171 Clinical Internship jobs in Vietnam
Clinical Pharmacologist
900000 Can Tho , Can Tho
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Posted 2 days ago
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Our client, a renowned pharmaceutical company, is seeking an experienced Clinical Pharmacologist to join their team, offering a hybrid work model combining remote flexibility with essential on-site collaboration in **Can Tho, Can Tho, VN**. This critical role involves contributing to the design, execution, and analysis of clinical trials to evaluate the safety and efficacy of new drug candidates. You will be responsible for developing clinical pharmacology strategies, including study design, dose selection, pharmacokinetic (PK) and pharmacodynamic (PD) assessments, and drug interaction studies. Your expertise will guide the development of optimal dosing regimens for various patient populations. You will interpret complex clinical data, prepare clinical study reports, and contribute to regulatory submissions. Collaboration with multidisciplinary teams, including clinical operations, biostatistics, regulatory affairs, and medical affairs, is essential. We are looking for a candidate with a Ph.D. or M.D. in Pharmacology, Clinical Pharmacology, or a related life science field, coupled with significant experience in clinical drug development within the pharmaceutical industry. A deep understanding of regulatory guidelines (e.g., ICH, FDA, EMA) and experience with PK/PD modeling and simulation is required. Excellent analytical, problem-solving, and communication skills are paramount. The ability to manage multiple projects and work effectively in both remote and on-site team environments is crucial. This is an exciting opportunity to make a significant impact on bringing novel therapies to patients while enjoying a flexible work arrangement.
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Clinical Pharmacologist
53000 Thuy Van
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Posted 2 days ago
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Our client is actively searching for a dedicated Clinical Pharmacologist to join their esteemed research division. This is a 100% remote position, offering unparalleled flexibility. The successful candidate will play a critical role in designing, executing, and analyzing clinical trials, focusing on the pharmacokinetic and pharmacodynamic properties of novel therapeutic agents. You will contribute to the strategic development of drugs by providing expert insights into human pharmacology.
Responsibilities:
Responsibilities:
- Design clinical pharmacology studies (Phase I-IV) in accordance with regulatory guidelines (FDA, EMA, etc.).
- Develop study protocols, investigator brochures, and informed consent forms.
- Oversee the conduct of clinical trials, ensuring data integrity and patient safety.
- Analyze pharmacokinetic (PK) and pharmacodynamic (PD) data using specialized software (e.g., NONMEM, Phoenix WinNonlin).
- Develop and validate population PK/PD models to characterize drug effects.
- Interpret study results and contribute to regulatory submissions (e.g., IND, NDA).
- Collaborate with cross-functional teams, including clinical operations, biostatistics, and regulatory affairs.
- Stay updated on advancements in clinical pharmacology, translational medicine, and therapeutic areas.
- Mentor junior team members and contribute to scientific knowledge sharing.
- Ph.D. or Pharm.D. with a specialization in Clinical Pharmacology, Pharmacokinetics, or a related field.
- Minimum of 3-5 years of experience in clinical drug development within the pharmaceutical or biotech industry.
- Demonstrated experience in designing and analyzing PK/PD studies.
- Proficiency with modeling and simulation software.
- Strong understanding of regulatory requirements for drug development.
- Excellent analytical, critical thinking, and problem-solving abilities.
- Exceptional written and verbal communication skills, with experience in preparing regulatory documents.
- Ability to work autonomously and collaboratively in a remote environment.
- Experience in specific therapeutic areas is a plus.
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1
Clinical Lead
Hanoi, Hanoi
Novotech Asia
Posted today
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Job Description
**Responsibilities**:
- Lead site identification and site selection activities.
- Lead set up of clinical components in CTMS
- Prepare for and attend investigator meetings; may present materials.
- Develop and distribute Clinical Monitorring Plan (CMP) and update as required
- Develop and distribute Site Initiation Visit (SIV) materials.
- Develop and distribute Source Data Verification/Monitoring tools and trackers.
- Develop and distribute annotated report templates and templates for visit confirmation/follow-up letters in accordance with any Sponsor requirements.
- Review Site Activation Forms and related essential documents; assist PM and/or Regulatory Start-up Manager (RSM) with Project and Country Activation Forms as requested across regions.
