What Jobs are available for Flexible Research in Thailand?

The research associate is responsible for assisting breeders in seed organizing/ administration, sowing and planting of trials, data collection, pollinations, seed harvesting and extraction. Develop basic plant breeding know-how and skills.

Roles and Responsibilities:

• Assist direct supervisor with all trial activities and special projects as assigned.
• Assist direct supervisor with management of breeding working collections and seed admin database.
• Search for information related to species breeding objectives.
• Assist direct supervisor with supervision, training and evaluation of breeding technicians and breeding workers.
• Submit reports to direct supervisor for review and discussion as required
• Ad-hoc projects or company events as assigned

Minimum Requirements:

• M.S. in Agriculture, Horticulture/Crop Sciences/Biological Sciences and related field; no/limited work experience
• Strong interest in plant breeding and molecular genetics.
• Ability to work under adverse conditions in the field
• Result Oriented
• Good command of English in both speaking and writing English language.
• Good interaction skill, mature, hard working, self Initiative, enthusiastic and service minded
• Stress tolerance
• Attention to details, organized and neat
• Integrity and accountability
• Able to handle multiple tasks at once and works well under pressure

Job Title:
 Research Associate

Location:
 Bangkok, Thailand (On-site)

Organisation:
 Asia Centre

About Asia Centre

Asia Centre is a regional think tank focused on advancing human rights, democracy, and sustainable development in Asia through rigorous research, policy analysis, and advocacy.

Position Overview

We are seeking a 
Research Associate
 with strong expertise in political science, human rights, or regional development to support our research projects. This role requires hands-on research, policy analysis, and publication work aligned with Asia Centre's focus areas. The ideal candidate is highly analytical, detail-oriented, and familiar with Southeast Asian political and social contexts.

Key Responsibilities

• Conduct 
  desk-based research and field research
   on topics such as human rights, governance, democracy, climate policy, or social development in Asia.
• Collect, analyse, and synthesise qualitative and quantitative data from credible sources (government reports, academic publications, NGOs, and news media).
• Draft 
  research reports, policy briefs, working papers, and academic articles
   that meet high-quality standards.
• Monitor developments in specific countries or thematic areas relevant to Asia Centre's projects.
• Support the design, organisation, and reporting of events, workshops, or roundtables related to research outputs.
• Collaborate with other researchers and staff to ensure alignment with project objectives.
• Assist with funding proposals, donor reports, and dissemination of research outputs.

Required Qualifications

• Master's degree
   in political science, international relations, law, human rights, public policy, or a closely related field.
• Minimum 
  2 years of relevant research experience
   in NGOs, think tanks, or academic institutions.
• Proven 
  track record of producing research outputs
  , including reports, policy briefs, or publications.
• Strong analytical, writing, and editing skills; able to present complex ideas clearly.
• Familiarity with 
  Southeast Asian political and social contexts
   is essential.
• Proficiency in 
  English
   (written and spoken); additional regional language(s) are a plus.
• Experience in 
  qualitative and quantitative research methods
   is highly desirable.
• Ability to work independently and meet deadlines under minimal supervision.

Preferred Attributes

• Knowledge of human rights, governance, or climate and social policy issues in Asia.
• Experience with 
  data collection, interviews, or field research
  .
• Strong attention to detail and ability to critically evaluate sources.

What We Offer

• Meaningful work in an internationally recognised think tank.
• Exposure to regional policy networks and decision-makers.
• Collaborative and intellectually stimulating work environment.
• Opportunities to publish and present research at conferences or workshops.

How to Apply

Interested candidates should submit the following to:

1. A 
   cover letter
    (max 1 page) explaining your motivation and relevant experience.
2. A 
   CV
    (max 2 pages).
3. A 
   recent writing sample
    (3–5 pages) demonstrating analytical and research skills.

Only shortlisted candidates will be contacted. More About Asia Centre visit

Job Title: Research Associate

Location: Bangkok, Thailand (On-site)

Organisation: Asia Centre

About Asia Centre

Asia Centre is a regional think tank focused on advancing human rights, democracy, and sustainable development in Asia through rigorous research, policy analysis, and advocacy.

Position Overview

We are seeking a Research Associate with strong expertise in political science, human rights, or regional development to support our research projects. This role requires hands-on research, policy analysis, and publication work aligned with Asia Centre's focus areas. The ideal candidate is highly analytical, detail-oriented, and familiar with Southeast Asian political and social contexts.

