3,582 Research Associate jobs in Indonesia
Remote Scientific Research Associate
76111 Balikpapan, East Kalimantan
IDR17000000 month
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Posted 4 days ago
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Job Description
Our client is seeking a dedicated and meticulous Remote Scientific Research Associate to contribute to groundbreaking research and development initiatives. This is a fully remote position, allowing you to conduct your work from anywhere. You will be responsible for designing and executing experiments, collecting and analyzing data, and contributing to the interpretation of research findings. Your duties will include performing literature reviews, developing experimental protocols, preparing research reports, and maintaining detailed laboratory notebooks (digitally). You will collaborate closely with senior scientists and researchers through virtual platforms, sharing insights and contributing to project planning. Proficiency in statistical analysis software, data visualization tools, and relevant scientific databases is essential. The ideal candidate will possess a strong foundation in scientific principles within their field, excellent analytical and problem-solving skills, and exceptional attention to detail. You must be a self-starter, capable of working independently, managing your time effectively, and meeting project deadlines in a remote setting. A Bachelor's or Master's degree in a relevant scientific discipline such as Biology, Chemistry, Physics, or a related field is required. Experience in a research environment, including data analysis and scientific writing, is highly valued. We are looking for an inquisitive and motivated individual who is passionate about scientific discovery and eager to contribute to innovative projects. Your ability to meticulously document and report research findings will be crucial for the success of our R&D efforts. This role offers an exciting opportunity to engage in cutting-edge research without the constraints of a traditional laboratory setting.
Responsibilities:
Qualifications:
Responsibilities:
- Design and conduct scientific experiments according to established protocols.
- Collect, analyze, and interpret research data using statistical methods.
- Perform comprehensive literature reviews to support research projects.
- Maintain accurate and detailed digital records of experiments and findings.
- Collaborate with research teams via virtual communication platforms.
- Prepare research reports, presentations, and publications.
- Stay current with scientific advancements and methodologies in the field.
- Assist in the development of new research methodologies and techniques.
- Contribute to the overall research strategy and project planning.
Qualifications:
- Bachelor's or Master's degree in Biology, Chemistry, Physics, or a related scientific field.
- Previous experience in scientific research or laboratory work.
- Proficiency in data analysis software (e.g., R, SPSS, Python for data science).
- Strong understanding of scientific methodologies and experimental design.
- Excellent analytical and critical thinking skills.
- Strong written and verbal communication skills for remote collaboration.
- Ability to work independently and manage research tasks efficiently.
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0
Clinical Research Associate
17111 Purwakarta, West Java
IDR12 month
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Posted 2 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated Clinical Research Associate (CRA) to join their dynamic team in Bekasi, West Java, ID . This is a vital, on-site role focused on ensuring the smooth and effective execution of clinical trials according to Good Clinical Practice (GCP) guidelines and regulatory standards. The CRA will be responsible for monitoring clinical trial sites, ensuring data integrity, patient safety, and protocol adherence. This includes performing site initiation visits, routine monitoring visits, and close-out visits, as well as verifying source data against the case report forms (CRFs). You will play a crucial role in managing relationships with principal investigators and site staff, providing essential training, and addressing any protocol-related queries or issues that arise. The ideal candidate will have a Bachelor's or Master's degree in a life science, nursing, or a related field, along with a proven track record of experience in clinical trial monitoring. Strong understanding of ICH-GCP, FDA regulations, and local regulatory requirements is paramount. Excellent organizational skills, meticulous attention to detail, and the ability to manage multiple priorities effectively are essential. You must be adept at problem-solving and possess strong interpersonal and communication skills to build and maintain positive relationships with clinical sites and internal stakeholders. The ability to travel to trial sites regularly is a requirement for this position. This role offers an excellent opportunity to contribute to the advancement of life-saving medicines and therapies within a reputable organization dedicated to improving global health. Join a team committed to excellence in clinical research and make a significant impact on patient well-being.
