6,490 Oncology Research jobs in Indonesia
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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0
Clinical Research Scientist - Oncology
29411 Batam, Riau Islands
IDR18000000 Annually
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Posted 3 days ago
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A prominent pharmaceutical company dedicated to advancing patient care is seeking a highly skilled Clinical Research Scientist specializing in Oncology to be based in Batam, Riau Islands, ID . This pivotal role involves the design, execution, and interpretation of clinical trials for novel cancer therapies. The successful candidate will collaborate closely with cross-functional teams, including R&D, regulatory affairs, and clinical operations, to ensure the successful progression of drug development programs. Responsibilities include developing clinical trial protocols, overseeing patient recruitment and data collection, analyzing trial results, and contributing to regulatory submissions. You will stay abreast of the latest scientific advancements in oncology and pharmaceutical research, applying this knowledge to optimize study designs and outcomes. This position requires a strong understanding of Good Clinical Practice (GCP) guidelines, regulatory requirements, and statistical analysis principles. The ideal candidate will possess excellent scientific acumen, meticulous attention to detail, and exceptional problem-solving abilities. A Ph.D. or Master's degree in a relevant life science discipline (e.g., Biology, Pharmacology, Medicine) is required, coupled with significant experience in clinical research within the pharmaceutical industry, particularly in oncology. Strong written and verbal communication skills are essential for interacting with internal teams, external investigators, and regulatory agencies. This is a challenging yet rewarding opportunity to contribute to the development of life-saving treatments and make a real difference in the lives of cancer patients worldwide. The role offers significant opportunities for professional growth and development within a leading organization committed to innovation and scientific excellence.
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1
Clinical Research Scientist - Oncology
76114 Balikpapan, East Kalimantan
IDR22000000 Monthly
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Posted 3 days ago
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Job Description
Our client, a prominent Pharmaceutical company, is looking for an experienced Clinical Research Scientist specializing in Oncology to be based in **Balikpapan, East Kalimantan, ID**. This role is integral to the advancement of novel cancer therapies, requiring a deep understanding of oncology drug development. You will be responsible for the design, execution, and interpretation of clinical trials, ensuring compliance with regulatory standards and ethical guidelines. This position demands a meticulous approach to data analysis, protocol development, and scientific reporting. You will collaborate with internal R&D teams, clinical operations, and external investigators to drive research forward. The ideal candidate will possess strong scientific acumen, excellent project management skills, and a proven track record in oncology clinical research. Responsibilities include:
- Designing and developing clinical trial protocols for oncology agents.
- Overseeing the conduct of clinical trials, ensuring adherence to protocol and regulatory requirements.
- Analyzing and interpreting clinical trial data, including statistical analysis review.
- Preparing scientific reports, publications, and presentations.
- Collaborating with statisticians, clinicians, and regulatory affairs personnel.
- Identifying and evaluating potential clinical investigators and sites.
- Managing budgets and timelines for clinical research projects.
- Staying abreast of scientific literature and advancements in oncology.
- Ensuring data integrity and quality throughout the research process.
- Advanced degree (M.S., Ph.D., M.D.) in life sciences, pharmacology, or a related field.
- Significant experience (5+ years) in clinical research, with a focus on oncology.
- Thorough understanding of GCP, ICH guidelines, and regulatory submission processes.
- Expertise in clinical trial design, data analysis, and interpretation.
- Strong scientific writing and presentation skills.
- Excellent project management and organizational abilities.
- Ability to work independently and effectively within a multidisciplinary team.
- Experience in pharmaceutical or biotechnology industry is highly desirable.
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2
Clinical Research Scientist - Oncology
70111 Banjarmasin, South Kalimantan
IDR18000000 Annually
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Posted 6 days ago
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Job Description
Our client, a dynamic pharmaceutical company at the forefront of medical innovation, is looking for an experienced Clinical Research Scientist specializing in Oncology to join their team in Banjarmasin, South Kalimantan, ID . This hybrid role offers the flexibility to balance remote work with essential on-site collaboration, fostering a productive and engaging research environment. You will play a critical role in the design, execution, and analysis of clinical trials, contributing to the development of life-saving cancer therapies.
