13 Scientific Advisor jobs in Vietnam
Remote Plant Pathologist - Research and Development
10000 An Cu, An Giang
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Our client is a cutting-edge agricultural biotechnology company seeking a highly qualified Plant Pathologist to lead their remote research and development efforts. This is a fully remote position that will allow you to contribute to vital projects aimed at enhancing crop health and disease resistance. You will be responsible for identifying, diagnosing, and developing innovative solutions for plant diseases affecting major crops. This role demands a strong scientific background, exceptional research skills, and the ability to collaborate effectively in a virtual environment.
Key Responsibilities:
Qualifications:
This is an unparalleled opportunity to contribute to global food security and sustainable agriculture through pioneering research in plant pathology.
Key Responsibilities:
- Conduct comprehensive research on plant diseases, their causal agents (fungi, bacteria, viruses, nematodes), and their epidemiology.
- Develop and implement molecular and morphological diagnostic techniques for accurate disease identification.
- Design and manage controlled experiments to evaluate the efficacy of novel disease control strategies, including biological, chemical, and genetic approaches.
- Analyze plant health data using advanced statistical methods and bioinformatics tools.
- Collaborate with plant breeders, geneticists, and agronomists to identify and introgress disease resistance genes into crop germplasm.
- Stay updated on emerging plant diseases and threats to agriculture worldwide.
- Publish research findings in peer-reviewed scientific journals and present at international conferences.
- Contribute to the patenting process for new disease management technologies.
- Provide technical guidance and support to regional field teams and external partners.
- Develop protocols for disease screening and management in diverse agricultural settings.
- Ensure research activities align with company objectives and regulatory requirements.
- Mentor junior researchers and contribute to a collaborative R&D culture.
Qualifications:
- Ph.D. in Plant Pathology, Botany, or a closely related field with a specialization in plant diseases.
- A minimum of 6 years of post-doctoral research experience in plant pathology or a related field.
- Demonstrated expertise in fungal, bacterial, and viral plant pathogens and their management.
- Proficiency in molecular biology techniques relevant to plant pathology (e.g., PCR, qPCR, sequencing, pathogen genomics).
- Strong statistical analysis skills and experience with relevant software (e.g., R, SPSS).
- Experience with bioinformatic tools for pathogen analysis is a significant advantage.
- Proven track record of scientific publications and presentations.
- Excellent analytical, critical thinking, and problem-solving abilities.
- Exceptional written and verbal communication skills for effective collaboration and dissemination of research findings.
- Ability to work independently, manage multiple research projects, and meet deadlines in a remote setting.
This is an unparalleled opportunity to contribute to global food security and sustainable agriculture through pioneering research in plant pathology.
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Research Scientist - Pharmaceutical Development
77000 Hoa Sơn
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Our client is a leading innovator in scientific research and development, seeking a highly qualified and dedicated Research Scientist to join their fully remote R&D team. This role is integral to the discovery and advancement of novel pharmaceutical compounds and therapeutic strategies. You will be involved in designing and conducting experiments, analyzing complex biological data, interpreting results, and contributing to the publication of findings. This is a fully remote position, requiring advanced research skills and the ability to collaborate effectively with a dispersed team of scientists and researchers through virtual platforms. The ideal candidate will possess a Ph.D. or Master's degree in a relevant scientific discipline, a strong background in molecular biology, pharmacology, or a related field, and a proven track record of impactful research. You should be adept at experimental design, data analysis using statistical software, and scientific writing. A passion for scientific discovery and a commitment to rigorous research methodologies are essential.
Responsibilities:
Responsibilities:
- Design, execute, and optimize in vitro and in vivo experiments to evaluate therapeutic candidates.
- Analyze and interpret complex biological and chemical data using statistical methods and specialized software.
- Develop and validate new assays and experimental protocols.
- Maintain meticulous records of experimental procedures, results, and observations.
- Contribute to the writing of research reports, manuscripts for publication, and patent applications.
- Collaborate with cross-functional teams, including medicinal chemists, biologists, and pharmacologists.
- Stay current with the latest scientific literature and advancements in relevant fields.
- Present research findings at internal meetings and external scientific conferences (virtually).
- Troubleshoot experimental challenges and propose innovative solutions.
- Ensure compliance with all relevant laboratory safety and ethical guidelines.
- Ph.D. or Master's degree in Biology, Chemistry, Pharmacology, Biotechnology, or a related field.
