51 Healthcare Project Management 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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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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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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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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3
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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Clinical Research Associate - Pharmaceutical Trials
06400 Hoi An
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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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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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Project Management Director
850000 An Thanh
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Our client, a prestigious organization within the oil and gas sector, is looking for a highly motivated and seasoned Project Management Director to lead critical initiatives in Vung Tau, Ba Ria–Vung Tau, VN . This is an on-site position demanding strong leadership and strategic planning capabilities. As the Project Management Director, you will be responsible for the overall success of multiple complex projects, from initiation through to closure. You will oversee project planning, resource allocation, budgeting, risk management, and stakeholder communication. Key duties include developing comprehensive project strategies, defining project scope and objectives, managing project timelines and deliverables, and ensuring projects are completed within scope, on time, and within budget. You will lead and mentor a team of project managers and coordinators, fostering a collaborative and high-performance work environment. The role requires building and maintaining strong relationships with internal departments, external vendors, and regulatory bodies. A proven track record of successfully managing large-scale projects in the energy industry is essential. The ideal candidate will possess a Bachelor's degree in a relevant field (e.g., Engineering, Business Administration), coupled with at least 10 years of progressive experience in project management, including significant leadership experience. PMP or equivalent certification is highly preferred. Exceptional organizational, negotiation, and decision-making skills are crucial. This is a challenging and rewarding opportunity to drive significant impact and growth for our client.
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7
Project Management Lead
550000 Hoa Sơn
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Our client is seeking a highly motivated and experienced Project Management Lead to spearhead key initiatives within their dynamic organization. This position is based in the vibrant coastal city of **Quy Nhon, Binh Dinh, VN**. As a Project Management Lead, you will be responsible for the planning, execution, and successful delivery of complex projects from inception to completion. This role requires a strategic thinker with exceptional leadership qualities and a proven ability to manage cross-functional teams and stakeholders effectively. You will oversee project timelines, budgets, and resources, ensuring that all project objectives are met with the highest standards of quality and efficiency.
Key responsibilities include developing detailed project plans, defining project scope, objectives, and deliverables, and managing project risks and issues proactively. You will establish and maintain strong working relationships with internal departments and external partners, facilitating clear and consistent communication throughout the project lifecycle. The Project Management Lead will also be responsible for monitoring project progress, reporting on key performance indicators, and making necessary adjustments to ensure project success. This includes managing change requests and ensuring adherence to project management methodologies and best practices. The role also involves mentoring junior project managers and team members, fostering a collaborative and high-performance work environment.
We are looking for candidates with a Bachelor's degree in a relevant field such as Business Administration, Engineering, or a related discipline. A Master's degree or PMP certification is a significant advantage. You should have a minimum of 7-10 years of progressive experience in project management, with a substantial portion of that experience leading significant projects. Proven experience in stakeholder management, risk assessment, and budget control is essential. Excellent communication, negotiation, and leadership skills are critical for success in this role. The ability to thrive in a fast-paced, results-driven environment and a commitment to delivering exceptional project outcomes are highly valued. Join a team that is shaping the future and make a tangible impact on our client's strategic goals.
Essential requirements include:
This is an outstanding opportunity to contribute to a forward-thinking company and advance your career in project leadership. We await your application.
Key responsibilities include developing detailed project plans, defining project scope, objectives, and deliverables, and managing project risks and issues proactively. You will establish and maintain strong working relationships with internal departments and external partners, facilitating clear and consistent communication throughout the project lifecycle. The Project Management Lead will also be responsible for monitoring project progress, reporting on key performance indicators, and making necessary adjustments to ensure project success. This includes managing change requests and ensuring adherence to project management methodologies and best practices. The role also involves mentoring junior project managers and team members, fostering a collaborative and high-performance work environment.
We are looking for candidates with a Bachelor's degree in a relevant field such as Business Administration, Engineering, or a related discipline. A Master's degree or PMP certification is a significant advantage. You should have a minimum of 7-10 years of progressive experience in project management, with a substantial portion of that experience leading significant projects. Proven experience in stakeholder management, risk assessment, and budget control is essential. Excellent communication, negotiation, and leadership skills are critical for success in this role. The ability to thrive in a fast-paced, results-driven environment and a commitment to delivering exceptional project outcomes are highly valued. Join a team that is shaping the future and make a tangible impact on our client's strategic goals.
Essential requirements include:
- Demonstrated success in managing multiple complex projects simultaneously.
- Expertise in project management software and tools.
- Strong understanding of various project management methodologies (e.g., Agile, Waterfall).
- Excellent problem-solving and decision-making capabilities.
- Ability to lead and motivate diverse teams.
- Exceptional organizational and time management skills.
This is an outstanding opportunity to contribute to a forward-thinking company and advance your career in project leadership. We await your application.
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8
Project Management Lead
25000 Phuong Son
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Our client is searching for an experienced and strategic Project Management Lead to spearhead critical projects in Thai Nguyen, Thai Nguyen, VN . This role demands a seasoned professional capable of guiding cross-functional teams, managing project lifecycles, and ensuring successful delivery on time and within budget. The ideal candidate will possess a strong understanding of project management methodologies (Agile, Waterfall), excellent leadership qualities, and exceptional communication and stakeholder management skills. You will be responsible for defining project scope, objectives, and deliverables, developing detailed project plans, and managing resources effectively. This position requires a proactive approach to risk management and problem-solving. You will work closely with various departments, including engineering, marketing, and operations, to ensure alignment and smooth execution. Our client values individuals who can inspire and motivate their teams, foster collaboration, and maintain a clear focus on project success. Experience in managing large-scale, complex projects is essential. The ability to adapt to changing priorities and stakeholder needs is crucial. We offer a dynamic work environment with opportunities for professional growth and impact. You will be instrumental in driving innovation and achieving strategic business objectives through effective project execution. Strong analytical skills and the ability to translate business requirements into actionable project plans are a must. The successful candidate will be a results-oriented leader committed to delivering excellence. This is an excellent opportunity for a motivated project manager to take on a leadership role and contribute significantly to our client's success.
Responsibilities:
Qualifications:
Responsibilities:
- Lead and manage multiple projects from initiation through to completion.
- Define project scope, goals, and deliverables in collaboration with stakeholders.
- Develop comprehensive project plans, timelines, and resource allocation.
- Manage project budgets and ensure financial objectives are met.
- Coordinate and lead project team meetings, ensuring clear communication.
- Identify, assess, and manage project risks and issues.
- Monitor project progress and performance, implementing corrective actions as needed.
- Communicate project status and updates to all relevant stakeholders.
- Ensure the quality of project deliverables.
- Foster a collaborative and high-performing project team environment.
Qualifications:
- Minimum 6 years of experience in project management, with at least 2 years in a leadership role.
- Proven experience in managing projects from start to finish, with successful delivery records.
- Strong knowledge of project management methodologies (e.g., PMP, Agile, Scrum).
- Excellent leadership, communication, and interpersonal skills.
- Proficiency in project management software (e.g., MS Project, Jira, Asana).
- Ability to manage multiple projects simultaneously and prioritize effectively.
- Strong risk management and problem-solving capabilities.
- Bachelor's degree in Business Administration, Engineering, or a related field.
- Experience in the relevant industry sector is a plus.
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