Responsibilities:
Responsibilities:
- Design and develop clinical trial protocols, ensuring alignment with regulatory requirements and scientific objectives.
- Oversee the planning and execution of clinical studies, managing timelines, budgets, and resources effectively.
- Collaborate closely with principal investigators, clinical site staff, and other stakeholders to ensure smooth trial operations.
- Monitor study progress, analyze clinical data, and interpret results to inform decision-making.
- Prepare regulatory submission documents, clinical study reports, and scientific publications.
- Ensure compliance with Good Clinical Practice (GCP) guidelines, regulatory standards, and company policies.
- Provide scientific and technical expertise on oncology drug development to internal teams and external partners.
- Identify and evaluate potential research collaborations and strategic partnerships.
- Contribute to the development of new research strategies and therapeutic areas.
- Present research findings at scientific conferences and internal meetings.
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Biology, Medicine).
- Minimum of 4 years of experience in clinical research within the pharmaceutical or biotechnology industry, with a strong focus on oncology.
- In-depth knowledge of oncology drug development, clinical trial design, and regulatory affairs.
- Proven experience in protocol development, data analysis, and interpretation of clinical trial results.
- Excellent understanding of GCP, ICH guidelines, and other relevant regulatory requirements.
- Strong analytical, critical thinking, and problem-solving skills.
- Exceptional written and verbal communication skills, with the ability to effectively communicate complex scientific information.
- Ability to work effectively in a hybrid environment, demonstrating strong self-discipline and time management.
- Experience with statistical analysis of clinical data and familiarity with biostatistics principles.
- Demonstrated ability to manage multiple projects simultaneously and meet deadlines.
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3
Clinical Research Scientist - Oncology
60111 Surabaya, East Java
IDR22000000 Annually
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Posted 8 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology to join their esteemed research and development team in Surabaya, East Java, ID . This role is crucial in advancing innovative cancer therapies through meticulous clinical trial design, execution, and data analysis. You will be responsible for contributing to the scientific strategy of clinical development programs, translating preclinical findings into human trials, and ensuring the integrity and quality of clinical research conducted. The ideal candidate possesses a strong scientific background in oncology, a deep understanding of clinical trial methodologies (Phase I-IV), regulatory requirements (e.g., ICH-GCP, FDA/EMA guidelines), and data interpretation. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and operations, to ensure seamless trial conduct. Responsibilities include protocol development, site selection and initiation, monitoring trial progress, analyzing clinical data, and contributing to regulatory submissions and scientific publications. We are looking for a detail-oriented, analytical, and results-driven individual with excellent scientific writing and communication skills. A passion for improving patient outcomes and a commitment to advancing cancer research are paramount. This position offers a significant opportunity to contribute to groundbreaking medical advancements and shape the future of cancer treatment.
Key Responsibilities:
Key Responsibilities:
- Contribute to the scientific strategy and design of oncology clinical trials.
- Develop clinical trial protocols, informed consent forms, and other study-related documents.
- Oversee the conduct of clinical trials, ensuring adherence to protocols and regulatory guidelines.
- Collaborate with clinical investigators, site staff, and CROs.
- Monitor trial progress, identify potential issues, and implement corrective actions.
- Analyze clinical trial data and contribute to study reports and publications.
- Stay abreast of the latest scientific advancements and research in oncology.
- Contribute to the preparation of regulatory submissions.
- Provide scientific expertise and support to internal and external stakeholders.
- Ensure compliance with GCP, regulatory requirements, and company SOPs.
- Ph.D. or M.D. in a relevant life science field (e.g., Oncology, Pharmacology, Biology).
- 5+ years of experience in clinical research, with a specific focus on oncology trials.
