13 Clinical Development jobs in Vietnam
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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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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1
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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2
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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3
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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4
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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5
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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6
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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7
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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8
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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