clinical research associate salary thailand

Average Clinical Research Associate (CRA) Salary in Thailand

The average annual salary of Clinical Research Associate (CRA) is THB 827,623.00

The starting salary of Clinical Research Associate (CRA) is between THB 516,545.00 and THB 607,700.00 whereas the maximum salary range is between THB 830,180.00 and THB 954,707.00.

• Currency : THB
• Annual Salary : THB 827,623.00
• Weekly Pay : THB 14,602.00
• Fortnightly Salary : THB 29,203.00
• Monthly Salary : THB 63,274.00

Clinical Research Associate (CRA) Salary Comparison by Gender

This pie chart demonstrates the gender share for Clinical Research Associate (CRA). As indicated, the golden colour represents the percentage share for women and the green represents the percentage share for men.

As shown via chart, female employees are involved 100% in contrast with male who possibly are not a part of this profession.

Prominent Skills Affecting Clinical Research Associate (CRA) Salary

The bar graph data indicates the importance of specific skills which can have a direct impact on Clinical Research Associate (CRA)'s salary. It clearly highlights the skills needed for a post of Clinical Research Associate (CRA) when hired by an employer. The skill that is required for Clinical Research Associate (CRA) is Clinical Research that affects the salary by 1%.

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Last updated: May 16, 2024

Clinical Research Associate Salary in Thailand

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THB 658,637

Explore our salary database, salary recap.

The average pay for a Clinical Research Associate is THB 658,637 a year and THB 317 an hour in Thailand. The average salary range for a Clinical Research Associate is between THB 463,681 and THB 798,927 . This compensation analysis is based on salary survey data collected directly from employers and anonymous employees in Thailand.

ERI's  compensation data  are based on  salary surveys  conducted and researched by ERI. Cost of labor  data in the Assessor Series are based on actual housing sales data from commercially available sources, plus rental rates, gasoline prices, consumables, medical care premium costs, property taxes, effective income tax rates, etc.

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Salary Potential

Estimated salary in 2029:, 5 year change:, shift differentials, calculate your shift differential, what is shift differential pay, about thailand, thailand cost of living score:, job summary.

• Designs, administers, researches, and studies designated clinical trials including investigator selection (who is responsible for the conduct of the trial at the trial site), analysis of potential patient recruitment, and preparation of trial related documentation, following company standard operating procedures and in accordance with Good Clinical Practice.
• Establishes, monitors throughout its duration, and closes down trial sites on completion of the trial.
• Coordinates with the ethics committee, which safeguards the rights, safety, and wellbeing of all trial subjects; and organizes ethics committee submissions with follow through to ensure successful outcome.
• Identifies and assesses the suitability of facilities to be used as the investigational/clinical trial site; sets up trial sites, which includes ensuring each center has the required trial materials, including the trial drug often known as the investigational medicinal product.

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Webinar recordings, stay up to date on hr news, clinical research associate, ฿646,312 (thb)/yr, ฿310.73 (thb) /hr, ฿14,413 (thb) /yr.

The average clinical research associate gross salary in Pattaya, Thailand is ฿646,312 or an equivalent hourly rate of ฿311. This is 2% lower (-฿10,672) than the average clinical research associate salary in Thailand. In addition, they earn an average bonus of ฿14,413. Salary estimates based on salary survey data collected directly from employers and anonymous employees in Pattaya, Thailand. An entry level clinical research associate (1-3 years of experience) earns an average salary of ฿466,149. On the other end, a senior level clinical research associate (8+ years of experience) earns an average salary of ฿803,180.

Data powered by ERI's Salary Expert Database .

This page is a promotion for SalaryExpert’s Assessor Platform and is not intended for professional use.

Professionals should subscribe to SalaryExpert’s Assessor Platform .

ERI’s compensation data are based on salary surveys conducted and researched by ERI. Cost of labor data in the Assessor Series are based on actual housing sales data from commercially available sources, plus rental rates, gasoline prices, consumables, medical care premium costs, property taxes, effective income tax rates, etc.

฿736,250 (THB)

Based on our compensation data, the estimated salary potential for Clinical Research Associate will increase 14 % over 5 years.

This chart displays the highest level of education for: Clinical Research Associate , the majority at 100% with bachelors.

Typical Field of Study: Community Organization and Advocacy

Pattaya, Thailand

The cost of living in Pattaya, Thailand is 1% less than the average cost of living in Thailand. Cost of living is calculated based on accumulating the cost of food, transportation, health services, rent, utilities, taxes, and miscellaneous.

Pattaya (Thai: พัทยา, RTGS: Phatthaya, pronounced [pʰát.tʰā.jāː] ) is a city in Eastern Thailand, the second-largest city in Chonburi province and the eighth-largest city in Thailand. It is on the east coast of the Gulf of Thailand, about 100 kilometres (62 mi) southeast of Bangkok, and has a population of 328,961 as of 2021. Pattaya City (Thai: เมืองพัทยา, RTGS: Mueang Phatthaya, pronounced [mɯ̄a̯ŋ pʰát.tʰā.jāː]) is a self-governing municipal area within, but not part of, Bang Lamung district and...

