7 Pharmaceutical jobs in Thailand

**Job Family:** Process Automation
**Req ID:**
Are you passionate about leveraging technology to transform manufacturing processes? We're looking for a **Senior Manufacturing Execution Systems Engineer** to join our team and drive digitalization initiatives across various industries. In this role, you'll be at the forefront of implementing cutting-edge solutions that optimize production, integrate systems, and enhance operational efficiency.
**You'll make a difference by:**
+ **Designing and proposing technical solutions:** You'll create and refine concepts for Manufacturing Execution Systems (MES) and other digital manufacturing opportunities, translating complex business needs into actionable technical designs.
+ **Defining detailed functional specifications:** You'll work closely with stakeholders to interpret business, process, and technical requirements, producing clear and comprehensive functional and design specifications (workflows, equipment classes, bill of material (BOM).
+ **Developing custom applications and integrations:** When necessary, you'll lead the development of specialized software, scripts, and interfaces to connect various systems like ERP and automation platforms.
+ **Leading testing and deployment activities:** You'll define test specifications, lead and participate in thorough testing, and oversee the successful deployment of engineered solutions at customer sites.
+ **Improving engineering processes and sharing knowledge:** You'll proactively identify opportunities to optimize our engineering processes for cost and quality, and share best practices through technical training.
+ **Providing expert technical guidance:** You'll serve as a key technical resource, advising engineers and project managers, clarifying requirements with customers, and actively seeking opportunities for project enhancement.
**Your defining qualities:**
+ **Proven software development expertise:** You have experience with various software development methods, programming languages (e.g., C#, Python, Java), and tools for designing, implementing, and testing systems.
+ **Strong database knowledge:** You're skilled in SQL database management and querying, with familiarity in other database tools such as Oracle, Postgres, MongoDB or MYSQL.
+ **Experience with web and integration technologies:** You have a solid understanding of front-end (e.g., JavaScript, HTML, CSS, JQuery, AngularJS, Bootstrap) and back-end development frameworks (e.g. NET, Web API), along with integration tools like REST API and XML.
+ **Prior experience in manufacturing software projects:** You have at least 3-5 years of proven experience in implementing Manufacturing Execution Systems (MES) or similar software solutions, ideally within process, pharmaceutical, or food and beverage industries.
+ **Good understanding of OT/IT development and integration frameworks:** You possess knowledge of how Operational Technology (OT) and Information Technology (IT) systems are developed and integrated, including relevant frameworks and protocols.
+ **Education:** Bachelor's degree in engineering, Computer Science, data/knowledge engineering or relevant field experience.
+ **Excellent problem-solving and analytical skills:** You can effectively analyze situations, anticipate problems, identify root causes, and develop practical, timely solutions.
+ **Strong collaborative and communication abilities:** You excel at working effectively within diverse teams, respecting others' contributions, contributing to collective decision-making, and communicating fluently in English.
**In return, we offer you**
+ **Flexible mobile working policy** that allows for time off for you to recharge and spend more time with your loved ones
+ **Attractive compensation and benefits**
+ **Values-driven work culture** with inclusive workplace policies and practices that prioritize diversity and inclusion
+ Endless **possibilities and opportunities** for progression and learning
**Recruitment Process:**
+ CV Screening
+ A session with our recruiter to understand your motivation & your past experiences
+ 1-3 Business Interviews
+ Offer Stage
**Transform the everyday with us!**
We value your unique identity and perspective and are fully committed to providing equitable opportunities and building a workplace that reflects the diversity of society. Come bring your authentic self and create a better tomorrow with us.
**Public Notice: Recruitment Fraud**
We wish to caution jobseekers that Siemens, as a policy, does not authorize external parties/agents to conduct employment drives or extend Offers of Employment on our behalf. We do not ask for bank details, payment of any kind nor personal financial information in return for assurance of employment. Please visit our job portal for all Siemens job openings, and apply via the portal.

