1 671 Svar Life Science jobs in Vietnam
Clinical Research Associate
55000 Hoa Sơn
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Job Description
Our client, a prominent pharmaceutical company focused on developing innovative healthcare solutions, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their team. This hybrid role offers a dynamic work environment, combining remote administrative tasks with essential on-site monitoring activities in **Da Nang, Da Nang, VN**, and surrounding areas. You will be responsible for ensuring the quality, integrity, and ethical conduct of clinical trials, adhering to strict protocols and regulatory guidelines. This is a critical position for driving forward life-saving research.
Key Responsibilities:
Key Responsibilities:
- Monitor clinical trial sites to ensure adherence to study protocols, GCP guidelines, and regulatory requirements.
- Verify the accuracy, completeness, and consistency of clinical data.
- Manage site initiation, routine monitoring, and close-out visits.
- Build and maintain strong relationships with investigators, site staff, and study participants.
- Ensure proper collection, storage, and reconciliation of Investigational Product (IP).
- Oversee the resolution of data queries and discrepancies.
- Train site personnel on study-specific procedures and regulatory compliance.
- Prepare and submit monitoring reports and other study-related documentation.
- Ensure all site activities are conducted ethically and in accordance with patient safety standards.
- Communicate effectively with the study team, sponsors, and regulatory authorities.
- Manage and maintain study supplies and essential documents.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- Thorough understanding of ICH-GCP guidelines and other relevant regulatory requirements.
- Experience in monitoring Phase I-IV clinical trials across various therapeutic areas.
- Excellent attention to detail and organizational skills.
- Strong communication, interpersonal, and problem-solving abilities.
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Ability to travel frequently to assigned clinical sites.
- Familiarity with the healthcare landscape in **Da Nang, Da Nang, VN** is advantageous.
- Commitment to patient safety and data integrity.
- Fluent in English, both written and spoken.
This advertiser has chosen not to accept applicants from your region.
0
Clinical Research Associate
36000 Thai Binh , Thai Binh
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Job Description
Our client, a leading pharmaceutical company, is looking for a dedicated and experienced Clinical Research Associate to join our global clinical operations team on a contract basis, with a fully remote working arrangement. This role is essential for the successful execution of clinical trials, ensuring compliance with regulatory standards and ethical guidelines. You will be responsible for monitoring clinical trial sites, verifying data accuracy, and ensuring adherence to study protocols. Key duties include site initiation visits, routine monitoring, and close-out visits, as well as maintaining effective communication with investigators, site staff, and study sponsors. The ideal candidate will possess a strong background in life sciences, nursing, or a related field, with prior experience as a CRA or in a similar clinical research role. Excellent understanding of ICH-GCP guidelines and regulatory requirements is paramount. We are seeking a highly organized, detail-oriented individual with strong analytical and problem-solving skills. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is required. This is a remote-first position, offering the flexibility to work from any location in Vietnam. You will play a crucial role in advancing pharmaceutical research and bringing life-saving medications to market. The ability to manage multiple sites, conduct thorough source data verification, and ensure the safety of study participants will be key to your success. This contract role offers a dynamic work environment and the opportunity to contribute to groundbreaking medical research. We value individuals who are proactive, possess excellent time management skills, and are committed to maintaining the highest standards of data integrity and patient safety.
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1
Research Associate - Nanotechnology
40000 Nam Dinh , Nam Dinh
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Our client is seeking an enthusiastic and detail-oriented Research Associate with expertise in Nanotechnology to join their cutting-edge research facility in Nam Dinh, Nam Dinh, VN . This role offers an excellent opportunity for individuals passionate about exploring the frontiers of nanoscience and its applications. The ideal candidate will possess a Master's or Ph.D. in Nanotechnology, Physics, Chemistry, or a related scientific discipline, coupled with practical experience in nanofabrication, characterization, and testing of nanomaterials. You will be involved in designing and conducting experiments, analyzing data, and contributing to the development of novel nanotechnological solutions. Collaboration with senior researchers and a commitment to scientific rigor are essential for success in this position.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Assist in the design and execution of experiments related to nanotechnology and nanomaterials.
- Prepare and characterize nanomaterials using various synthesis and fabrication techniques.
- Utilize specialized equipment for the analysis and testing of nanomaterials.
- Collect, analyze, and interpret experimental data using statistical methods.
- Contribute to the development of new research methodologies and protocols.
- Maintain accurate and detailed laboratory notebooks and records.
- Collaborate with senior scientists and researchers on project tasks.
- Prepare technical reports, presentations, and contribute to scientific publications.
- Ensure compliance with laboratory safety procedures and ethical standards.
- Troubleshoot experimental setups and resolve technical challenges.
Qualifications:
- Master's or Ph.D. in Nanotechnology, Physics, Chemistry, Materials Science, or a related field.
- Hands-on experience in nanofabrication techniques (e.g., lithography, deposition).
- Proficiency in nanomaterial characterization methods (e.g., SEM, AFM, TEM, UV-Vis spectroscopy).
- Strong understanding of fundamental principles of nanoscience and nanotechnology.
- Excellent data analysis and interpretation skills.
- Good written and verbal communication skills.
- Ability to work both independently and as part of a research team.
- Familiarity with scientific literature search databases.
- Prior experience in a research and development environment is advantageous.