- Minimum of 3-5 years of post-graduate research experience.
- Proven expertise in experimental design and data analysis.
- Proficiency with relevant laboratory techniques and scientific instrumentation.
- Strong understanding of drug discovery and development processes.
- Experience with scientific software (e.g., GraphPad Prism, R, Python for data analysis) is highly desirable.
- Excellent scientific writing and presentation skills.
- Strong problem-solving and critical thinking abilities.
- Ability to work independently and manage research projects in a remote environment.
- Effective communication and collaboration skills within a virtual team.
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1
Research Scientist, Pharmaceutical Development
61000 Hoi An
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Our client is actively recruiting for a dedicated and innovative Research Scientist to join their pharmaceutical development team on a fully remote basis. This role focuses on discovery and early-stage research, contributing to the development of novel therapeutic agents. The ideal candidate will possess a strong background in pharmaceutical sciences, excellent laboratory skills (even if managing remote lab work), and a proven ability to conduct independent research.
Responsibilities:
Responsibilities:
- Design and conduct experiments to identify and validate new drug targets and therapeutic compounds.
- Develop and optimize assays for screening and characterization of potential drug candidates.
- Analyze experimental data, interpret results, and draw meaningful conclusions.
- Prepare comprehensive reports, scientific presentations, and contribute to research publications.
- Collaborate with chemists, biologists, and other scientists to advance drug discovery projects.
- Stay updated on the latest scientific literature and technological advancements in the pharmaceutical industry.
- Manage and maintain laboratory equipment and consumables, ensuring a well-equipped research environment.
- Contribute to the development of intellectual property and patent applications.
- Work effectively in a virtual team environment, communicating research progress and challenges.
- Adhere to all safety protocols and ethical guidelines in research conduct.
- Ph.D. or Master's degree in Pharmacology, Biochemistry, Molecular Biology, Chemistry, or a related life science discipline.
- Minimum of 3-5 years of relevant post-doctoral or industry research experience.
- Proven experience in drug discovery, assay development, or preclinical research.
- Strong understanding of molecular biology techniques, cell culture, and various analytical methods.
- Excellent data analysis and interpretation skills, with proficiency in relevant software.
- Demonstrated ability to work independently, manage multiple projects, and meet deadlines in a remote setting.
- Exceptional written and verbal communication skills in English.
- Experience with high-throughput screening (HTS) methodologies is a plus.
- Knowledge of regulatory requirements for drug development is advantageous.
- A passion for scientific innovation and a commitment to improving patient health.
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2
Pharmaceutical Research Scientist - Formulation Development
630000 Hoi An
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Our client, a prominent pharmaceutical company, is seeking a dedicated Pharmaceutical Research Scientist to join their Formulation Development team. This role is based at their facility in **Buon Ma Thuot, Dak Lak, VN**. You will be responsible for developing and optimizing pharmaceutical formulations for various dosage forms, ensuring product stability, efficacy, and bioavailability. Your primary duties will include conducting pre-formulation studies, selecting appropriate excipients, designing experimental protocols for formulation development, and performing characterization of drug products. You will work closely with analytical chemists and process engineers to ensure smooth technology transfer from lab to manufacturing. The ideal candidate will have a strong understanding of pharmaceutics, drug delivery systems, and solid dosage form development. Experience with techniques such as granulation, tablet compression, capsule filling, and coating is highly desirable. Proficiency in relevant laboratory equipment and analytical techniques is essential. You should possess excellent scientific thinking, problem-solving abilities, and meticulous attention to detail. Strong communication and interpersonal skills are crucial for effective collaboration within the R&D department and with cross-functional teams. This position requires a Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related field, with hands-on experience in formulation development. We are looking for a proactive, results-oriented individual committed to advancing pharmaceutical innovation.
Responsibilities:
Responsibilities:
- Develop and optimize pharmaceutical formulations.
- Conduct pre-formulation studies and excipient compatibility testing.
- Design and execute experimental plans for dosage form development.
- Characterize drug products using various analytical techniques.
- Troubleshoot formulation and process-related issues.
- Collaborate with analytical and process development teams.
- Ensure compliance with regulatory guidelines (e.g., GMP).
- Document research findings and prepare reports.
- Support technology transfer activities.
- Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related field.
- 3+ years of experience in pharmaceutical formulation development.
- Knowledge of pharmaceutics and drug delivery systems.