- In-depth knowledge of clinical trial design, conduct, and data analysis.
- Familiarity with regulatory requirements (ICH-GCP, FDA/EMA).
- Strong scientific writing and presentation skills.
- Excellent analytical and problem-solving abilities.
- Proven ability to collaborate effectively with cross-functional teams.
- Experience in data interpretation and report generation.
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4
Clinical Research Scientist - Oncology
60111 Surabaya, East Java
IDR12000000 Monthly
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Posted 8 days ago
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Job Description
Our client, a leading pharmaceutical company renowned for its commitment to innovation in cancer treatment, is looking for a talented Clinical Research Scientist to join their team in **Surabaya, East Java**. This hybrid role offers the flexibility to work remotely on certain days, balancing focused research with collaborative team efforts. The successful candidate will play a crucial role in the design, execution, and interpretation of clinical trials for novel oncology therapies. Responsibilities include developing study protocols, overseeing data collection and analysis, ensuring compliance with regulatory guidelines (e.g., GCP), and contributing to scientific publications and presentations. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and clinical operations, to ensure the successful progression of research programs. A strong understanding of oncology, clinical trial methodologies, and regulatory requirements is essential. The ideal candidate will possess excellent analytical skills, attention to detail, and the ability to critically evaluate scientific data. You will also be involved in identifying and evaluating new research opportunities and maintaining up-to-date knowledge of scientific literature and industry trends. This position requires a PhD or Master's degree in a relevant life science discipline (e.g., Pharmacology, Biology, Biochemistry, Medicine) and a minimum of 3-5 years of experience in clinical research within the pharmaceutical industry or a related field. Proficiency in statistical analysis software and strong communication skills, both written and verbal, are required. The ability to manage multiple projects simultaneously and work effectively in a team environment, both in-person and remotely, is key to success in this role. Join a company that is at the forefront of medical advancement and contribute to improving the lives of cancer patients.
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5
Clinical Research Scientist - Oncology
76111 Balikpapan, East Kalimantan
IDR18000000 Annually
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Posted 8 days ago
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Job Description
Our client is seeking a dedicated and skilled Clinical Research Scientist specializing in Oncology to join their innovative team in Balikpapan, East Kalimantan, ID . This role focuses on designing, implementing, and managing clinical trials for novel cancer therapies. You will be instrumental in advancing cancer treatment through rigorous scientific research and meticulous data analysis. The Clinical Research Scientist will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, and data management, to ensure the successful execution of clinical development programs. This includes developing comprehensive study protocols, investigator brochures, and clinical study reports in alignment with regulatory requirements and scientific objectives.
Key responsibilities involve overseeing the conduct of clinical trials at investigational sites, ensuring compliance with Good Clinical Practice (GCP) guidelines and relevant regulations. You will be responsible for reviewing and interpreting clinical data, identifying trends, and making recommendations for study adjustments or further research. The Scientist will also play a vital role in site selection, initiation, monitoring, and closure activities, ensuring data integrity and patient safety. Contributing to the preparation of regulatory submissions and interacting with health authorities are also key functions. Furthermore, the position requires staying abreast of the latest scientific advancements and competitor activities within the oncology field. Presenting research findings at scientific conferences and contributing to publications in peer-reviewed journals will be expected.
Qualifications include a Ph.D. or M.D. in a life science, biomedical, or related field, with a strong emphasis on oncology research. A minimum of 5 years of experience in clinical trial management and drug development, preferably within the pharmaceutical or biotechnology industry. Proven expertise in oncology clinical research, including understanding of various cancer types and therapeutic approaches. Strong knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials (e.g., FDA, EMA). Excellent analytical, critical thinking, and problem-solving skills, with a meticulous attention to detail. Superior written and verbal communication skills, with the ability to present complex scientific information clearly and concisely. Experience in data analysis and interpretation using statistical software is a plus. This is a hybrid role, requiring regular attendance at the Balikpapan, East Kalimantan, ID office for team collaboration and strategic planning, with flexibility for remote work.
