6,490 Medical Research jobs in Indonesia
Clinical Research Scientist
60211 Balikpapan, East Kalimantan
IDR18000000 Annually
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Posted 6 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly motivated and experienced Clinical Research Scientist to join their dynamic team. This role offers a hybrid work arrangement, combining the flexibility of remote work with essential in-person collaboration. The Clinical Research Scientist will play a vital role in the design, execution, and interpretation of clinical trials, contributing to the development of innovative new therapies. You will be responsible for overseeing various aspects of clinical research projects, ensuring adherence to scientific rigor, ethical standards, and regulatory requirements. Key responsibilities include developing study protocols, designing case report forms (CRFs), and managing data collection and analysis. You will collaborate closely with cross-functional teams, including biostatistics, medical affairs, and regulatory affairs, to ensure the successful progression of clinical development programs. The ideal candidate will possess a Ph.D. or Master's degree in a relevant scientific discipline (e.g., Pharmacy, Biology, Medicine) with a minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry. Strong knowledge of clinical trial design, GCP guidelines, and regulatory submission processes is essential. Excellent scientific writing, analytical, and communication skills are required, along with the ability to interpret complex scientific data. You should be adept at problem-solving and possess a strong understanding of drug development processes. Responsibilities encompass:
- Designing and developing clinical trial protocols and study plans.
- Overseeing the execution of clinical trials, ensuring compliance with GCP and regulatory guidelines.
- Managing data collection, monitoring, and analysis to ensure data integrity.
- Interpreting clinical data and contributing to the preparation of study reports and publications.
- Collaborating with internal and external stakeholders, including investigators, site staff, and regulatory agencies.
- Providing scientific expertise and guidance on clinical development strategies.
- Evaluating and selecting appropriate endpoints and biomarkers for clinical studies.
- Contributing to the preparation of regulatory submissions and scientific presentations.
- Staying abreast of scientific advancements and emerging trends in relevant therapeutic areas.
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Clinical Research Scientist
50241 Semarang, Central Java
IDR18000000 Annually
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Posted 7 days ago
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Job Description
Our client, a leading pharmaceutical innovator based in **Semarang, Central Java, ID**, is seeking a highly skilled and dedicated Clinical Research Scientist to join their growing research and development team. This hybrid role offers the flexibility of working both remotely and from our state-of-the-art facilities, allowing for optimal collaboration and scientific exploration. The successful candidate will be instrumental in designing, executing, and analyzing clinical trials, contributing significantly to the advancement of novel therapeutics. Your responsibilities will include developing clinical trial protocols, overseeing study conduct, ensuring compliance with regulatory guidelines (GCP, ICH), and interpreting complex data sets. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management, to ensure the successful progression of clinical programs. Key duties involve identifying potential risks and challenges in trial execution, implementing mitigation strategies, and preparing comprehensive study reports. The ideal candidate will possess a strong scientific background, excellent analytical and problem-solving skills, and a proven track record in clinical research. A Ph.D. or Master's degree in a relevant life science discipline (e.g., Pharmacology, Biochemistry, Molecular Biology) is essential. Prior experience in a pharmaceutical or biotechnology setting is highly desirable. You should be proficient in data analysis software and possess exceptional written and verbal communication skills. The ability to work independently and as part of a team, coupled with a meticulous attention to detail, is critical for success in this role. This is a unique opportunity to contribute to groundbreaking medical research and development within a supportive and innovative environment. The role requires a proactive approach to scientific inquiry and a commitment to achieving research excellence. The candidate will be expected to stay abreast of the latest scientific literature and industry trends, bringing fresh perspectives to ongoing projects. We are looking for individuals who are passionate about making a difference in patient care through scientific discovery.
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1
Clinical Research Scientist
41111 Bekasi, West Java
IDR18000000 Annually
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Posted 8 days ago
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Job Description
Our client is seeking a highly motivated and experienced Clinical Research Scientist to join their innovative pharmaceutical team. This is a fully remote position, allowing you to contribute to groundbreaking research from the comfort of your home office. You will play a critical role in the design, execution, and analysis of clinical trials, ensuring adherence to regulatory standards and scientific integrity. The ideal candidate will have a strong background in clinical pharmacology, experimental design, and data interpretation within the pharmaceutical industry.