Key Responsibilities

• Conduct desk-based research and field research on topics such as human rights, governance, democracy, climate policy, or social development in Asia.
• Collect, analyse, and synthesise qualitative and quantitative data from credible sources (government reports, academic publications, NGOs, and news media).
• Draft research reports, policy briefs, working papers, and academic articles that meet high-quality standards.
• Monitor developments in specific countries or thematic areas relevant to Asia Centre's projects.
• Support the design, organisation, and reporting of events, workshops, or roundtables related to research outputs.
• Collaborate with other researchers and staff to ensure alignment with project objectives.
• Assist with funding proposals, donor reports, and dissemination of research outputs.

Required Qualifications

• Master's degree in political science, international relations, law, human rights, public policy, or a closely related field.
• Minimum 2 years of relevant research experience in NGOs, think tanks, or academic institutions.
• Proven track record of producing research outputs, including reports, policy briefs, or publications.
• Strong analytical, writing, and editing skills; able to present complex ideas clearly.
• Familiarity with Southeast Asian political and social contexts is essential.
• Proficiency in English (written and spoken); additional regional language(s) are a plus.
• Experience in qualitative and quantitative research methods is highly desirable.
• Ability to work independently and meet deadlines under minimal supervision.

Preferred Attributes

• Knowledge of human rights, governance, or climate and social policy issues in Asia.
• Experience with data collection, interviews, or field research.
• Strong attention to detail and ability to critically evaluate sources.

What We Offer

• Meaningful work in an internationally recognised think tank.
• Exposure to regional policy networks and decision-makers.
• Collaborative and intellectually stimulating work environment.
• Opportunities to publish and present research at conferences or workshops.

How to Apply

Interested candidates should submit the following to:

1. A cover letter (max 1 page) explaining your motivation and relevant experience.
2. A CV (max 2 pages).
3. A recent writing sample (3–5 pages) demonstrating analytical and research skills.

Only shortlisted candidates will be contacted. More About Asia Centre visit

1. Job Purpose

1.1 This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations.

1.2 The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget.

2.Responsibilities

(a) Site management

• Study site selection, initiation (SIV) and clinical monitoring.

• Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.

• Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.

• Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.

• Track study recruitment to ensure recruitment target is achieved in all studies.

• Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating.

• Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.

• Assemble site specific EC submission dossier, and ensure submission to EC.

Training

• Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.

• Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements.

Documentation

• Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files.

• Prepare/complete study records' archiving according to protocol and sponsor requirements.

(b) Drug Safety

• Ensure safety information is disseminated to all sites according SOP and applicable regulations.

• Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations.

(c) Finance and Administration

• Finalize budget and obtain signed contract from site, prior to site initiation visit.

• Ensure Study Payment Schedule is executed and retain relevant documents/receipts.

(d) Study Tools and system

• Update and maintain Study tools/systems in a timely manner.

1. Qualifications

3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. The excellent candidates will not be restricted to the current requirements;

3.2 At least 2 year of CRA experience including experience in SSU part such as SSV, SSU (preparation submission package) and site monitor.

3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;

3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

Mahidol Oxford Tropical Medicine Research Unit (MORU)

Faculty of Tropical Medicine, Mahidol University

Position:  Research Scientist

Team structure

This post is based at the Malaria Laboratory of the Mahidol Oxford Tropical Medicine Research Unit (MORU). MORU is a collaboration between Mahidol University and the University of Oxford, principally funded by the Wellcome Trust. MORU conducts targeted clinical trials and public health research that aim to discover and develop appropriate, affordable interventions that measurably improve the health of people living in resource-limited parts of the world. MORU's Malaria Department focuses on approaches to malaria elimination, i.e. the genetics, biology and epidemiology of antimalarial drug resistance; the treatment of multidrug resistant falciparum malaria; pathobiology; treatment and management of severe falciparum malaria; radical treatment of vivax malaria and the development of a Plasmodium vivax Controlled Human Infection Model.

The successful candidate will work in collaboration with a senior postdoctoral researcher and be responsible for routine asexual and sexual malaria cell culture, biochemical and phenotypic antimalarial drug screening assays and in vitro antimalarial drug metabolism. They will contribute to data analysis and preparations of research manuscripts. In addition, there will be opportunities to join weekly scientific seminars and journal clubs across the MORU Tropical Health Network as well as participate in a variety of training courses.

A Research Scientist typically engages in advanced research and development within a specific field, such as biology, pathophysiology, pharmacodynamics, immunology etc.