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
**A Day in the Life**
Responsibilities may include the following and other duties may be assigned.
+ Provides oversight for the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and that the performance and quality of services conform to established internal and external standards and guidelines.
+ Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
+ Works directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.
+ Leads audit and inspection preparation, resolution of audit and inspection findings and liaises with auditing groups and inspectors through all stages of the audits.
+ Prepares reports and/or necessary documentation (ex Corrective and Preventative Actions) and provides to applicable stakeholders, both internal and external.
+ Co-ordinates legal requests in support of government investigations or litigations.
+ Ensures the quality assurance programs and policies are maintained and modified regularly.
+ Facilitates uniform standards worldwide and enables best practice sharing, thereby fostering the achievement of company's mission globally.
**SPECIALIST CAREER STREAM:** Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects - from design to implementation - while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education.
**DIFFERENTIATING FACTORS**
**Autonomy:** Entry-level individual contributor on a project or work team.
Works with close supervision.
**Organizational Impact:** Delivers work of limited scope, typically smaller, less complex projects or related activities.
**Innovation and Complexity:** Identifies, defines and addresses problems that are not immediately evident but typically not difficult or complex.
Makes minor changes in systems and processes to solve problems .
**Communication and Influence:** Communicates primarily with internal contacts within immediate group.
Contacts others to gather, confirm and convey information.
**Leadership and Talent Management:** N / A - job at this level is focused on self-development .
**Required Knowledge and Experience:** Requires broad theoretical job knowledge typically obtained through advanced education.
Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A), 0 years of experience required.
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
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Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care.
With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec's revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC).
To learn more please visit will be responsible for the regulatory activities for all Convatec products including product registration (new, renewal and amendment), product promotional activities, labeling review activities, product registration and listing database. The incumbent will provide other regulatory support as assigned by supervisor.
The responsible countries include Thailand and other South East Asia countries as assigned by supervisor.
**Key duties and responsibilities:**
+ Ensure regulatory compliance with local laws.
+ Prepare and submit documents to health authorities for product approvals.
+ Support regulatory strategy and update based on changes.
+ Handle post-approval activities and product lifecycle tasks (renewals, changes, listings).
+ Review and approve product changes, labeling, and promotional materials.
+ Communicate with health authorities to ensure timely approvals.
+ Participate in audits and support post market reporting.
+ Maintain regulatory databases and provide documents for reimbursement/tenders.
+ Stay updated on regulatory changes and inform relevant teams.
+ Collaborate with supply chain, marketing, and country manager on regulatory projects
**Skills & Experience:**
+ Bachelor's degree in related field or higher; RAC certification is a plus.
+ Minimum 3 years in medical device regulatory affairs.
+ Experience with regulatory submissions and quality systems.
+ Knowledge of GDPMDS and ISO13485 preferred.
+ Strong communication skills in English
At Convatec, we're pioneering trusted medical solutions to improve the lives we touch. If you're ready to make a real impact, apply today and help us bring our Forever Caring promise to life.
#LI-SA1
#LI-Hybrid
**Beware of scams online or from individuals claiming to represent Convatec**
A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.
If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you're unsure, please contact us at .
**Equal opportunities**
Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
**Notice to Agency and Search Firm Representatives**
Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
**Already a Convatec employee?**
**If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!**