- Experience with solid dosage forms (tablets, capsules).
- Familiarity with laboratory equipment and analytical methods.
- Strong problem-solving and analytical skills.
- Excellent written and verbal communication abilities.
- Ability to work effectively in a laboratory environment.
- Understanding of GMP principles.
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3
Senior Research Scientist - Pharmaceutical Development
55000 Hoa Sơn
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Our client, a leading pharmaceutical company at the forefront of medical innovation, is seeking a highly skilled Senior Research Scientist to join their completely remote research and development team. This role is critical in driving the discovery and development of novel pharmaceutical compounds and therapies. As a Senior Research Scientist, you will lead research projects, design and execute complex experiments, analyze data, and contribute to the advancement of drug candidates from early-stage research through preclinical development. You will collaborate closely with cross-functional teams, including medicinal chemists, pharmacologists, and toxicologists, to achieve research milestones. This position demands a deep understanding of pharmaceutical sciences, excellent laboratory and analytical skills, and a passion for advancing healthcare.
Key Responsibilities:
Key Responsibilities:
- Design and conduct sophisticated in vitro and in vivo experiments to evaluate drug efficacy and safety.
- Develop and optimize assays for target identification and validation.
- Analyze experimental data using statistical methods and interpret results to guide research direction.
- Contribute to the formulation development and characterization of drug candidates.
- Stay abreast of the latest scientific literature, technological advancements, and industry trends in pharmaceutical research.
- Lead specific research projects, manage timelines, and troubleshoot experimental challenges.
- Collaborate effectively with internal and external research partners.
- Prepare research reports, scientific presentations, and contribute to patent applications and regulatory filings.
- Mentor junior scientists and contribute to a collaborative research environment.
- Ensure compliance with all relevant safety, ethical, and regulatory guidelines.
- Ph.D. in Pharmacology, Pharmaceutical Sciences, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 5 years of post-doctoral or industry research experience in drug discovery and development.
- Proven track record of leading research projects and delivering impactful scientific results.
- Extensive experience with various biochemical, cellular, and molecular biology techniques.
- Proficiency in data analysis software and statistical tools.
- Strong understanding of drug discovery processes, pharmacokinetics, and pharmacodynamics.
- Excellent scientific writing and presentation skills.
- Demonstrated ability to work independently and collaboratively in a remote research setting.
- Strong problem-solving skills and a creative approach to scientific challenges.
- A genuine passion for scientific discovery and improving patient outcomes.
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4
Clinical Research Associate - Pharmaceutical Development
47000 Nam Dinh , Nam Dinh
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Our client is seeking a highly skilled and motivated Clinical Research Associate (CRA) to join their pharmaceutical development team. This fully remote position offers the exciting opportunity to contribute to the advancement of novel therapies by monitoring clinical trials. As a CRA, you will play a crucial role in ensuring the quality, integrity, and compliance of clinical research conducted in accordance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. Your primary responsibilities will include site selection and initiation, regular monitoring of clinical trial sites (virtually or through remote data review where applicable), and ensuring accurate and timely data collection. You will conduct source data verification (SDV), review case report forms (CRFs), and verify the safety and rights of study participants. You will also be responsible for training site personnel on study protocols and procedures, troubleshooting issues that arise at clinical sites, and ensuring proper drug accountability and management. Effective communication and relationship-building with investigators, study coordinators, and internal project teams are essential for success. You will prepare monitoring reports, follow-up on action items, and contribute to the overall management of clinical trial timelines and deliverables. This role requires a strong understanding of clinical trial processes, pharmaceutical regulations, and medical terminology. The ideal candidate will possess excellent analytical and problem-solving skills, a keen eye for detail, and the ability to manage multiple tasks and priorities in a remote environment. A background in life sciences, healthcare, or a related field, coupled with direct experience as a CRA or in a similar clinical research role, is essential. You will need to be proficient with clinical trial management systems (CTMS) and electronic data capture (EDC) systems. This is a fantastic opportunity to make a tangible difference in patient health by contributing to the development of life-saving medications.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Monitor clinical trial sites for protocol adherence and data accuracy.
- Ensure compliance with GCP, ICH guidelines, and regulatory requirements.
- Conduct source data verification (SDV) and review case report forms (CRFs).
- Train and support site personnel on study conduct.
- Oversee drug accountability and investigational product management.
- Identify, track, and resolve site issues and deviations.
