129 Icon Plc jobs in Vietnam
Senior Research Scientist - Oncology Drug Development
200000 Phuong Son
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
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.
This advertiser has chosen not to accept applicants from your region.
0
Clinical Research Associate
70000 Can Tho , Can Tho
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a diligent and experienced Clinical Research Associate (CRA) to support their ongoing clinical trials. This is a field-based role requiring significant travel to clinical sites. You will be responsible for monitoring the progress of clinical studies at investigational sites, ensuring that they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
Key responsibilities include site selection and initiation, conducting routine monitoring visits, performing source data verification, and ensuring the accuracy and completeness of clinical trial documentation. You will serve as the primary liaison between the sponsor and the investigative sites, addressing any questions or issues that arise during the trial. The CRA will also be responsible for training site personnel on study procedures and regulatory requirements, and ensuring the safety of study participants.
We are looking for a candidate with a Bachelor's degree in a life science or healthcare-related field. A minimum of 3 years of experience as a CRA is required, with a strong understanding of ICH-GCP guidelines and regulatory requirements. Excellent organizational, communication, and interpersonal skills are essential. The ability to manage multiple sites and priorities effectively, along with strong analytical and problem-solving skills, is crucial. Proficiency in clinical trial management software and electronic data capture (EDC) systems is necessary. This role requires a dedicated professional committed to the highest standards of clinical research ethics and execution.
Key responsibilities include site selection and initiation, conducting routine monitoring visits, performing source data verification, and ensuring the accuracy and completeness of clinical trial documentation. You will serve as the primary liaison between the sponsor and the investigative sites, addressing any questions or issues that arise during the trial. The CRA will also be responsible for training site personnel on study procedures and regulatory requirements, and ensuring the safety of study participants.
We are looking for a candidate with a Bachelor's degree in a life science or healthcare-related field. A minimum of 3 years of experience as a CRA is required, with a strong understanding of ICH-GCP guidelines and regulatory requirements. Excellent organizational, communication, and interpersonal skills are essential. The ability to manage multiple sites and priorities effectively, along with strong analytical and problem-solving skills, is crucial. Proficiency in clinical trial management software and electronic data capture (EDC) systems is necessary. This role requires a dedicated professional committed to the highest standards of clinical research ethics and execution.
This advertiser has chosen not to accept applicants from your region.
1
Clinical Research Associate
57000 An Thanh
WhatJobs
Posted today
Job Viewed
Job Description
Our client is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their dedicated pharmaceutical team. This vital role involves monitoring clinical trials to ensure data integrity, adherence to protocols, and compliance with regulatory standards. You will be responsible for site selection, initiation, monitoring, and closing visits, as well as ensuring that study conduct is in accordance with Good Clinical Practice (GCP) guidelines and applicable regulations. The ideal candidate possesses a strong scientific background, excellent organizational skills, and a keen eye for detail. You will liaise with investigators, site staff, and internal project teams to facilitate the smooth running of clinical trials. This position requires travel to clinical trial sites for monitoring and verification purposes. Your responsibilities will include reviewing essential documents, tracking study progress, reporting adverse events, and ensuring accurate record-keeping. You will play a key role in the successful execution of clinical research, contributing to the development of life-saving therapies. A thorough understanding of the drug development process and clinical trial management is essential for success in this demanding yet rewarding position.
Key Responsibilities:
Qualifications:
This position offers a significant opportunity to contribute to groundbreaking pharmaceutical research and development.
Key Responsibilities:
- Conduct site visits (selection, initiation, monitoring, close-out) according to study requirements.
- Verify the accuracy, completeness, and validity of clinical trial data.
- Ensure compliance with study protocols, SOPs, and regulatory guidelines (e.g., GCP, ICH).
- Train and support site staff on study-related procedures.
- Monitor study drug accountability and dispensing.
- Review source documents and case report forms (CRFs).
- Report and track adverse events and serious adverse events (SAEs).
- Communicate effectively with investigators, site staff, and internal project teams.
- Prepare monitoring visit reports and follow-up actions.
- Contribute to the development of study-related documents.
Qualifications:
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial management role.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Strong understanding of the clinical trial process and pharmaceutical industry.
- Excellent clinical monitoring skills and attention to detail.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong written and verbal communication skills.
- Ability to travel frequently to clinical trial sites.
- Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
This position offers a significant opportunity to contribute to groundbreaking pharmaceutical research and development.
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Associate
950000 Long Xuyen, An Giang
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is looking for a dedicated Clinical Research Associate (CRA) to join their remote team. This position is fully remote, allowing you to contribute from anywhere. You will be responsible for monitoring clinical trials, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your duties will include site initiation visits, routine monitoring visits, close-out visits, and reviewing essential documents. You will also be tasked with tracking patient recruitment, data collection, and resolving data queries. Strong communication and interpersonal skills are vital for building and maintaining positive relationships with investigators, study coordinators, and internal teams. The ideal candidate will have a Bachelor's degree in a life science, nursing, or a related field, coupled with at least 3 years of experience as a CRA or in a similar clinical trial role. A thorough understanding of ICH-GCP and applicable regulatory guidelines is mandatory. Experience with various therapeutic areas is a plus. The ability to manage multiple projects simultaneously, maintain meticulous records, and adapt to changing project needs is crucial. This is an excellent opportunity to advance your career in pharmaceutical research while enjoying the benefits of a remote work environment. Apply today to make a difference in bringing life-saving therapies to patients.