The key responsibilities include:

• Contribute significantly to their field through innovative research and updates on advances in science and technology such as cell and tissue culture, cell biology, molecular biology

• Research Design: Developing experimental protocols and methodologies to explore scientific questions.

• Data Analysis: Analyzing data sets using statistical tools and techniques to derive meaningful conclusions.

• Publication: Writing and publishing research findings in peer-reviewed journals.

• Project Management: Leading research projects, scheduling, and resource management.

• Mentorship: Supervising and training junior researchers and students.

Essential

• Bachelor's, Master's, or PhD degree in Biology or a related subject, plus 1–3 years of previous research laboratory experience

• Previous experience with cell culture

• Experience with biochemical cell biology or biochemistry or general drug screening

• Ability to work independently

• Proven ability to contribute to the development of new lab protocols

• Good spoken and written English

• Excellent team player and open communication

• Critical thinking

Desirable

• Prior experience with in vitro malaria work

• Experience with independent data analysis

Terms & conditions

The post is based in Bangkok at the Mahidol Oxford Research unit ).

The salary will be based on MORU scales and will depend on experience and qualifications.

The salary package includes:

• 13th months of salary

• health and life insurance

• social Security

• provident Fund

• 20 days of annual leave

The successful applicant should have good communication skills. Interested applicants, please submit your application with detailed resumé to

Head of Malaria Laboratory

Kesinee Chotivanich

Mahidol-Oxford Tropical Medicine Research Unit (MORU)

Faculty of Tropical Medicine, Mahidol University

420/6 Rajvithi Road, Bangkok 10400

MORU's Commitment to Equity, Diversity, and Inclusion

MORU is committed to creating an inclusive culture and a respectful environment, and values diversity and promoting equity for all its members. MORU does not tolerate any form of harassment or victimisation and expects all members, visitors and contractors to treat each other with respect, courtesy and consideration. Successful candidates are expected to adhere to these standards and principles.

We are currently seeking a full-time, experienced Clinical Research Associate to join our Clinical Monitoring team in the Thailand. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company's success. If you are interested in an exciting career where you can use your expertise and develop and grow your career even further, then this is the opportunity for you.

Our culture is of expertise, and we empower our teams to employ their unique talents and experience to take an assertive approach to research, problem solving, and ultimately supporting our business partners. At Medpace, our employees embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return they are rewarded with interesting projects, career advancement, and recognition and exposure to our international footprint. These are just a few reasons why talented individuals join the Medpace team.

Through our PACE

Training Program, you will join other Professionals Achieving CRA Excellence and receive customized, expedited training, and efficient onboarding to familiarize experienced CRAs with Medpace systems.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
• Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
• Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
• Verification that the investigator is enrolling only eligible subjects;
• Regulatory document review;
• Investigational product/drug accountability and inventory;
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
• Assessing the clinical research site's patient recruitment and retention success and offering suggestions for improvement;
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

• Bachelor's degree with at least 2-4 years of Experience as a Clinical Research Associate;
• Must have a minimum of a bachelor's degree in a health or science related field;
• Proficient knowledge of Microsoft Office;
• Outstanding communication skills; and
• Must be detail-oriented and efficient in time management
• Demonstrated ability to independently function as a Lead CRA (on more complex studies as applicable), including the ability to effectively plan, delegate, and review the work of others;
• Demonstrated ability to present at meetings, including the ability to seek, make, and develop suggestions; and
• Knowledgeable enough about Clinical Monitoring practices and procedures to represent the function in internal and external (e.g., business development) meetings.

Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What To Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

About the role:

The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech, and Sponsor. Key responsibility of a CRA is as a site relationship manager ensuring that clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs.

Minimum Qualifications & Experience:

• Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate.
• Preferably experience of working in the research, pharmaceutical industry or a related field per job level as follows.
• At least 3-5 years of Clinical Research Associate experience in the Clinical industry.

Responsibilities:

• CRAs primary responsibility is to build relationships with Principal Investigators, study co-ordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited, and smooth management of clinical trials.
• Foster internal and external customer relationships to ensure focus on efficient, timely and productive project delivery as per study requirements and timelines.
• In collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start-Up Associate (RSA), prepare site essential documents, and support the ethics and regulatory submission and approval processes as needed.
• In collaboration with Regulatory Start-up (RSU) Team, understand the requirements of applicable local and international regulatory requirements as relevant to specific clinical trials.
• Ensure recruitment of participants as per the site target. Drive site recruitment and engagement initiatives and prepare site-specific recruitment plan(s) and update as required.
• Monitoring of investigational sites as per ICH GCP §5.18 (Monitoring) and the Clinical Monitoring Plan (CMP) for each study. This includes all monitoring visit types across all phases of a clinical trial including Site Selection, Site Initiation, Site Monitoring and Site Close Out, unblinded pharmacy visits, and co-monitoring visits. Visits can be conducted either onsite or remote as per CMP.