- Prepare monitoring visit reports and follow-up on action items.
- Ensure the safety and rights of study participants.
- Liaise between clinical sites and internal project teams.
- Manage multiple clinical trial sites effectively in a remote setting.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum 3 years of experience as a Clinical Research Associate (CRA).
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with CTMS and EDC systems.
- Excellent understanding of clinical trial processes and documentation.
- Strong analytical, problem-solving, and organizational skills.
- Proficiency in medical terminology.
- Excellent written and verbal communication skills.
- Ability to travel occasionally for site visits if required, though the role is primarily remote.
- Demonstrated ability to work independently and manage time effectively remotely.
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5
Clinical Research Associate - Pharmaceutical Development
10000 An Cu, An Giang
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Our client, a globally recognized pharmaceutical company, is actively seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join our esteemed team in **Hanoi, Hanoi, VN**. This vital role involves the monitoring and management of clinical trials to ensure data integrity, patient safety, and compliance with regulatory standards (GCP, ICH). You will be responsible for site selection, initiation, routine monitoring, and close-out of clinical trial sites, working closely with investigators and site staff to ensure adherence to protocols.
Key responsibilities include verifying the accuracy and completeness of clinical data, ensuring that all study-related procedures are conducted according to the approved protocol, and maintaining essential regulatory documents. You will conduct site visits, both pre-study, initiation, and close-out, as well as periodic 'in-house' or 'at-home' visits. The CRA will also be responsible for identifying and reporting adverse events, managing study supplies, and resolving any issues that arise during the trial. Effective communication with study sponsors, site personnel, and internal teams is crucial for the successful execution of clinical research studies.
The ideal candidate will possess a strong understanding of clinical trial processes, regulatory requirements, and medical terminology. Proven experience as a CRA or in a similar clinical research role is essential. Excellent organizational skills, meticulous attention to detail, and strong analytical abilities are required. You must possess excellent written and verbal communication skills, proficiency in English, and the ability to travel frequently to assigned clinical sites. A Bachelor's degree in a life science, nursing, or a related scientific field is required. Advanced degrees or relevant certifications are a plus. This is an excellent opportunity to contribute to the development of life-saving therapies within a supportive and dynamic research environment.
Key responsibilities include verifying the accuracy and completeness of clinical data, ensuring that all study-related procedures are conducted according to the approved protocol, and maintaining essential regulatory documents. You will conduct site visits, both pre-study, initiation, and close-out, as well as periodic 'in-house' or 'at-home' visits. The CRA will also be responsible for identifying and reporting adverse events, managing study supplies, and resolving any issues that arise during the trial. Effective communication with study sponsors, site personnel, and internal teams is crucial for the successful execution of clinical research studies.
The ideal candidate will possess a strong understanding of clinical trial processes, regulatory requirements, and medical terminology. Proven experience as a CRA or in a similar clinical research role is essential. Excellent organizational skills, meticulous attention to detail, and strong analytical abilities are required. You must possess excellent written and verbal communication skills, proficiency in English, and the ability to travel frequently to assigned clinical sites. A Bachelor's degree in a life science, nursing, or a related scientific field is required. Advanced degrees or relevant certifications are a plus. This is an excellent opportunity to contribute to the development of life-saving therapies within a supportive and dynamic research environment.
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Clinical Research Associate - Pharmaceutical Development
51000 Thuy Van
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Our client, a leader in the pharmaceutical industry, is seeking a meticulous and dedicated Clinical Research Associate (CRA) for their operations in **Hue, Thua Thien–Hue, VN**. This role requires on-site presence to ensure the highest standards of clinical trial conduct. As a CRA, you will be responsible for monitoring clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and regulatory requirements. You will play a vital role in bringing new and innovative pharmaceutical treatments to market. The ideal candidate will have a strong understanding of clinical trial processes, GCP (Good Clinical Practice) guidelines, and a passion for contributing to medical advancements. Responsibilities include: monitoring clinical trial sites to ensure compliance with protocols and regulations; verifying the accuracy and completeness of source data and patient records; managing investigational product accountability; serving as the primary liaison between the study sites and the sponsor; identifying and reporting adverse events and serious adverse events; ensuring timely completion of study-related activities; providing training and support to study site personnel; assisting with regulatory submissions and audits. 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 clinical research role; thorough understanding of ICH-GCP guidelines and other relevant regulatory requirements; strong medical knowledge and understanding of clinical trial methodology; excellent communication, interpersonal, and organizational skills; ability to travel to clinical trial sites as needed. This is a challenging yet rewarding opportunity to contribute to critical pharmaceutical research and development efforts within our client's organization.