Key responsibilities will include:
Qualifications for this role include a PhD or PharmD degree in a relevant scientific discipline (e.g., pharmacology, biology, medicine), coupled with a minimum of 5 years of hands-on experience in clinical research within the pharmaceutical or biotechnology sectors. A proven track record of successful clinical trial management and regulatory interactions is essential. Exceptional written and verbal communication skills are required, along with strong critical thinking and problem-solving abilities. The ability to work independently and collaboratively in a remote team environment is paramount. This remote role offers a unique opportunity to significantly impact patient lives through innovative pharmaceutical research.
Key responsibilities will include:
- Designing and developing clinical trial protocols, including study objectives, endpoints, and statistical considerations.
- Overseeing the day-to-day operational aspects of clinical studies conducted across multiple sites.
- Collaborating with internal and external stakeholders, including investigators, site staff, regulatory authorities, and CROs.
- Analyzing clinical trial data, interpreting results, and contributing to the preparation of study reports, manuscripts, and regulatory submissions.
- Ensuring compliance with Good Clinical Practice (GCP), ICH guidelines, and other relevant regulations.
- Evaluating the safety and efficacy of investigational medicinal products.
- Contributing to the development of scientific and clinical strategy for assigned drug development programs.
- Staying abreast of the latest scientific literature, industry trends, and regulatory developments in pharmaceutical research.
- Mentoring and providing guidance to junior research staff.
Qualifications for this role include a PhD or PharmD degree in a relevant scientific discipline (e.g., pharmacology, biology, medicine), coupled with a minimum of 5 years of hands-on experience in clinical research within the pharmaceutical or biotechnology sectors. A proven track record of successful clinical trial management and regulatory interactions is essential. Exceptional written and verbal communication skills are required, along with strong critical thinking and problem-solving abilities. The ability to work independently and collaboratively in a remote team environment is paramount. This remote role offers a unique opportunity to significantly impact patient lives through innovative pharmaceutical research.
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2
Clinical Research Scientist
16111 Bogor, West Java
IDR15000000 Annually
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Posted 8 days ago
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Job Description
Our client is actively searching for a talented and dedicated Clinical Research Scientist to join their innovative pharmaceutical team. This is a fully remote position, offering flexibility and the opportunity to contribute to groundbreaking medical advancements from anywhere. The successful candidate will be instrumental in the design, execution, and interpretation of clinical trials, ensuring adherence to regulatory guidelines and ethical standards. Responsibilities include developing study protocols, selecting and overseeing clinical trial sites, and managing data collection and analysis. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and drug safety, to ensure seamless trial progression. A critical aspect of this role involves interpreting complex clinical data, identifying trends, and contributing to scientific publications and regulatory submissions. The ideal candidate will have a strong background in clinical research methodology, a solid understanding of pharmaceutical development, and a passion for advancing patient care. Experience in therapeutic areas such as oncology, cardiology, or immunology is highly desirable. You will be expected to stay abreast of the latest scientific literature and emerging trends in clinical research. Excellent written and verbal communication skills are essential, as you will be presenting findings to internal stakeholders and external scientific communities. This role requires meticulous attention to detail, strong organizational skills, and the ability to manage multiple projects concurrently. A Ph.D. or Master's degree in a relevant life science discipline (e.g., Pharmacology, Biology, Medicine) is required, along with a minimum of 5 years of experience in clinical trial management and scientific research. Proficiency in statistical analysis software and electronic data capture (EDC) systems is a plus. This remote opportunity allows you to leverage your expertise in a challenging and rewarding environment, contributing directly to the development of life-saving therapies. We are looking for individuals who are proactive, innovative, and possess a strong commitment to scientific integrity and patient well-being. The ability to work independently and as part of a dispersed global team will be key to success.