- Work with PM and/or RSM to coordinate initial shipment of both IP and non IP supplies across regions. Work with PM for re-supply of IP and non-IP.
- Lead the CRA team to ensure all study materials are in place before SIV.
- Lead internal meetings/teleconferences with the CRA team.
- Ensure the clinical team are adequately trained on project-specific requirements.
- Review CTMS compliance reports for clinical project team and follow up on gaps.
- Review Monitoring Visit Reports (MVR) and follow-up letters for compliance with ICH-GCP and the CMP; provide final approved documents to Sponsor as required and track report metrics in CTMS.
- Track the resolution of follow-up issues from site visits.
- Maintain protocol deviation tracking in CTMS
- Ensure appropriate issue escalation and tracking of these to resolution, proactive identification of areas of risk, and develop risk management strategies.
- Oversee safety reporting processes to ensure in line with regulatory requirements.
- Provide guidance to CRAs and IHCRAs through mentoring.
- Oversee data collection and query resolution throughout the projects.
- Oversee and coordinate the timely review and documented reconciliations of the TMF at the indicated timepoints per the project filing plan.
- Assist PM with response to audit findings and assist the clinical team with completion of any CAPA review and documentation.
- Work with PM to manage clinical resources to ensure monitoring activities are within budget and notify the PM of any changes required or changes in scope.
- Assist PM to oversee the timely completion of site and investigator payment in accordance with the schedule detailed in the Clinical Trial Agreement.
- May perform co-monitoring visits for ensuring site quality and CRA's monitoring performance as request.
- Oversees study transition plans of CRAs, ensures filing of the transition document/checklist.
- Coordinate with PM and CRAs for Database Lock (DBL) and all close-out activities.
- Oversee site close-out activities of the CRA team
- Lead site identification and site selection activities.
- Lead set up of clinical components in CTMS
- Prepare for and attend investigator meetings; may present materials.
- Develop and distribute Clinical Monitorring Plan (CMP) and update as required
- Develop and distribute Site Initiation Visit (SIV) materials.
- Develop and distribute Source Data Verification/Monitoring tools and trackers.
- Develop and distribute annotated report templates and templates for visit confirmation/follow-up letters in accordance with any Sponsor requirements.
- Review Site Activation Forms and related essential documents; assist PM and/or Regulatory Start-up Manager (RSM) with Project and Country Activation Forms as requested across regions.
- Work with PM and/or RSM to coordinate initial shipment of both IP and non IP supplies across regions. Work with PM for re-supply of IP and non-IP.
- Lead the CRA team to ensure all study materials are in place before SIV.
- Lead internal meetings/teleconferences with the CRA team.
- Ensure the clinical team are adequately trained on project-specific requirements.
- Review CTMS compliance reports for clinical project team and follow up on gaps.
- Review Monitoring Visit Reports (MVR) and follow-up letters for compliance with ICH-GCP and the CMP; provide final approved documents to Sponsor as required and track report metrics in CTMS.
- Track the resolution of follow-up issues from site visits.
- Maintain protocol deviation tracking in CTMS
- Ensure appropriate issue escalation and tracking of these to resolution, proactive identification of areas of risk, and develop risk management strategies.
- Oversee safety reporting processes to ensure in line with regulatory requirements.
- Provide guidance to CRAs and IHCRAs through mentoring.
- Oversee data collection and query resolution throughout the projects.
- Oversee and coordinate the timely review and documented reconciliations of the TMF at the indicated timepoints per the project filing plan.
- Assist PM with response to audit findings and assist the clinical team with completion of any CAPA review and documentation.
- Work with PM to manage clinical resources to ensure monitoring activities are within budget and notify the PM of any changes required or changes in scope.
- Assist PM to oversee the timely completion of site and investigator payment in accordance with the schedule detailed in the Clinical Trial Agreement.
- May perform co-monitoring visits for ensuring site quality and CRA's monitoring performance as request.
- Oversees study transition plans of CRAs, ensures filing of the transition document/checklist.
- Coordinate with PM and CRAs for Database Lock (DBL) and all close-out activities.