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
+ Lead Allergan Aesthetic portfolio to ensure prioritized objectives that focus on the critical activities are successfully delivered on time and to quality.
+ Regulatory activities, including new product registrations, renewal registration, variations and maintenance of registered products, for Allergan Aesthetics with AbbVie's policies compliance.
+ Procedures are expected to meet statutory, quality and business requirements.
+ Develop regulatory strategies and provide regulatory assessment for submission and approval plan.
+ Responsible for review and approval of advertising/promotional material from regulatory perspective
+ Support business and cross functional teams from regulatory perspective.
+ Support maintenance of local SOPs and ensuring compliance with regulations.
+ Monitor emerging trends regarding industry regulations.
+ Other regulatory projects and tasks assigned by RA Head.
CORE JOB RESPONSIBILITIES
Product Registration and maintenance
+ Primary contact with Regulatory Authority in Thailand for responsible products.
+ Facilitate communication between Area Regulatory lead and the local regulatory authority.
+ Develop registration strategies, prioritizing assignments; implement regulatory plan and coordinate multiple projects and activities in accordance with strategic company objectives, annual plan and targets.
+ Ensure that the regulatory strategy is designed to deliver timely approval with desired labeling.
+ Execute manage new product submissions, line extensions, variations, renewal registration according to priorities and responses to deficiency letters. Ensure that the content comply with government regulations prior to submission to Regulatory Authority.
+ Keep up to date for product registration, variation, line extension and other related law & regulations knowledge.
+ Monitor and disseminate information on changes related to the Regulatory Authority Department: law & regulations affecting registration, manufacture, distribution and sale & marketing of Allergan Aesthetic products.
+ Liaise and negotiate with the relevant authorities to facilitate and secure expeditious regulatory approvals.
+ Provide regular registration status to RA Head.
+ Communicate regulatory issues and evaluate the impact on the business to management, Business Unit, where applicable.
+ Manage labelling changes, artwork development and artwork approval of packaging material components.
Business Support
+ Work cross-functionally as required to meet business needs.
+ Support local business teams in activities such as tenders, as required, from a regulatory perspective.
+ Review and provide input and approval on promotional materials, from regulatory perspective.
+ Provide regulatory input and support for marketing plans, product launches and other cross-functional activities.
+ Provide regulatory leadership as needed in product in-license/due diligence review, product divestment and product withdrawal.
+ Monitor the progress of marketing applications and provide management with a monthly registration status in (Sales & Operation Planning) S&OP meeting and during brand team meetings as applicable.
+ Implement regulatory activities in support of lifecycle management in line with business needs.
+ Collaborative with supply chain to ensure timely maintenance of product labels to ensure compliance to Abbvie requirements, and continuity in supply.
Processes
+ Maintain global systems and databases to ensure that all relevant regulatory information is updated.
+ Manage Allergan Aesthetic regulatory systems and SOPs to comply the corporate policy.
+ Lead or participate in projects to streamline RA processes to increase productivity, where applicable.
Compliance
+ Responsible for review and approval of advertising and promotional materials and campaign/events from regulatory perspective, collaborating with business partners.
+ Maintain good knowledge of relevant regulatory corporate policies and ensure compliance.
+ Update local SOPs and policies relevant to Regulatory Affairs to comply with AbbVie global SOPs & policies and Regulatory Authority requirements.
+ Provide timely and accurate input to regulatory assessments of products where requested.
+ Support sales and marketing colleagues by providing adequate and relevant regulatory information.
+ Hold pharmacist licence for company, if required and where applicable.
Regulatory Intelligence
+ Keep up to date for product registration, variation, line extension and other related law & regulations knowledge.
+ Keep abreast of changes in the regulatory environment to assure accuracy and effectiveness in regulatory submissions.
+ Monitor on changes related to the Regulatory Authority on law & regulations affecting registration, manufacture, distribution, and sale & marketing of AbbVie products.
+ Maintain an awareness of country's regulatory legislation and assess its impact on AbbVie's business
People/Contractor Management (where applicable)
+ Lead and provide guidance to team member/contractor to prioritize and meet target goals and objectives in a timely manner
Qualifications
+ University degree in Pharmacy or Pharmaceutical Science, or related disciplines.
+ At least 7 years of regulatory experience in the pharmaceutical industry and/or medical device industry. Knowledge of Thailand regulations in medical device. Pharmaceutical knowledge would be an added advantage.
+ Excellent analytical skills and ability to think strategically with local, regional, and global perspectives.
+ High affinity in regulatory affairs intelligence with strong ability to provide sound advices and suggestions to the team.
+ Ability to manage cross-functional team to achieve the goals and objectives with excellence of interpersonal skills, enthusiastic and a team player with positive attitude.
+ Result oriented, agility and ability to work in a fast-paced environment
+ Strong communication skills - both oral and written and proficiency in English and Thai to su the market requirements.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
This position is responsible for:
+ Current and upcoming Medical Aesthetics portfolios and their associate indications.
+ Own and drive Key Opinion Leaders (KOL) engagement
+ Lead scientific exchange with HCPs and report/advise cross-functional team on future medical activities
+ Advise and share feedback on brand strategy, development of tactical planning in collaboration with brand team in marketing department
+ Contribute to the total competency of the Medical Affairs, not limited to technical aspects.
+ Contribute towards medical-marketing messaging and approval procedures required.
Position Overview
+ Develops and maintains professional relationships with internal and external customers to provide comprehensive medical and scientific support to Allergan initiatives in assigned therapeutic areas.