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7
Clinical Research Associate - Pharmaceutical Development
53000 Thuy Van
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Our client, a leading pharmaceutical company committed to advancing healthcare solutions, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their dynamic team in Hue, Thua Thien–Hue, VN . This role is instrumental in managing and overseeing clinical trials, ensuring compliance with protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. You will be responsible for monitoring study sites, ensuring data accuracy and integrity, and safeguarding the rights and well-being of study participants.
Key responsibilities include selecting, training, and managing investigators and study staff at clinical trial sites. You will conduct site initiation visits, routine monitoring visits, and close-out visits, ensuring all regulatory and protocol requirements are met. The CRA will review case report forms (CRFs), source documents, and other trial-related records to verify data accuracy and completeness. You will also be responsible for managing study supplies, ensuring proper storage and accountability of investigational products. Furthermore, you will liaise with study participants, investigators, and internal teams to address any issues or queries that arise during the trial. The role also involves preparing and maintaining essential trial documentation and contributing to the preparation of study reports.
The ideal candidate will possess a Bachelor's degree in a life science, pharmacy, or related field, with a minimum of 3-5 years of experience as a CRA in the pharmaceutical or biotechnology industry. A strong understanding of ICH-GCP guidelines and regulatory affairs is essential. Excellent monitoring skills, attention to detail, and the ability to manage multiple priorities in a fast-paced environment are required. Strong written and verbal communication skills, along with proficiency in clinical trial management software and data entry systems, are necessary. The ability to travel to clinical sites (estimated 50-70%) is required. This is a significant opportunity for a dedicated clinical research professional to contribute to life-saving drug development within a reputable pharmaceutical organization based in Hue, Thua Thien–Hue, VN .
Key responsibilities include selecting, training, and managing investigators and study staff at clinical trial sites. You will conduct site initiation visits, routine monitoring visits, and close-out visits, ensuring all regulatory and protocol requirements are met. The CRA will review case report forms (CRFs), source documents, and other trial-related records to verify data accuracy and completeness. You will also be responsible for managing study supplies, ensuring proper storage and accountability of investigational products. Furthermore, you will liaise with study participants, investigators, and internal teams to address any issues or queries that arise during the trial. The role also involves preparing and maintaining essential trial documentation and contributing to the preparation of study reports.
The ideal candidate will possess a Bachelor's degree in a life science, pharmacy, or related field, with a minimum of 3-5 years of experience as a CRA in the pharmaceutical or biotechnology industry. A strong understanding of ICH-GCP guidelines and regulatory affairs is essential. Excellent monitoring skills, attention to detail, and the ability to manage multiple priorities in a fast-paced environment are required. Strong written and verbal communication skills, along with proficiency in clinical trial management software and data entry systems, are necessary. The ability to travel to clinical sites (estimated 50-70%) is required. This is a significant opportunity for a dedicated clinical research professional to contribute to life-saving drug development within a reputable pharmaceutical organization based in Hue, Thua Thien–Hue, VN .
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8
Clinical Research Associate - Pharmaceutical Development (Remote)
500000 An Thanh
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Our client, a leading pharmaceutical company dedicated to advancing healthcare, is looking for a meticulous and proactive Clinical Research Associate (CRA) to join their remote global clinical operations team. This critical role supports the planning, execution, and monitoring of clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The remote CRA will be responsible for site selection and initiation, monitoring trial progress at investigational sites, ensuring data accuracy and integrity, and managing regulatory documentation. You will serve as the primary point of contact for clinical investigators and site staff, providing training on study procedures and addressing any queries or issues that arise. Key responsibilities include conducting source data verification, reviewing case report forms (CRFs), and ensuring all trial-related activities are documented comprehensively. The ideal candidate will have a strong background in life sciences, a Bachelor's or Master's degree in a relevant field such as Pharmacy, Biology, or Medicine, and several years of experience as a CRA or in a similar clinical trial management role. Excellent understanding of ICH-GCP guidelines and regulatory affairs is mandatory. Superior organizational, analytical, and communication skills are essential for success in this remote position, which offers the flexibility to contribute significantly to life-saving drug development from anywhere.
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