534 Icon Plc jobs in Vietnam

• Lead the design and synthesis of novel small molecule compounds targeting specific disease pathways.
• Apply principles of medicinal chemistry, structure-activity relationships (SAR), and computational chemistry to optimize lead compounds.
• Oversee the synthesis of target molecules and intermediates, utilizing a wide range of modern organic chemistry techniques.
• Collaborate closely with biologists, pharmacologists, and other medicinal chemists in a remote setting to define project goals and strategies.
• Analyze spectroscopic data (NMR, MS, HPLC) to confirm compound structures and purity.
• Manage external collaborations with CROs for synthesis and screening activities.
• Prepare detailed reports on synthesis strategies, experimental results, and project progress.
• Contribute to intellectual property generation through patent applications.
• Mentor junior chemists and foster a culture of scientific excellence and innovation.
• Stay current with the latest advancements in synthetic organic chemistry and medicinal chemistry.

• Ph.D. in Organic Chemistry or Medicinal Chemistry from a leading institution.
• A minimum of 6 years of post-doctoral or industry experience in medicinal chemistry, with a strong track record in small molecule drug discovery.
• Demonstrated expertise in designing and synthesizing diverse chemical libraries.
• Proficiency in modern synthetic organic chemistry techniques and instrumentation.
• Strong understanding of drug design principles, ADME/Tox properties, and SAR analysis.
• Experience with computational chemistry tools and databases is highly desirable.
• Excellent analytical, problem-solving, and organizational skills.
• Superb written and verbal communication skills, with the ability to articulate complex scientific concepts clearly in a remote context.
• Proven ability to work independently and as part of a distributed team.
• Experience in managing research projects and mentoring junior scientists.

• Lead and manage drug discovery research programs from target identification to lead optimization.
• Design and execute complex in vitro and in vivo experiments to validate targets and assess compound efficacy and safety.
• Develop and implement novel assays and screening strategies.
• Interpret complex biological and chemical data, and make strategic recommendations for project progression.
• Collaborate with medicinal chemists to design and synthesize novel drug candidates.
• Oversee preclinical development activities, including PK/PD studies and toxicology assessments.
• Mentor and guide a team of research scientists and technicians.
• Author scientific publications, patent applications, and regulatory submission documents.
• Build and maintain relationships with external scientific collaborators and key opinion leaders.
• Contribute to the strategic planning and portfolio management of the R&D pipeline.

• PhD in Pharmacology, Molecular Biology, Biochemistry, Medicinal Chemistry, or a related life science discipline.
• 10+ years of post-doctoral research experience in the pharmaceutical or biotechnology industry.
• Proven track record of successfully advancing drug candidates through the discovery pipeline.
• Expertise in specific therapeutic areas and modalities (e.g., small molecules, biologics).
• Strong understanding of drug discovery processes, including target validation, assay development, lead optimization, and preclinical testing.
• Excellent track record of scientific publications and presentations.
• Demonstrated leadership and team management skills.
• Exceptional analytical, problem-solving, and critical thinking abilities.
• Experience with project management and cross-functional team collaboration.

• Lead and manage complex research projects focused on the discovery and preclinical development of novel therapeutics for challenging diseases.
• Design and execute in vitro and in vivo studies to evaluate the efficacy, safety, and pharmacokinetic profiles of drug candidates.
• Develop and optimize assays for high-throughput screening (HTS) and target validation.
• Provide scientific leadership and mentorship to a team of research scientists and technicians.
• Analyze and interpret complex biological and chemical data, drawing insightful conclusions and making data-driven decisions.
• Collaborate closely with cross-functional teams, including medicinal chemistry, DMPK, toxicology, and clinical development.
• Stay abreast of the latest scientific literature, technological advancements, and competitive landscape in relevant therapeutic areas.
• Contribute to the strategic planning and prioritization of the drug discovery pipeline.
• Prepare and present research findings at internal meetings and external scientific conferences.
• Contribute to the preparation of regulatory submissions (e.g., IND applications) and patent filings.