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1
Clinical Research Associate
30114 Palembang, South Sumatra
IDR18000000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is looking for a diligent and organized Clinical Research Associate (CRA) to join our expanding remote team. This role is vital in supporting the execution of clinical trials, ensuring data integrity, patient safety, and compliance with regulatory standards. As a fully remote CRA, you will be responsible for monitoring study sites, verifying data accuracy through source data verification (SDV), and ensuring adherence to protocols and Good Clinical Practice (GCP) guidelines. Your duties will include site initiation visits, routine monitoring visits, and site closure visits, all conducted virtually or at the designated sites as required by the study protocol. You will serve as the primary point of contact for investigative sites, providing guidance and support to study coordinators and investigators. Building and maintaining strong relationships with site personnel is crucial for successful trial conduct. This position requires meticulous attention to detail in managing trial documentation, including Investigator Site Files (ISFs) and clinical study reports. You will also play a key role in identifying and resolving site-level issues, escalating them when necessary, and ensuring corrective actions are implemented effectively. A strong understanding of pharmaceutical drug development processes and various therapeutic areas is highly desirable. The ideal candidate will possess excellent written and verbal communication skills, proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems. A Bachelor's degree in a life science, nursing, or a related field, along with at least 2-3 years of direct CRA experience, is mandatory. This remote-first position offers the flexibility to work from any location within Indonesia, with occasional travel to clinical trial sites as needed.
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2
Clinical Research Associate
25132 Padang, West Sumatra
IDR9000000 month
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Posted 3 days ago
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Job Description
Our client, a prominent pharmaceutical research organization, is seeking a meticulous and organized Clinical Research Associate (CRA) to contribute to groundbreaking drug development. This is a fully remote position, allowing you to conduct vital research activities from anywhere. The CRA will be instrumental in ensuring the smooth execution of clinical trials, adhering to strict regulatory guidelines and ethical standards. Your primary responsibilities will include monitoring clinical trial sites, ensuring data integrity, and verifying compliance with study protocols and Good Clinical Practice (GCP) guidelines. You will liaise directly with investigators, study coordinators, and other site personnel to facilitate trial operations. This role demands extensive travel to clinical sites (though the core work is remote), for monitoring and essential oversight activities. Qualifications include a Bachelor's degree in a life science, nursing, or a related field, with a minimum of three years of experience as a CRA or in a similar clinical research role. A thorough understanding of FDA regulations, ICH-GCP, and clinical trial methodologies is essential. Excellent written and verbal communication skills are required, along with strong organizational abilities and the capacity to manage multiple tasks efficiently. You must be adept at problem-solving and possess a keen eye for detail to ensure the accuracy and completeness of trial data. The ability to work independently, manage your time effectively, and maintain a high level of professionalism in all interactions is crucial. This remote opportunity offers the chance to be at the forefront of pharmaceutical innovation, contributing to the development of new therapies that improve patient lives, all while working in a flexible environment. Join our client's dynamic team and advance your career in clinical research.
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3
Clinical Research Associate
34114 Bandar Lampung, Lampung
IDR8000000 month
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Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a detail-oriented Clinical Research Associate to join their operations in Bandar Lampung, Lampung, ID . This role involves overseeing and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures, and regulatory requirements. You will be responsible for site selection, initiation, monitoring, and close-out visits to ensure data integrity and patient safety. The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) guidelines and relevant regulatory frameworks. Excellent organizational skills, a meticulous approach to data management, and the ability to travel to clinical sites within Bandar Lampung, Lampung, ID and surrounding areas are essential. You will also be tasked with training site staff on study protocols and ensuring compliance. This position requires strong analytical skills to review clinical trial data and identify any discrepancies or issues. Your ability to communicate effectively with investigators, site staff, and internal stakeholders will be critical to the success of the trials. A background in life sciences or a related field, along with prior experience in clinical research, is highly preferred. You will play a vital role in bringing new pharmaceutical products to market, contributing to advancements in healthcare.
Responsibilities:
Qualifications:
Responsibilities:
- Monitor clinical trial sites to ensure compliance with protocols and regulations.
- Perform site initiation, routine monitoring, and close-out visits.
- Verify accuracy and completeness of clinical data.
- Manage and resolve data queries.
- Ensure adherence to Good Clinical Practice (GCP) standards.
- Train site personnel on study procedures.
- Liaise between investigators, site staff, and the study team.
- Prepare monitoring visit reports.
- Ensure all study-related documentation is maintained.
Qualifications:
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related field.
- Proven experience as a Clinical Research Associate or in a similar role.
- In-depth knowledge of clinical trial processes and GCP guidelines.
- Strong understanding of regulatory requirements.
- Excellent attention to detail and analytical skills.
- Proficiency in clinical trial management software.
- Ability to travel to clinical sites.
- Effective communication and interpersonal skills.