- Oversee site close-out activities of the CRA team
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2
Clinical Research Associate
60000 Pleiku, Gia Lai
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Our client is a leading pharmaceutical company seeking a dedicated Clinical Research Associate (CRA) to join their team. This hybrid role offers a balance between remote work flexibility and essential on-site responsibilities to ensure the integrity and success of clinical trials. As a CRA, you will play a critical role in monitoring clinical trial sites, ensuring compliance with protocols, and safeguarding patient safety and data accuracy.
Key Responsibilities:
Key Responsibilities:
- Conduct site initiation visits, interim monitoring visits, and site termination visits.
- Verify that the clinical trial is conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and applicable regulatory requirements.
- Ensure the safety of study participants and the quality of data collected.
- Train and support study site staff on trial-related matters.
- Review essential documents and study-related records for completeness and accuracy.
- Communicate effectively with study site personnel and internal project teams.
- Identify and report deviations, adverse events, and serious adverse events.
- Participate in the preparation and presentation of study-related materials.
- Maintain detailed records of site visits and communications.
- Collaborate with project managers and other team members to ensure the smooth progression of clinical trials.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 2-3 years of experience as a Clinical Research Associate or in a similar role within the pharmaceutical or biotechnology industry.
- Thorough understanding of GCP, ICH guidelines, and relevant regulatory requirements.
- Strong monitoring skills and attention to detail.
- Excellent communication, interpersonal, and organizational skills.
- Ability to travel to clinical trial sites as required.
- Proficiency in electronic data capture (EDC) systems and clinical trial management software (CTMS).
- Ability to work independently and manage multiple priorities effectively.
- Strong problem-solving abilities.
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3
Clinical Research Associate
53000 Thuy Van
WhatJobs
Posted today
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Job Description
Our client is looking for a meticulous and dedicated Clinical Research Associate (CRA) to join their pharmaceutical team, working in a fully remote capacity. This role is critical for ensuring the successful execution of clinical trials, adhering to strict regulatory and ethical guidelines. You will be responsible for monitoring clinical trial sites, verifying data accuracy and integrity, and ensuring patient safety and protocol compliance. Key duties include conducting site visits, training site staff, managing study documentation, and resolving data discrepancies. The ideal candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements in the pharmaceutical industry. This remote position requires exceptional organizational skills, attention to detail, and the ability to work independently while maintaining clear communication with study teams and site personnel. A Bachelor's degree in a life science, nursing, or a related field is required, along with at least 3 years of experience as a Clinical Research Associate or in a similar clinical trial role. Strong knowledge of medical terminology and therapeutic areas is essential. You will play a vital role in bringing new and innovative medicines to patients, ensuring the quality and reliability of clinical data collected during trials, and contributing to advancements in healthcare.
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4
Clinical Research Associate
30000 An Thanh
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Posted today
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Our client is looking for a dedicated and detail-oriented Clinical Research Associate (CRA) to join their pharmaceutical team in Vung Tau, Ba Ria–Vung Tau, VN . As a CRA, you will be responsible for monitoring clinical trials to ensure adherence to protocols, regulatory requirements, and good clinical practice (GCP) guidelines. Your duties will include site selection, initiation, monitoring, and close-out visits; reviewing and verifying case report forms (CRFs); ensuring data accuracy and integrity; managing investigational product; and acting as a liaison between the sponsor and clinical trial sites. The ideal candidate will have a strong understanding of clinical trial processes, excellent communication and interpersonal skills, and the ability to work independently and manage multiple priorities effectively. Experience with electronic data capture (EDC) systems and a background in healthcare, life sciences, or a related field are essential. You should possess strong organizational skills and a meticulous approach to documentation and reporting. The ability to travel to clinical sites as required is necessary. This role requires a high level of professionalism and a commitment to ethical conduct in clinical research. You will play a critical role in the successful execution of clinical studies, contributing to the development of new pharmaceutical products. A proactive approach to problem-solving and the ability to build rapport with investigators and site staff are key to success. Our client offers a supportive work environment and opportunities for professional growth within the pharmaceutical industry. Bachelor's degree in life sciences, nursing, pharmacy, or a related field is required. Previous experience as a CRA or in a related clinical research role is highly preferred.