Key responsibilities involve overseeing the conduct of clinical trials at investigational sites, ensuring compliance with Good Clinical Practice (GCP) guidelines and relevant regulations. You will be responsible for reviewing and interpreting clinical data, identifying trends, and making recommendations for study adjustments or further research. The Scientist will also play a vital role in site selection, initiation, monitoring, and closure activities, ensuring data integrity and patient safety. Contributing to the preparation of regulatory submissions and interacting with health authorities are also key functions. Furthermore, the position requires staying abreast of the latest scientific advancements and competitor activities within the oncology field. Presenting research findings at scientific conferences and contributing to publications in peer-reviewed journals will be expected.
Qualifications include a Ph.D. or M.D. in a life science, biomedical, or related field, with a strong emphasis on oncology research. A minimum of 5 years of experience in clinical trial management and drug development, preferably within the pharmaceutical or biotechnology industry. Proven expertise in oncology clinical research, including understanding of various cancer types and therapeutic approaches. Strong knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials (e.g., FDA, EMA). Excellent analytical, critical thinking, and problem-solving skills, with a meticulous attention to detail. Superior written and verbal communication skills, with the ability to present complex scientific information clearly and concisely. Experience in data analysis and interpretation using statistical software is a plus. This is a hybrid role, requiring regular attendance at the Balikpapan, East Kalimantan, ID office for team collaboration and strategic planning, with flexibility for remote work.
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6
Clinical Research Scientist - Oncology
10260 Jakarta Pusat, Jakarta
IDR30000000 Monthly
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Posted 8 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly skilled and dedicated Clinical Research Scientist specializing in Oncology to join their growing team in **Jakarta**. This role involves significant hands-on work in clinical trials and research, requiring a blend of laboratory expertise and clinical understanding. You will be instrumental in designing, executing, and interpreting studies that advance cancer therapies. This position offers a hybrid work model, balancing crucial in-office collaboration with the flexibility of remote work.
Key Responsibilities:
Key Responsibilities:
- Design and develop clinical trial protocols in oncology, ensuring scientific rigor and compliance with regulatory guidelines.
- Oversee the conduct of clinical trials, including site selection, monitoring, and data interpretation.
- Analyze and interpret complex clinical data, generating reports and publications.
- Collaborate with cross-functional teams, including R&D, regulatory affairs, medical affairs, and commercial departments.
- Stay abreast of the latest advancements in oncology research, emerging therapies, and competitive landscape.
- Prepare regulatory submission documents and respond to queries from health authorities.
- Present research findings at scientific meetings and conferences.
- Manage relationships with key opinion leaders and external investigators.
- Contribute to the strategic planning and pipeline development for oncology assets.
- Ensure adherence to Good Clinical Practice (GCP) and all relevant ethical and regulatory standards.
- Develop and manage study budgets and timelines effectively.
- Advanced degree (Ph.D., M.D., Pharm.D.) in a relevant life science discipline (e.g., Oncology, Pharmacology, Biology, Medicine).
- Minimum of 5 years of experience in clinical research, preferably within the pharmaceutical industry or a contract research organization (CRO).
- In-depth knowledge of oncology, cancer biology, and current treatment modalities.
- Demonstrated experience in clinical trial design, execution, and data analysis.
- Strong understanding of regulatory requirements (e.g., FDA, EMA, BPOM) and ICH-GCP guidelines.
- Excellent scientific writing and presentation skills.
- Proven ability to collaborate effectively in a multidisciplinary team environment.
- Strong analytical and problem-solving skills.
- Experience with statistical analysis and interpretation of clinical data.
- Excellent project management and organizational skills.
- Must be able to work effectively in a hybrid setting, balancing remote and in-office responsibilities.