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate
76112 Balikpapan, East Kalimantan
IDR9 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a leading innovator in the pharmaceutical industry, is looking for a diligent and experienced Clinical Research Associate (CRA) for a fully remote position. You will be instrumental in the planning, execution, and monitoring of clinical trials across various therapeutic areas, contributing to the development of life-saving medications. Your core responsibilities will include site selection and initiation, ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements, and monitoring subject recruitment and retention. You will conduct regular site visits (virtual or on-site as needed, but primarily remote coordination) to assess the progress of clinical trials, verify data accuracy, and ensure patient safety. This role requires a meticulous approach to documentation, including source data verification and source document review. You will serve as the key liaison between the sponsor, research sites, and ethics committees, fostering collaborative relationships and resolving any issues that may arise. The ideal candidate will possess strong analytical and problem-solving skills, with the ability to interpret complex data sets. Excellent organizational skills and the capacity to manage multiple projects concurrently are essential, given the remote nature of this role. You must be proficient in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems. A Bachelor's degree in a life science, nursing, or a related field is required, along with a minimum of 2-3 years of direct CRA experience. Knowledge of regulatory frameworks such as ICH-GCP is paramount. This position offers the opportunity to work with cutting-edge research and make a significant contribution to advancing global health from the comfort of your home.
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5
Clinical Research Associate
29431 Batam, Riau Islands
IDR14000000 month
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Posted 4 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join their fully remote team. This role is vital in supporting the planning, execution, and monitoring of clinical trials to ensure data integrity and patient safety. The ideal candidate will have a strong background in clinical research and a proven ability to manage studies effectively from a distance.
Key Responsibilities:
Qualifications:
This exciting remote opportunity for a CRA is based in **Batam, Riau Islands, ID**. Our client offers a competitive compensation package and the chance to contribute to life-saving pharmaceutical research.
Key Responsibilities:
- Conduct site initiation visits, interim monitoring visits, and close-out visits according to protocol and regulatory requirements.
- Monitor clinical trial progress and ensure compliance with Good Clinical Practice (GCP) and other applicable regulations.
- Verify the accuracy, completeness, and quality of clinical data through source data verification.
- Manage trial-related documentation and essential regulatory documents.
- Serve as a primary contact for investigative sites and provide ongoing support to study staff.
- Ensure timely resolution of data queries and protocol deviations.
- Prepare monitoring reports and communicate findings to the study team and management.
- Identify and report adverse events and safety issues promptly.
- Manage investigational product accountability at clinical sites.
- Facilitate communication between investigators, site staff, and the sponsor.
- Ensure sites are adequately supplied with study materials.
- Maintain strong relationships with clinical investigators and site personnel.
- Contribute to the development of clinical trial protocols and study plans.
- Stay current with regulatory guidelines and industry best practices in clinical research.
- Support the review and archiving of study-related documents.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate (CRA) or in a similar clinical trial monitoring role.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Proven ability to conduct site monitoring visits, including initiation, interim, and close-out visits.
- Strong skills in source data verification and regulatory document management.
- Excellent written and verbal communication skills.
- Exceptional organizational and time-management skills, with the ability to manage multiple sites and priorities remotely.
- Proficiency in Microsoft Office Suite.
- Ability to work independently with minimal supervision and as part of a virtual team.
- Strong problem-solving and critical-thinking abilities.
- Detail-oriented with a commitment to accuracy and quality.
- Travel may be required occasionally, but the role is primarily remote.
This exciting remote opportunity for a CRA is based in **Batam, Riau Islands, ID**. Our client offers a competitive compensation package and the chance to contribute to life-saving pharmaceutical research.
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6
Clinical Research Associate
10110 Jakarta Pusat, Jakarta
IDR13 month
WhatJobs
Posted 4 days ago
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Job Description
Our client, a leading pharmaceutical company based in **Jakarta, Jakarta, ID**, is actively seeking a highly qualified Clinical Research Associate (CRA) to join their dedicated clinical development team. This hybrid role requires a balance of on-site monitoring and remote data management, offering a dynamic career path in pharmaceutical research. As a CRA, you will play a crucial role in ensuring the quality and integrity of clinical trials, adhering to regulatory requirements and company protocols.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct site initiation, interim, and close-out visits for clinical trials in accordance with clinical trial protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Monitor clinical trial activities to ensure patient safety, data accuracy, and protocol compliance.
- Verify the accuracy and completeness of source documents and case report forms (CRFs).