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3
Clinical Research Scientist
16511 Magelang, Central Java
IDR18000000 Monthly
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Posted 8 days ago
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Our client, a leading pharmaceutical innovator, is seeking a dedicated Clinical Research Scientist to join their expanding team in Depok, West Java, ID . This hybrid role offers the flexibility to work both remotely and from our state-of-the-art facilities. You will play a pivotal role in the design, execution, and monitoring of clinical trials, ensuring compliance with regulatory standards and ethical guidelines. Responsibilities include developing clinical trial protocols, selecting and managing clinical investigator sites, and overseeing data collection and analysis. The ideal candidate will have a strong background in pharmaceutical sciences, medicine, or a related field, with proven experience in clinical trial management. You will collaborate with cross-functional teams, including medical affairs, regulatory affairs, and project management, to ensure the successful progression of drug development programs. Key duties involve troubleshooting clinical trial issues, providing scientific and medical expertise, and contributing to the interpretation of trial results. You will be involved in preparing scientific publications and presentations to disseminate research findings. We are looking for a highly motivated individual with excellent communication, interpersonal, and organizational skills. A keen eye for detail and a commitment to scientific rigor are essential. This hybrid position requires candidates to be based in or willing to commute to Depok, West Java, ID , while also offering the flexibility of remote work days. You will contribute to the advancement of innovative therapies that improve patient outcomes. The role demands a thorough understanding of Good Clinical Practice (GCP) guidelines and relevant regulatory requirements. You will also be responsible for training and supporting clinical research staff. A proactive approach to identifying and addressing potential challenges in clinical research is highly valued. This is an exciting opportunity to contribute to cutting-edge pharmaceutical research and development within a supportive and collaborative environment. The successful candidate will demonstrate strong leadership potential and the ability to work effectively in a fast-paced setting. Our client is committed to fostering a culture of scientific excellence and innovation. Your expertise will be instrumental in bringing new medicines to patients in need.
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4
Clinical Research Scientist
10220 Jakarta Pusat, Jakarta
IDR150000000 Annually
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Posted 8 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and innovative Clinical Research Scientist to join their esteemed team in **Jakarta, Jakarta, ID**. This role offers a hybrid work model, allowing for a blend of in-office collaboration and remote flexibility. The Clinical Research Scientist will be instrumental in designing, executing, and overseeing clinical trials for novel therapeutic agents. You will contribute to the entire lifecycle of clinical research, from protocol development to data analysis and reporting. This position requires a strong scientific background, meticulous attention to detail, and a comprehensive understanding of regulatory guidelines governing pharmaceutical research. You will work with cross-functional teams, including medical affairs, regulatory affairs, data management, and clinical operations, to ensure the successful conduct of clinical studies.
Key Responsibilities include:
Key Responsibilities include:
- Designing and developing clinical trial protocols, informed consent forms, and other essential study documents.
- Selecting and managing clinical investigator sites, ensuring adherence to protocols and good clinical practice (GCP) standards.
- Overseeing the conduct of clinical trials, monitoring patient safety and data integrity.
- Collaborating with biostatisticians and data managers for data analysis and interpretation.
- Preparing clinical study reports (CSRs), manuscripts for publication, and regulatory submission documents.
- Staying abreast of scientific literature, emerging technologies, and competitive landscape relevant to therapeutic areas.
- Participating in the evaluation of new drug candidates and therapeutic strategies.
- Presenting study results at scientific meetings and conferences.
- Ensuring compliance with all applicable regulatory requirements (e.g., FDA, EMA, BPOM).
- Providing scientific expertise and support to project teams.
- Ph.D. or M.D. in a relevant life science discipline (e.g., Pharmacology, Biology, Medicine).
- Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry.
- Demonstrated experience in clinical trial design and execution across various phases (Phase I-IV).
- In-depth knowledge of GCP, ICH guidelines, and regulatory submission processes.
- Strong analytical and critical thinking skills with the ability to interpret complex scientific data.
- Excellent written and verbal communication skills.
- Proven ability to manage multiple projects simultaneously and meet deadlines.
- Experience with medical writing and report generation.
- Proficiency in statistical analysis concepts and interpretation.
- Ability to work effectively in a collaborative, multidisciplinary environment.