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Associate
600000 Hoi An
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
We are seeking a meticulous and dedicated Clinical Research Associate to join our pharmaceutical research and development team. You will be responsible for overseeing clinical trials, ensuring adherence to protocols, regulatory guidelines, and Good Clinical Practice (GCP) standards. Your duties will include site initiation, monitoring, and close-out visits, ensuring accurate data collection and reporting, and maintaining effective communication with investigators, study coordinators, and regulatory authorities. This role requires a strong understanding of pharmaceutical research, clinical trial management, and regulatory compliance. The ideal candidate will possess excellent organizational skills, attention to detail, and the ability to manage multiple projects simultaneously. You will conduct source data verification, review case report forms, and ensure the safety and well-being of study participants. Experience in managing clinical trial timelines, budgets, and resources is essential. You will also be involved in selecting and qualifying study sites and providing training to site staff. This position offers a challenging and rewarding opportunity to contribute to the development of life-saving medications. We are committed to advancing healthcare through innovative pharmaceutical research. Your role will be critical in ensuring the integrity and validity of clinical trial data, which is fundamental to bringing new therapies to patients. Collaboration with internal teams, including medical affairs, regulatory affairs, and biostatistics, will be a key aspect of your work. You will actively participate in trial team meetings and contribute to the development of study-related documents. Join us and be part of a team dedicated to improving patient outcomes and making a difference in global health. Location: Buon Ma Thuot, Dak Lak, VN
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate
24000 Phuong Son
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a leader in the pharmaceutical sector, is looking for a dedicated and experienced Clinical Research Associate (CRA) to join our fully remote team. This role is crucial in ensuring the quality and integrity of clinical trials, from initiation to close-out. You will be responsible for monitoring clinical trial sites, verifying data accuracy, ensuring compliance with protocols and regulatory guidelines, and managing patient recruitment and retention efforts. Key responsibilities include conducting site visits, training site staff, resolving data discrepancies, and preparing regulatory submissions. The ideal candidate will have a strong background in clinical research, a deep understanding of Good Clinical Practice (GCP) guidelines, and prior experience as a CRA or in a similar role within the pharmaceutical or biotechnology industry. Excellent organizational, communication, and interpersonal skills are essential. You must be proficient in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems. This remote position requires a high degree of self-motivation, the ability to travel occasionally as needed for site visits, and a commitment to maintaining the highest standards of ethical conduct and scientific rigor. If you are passionate about advancing medical treatments and thrive in a remote, dynamic work environment, we invite you to apply.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate
530000 Thuy Van
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client is seeking a meticulous and organized Clinical Research Associate (CRA) to join their team in Hue, Thua Thien–Hue, VN . This role is integral to the successful execution of clinical trials, ensuring adherence to protocols, regulations, and ethical standards. The CRA will be responsible for site selection, initiation, monitoring, and close-out activities, as well as ensuring the quality and integrity of data collected. You will build and maintain strong relationships with investigative sites, providing training and support to study personnel. The ideal candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements. This position demands excellent communication, interpersonal, and organizational skills, with a keen eye for detail. You will be involved in reviewing case report forms (CRFs), source documents, and query resolution, ensuring data accuracy and completeness. The CRA plays a vital role in patient safety and data integrity throughout the trial lifecycle. Responsibilities include:
Qualifications:
- Conducting site visits for qualification, initiation, routine monitoring, and close-out.
- Ensuring compliance with study protocols, GCP, and regulatory requirements.
- Monitoring subject recruitment and retention at clinical sites.
- Reviewing and verifying clinical trial data, CRFs, and source documents.
- Resolving data discrepancies and ensuring timely query resolution.
- Managing essential trial documents and maintaining site files.
- Providing training and ongoing support to site staff.
- Reporting on site status, risks, and issues to project management.
- Ensuring adherence to safety reporting requirements.
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 knowledge of GCP guidelines and clinical trial processes.
- Experience with electronic data capture (EDC) systems.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills.
- Ability to travel to clinical sites as required.
This advertiser has chosen not to accept applicants from your region.
Be The First To Know
About the latest Icon plc Jobs in Vietnam !