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Clinical Research Associate (CRA) ID:65942

50,000 THB ~ 75,000 THB

Job Description

【Job Summary】 CRA is responsible to ensure that the trial is conducted and documented properly by carrying out the following activities when relevant and necessary to the trial and the trial site in order to verify that: 〇The rights and well-being of human subjects are protected. 〇The reported trial data are accurate, complete, and verifiable from source documents. 〇The conduct of the trial is in compliance with the currently approved protocol/amendment(s), with GCP, and with applicable regulatory requirement(s). 【Responsibilities】 ‐ Acting as the main line of communication between company and the Thai investigator. - Communicate with study team and third-party vendors as needed. - Conduct site selection activities for verifying adequate qualifications. - Manage and monitor the responsible sites and ensure their quality appropriately, agreed cost spent and on a timely basis. - Manage the contracts of clinical trial with the responsible site and ensure the compliance with regulations and company-wide governance controls such as Ethical Interactions policy or company-legal standard. - Input appropriate information in order to create clinical trial related documents (ex. CSP, IND). - Ensure a steady implementation of supplying clinical site with study materials. - Provide Thai investigators and site staff with education and training regarding study specific procedures including EDC system. - Manage the patient recruitment status and request acceleration of patient recruitment for Investigators and site staff. - Conduct source data verification and ensure data quality to collect appropriate clinical study data. - If necessary, support sites to ensure sites understand and resolve data queries in a timely manner. - Ensure that essential documents and source data are appropriately stored in a clinical site. - Produce monitoring activity reports appropriately and in a timely manner. - Confirm and ensure status of GCP/ICH guidelines. - Report critical and/or serious issues relating to site management to the study team and line manager in a timely manner. - Participate in-house and/or external clinical trial related meeting (ex. Study team meeting, CRA’s meeting, Investigators’ meeting) including the preparations. - Cooperate with site audit in liaison with QA and a site inspection by regulatory authority. - Cooperate with resolving the result of SAE reconciliation.

Qualifications

Requirement.

【Must】 - Bachelor’s degree (or equivalent), preferably in biological science or discipline associated with clinical research - At least 2 years of CRA experience (negotiable) - Experience in Clinical Trial/ Clinical Research at University medical center, Pharmaceutical company or Drug Development Services company(CRO) - Good command of English 【Advantage】 - Top university would be advantage - Graduated from Life Sciences, Biotechnology or any replated fields - Over 2 years experience as Clinical Research Associate (CRA) - Good computer skills (especially in MS Excel and Power Point)

English Level

Level 3 - Business Level

Other Language

Additional information.

- Transporation: Paid actial(Maximum 2000THB/month) - OT - Social security - Medical insurance - Bonus (avarage 4 months) - Others

Working Hour

8:30 ~ 17:15

- Sat,Sun - Public holidays

Job Function

Other (Medical)

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- Visit customers and earn sales of medical products- Introduce products and making related documents such as quotation to expand market- Schedule and documentation about the above activities- Handle phone calls and emails from clients- Create products’ catalogs in Thai and English- Create quotation and other documents- Other administrative activities requested by the management team

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Thailand Clinical Research Associate

• Job type: Permanent
• Discipline: Clinical Research Associate (CRA)
• Location: Thailand

This vacancy has now expired. Please see similar roles below...

Proclinical is excited to announce a new vacancy for a home-based CRA role in Thailand . This is a great chance to join a passionate, innovative and committed team and make some positive contributions to medicine.

Job Responsibilities

• Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.
• Performs site qualification, site initiation, interim monitoring, site management and close-out visits, ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practices (GPP) and protocol compliance.
• Assesses factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
• Assesses site processes, Conducts Source Document Review of appropriate site source documents and medical records
• Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF).

Skills and Requirements

• Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment is essential.
• A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
• You will be educated to degree level in a life science discipline or be a licensed healthcare professional.

Please click on the Apply button.

In case you have difficulty in applying or if you have any questions, please contact Mandy Fang on [email protected] or upload your CV on our website - www.proclinical.com/send-cv

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Clinical Research Associate

• Location: Thailand
• Categories Clinical Monitoring
• __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
• __vacancyopjusttionswidget.opt-Remote Working __ Remote

About the role

This vacancy has now expired. please see similar roles below....

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

The responsibilities of the Clinical Research Associate include, but are not limited to:

• Conduct of clinical research activities independently in accordance to ICH GCP and SOP’s.
• Act in a lead role on a study, assuming additional responsibilities as detailed/documented by the PM, if appropriate
• Project coordination, planning and logistics, including overview of budget and timelines
• Effective Communication
• Recognize, exemplify and adhere to company’ values which center around our commitment to People, Clients and Performance.
• Ability and willingness to travel as and when required by the company.
• Participate in training and mentoring new staff up to Clinical Research Associate level as required
• Assist with marketing the company if and when appropriate
• Other duties as assigned
• Degree, Masters or PhD in Life Science, Nursing or Health Related
• Approximately, 3~ 4 years experience as a CRA (level 2 and 3) and special knowledge in a therapeutic area
• Strong knowledge of ICH-GCP and a strong interest in clinical research
• Professional use of the English language; both written and oral

Benefits of Working in ICON: 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. At 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. 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, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

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