• Ph.D. in Pharmacology, Molecular Biology, Biochemistry, Medicinal Chemistry, or a related life science discipline.
• Minimum of 8 years of post-doctoral research experience in the pharmaceutical or biotechnology industry, with a proven track record in drug discovery and preclinical development.
• Extensive experience in designing and executing a variety of biological assays and animal models relevant to drug discovery.
• Strong understanding of target identification, validation, lead optimization, and candidate selection processes.
• Demonstrated leadership skills with experience in managing and mentoring research teams.
• Expertise in at least one major therapeutic area (e.g., oncology, immunology, neuroscience).
• Proficiency in data analysis software and interpretation of complex datasets.
• Excellent written and verbal communication skills, with the ability to articulate scientific concepts clearly and concisely.
• Strong collaborative spirit and ability to work effectively in a fast-paced, remote research environment.
• Experience with biostatistics and pharmacokinetics/pharmacodynamics (PK/PD) modeling is highly desirable.

• Lead the design and execution of groundbreaking research projects aimed at identifying and validating new drug targets.
• Develop and implement innovative strategies for small molecule and/or biologic drug discovery.
• Oversee and interpret complex experimental data, drawing meaningful conclusions to guide project direction.
• Collaborate closely with medicinal chemists, biologists, pharmacologists, and toxicologists to advance lead candidates.
• Manage research collaborations with academic institutions and contract research organizations (CROs).
• Author high-impact scientific publications and present findings at international conferences.
• Provide scientific leadership and mentorship to junior researchers and scientists.
• Ensure adherence to rigorous scientific standards, ethical guidelines, and regulatory requirements.
• Contribute to the development of intellectual property strategies and patent filings.
• Evaluate new technologies and methodologies to enhance drug discovery capabilities.
• Prepare comprehensive research reports and regulatory submission documents.

• Ph.D. in a relevant scientific discipline (e.g., Molecular Biology, Pharmacology, Biochemistry, Chemistry).
• Minimum of 10 years of progressive research experience in the pharmaceutical or biotechnology industry, with a strong emphasis on drug discovery.
• Demonstrated success in leading research programs and delivering preclinical drug candidates.
• Expertise in multiple therapeutic areas or specific disease mechanisms.
• In-depth knowledge of target validation, assay development, high-throughput screening, and lead optimization.
• Exceptional analytical, problem-solving, and critical thinking skills.
• Strong publication record in peer-reviewed journals.
• Excellent leadership, communication, and interpersonal skills, with the ability to foster a collaborative research environment.
• Experience in managing CROs and academic collaborations is highly desirable.
• Proficiency in relevant scientific software and data analysis tools.
• This role is based in Vung Tau, Ba Ria–Vung Tau, VN , but operates entirely remotely. We are committed to creating a connected and productive remote workforce where scientific excellence is paramount.

• Design and develop robust pharmaceutical formulations for various dosage forms (e.g., oral solids, injectables, topicals).
• Conduct pre-formulation studies, including solubility, stability, and compatibility assessments.
• Develop and optimize manufacturing processes for drug products, ensuring scalability and reproducibility.
• Characterize formulations using various analytical techniques (e.g., HPLC, DSC, XRPD, dissolution testing).
• Troubleshoot formulation and process-related issues, implementing effective solutions.
• Collaborate with analytical development teams to establish appropriate quality control methods.
• Prepare technical documentation, including formulation development reports, development summaries, and regulatory submissions.
• Stay abreast of the latest advancements in drug delivery technologies, pharmaceutics, and regulatory guidelines.
• Manage external contract research organizations (CROs) for specific formulation development activities.
• Mentor junior scientists and contribute to the growth of the formulation development team.
• Participate in cross-functional team meetings, providing expertise on formulation development.
• Evaluate and select appropriate excipients and technologies for formulation development.
• Contribute to the strategic planning of the drug product development pipeline.
• Ensure adherence to Good Manufacturing Practices (GMP) and other relevant regulatory standards.
• Assist in the preparation of Investigational New Drug (IND) and New Drug Application (NDA) filings.

• Ph.D. or Master's degree in Pharmaceutics, Pharmaceutical Chemistry, Chemical Engineering, or a related scientific discipline.
• Minimum of 6 years of progressive experience in pharmaceutical formulation development.
• Extensive knowledge of drug delivery systems, dosage form design, and pharmaceutical manufacturing processes.
• Proficiency in a wide range of analytical techniques used for formulation characterization.
• Strong understanding of biopharmaceutics, pharmacokinetics, and drug metabolism.
• Experience with solid-state chemistry, polymorphism, and salt screening is highly desirable.
• Proven ability to manage complex research projects from conception to completion.
• Excellent problem-solving, critical-thinking, and analytical skills.
• Exceptional written and verbal communication skills, with the ability to present scientific data effectively in a remote environment.
• Familiarity with regulatory requirements (FDA, EMA) related to drug product development.
• Experience with sterile product development or specialized delivery systems is a plus.
• Ability to work independently, prioritize tasks, and meet deadlines.
• A proactive approach to innovation and continuous learning.