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5
Principal Clinical Research Scientist
16114 Bogor, West Java
IDR30000000 Annually
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Posted today
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly accomplished Principal Clinical Research Scientist to join their esteemed global research and development team. This is a fully remote position, designed for experienced professionals who thrive in an independent, research-focused environment. You will play a pivotal role in the design, execution, and interpretation of clinical trials for novel therapeutic agents. Your expertise will be crucial in developing clinical development strategies, writing protocols, analyzing study data, and contributing to regulatory submissions. Responsibilities include overseeing the scientific integrity of clinical studies, collaborating with internal and external stakeholders (including investigators, CROs, and regulatory agencies), and ensuring adherence to Good Clinical Practice (GCP) guidelines. You will be expected to lead cross-functional teams, mentor junior scientists, and present complex scientific findings at internal and external forums. The ideal candidate will possess a deep understanding of drug development processes, statistical analysis, and the regulatory landscape within the pharmaceutical industry. A strong publication record and experience in a specific therapeutic area are highly desirable. This role requires exceptional analytical, critical thinking, and communication skills, with the ability to translate complex biological and clinical data into actionable insights. You will be instrumental in shaping the future of our client's drug pipeline. This is a remote-first opportunity, offering significant autonomy and the chance to make a substantial impact on global health from your home office. The role, while remote, is associated with our Bogor, West Java, ID research hub.
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Clinical Research Scientist - Oncology
50132 Semarang, Central Java
IDR28000000 Monthly
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Posted today
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Job Description
Our client, a pioneering pharmaceutical company, is seeking a highly motivated Clinical Research Scientist specializing in Oncology to join their team in Semarang, Central Java, ID . This hybrid role offers the chance to contribute to groundbreaking research and development in cancer therapeutics. You will play a pivotal role in the design, execution, and interpretation of clinical trials, collaborating with a multidisciplinary team of scientists, clinicians, and statisticians. The ideal candidate possesses a strong scientific background in oncology, a deep understanding of clinical trial methodologies, and excellent analytical and problem-solving skills. You will be responsible for ensuring the scientific integrity of trials, managing data, and contributing to regulatory submissions. This position demands a rigorous scientific approach, meticulous attention to detail, and the ability to communicate complex findings effectively. Responsibilities include:
- Designing and developing clinical trial protocols for oncology therapeutics.
- Overseeing the execution of clinical trials, ensuring compliance with regulatory guidelines (e.g., GCP, ICH).
- Analyzing clinical trial data, including efficacy and safety endpoints.
- Interpreting study results and contributing to scientific publications and presentations.
- Collaborating with statisticians and data managers to ensure data quality and integrity.
- Providing scientific expertise to cross-functional teams, including regulatory affairs, medical affairs, and R&D.
- Preparing study reports, investigator brochures, and other essential trial documents.
- Identifying and evaluating potential new drug candidates and therapeutic strategies.
- Engaging with key opinion leaders (KOLs) and clinical investigators.
- Contributing to the development of clinical development strategies for new oncology assets.
- Staying current with the latest scientific literature and advancements in oncology and clinical research.
- Ph.D. in Oncology, Pharmacology, Molecular Biology, or a related life science discipline.
- Minimum of 5 years of experience in clinical research, preferably within the pharmaceutical industry or a CRO.
- Extensive knowledge of oncology drug development and clinical trial design.
- Strong understanding of biostatistics and data analysis methodologies.
- Experience with regulatory requirements for clinical trials.
- Excellent written and verbal communication skills, with the ability to present complex scientific information clearly.
- Proven ability to work effectively in a collaborative, team-oriented environment.
- Proficiency in relevant scientific literature databases and clinical trial management systems.
- Ability to manage multiple projects and meet deadlines in a fast-paced environment.
- Experience with data interpretation and report generation.