-Ensure the rights & wellbeing of trial participants are protected, including consent form checks, patient eligibility confirmation, protocol compliance, investigational drug compliance, and review of Adverse Events/SAEs.

-Ensure safety issues are reported to the sponsor promptly. ü Verify trial data are accurate and complete, ensure CRF data and queries are completed and resolved as per the study timelines documented in the Clinical Monitoring Plan.

-Ensure all study drug is appropriately stored, dispensed, accounted for, and reconciled as per the Clinical Monitoring Plan and the Protocol.
- In collaboration with IHCRA or DMA team, ensure the project Trial Master File (TMF) is up to date, current and complete always throughout duration of the study.
- Support sites to be always audit and inspection ready. · Ensure all clinical trial management systems are always current and up to date with all relevant trial data. · Provide written and verbal site updates (including monitoring visit reports) on study progress to the PM/LCRA according to the study requirements/timelines as documented in the Clinical Monitoring Plan and Sponsor/Novotech SOPs. Escalate all key issues as per Issue Escalation SOP. · Collaborate with IHCRA and Site Contract Associates, as applicable, on-site payments, taking ultimate responsibility on site payments to ensure payment execution as per term stated in Clinical Trial Agreement.
- Assist the PM with the development of study related project plans and templates as per study requirements and support tasks as needed for successful study execution. · Demonstrate a thorough understanding of ICH GCP, The Declaration of Helsinki, and any local guidelines as they apply to the investigator, sponsor, monitor, and IEC. · Be aware of and adhere to company processes in areas relevant to a CRA. Be quality focused on the performance of duties. Assist in the review and development of clinical SOPs and processes.
- Participate in activities of the Clinical Services Department, including presentations at clinical department meetings, and assisting with the development of clinical processes and SOPs.
- In collaboration with Business Development (BD), foster relationships with sites to provide feasibility information, as requested, and in accordance with documented feasibility processes. Highlight any BD opportunities to the group
- Understand the responsibilities of Novotech as a service provider in the pharmaceutical and biotech industry and ensure all communications with external and internal customers present a positive professional image of the company.
Senior CRA (SCRA) · Provide mentorship to junior staff and can also provide support to the line manager or project manager in the role of Lead Clinical Research Associate. · Provide the support on ad hoc visits and can be assigned to evaluate and assess junior CRA staff as needed. · Participate in activities of the Clinical Services department, including presenting at clinical department meetings, assisting with the development of clinical processes and SOPs. Identify areas of inefficiency in processes and make recommendations for improvements.

Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.

We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.

We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.

Overview:

IDC is seeking a Market Analyst to join the consumer device team. In this role, you will have the opportunity to work on several of IDC's device programs, including mobile phones, wearables, and personal computing devices. The candidate will be responsible for fieldwork interviews, analyzing data, and providing actionable recommendations to customers. The candidate should demonstrate the ability to ask inquisitive questions, interpret complex data from both quantitative and qualitative sources, and delivering meaningful insights.

Why IDC?

IDG is a dynamic and innovative data, research, and services company at the forefront of guiding the global technology market ecosystem. Our mission is to help companies grow by putting technology insights into action, and empowering businesses to make better decisions and thrive in the digital-first age.

Recruitment Fraud Notice: IDC would like to inform you that we conduct our formal communications via corporate email, our Applicant Tracking System iCIMS, LinkedIn messaging, or directly by phone. We do not use any other platform (including Telegram, WhatsApp, Signal, text, instant message, etc.) to communicate with prospective candidates. If you receive any communication outside of our formal communications channels, please ignore it and block the sender or caller. In addition, we do not ask candidates to provide sensitive personally identifiable information such as bank account or social security numbers. If you have been contacted by someone claiming to represent a job offer, please report it as potential job fraud to law enforcement.