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Associate
Hanoi, Hanoi
IQVIA
Posted today
Job Viewed
Job Description
As you develop your career as a Senior CRA or CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a 'career ceiling.' You will be exposed to wider opportunities like operations management, dedicated customer solutions, project management and more. And you won't do it alone - you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion opportunities and awards. Joining IQVIA will give you access to cutting-edge in-house technology and provide opportunities to work on global projects/ trials. You will be building a flexible, meaningful and fulfilling career with no limits.
**Your responsibilities will include:**
+ Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation
+ Supporting the development of a subject recruitment plan
+ Establishing regular lines of communication plus administering protocol and related study training to assigned sites
+ Evaluating the quality and integrity of site practices - escalating quality issues as appropriate
+ Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
+ You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You will need to have a good knowledge of applicable clinical research regulatory requirements.
**Qualifications:**
+ University degree in scientific discipline or healthcare
+ At least 1 year of on-site monitoring experience
+ Good knowledge of GCP and clinical research regulatory requirements
+ Good computer skills including MS Office
+ Excellent command of English language
+ Organizational, time management and problem-solving skills
+ Ability to establish and maintain effective working relationships with colleagues, managers, and customers.
+ Flexibility to travel.
**What you can expect:**
+ Working with different customers on global trials
+ Career development opportunities for those who are passionate in wanting to grow as part of the organization.
+ Leaders that support flexible work schedules/arrangement
+ Excellent working environment in a stable, international, reputable company
+ Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape
+ Attractive remuneration package.
#LI-Hybrid
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**Your responsibilities will include:**
+ Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation
+ Supporting the development of a subject recruitment plan
+ Establishing regular lines of communication plus administering protocol and related study training to assigned sites
+ Evaluating the quality and integrity of site practices - escalating quality issues as appropriate
+ Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
+ You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You will need to have a good knowledge of applicable clinical research regulatory requirements.
**Qualifications:**
+ University degree in scientific discipline or healthcare
+ At least 1 year of on-site monitoring experience
+ Good knowledge of GCP and clinical research regulatory requirements
+ Good computer skills including MS Office
+ Excellent command of English language
+ Organizational, time management and problem-solving skills
+ Ability to establish and maintain effective working relationships with colleagues, managers, and customers.
+ Flexibility to travel.
**What you can expect:**
+ Working with different customers on global trials
+ Career development opportunities for those who are passionate in wanting to grow as part of the organization.
+ Leaders that support flexible work schedules/arrangement
+ Excellent working environment in a stable, international, reputable company
+ Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape
+ Attractive remuneration package.
#LI-Hybrid
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Associate
Ho Chi Minh, Ho Chi Minh
IQVIA
Posted today
Job Viewed
Job Description
As you develop your career as a Senior CRA or CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a 'career ceiling.' You will be exposed to wider opportunities like operations management, dedicated customer solutions, project management and more. And you won't do it alone - you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion opportunities and awards. Joining IQVIA will give you access to cutting-edge in-house technology and provide opportunities to work on global projects/ trials. You will be building a flexible, meaningful and fulfilling career with no limits.
**Your responsibilities will include:**
+ Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation
+ Supporting the development of a subject recruitment plan
+ Establishing regular lines of communication plus administering protocol and related study training to assigned sites
+ Evaluating the quality and integrity of site practices - escalating quality issues as appropriate
+ Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
+ You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You will need to have a good knowledge of applicable clinical research regulatory requirements.
**Qualifications:**
+ University degree in scientific discipline or healthcare
+ At least 1 year of on-site monitoring experience
+ Good knowledge of GCP and clinical research regulatory requirements
+ Good computer skills including MS Office
+ Excellent command of English language
+ Organizational, time management and problem-solving skills
+ Ability to establish and maintain effective working relationships with colleagues, managers, and customers.
+ Flexibility to travel.
**What you can expect:**
+ Working with different customers on global trials
+ Career development opportunities for those who are passionate in wanting to grow as part of the organization.
+ Leaders that support flexible work schedules/arrangement
+ Excellent working environment in a stable, international, reputable company
+ Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape
+ Attractive remuneration package.
#LI-Hybrid
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**Your responsibilities will include:**
+ Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation
+ Supporting the development of a subject recruitment plan
+ Establishing regular lines of communication plus administering protocol and related study training to assigned sites
+ Evaluating the quality and integrity of site practices - escalating quality issues as appropriate
+ Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
+ You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You will need to have a good knowledge of applicable clinical research regulatory requirements.
**Qualifications:**
+ University degree in scientific discipline or healthcare
+ At least 1 year of on-site monitoring experience
+ Good knowledge of GCP and clinical research regulatory requirements
+ Good computer skills including MS Office
+ Excellent command of English language
+ Organizational, time management and problem-solving skills
+ Ability to establish and maintain effective working relationships with colleagues, managers, and customers.
+ Flexibility to travel.
**What you can expect:**
+ Working with different customers on global trials
+ Career development opportunities for those who are passionate in wanting to grow as part of the organization.
+ Leaders that support flexible work schedules/arrangement
+ Excellent working environment in a stable, international, reputable company
+ Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape
+ Attractive remuneration package.
#LI-Hybrid
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate
60000 Pleiku, Gia Lai
WhatJobs
Posted today
Job Viewed
Job Description
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.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate
53000 Thuy Van
WhatJobs
Posted today
Job Viewed
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.
This advertiser has chosen not to accept applicants from your region.
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6
Clinical Research Associate
30000 An Thanh
WhatJobs
Posted today
Job Viewed
Job Description
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.
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Associate
70000 Can Tho , Can Tho
WhatJobs
Posted 1 day ago
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.
8
Clinical Research Associate
57000 An Thanh
WhatJobs
Posted 1 day ago
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.
9