6
Clinical Research Associate
18000 Haiphong , Haiphong
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client seeks a meticulous and dedicated Clinical Research Associate (CRA) to join their global, fully remote research operations. This critical role involves overseeing the planning, implementation, and execution of clinical trials in accordance with Good Clinical Practice (GCP) guidelines and regulatory requirements. The successful candidate will be responsible for site selection, initiation, monitoring, and close-out visits to ensure data integrity, patient safety, and protocol adherence. You will act as the primary point of contact for clinical sites, providing essential training and support to investigators and site staff. Key responsibilities include reviewing and verifying source documents, ensuring accurate and timely entry of clinical data into databases, and managing trial-related documentation. This position requires a strong understanding of clinical trial processes, therapeutic areas, and relevant regulatory frameworks. Excellent communication, interpersonal, and organizational skills are paramount, especially in a remote capacity. You must be adept at building rapport with site personnel and stakeholders, even without in-person interaction. The ability to manage multiple sites and projects concurrently, coupled with a keen eye for detail and a commitment to quality, is essential. As a fully remote role, you will have the flexibility to manage your workload and travel to sites as needed from your home base in **Haiphong, Hai Phong, VN**, or anywhere else that supports your productive work. Our client is committed to advancing healthcare through rigorous and ethical clinical research, and this role is integral to that mission. We offer a supportive remote work environment, opportunities for professional development, and the chance to contribute to life-changing medical advancements.
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Associate
59000 Nha Trang, Khanh Hoa
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their team in **Nha Trang, Khanh Hoa, VN**. This role offers a hybrid work arrangement, balancing remote flexibility with essential on-site responsibilities. As a CRA, you will play a critical role in ensuring the quality, integrity, and timeliness of clinical trials. You will be responsible for monitoring clinical trial sites to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. This includes conducting site initiation visits, routine monitoring visits, and close-out visits. Key duties involve verifying data accuracy, ensuring proper source document verification, managing essential trial documents, and facilitating communication between study sites, investigators, and the study team. You will also be involved in training site staff on study protocols and procedures, identifying and resolving site-specific issues, and ensuring the safety of study participants. The ideal candidate will possess a strong understanding of clinical trial processes, excellent attention to detail, and superior organizational skills. A background in life sciences or a related healthcare field is essential. You must be adept at interpreting complex data and communicating effectively with diverse stakeholders, including healthcare professionals and regulatory bodies. This position requires a proactive approach to problem-solving and a commitment to maintaining the highest standards of research ethics and data integrity. The ability to travel to designated clinical trial sites as needed is a requirement for this hybrid role. We are looking for an individual who is passionate about advancing medical research and contributing to the development of innovative therapies. This is an excellent opportunity to grow your career within the pharmaceutical industry in a supportive and collaborative environment.
Responsibilities:
Responsibilities:
- Conduct pre-study, initiation, routine monitoring, and close-out visits at clinical trial sites.
- Ensure compliance with study protocols, standard operating procedures (SOPs), and regulatory guidelines (e.g., GCP).
- Verify the accuracy, completeness, and consistency of clinical data by reviewing source documents.
- Manage and maintain essential study documents at trial sites and within the company's systems.
- Provide training and ongoing support to clinical site staff.
- Identify, track, and ensure resolution of study-related issues and deviations.
- Facilitate communication between the sponsor, investigators, and study personnel.
- Ensure the timely submission of study-related documents and data.
- Monitor subject safety and reporting of adverse events.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Previous experience as a Clinical Research Associate or in a similar clinical trial role.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Strong understanding of clinical trial processes and methodologies.
- Excellent analytical, organizational, and problem-solving skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Effective written and verbal communication skills.
- Ability to travel to clinical trial sites as required.
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Associate
59000 Phan Thiet, Binh Thuan
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical research organization, is seeking a diligent and organized Clinical Research Associate (CRA) to contribute to groundbreaking medical studies. This hybrid role requires a balance of remote work and on-site presence at our facilities in Phan Thiet, Binh Thuan, Vietnam. As a CRA, you will play a vital role in ensuring the quality and integrity of clinical trials by monitoring study sites, verifying data accuracy, and ensuring compliance with protocols and regulatory requirements. Your responsibilities will span the entire trial lifecycle, from site initiation to close-out.
Key responsibilities will include:
Key responsibilities will include:
- Performing site visits (initiation, monitoring, and close-out) according to protocol and regulatory guidelines.
- Ensuring that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and regulatory requirements (e.g., ICH-GCP, local regulations).
- Verifying the accuracy, completeness, and consistency of clinical data by reviewing source documents and case report forms (CRFs).
- Identifying and reporting deviations from protocol or regulatory requirements, and ensuring that corrective and preventive actions (CAPAs) are implemented.
- Managing communication with investigators and site staff to address queries and ensure the smooth running of the trial.
- Maintaining essential trial documents and ensuring regulatory compliance at all study sites.
- Recruiting, training, and providing ongoing support to study coordinators and site personnel.
- Preparing monitoring visit reports and ensuring timely distribution.
- Escalating any issues or concerns related to study conduct or data integrity to the appropriate management level.
- Participating in study team meetings and contributing to the overall success of the clinical trial.
This advertiser has chosen not to accept applicants from your region.
9