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7
Principal Clinical Research Scientist
40111 Bandung, West Java
IDR450000000 Annually
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Posted today
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Job Description
Our client, a globally recognized leader in pharmaceutical innovation, is seeking a highly accomplished Principal Clinical Research Scientist for a fully remote position. This senior role is integral to the design, execution, and interpretation of clinical trials that advance novel therapeutics. The ideal candidate will possess a profound scientific background, extensive experience in clinical development, and a deep understanding of regulatory requirements within the **pharmaceutical industry**. You will lead complex research projects, contribute to the scientific strategy, and collaborate with cross-functional teams to bring life-changing medicines to patients. Responsibilities include designing clinical trial protocols, developing statistical analysis plans, overseeing data interpretation, authoring clinical study reports and regulatory submissions, staying abreast of scientific literature and emerging trends, providing scientific and strategic guidance to project teams, and ensuring compliance with all relevant guidelines and regulations. You will also play a key role in identifying and evaluating new drug targets and therapeutic approaches. This is a remote-first position, requiring exceptional self-management skills and the ability to foster strong working relationships through virtual communication channels. The Principal Clinical Research Scientist will be a key scientific advisor, contributing to critical decisions in drug development. Qualifications include a Ph.D. or M.D. in a relevant life science discipline. A minimum of 10 years of experience in clinical research and drug development within the pharmaceutical or biotechnology sector. Proven track record of successfully leading clinical trials from concept to completion. In-depth knowledge of clinical trial design, biostatistics, data management, and regulatory affairs (FDA, EMA, etc.). Excellent scientific writing and presentation skills. Strong leadership and interpersonal skills, with the ability to influence and collaborate effectively with diverse teams. Experience in therapeutic areas such as oncology, immunology, or neurology is highly desirable. Demonstrated ability to think critically and strategically, and to translate complex scientific data into actionable insights. This role offers a unique opportunity to make a substantial impact on patient health through groundbreaking pharmaceutical research.
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8
Remote Clinical Research Scientist
25111 Padang, West Sumatra
IDR20000000 Annually
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Posted today
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Job Description
Our client is seeking a highly motivated and detail-oriented Remote Clinical Research Scientist to contribute to groundbreaking pharmaceutical research. This fully remote position allows you to work from anywhere, focusing on designing, implementing, and analyzing clinical trials to advance novel therapeutics. You will play a crucial role in all phases of clinical development, from protocol design and site selection to data interpretation and regulatory submission support.
Your responsibilities will include developing comprehensive clinical study protocols, investigator brochures, and other essential study documents. You will collaborate with internal teams, including regulatory affairs, biostatistics, and data management, as well as external partners such as contract research organizations (CROs) and clinical investigators. A key part of your role will be to monitor study progress, ensure adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements, and proactively identify and address any study-related issues. You will be responsible for analyzing complex clinical data, interpreting results, and preparing comprehensive reports for internal stakeholders and regulatory agencies.
This role demands a strong scientific background, excellent analytical skills, and the ability to think critically and solve problems. You must be adept at managing multiple projects concurrently in a fast-paced, remote environment, maintaining clear and concise communication with a geographically dispersed team. A passion for drug development and a commitment to patient safety are essential.
Qualifications:
Your responsibilities will include developing comprehensive clinical study protocols, investigator brochures, and other essential study documents. You will collaborate with internal teams, including regulatory affairs, biostatistics, and data management, as well as external partners such as contract research organizations (CROs) and clinical investigators. A key part of your role will be to monitor study progress, ensure adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements, and proactively identify and address any study-related issues. You will be responsible for analyzing complex clinical data, interpreting results, and preparing comprehensive reports for internal stakeholders and regulatory agencies.
This role demands a strong scientific background, excellent analytical skills, and the ability to think critically and solve problems. You must be adept at managing multiple projects concurrently in a fast-paced, remote environment, maintaining clear and concise communication with a geographically dispersed team. A passion for drug development and a commitment to patient safety are essential.
Qualifications:
- Ph.D. or Master's degree in a relevant scientific discipline (e.g., Pharmacology, Biochemistry, Molecular Biology, Pharmacy).
- Minimum of 5 years of progressive experience in clinical research within the pharmaceutical industry or a CRO.
- In-depth knowledge of drug development processes, clinical trial design, and regulatory requirements (e.g., FDA, EMA, ICH GCP).
- Proven experience in data analysis and interpretation of clinical trial results.
- Exceptional written and verbal communication skills, with the ability to present complex scientific information clearly.
- Strong project management and organizational skills.
- Proficiency in relevant software and databases used in clinical research.
- Ability to work independently and collaboratively in a remote setting.
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