chemistry, biology, or a related life science discipline, with a strong publication record. Proven experience in preclinical drug development, including in vitro and in vivo study design and execution, is essential. Expertise in specific therapeutic areas and a deep understanding of molecular biology and pharmacology principles are highly valued. Excellent critical thinking, problem-solving, and written and verbal communication skills are required. This is a fully remote position, allowing you to contribute your scientific expertise from the convenience of your home office, collaborating with a world-class team dedicated to improving human health.
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