+ Executes against the Medical Affairs plan for Thailand.
+ Provides scientific education and training initiatives across Allergan Aesthetics portfolio.
+ Performs field visits with key physicians and stakeholders, organizing advisory board meetings, facilitating clinical trials, and serving as the medical resource for both external and internal stakeholders.
+ This position is a non-promotional role. The primary focus is providing Healthcare Professionals with fair and balanced scientific information.
+ Facilitates information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies in development or commercialized by Allergan. Works closely with other Allergan personnel to ensure information, education, and research needs of healthcare professionals are met and to ensure scientific and technical training needs of commercial organizations are identified and met.
Key duties and responsibilities:
Business Planning:
+ Work closely with the Commercial counterparts and leaders, Scientific and Medical Affairs manager, and Associate Dir, Medical Affairs to set priorities, and activities.
+ Develop strategies and Tactics for Medical Aesthetics portfolio and implement/execute them within timely manner to align to commercial strategies as budgeted.
+ Demonstrate ownership and initiative in identifying opportunities for improvement within Medical Affairs activities.
+ Develop and maintain awareness and understanding of competitor issues/intelligence.
+ Contribute to the development of and maintain competitiveness and growth within the market and communicate intelligence to the commercial team as appropriate.
Internal Training:
+ Facilitate training to Allergan field sales teams and others to ensure up-to-date knowledge of Allergan's Aesthetic products, relevant disease states and conditions.
+ Provide interpretation and perspective to competitor activities.
+ Assist in the evaluation of sales team members' skill and knowledge.
+ Assist in the development of training materials, exams and evaluative process for field sales teams.
External Training and Education:
+ Through field visits, improve doctors' awareness of Allergan's Aesthetic products. Share scientific data supporting their use, train professionals in their proper use, and develop physician's expertise and comfort in prescribing their use.
+ Work closely with the commercial team to facilitate training to physicians and provide proper engagement to thought leaders and doctors externally. Help shape the company's leadership image within the specialty area.
+ Ensure the future success of Allergan by identifying doctors-in-training with specialty interests which lie within the company's therapeutic range and fostering relationships through educational initiatives.
+ Provide scientific and clinical information to Healthcare Professionals on request.
Thought Leadership:
+ Identify key researchers and physicians critical to the knowledge base and disease awareness relevant to the success of each of Allergan's Aesthetic products in the specialty area.
+ Facilitate greater understanding of medical practice patterns, educational and training needs; organize local activities with the key stakeholders.
+ Present and communicate Allergan's scientific perspective and vision at customer meetings; plan meeting agendas with key stakeholders; interpret feedback and results.
+ Ensure the maintenance of key relationships with physicians and administrators of specialty societies.
Phase IV trials/Clinical Studies:
+ Identify and prioritize phase IV and investigator-initiated study needs; ensure that the approval process and execution of all phase IV and IITs follow Allergan guidelines and policies.
Pharmacovigilance/Compliance:
+ Responsible for providing support to Local Safety Officers (LSOs) on local PV issues and actions as required. Liaises with Regional PV Lead (RPL) on which support is needed e.g. assistance in product safety issues, HA inspections/audits, CAPAs, and training activities as required
Clinical Expertise:
+ Keep up-to-date on the status of the scientific developments in the specialty areas within own country, Asia-Pacific and globally.
+ Attend key relevant medical congresses locally, and as required, internationally for the purpose of extending medical knowledge, supporting the commercial team with medical expertise, establishing new business relationships, and strengthening existing relationships.
Qualifications
Educational Qualifications:
+ Strong preference for candidates with a medical degree (MD), advanced degree in science (PhD), or other healthcare-related credentials (e.g., PharmD, RN, DNP, or equivalent clinical qualification). Candidates with master's/bachelor's degree in a scientific or healthcare discipline can be considered in certain cases.
Relevant experience:
+ Minimum of 2 - 5 years of experience in the pharmaceutical industry, with specialized therapeutic area expertise.
+ Related specialist or experienced in medical aesthetics therapeutic area is preferred.
+ Medical affairs experience in various activities such as advisory board management, publication, and other scientific exchange.
+ Good understanding of domestic market.
+ Experience in establishing strong influential relationships with KOLs.
+ Good understanding on multinational culture and ways of working.
Essential Skills, Experience, and Competencies:
+ Good leadership skills and able to persuade at all levels within the organization (including Commercial team) as well as with external customers (KOLs, HCPs, etc.)
+ Strong presentation and interpersonal communication skills along with a positive attitude on learning.
+ Demonstrates agility and resilience, comfortable with change and ambiguity.
+ Strong problem-solving skills and an innovative mindset.
+ Highly self-driven with a track record of proactively acquiring new skills and knowledge in fast-paced environments.
+ Thinking strategically and being able to develop and execute plans at country level. Specifically, able to understand in-depth knowledge and clinical aspects of medical aesthetics.
+ Excellent presentation skills, strong interpersonal skills.
+ Able to engage HCPs and communicate effectively with them as well as medical institution and/or association.
+ Comply to all business ethics and all applicable regulations to secure personal credibility and integrity as well as Allergan
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

As a
**In-House Clinical Research Associate**) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

**Country: Thailand**

**What you will be doing**:

- EC Submission
- TMF upload & managing binders
- Supporting CRAs & CTMs with clinical research related administrative work

**You are**:

- Holds more than 1 year of CTA experience
- Holds EC Submission expereince
- Independant & resonsible
- English & Thai

**Why ICON?**

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.