• Lead and design innovative drug discovery research programs from target identification to preclinical candidate selection.
• Develop and optimize novel small molecules, biologics, or other therapeutic modalities.
• Conduct in vitro and in vivo studies to assess drug efficacy, safety, and pharmacokinetics/pharmacodynamics (PK/PD).
• Validate novel drug targets and mechanisms of action.
• Analyze complex experimental data, interpret results, and draw robust conclusions.
• Mentor and guide a team of research associates and scientists.
• Collaborate effectively with cross-functional teams, including medicinal chemistry, biology, DMPK, toxicology, and regulatory affairs.
• Prepare high-quality research reports, regulatory documents, and scientific publications.
• Stay current with the latest advancements in pharmaceutical research and relevant therapeutic areas.
• Contribute to the strategic direction of the company's research pipeline.

• Ph.D. in Pharmacology, Medicinal Chemistry, Biochemistry, Molecular Biology, or a related field.
• 8+ years of post-doctoral research experience in pharmaceutical R&D.
• Proven track record in leading successful drug discovery projects and advancing candidates into development.
• Extensive experience in target validation, assay development, lead optimization, and preclinical studies.
• Strong knowledge of various therapeutic areas (e.g., oncology, immunology, infectious diseases).
• Proficiency in relevant scientific techniques and instrumentation.
• Excellent scientific judgment, problem-solving, and analytical skills.
• Exceptional leadership, communication, and interpersonal skills.
• Ability to thrive in a fast-paced, remote research environment.

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.

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

HCM & Hanoi - CRC Recruitment Announcement

We are currently seeking highly motivated individuals to join our team. As a leading SMO company in our industry, we offer challenging and rewarding opportunities for those who are dedicated and passionate about their work.

Position: Clinical Research Coordinator

Location

This post is based in HCM & Hanoi, Viet Nam. There will be a requirement to travel within Viet Nam to support projects.

Hours of Work

Full time Monday – Friday, 40 hours per week, extra hours may be required.

Tenure

Initially for 01 years, excluding a 02-month probation period, with possibility of extension based on annual performance appraisal and research approval

Report to

SSD Director

Tasks

CRC assists the sponsors/PIs in doing the following tasks:

• Support screening and selecting patients

• Support the establishment of "Patient file" (patient records) (if any)

• Support PIs to import data into CRF/eCRF

• Supports storage, management of source data, as well as all records and related document // Support in drafting SOPs

• Support the implementation of research in accordance with the protocol, SOP and GCP (monitoring and guiding procedures to ensure the proper implementation)

• Check and prepare necessary testing equipment for the study

• Support for checking and updating information into required records (such as Update investigator file, patient binder .)

• Support the monitoring of patients (schedule and remind schedule of visits .)

• Support AE / SAE report

• Support login, activate, update to the research system (web-based system) if any

• Preparing documents, necessary files to meet the supervision and inspection

• Other by PI requests

Essential Criteria:

• Medical Doctor, Public health, Pharmacy, Nurse, Biology, Bio-technology or related

• High Intermediate level of English comprehension, including the ability to do translations from English to Vietnamese

• Excellent interpersonal communication/diplomatic skills with people of different backgrounds and social positions

• Excellent Vietnamese language skills: listening, speaking, reading, writing.

Benefits

• Contracted salary: Negotiate (depending on actual experience and education)

• Personal insurance: In-patient and out-patient medical coverage // Personal accident insurance coverage

• 13th month salary (annual bonus), Tet bonus and others

• Annual leave 12 days/year

• Vietnam Social & Health insurance, Sick leave, Maternity leave and National holidays will be based on Vietnam Labor Law

• Company teambuilding trip & Office outing activities

How to Apply

Interested candidates are invited to send curriculum vitae, application and copies of relevant certificates, either by email:

If you have any questions or concerns regarding our job recruitment announcement, please contact us via this Facebook. We will promptly respond and assist you throughout the application process. Thank you for your interest in employment opportunities at our company.