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7
Clinical Research Scientist - Oncology
70112 Banjarmasin, South Kalimantan
IDR170000000 Annually
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Posted 8 days ago
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Job Description
Our client, a prominent pharmaceutical company, is seeking a dedicated Clinical Research Scientist specializing in Oncology to join their team in Banjarmasin, South Kalimantan, ID . This critical role involves contributing to the design, execution, and analysis of clinical trials for novel cancer therapies. The successful candidate will work closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and clinical operations, to ensure the successful progression of research programs. Responsibilities will include developing clinical trial protocols, preparing regulatory submissions, overseeing study conduct at clinical sites, and interpreting complex clinical data. You will play a key role in the scientific evaluation of drug candidates, assessing their efficacy and safety profiles. The ideal candidate will possess a deep understanding of oncology, clinical trial methodologies, and regulatory requirements (e.g., GCP, ICH guidelines). A Ph.D. or M.D. in a relevant life science or medical field is required, along with a minimum of 5 years of experience in clinical drug development, with a specific focus on oncology. Strong analytical and critical thinking skills, excellent written and verbal communication abilities, and the capacity to collaborate effectively in a multidisciplinary environment are essential. Experience with data analysis, manuscript preparation, and scientific presentations is highly desirable. This hybrid role offers a balanced approach, combining essential in-office collaboration with remote work flexibility, allowing for efficient contribution to groundbreaking cancer research.
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8
Clinical Research Scientist - Oncology
28281 Pekanbaru, Riau
IDR25000000 Monthly
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Posted 8 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is searching for a highly motivated and experienced Clinical Research Scientist specializing in Oncology to contribute to groundbreaking research based in Pekanbaru, Riau, ID . This is a critical role focused on the design, execution, and interpretation of clinical trials for novel cancer therapies. The ideal candidate will possess a strong scientific background, extensive knowledge of oncology drug development, and a proven ability to manage complex research projects. Responsibilities include contributing to the development of clinical trial protocols, selecting clinical sites, and collaborating with investigators and study teams to ensure the efficient and ethical conduct of trials. You will be responsible for analyzing study data, interpreting results, and preparing scientific reports and publications. This role requires a deep understanding of cancer biology, therapeutic strategies, and regulatory requirements for drug approval. The Clinical Research Scientist will play a key role in evaluating the safety and efficacy of investigational drugs, making critical contributions to advancing patient care. Strong collaboration skills are essential, as you will work closely with cross-functional teams, including regulatory affairs, medical affairs, and data management. The ability to stay abreast of the latest scientific literature and emerging trends in oncology research is paramount. This position offers an exciting opportunity to be at the forefront of pharmaceutical research and development, driving the discovery of new treatments for cancer patients. We are looking for a strategic thinker with excellent analytical and problem-solving skills, dedicated to making a difference in oncology.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and oversee clinical trial protocols for oncology therapeutics.
- Collaborate with investigators and clinical sites to ensure trial integrity and compliance.
- Analyze and interpret clinical trial data, generating comprehensive study reports.
- Contribute to the preparation of regulatory submission documents.
- Stay current with scientific advancements and competitive landscape in oncology.
- Develop scientific presentations and publications for conferences and journals.
- Provide scientific and medical expertise to cross-functional teams.
- Evaluate the safety and efficacy profiles of investigational products.
- Ensure adherence to Good Clinical Practice (GCP) guidelines and all applicable regulations.
- Identify and recommend potential new research opportunities.
Qualifications:
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Biology).
- Minimum of 5 years of experience in clinical research within the pharmaceutical industry or academia, with a focus on oncology.
- In-depth knowledge of cancer biology, tumor types, and therapeutic approaches.
- Proven experience in clinical trial design, execution, and data analysis.
- Familiarity with regulatory guidelines (e.g., FDA, EMA, BPOM) for drug development.
- Excellent scientific writing and communication skills.
- Strong analytical and critical thinking abilities.
- Ability to manage multiple projects and work effectively in a team environment.
- Experience with biostatistics and data management principles.
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