- Manage communication between study sites and the sponsor, addressing any queries or issues that arise.
- Ensure adherence to study protocols, standard operating procedures (SOPs), and applicable regulatory guidelines.
- Maintain accurate and timely documentation, including site visit reports and essential trial documents.
- Identify and report adverse events and deviations from protocol.
- Train and mentor site staff on study-specific procedures and data collection.
- Participate in Investigator Meetings and other relevant training sessions.
- Collaborate with data management, regulatory affairs, and other functional groups to ensure successful trial execution.
- Track study progress and identify potential risks or challenges, implementing mitigation strategies as needed.
- Ensure proper drug accountability and storage at investigational sites.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials in Indonesia.
- Experience with various therapeutic areas is desirable.
- Proficiency in clinical trial management software (CTMS) and electronic data capture (EDC) systems.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills, with meticulous attention to detail.
- Ability to travel to clinical trial sites as required (up to 50% travel).
- Adaptability to work effectively in both remote and on-site environments.
- Professional certifications (e.g., ACRP, SoCRA) are a plus.
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7
Clinical Research Associate
28111 Pekanbaru, Riau
IDR9500000 month
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Posted 4 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated Clinical Research Associate to support their groundbreaking research efforts in Pekanbaru, Riau, ID . This hybrid role will involve both field visits to study sites and remote administrative tasks. The Clinical Research Associate will be responsible for monitoring clinical trials to ensure compliance with protocols, regulations, and good clinical practice (GCP) guidelines. You will perform site visits to assess patient recruitment, data accuracy, and regulatory compliance. Key duties include verifying source documentation, ensuring proper drug accountability, and managing study-related files and correspondence. The role involves establishing and maintaining communication with investigators and site staff, resolving any issues that arise during the trial, and ensuring timely completion of study milestones. You will also be responsible for preparing study-related documents, including monitoring visit reports and essential regulatory documents. Required qualifications include a Bachelor's degree in a life science, nursing, or related field. A minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial role is essential. Strong knowledge of ICH-GCP guidelines and local regulatory requirements is mandatory. Excellent organizational, communication, and interpersonal skills are required, along with the ability to travel to study sites as needed. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a plus. This is an excellent opportunity to contribute to the development of life-saving therapies within a collaborative and supportive environment.
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8
Clinical Research Associate
20152 Medan, North Sumatra
IDR12000000 month
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to advancing healthcare through innovative research and development, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their team in Medan, North Sumatra, ID . This role is fundamental to ensuring the successful execution of clinical trials, adhering strictly to Good Clinical Practice (GCP) guidelines, regulatory requirements, and company protocols. As a CRA, you will be responsible for monitoring clinical trial sites, ensuring accurate data collection, patient safety, and protocol compliance. Your duties will include conducting site initiation visits, routine monitoring visits, and close-out visits, as well as verifying source documentation against case report forms (CRFs). You will also be responsible for training site personnel, resolving data queries, and ensuring timely submission of study-related documents. The ideal candidate possesses a strong understanding of clinical trial processes, excellent organizational skills, and a keen eye for detail. Experience as a nurse, medical assistant, or in a related healthcare role is highly beneficial. This position requires significant travel to clinical sites within the designated region and requires your presence on-site. The ability to build strong working relationships with investigators and site staff is crucial for success.
Key Responsibilities:
Key Responsibilities:
- Monitor assigned clinical trial sites to ensure adherence to GCP, protocol, and regulatory requirements.
- Verify the accuracy, completeness, and integrity of clinical data.
- Conduct site initiation, routine monitoring, and close-out visits.
- Ensure proper study documentation is maintained at the trial sites.
- Train site staff on study protocols, procedures, and data collection.
- Resolve data discrepancies and queries in collaboration with site personnel.
- Oversee patient safety and report adverse events according to protocol.
- Manage the investigational product accountability at study sites.
- Liaise with investigators, study coordinators, and other site staff.
- Ensure timely submission of all study-related documentation.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical research role.
- In-depth knowledge of GCP, ICH guidelines, and clinical trial methodologies.
- Experience with electronic data capture (EDC) systems.
- Strong understanding of medical terminology and disease processes.
- Excellent organizational and time management skills.
- Proficiency in written and verbal communication in Bahasa Indonesia and English.
- Ability to travel regularly to clinical trial sites.
- Detail-oriented with strong problem-solving capabilities.
- Ability to work independently and manage a site workload effectively.
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