Responsibilities:

• Conduct primary research to gather data on consumer devices sales trends while developing a network of industry contacts
• Evaluate competitive positioning in the industry and update databases with relevant data and findings
• Develop market forecasts by utilizing statistical methods and tools to anticipate future trends and consumer behavior
• Prepare detailed reports and presentations to communicate findings to stakeholders
• Ensure the timely and accurate delivery of all program deliverables
• Engage in marketing activities including media engagements where appropriate
• Collaborate with cross-functional teams to develop customized market models

Qualifications:

• Bachelor's degree or equivalent in finance/economics, statistics, or engineering with a strong understanding of economic principles and their application to market analysis
• 2+ years of work experience, preferably in the market research or technology industry. Experience or interest in the devices sector is a bonus.
• Capable of conducting primary research in Thai, particularly in-person interviews and an ability to build relationships over time
• Skilled in analyzing datasets and developing predictive models. Familiarity in statistical tools and methodologies is a bonus.
• High attention to detail in data creation, analysis, and report preparation
• Efficient in managing multiple research projects and meeting deadlines. Excellent in problem-solving while working in a team-based environment.
• Strong English written and verbal communication skills, preferably with presentation experience. Fluency in a second language, particularly Mandarin Chinese, Korean, or Japanese, is a bonus.
• Advanced Microsoft Excel and PowerPoint skills required. PowerBI, Python, and other technical skills are a bonus.
• Hybrid work model with occasional travel

IDC is an Equal Opportunity Employer. Applicants and employees are considered for positions and are evaluated without regard to mental or physical disability, handicap, race, color, religion, gender, gender identity and expression, ancestry, national origin, age, genetic.

ABOUT PERCEPTRA

Perceptra is the leading deep health tech startup in Thailand. Our aim is to develop an artificial intelligence platform for the healthcare industry. Our first product Inspectra CXR is currently the best AI software for chest x-ray analysis in the SEA market, with 8 deep learning services deployed on the cloud supporting Radiologists' workflow, through a website interface and API services connected directly to the hospital's IT systems. Today, our platform is actively used by 30+ hospitals nationwide.

ABOUT THE ROLE

Perceptra is Thailand's leading deep health tech startup, pioneering artificial intelligence solutions for the healthcare industry. Our flagship product, Inspectra CXR, is a state-of-the-art AI software for chest x-ray analysis, currently deployed in over 30 hospitals nationwide.

As a Research Assistant within our AI Research team, you will support the development and advancement of medical AI by assisting in data preparation, analysis, and experimentation. You will work closely with AI researchers, engineers, and clinicians to ensure high-quality research outcomes that contribute directly to improving healthcare through innovative AI technologies.

ROLES & RESPONSIBILITIES

• Assist in organizing, cleaning, annotating, and formatting medical imaging datasets to prepare for AI model development.
• Work closely with ML engineers to drive data analysis workflows, taking primary responsibility for data analysis through data visualization, pattern recognition, anomaly detection, and clinical expertise, while providing comprehensive summarization of findings to support model improvements
• Conduct literature reviews and maintain documentation of relevant academic papers in deep learning and medical imaging, while assisting with scientific manuscript preparation, submission processes, and IRB requests.
• Help design and conduct small-scale experiments and evaluations under the supervision of senior researchers.
• Write and maintain clear documentation, reports, and presentations to communicate research progress and findings.
• Lead automation initiatives for data processing, labeling, and testing activities by identifying needs and coordinating with ML engineers for tool development and maintenance in support of research objectives.
• Collaborate effectively with researchers, engineers, and healthcare professionals to streamline workflows and optimize research outcomes.
• Stay updated on new developments in AI and medical imaging to support continuous learning within the team.
• Independently manage personal workload and project timelines, proactively communicating capacity constraints or availability for additional responsibilities to ensure optimal team productivity.

QUALIFICATIONS & SKILLS

• Bachelor's degree in computer science, Data Science, Biomedical Engineering, or related fields; recent graduates are welcome to apply.
• Strong attention to detail with good organizational, time-management, and analytical skills.
• Ability to learn quickly, work independently, and collaborate within a multidisciplinary team.
• Good communication skills in English and/or Thai for documenting and sharing research progress.
• Proactive attitude with eagerness to support cutting-edge AI research in healthcare.
• Thai citizen only.

Preferred Qualifications

• Familiarity with Python programming and scripting for data processing is preferred but not mandatory.
• Basic understanding of deep learning concepts and medical imaging modalities is a plus.

BENEFITS AND PERKS

• Salary : depending on availability and performance. ~
• Life & health insurance package.
• Perks : computer budget, annual company retreat.
• Office close to BTS Thonburi.
• Work from home 1-3 days per week.