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5
Clinical Case Manager
42000 Hoang Hoa
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Our client is seeking a compassionate and highly organized Clinical Case Manager to join their dedicated remote team, supporting individuals within the community social care sector. This role is crucial in providing holistic support and advocacy for clients, ensuring they receive the necessary care and resources to improve their well-being and quality of life. As a Clinical Case Manager, you will be responsible for conducting comprehensive client assessments, developing personalized care plans, and coordinating services with various healthcare providers, social services agencies, and community resources. You will act as a primary point of contact for clients and their families, offering guidance, support, and assistance in navigating complex systems. This remote position requires excellent communication and interpersonal skills, as you will be interacting with diverse populations and stakeholders via phone, video conferencing, and electronic communication. The ideal candidate will have a Bachelor's or Master's degree in Social Work, Psychology, Nursing, or a related field, coupled with a minimum of 3 years of experience in case management, social work, or healthcare coordination. A strong understanding of mental health, substance abuse, and chronic illness management is essential. You must be adept at client advocacy, crisis intervention, and resource linkage. Proficiency in electronic health record (EHR) systems and case management software is required. This role demands empathy, resilience, and a commitment to ethical practice. The ability to work independently, manage a caseload effectively, and maintain accurate client records is paramount. This is an excellent opportunity for a dedicated professional looking to make a meaningful difference in people's lives while enjoying the flexibility of a fully remote work arrangement. Join a supportive team dedicated to client-centered care.
Key Responsibilities:
Key Responsibilities:
- Conduct comprehensive assessments of client needs and strengths.
- Develop and implement individualized care plans in collaboration with clients.
- Coordinate services with healthcare providers, social services, and community agencies.
- Provide ongoing support, counseling, and advocacy for clients.
- Monitor client progress and adjust care plans as needed.
- Maintain accurate and confidential client records and documentation.
- Connect clients with appropriate community resources and services.
- Facilitate communication between clients, families, and service providers.
- Respond to client crises and provide immediate support and intervention.
- Bachelor's or Master's degree in Social Work, Psychology, Nursing, or a related field.
- Minimum 3 years of experience in case management or social work.
- Experience with specific client populations (e.g., mental health, elderly, disabled).
- Strong knowledge of community resources and social services.
- Excellent assessment, planning, and intervention skills.
- Proficiency in EHR systems and case management software.
- Strong communication, interpersonal, and organizational skills.
- Ability to work independently and manage time effectively.
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6
Senior Clinical Esthetician
95000 Long Xuyen, An Giang
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Posted today
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Our client, a leading name in the beauty and wellness sector, is looking for a highly skilled and experienced Senior Clinical Esthetician to join their esteemed, fully remote team. This role offers the unique opportunity to provide expert skincare consultations and treatments to a diverse clientele, utilizing advanced techniques and personalized care plans, all from the comfort of your own home office. You will be instrumental in delivering exceptional client experiences and achieving outstanding results, contributing to our client's reputation for excellence.
Responsibilities:
Qualifications:
Responsibilities:
- Conduct in-depth skin analysis and client consultations via video conferencing to assess needs and recommend appropriate treatments.
- Perform a wide range of advanced esthetic treatments including facials, chemical peels, microdermabrasion, and LED therapy.
- Develop customized skincare routines and product recommendations for clients.
- Educate clients on proper skincare practices and the benefits of recommended treatments and products.
- Maintain detailed and accurate client records and treatment progress notes.
- Stay updated on the latest trends, technologies, and product advancements in the esthetics industry.
- Manage client appointments and follow-ups effectively.
- Ensure all client interactions adhere to the highest standards of professionalism and client care.
- Contribute to the development of new treatment protocols and service offerings.
- Achieve and exceed client satisfaction and retention goals.
Qualifications:
- State-issued Esthetician license or equivalent certification.
- Minimum of 5 years of experience as a practicing esthetician, with a focus on clinical or medical esthetics.
- Proven expertise in performing advanced skincare treatments and utilizing various esthetic equipment.
- Strong knowledge of skin physiology, conditions, and ingredients.
- Excellent communication, interpersonal, and client relationship management skills.
- Ability to conduct virtual consultations effectively and build rapport with clients remotely.
- Self-motivated, organized, and able to manage time efficiently in a remote setting.
- Proficiency with skincare software and virtual consultation platforms.
- A passion for continuous learning and professional development in the beauty and wellness field.
- Experience with luxury skincare brands or medi-spa environments is a plus.
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7
Clinical Social Worker
71000 Rach Gia, Kien Giang
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Posted today
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Our client is seeking a dedicated and licensed Clinical Social Worker to join our fully remote behavioral health team. This role is crucial in providing comprehensive mental health services and support to individuals and families facing various challenges. You will be responsible for conducting client assessments, developing individualized treatment plans, and providing therapeutic interventions, including psychotherapy and counseling, via telehealth platforms. Key responsibilities include diagnosing mental health conditions using DSM-5 criteria, implementing evidence-based treatment modalities, and providing crisis intervention when necessary. You will work collaboratively with other healthcare professionals to ensure holistic client care. A strong understanding of therapeutic frameworks such as CBT, DBT, and trauma-informed care is essential. This position requires exceptional communication and active listening skills, coupled with a deep sense of empathy and commitment to client well-being. The ability to build rapport and trust with clients remotely is paramount. The ideal candidate will possess excellent organizational skills, meticulous record-keeping abilities, and a proactive approach to case management and documentation. Experience with electronic health record (EHR) systems and telehealth platforms is a must. This is a rewarding opportunity to make a significant impact on mental health outcomes while enjoying the flexibility of a fully remote work environment. You will also be involved in peer supervision and contributing to program development. A Master's degree in Social Work (MSW) from an accredited institution and a valid LCSW or equivalent license are required. A minimum of 3 years of post-MSW clinical experience is necessary. Join our mission-driven, remote team to provide vital mental health support.
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8
Remote Clinical Aromatherapist
530000 Thuy Van
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Posted today
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Our client, a leader in holistic health and natural therapies, is seeking a qualified and compassionate Remote Clinical Aromatherapist to join our Beauty & Wellness practice. This fully remote position involves providing expert guidance on the therapeutic use of essential oils to clients seeking to improve their physical, emotional, and mental well-being. You will conduct thorough virtual consultations, assessing client needs and health histories to create personalized aromatherapy treatment plans. The ideal candidate will possess in-depth knowledge of essential oil properties, safety protocols, contraindications, and blending techniques. Certification from a recognized aromatherapy organization (e.g., NAHA, IFPA) is a prerequisite. Responsibilities include educating clients on the safe and effective application of essential oils for various conditions such as stress, anxiety, sleep disturbances, pain management, and skin health. You will guide clients on creating custom blends for diffusion, topical application, or inhalation. This role requires excellent communication skills to explain complex information clearly and empathetically, fostering a supportive therapeutic relationship. You will need to maintain meticulous client records, track progress, and adjust recommendations as necessary. Experience with telemedicine platforms and a strong understanding of natural health principles are essential. We are looking for a dedicated practitioner who can empower clients with the knowledge and tools to integrate aromatherapy safely and effectively into their self-care routines. Strong organizational skills are needed to manage client schedules and consultations effectively. The ability to work independently, manage your workload proactively, and maintain a high standard of professional practice in a remote environment is crucial. We aim to provide clients with evidence-based, personalized aromatherapy solutions, and your expertise will be key to achieving this goal. Continuous professional development and staying abreast of aromatherapy research are expected.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct virtual consultations to assess client needs for aromatherapy.
- Develop personalized aromatherapy treatment plans and custom blends.
- Educate clients on the safe and effective use of essential oils.
- Provide recommendations for diffusion, inhalation, and topical application.
- Address client concerns related to stress, anxiety, sleep, pain, and other conditions.
- Maintain detailed client records and track progress.
- Stay updated on essential oil research, safety guidelines, and therapeutic applications.
- Advise on proper storage and handling of essential oils.
- Promote holistic well-being through the use of aromatherapy.
Qualifications:
- Certified Clinical Aromatherapist from a recognized institution.
- Minimum 3 years of experience practicing aromatherapy.
- In-depth knowledge of essential oil chemistry, properties, and safety.
- Excellent communication, interpersonal, and counseling skills.
- Ability to work independently and manage remote client caseloads.
- Proficiency with virtual communication and record-keeping tools.
- Understanding of holistic health principles.
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