What Jobs are available for Cancer Research in Bahrain?
Showing 5000+ Cancer Research jobs in Bahrain
Clinical Research Scientist
20121 Hamad Town, Northern
BHD95000 Annually
WhatJobs Direct
Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical company, is looking for a dedicated and skilled Clinical Research Scientist to join their dynamic team. This role is integral to the planning, execution, and analysis of clinical trials, contributing to the development of innovative new medicines. The successful candidate will be responsible for designing study protocols, managing data collection and analysis, ensuring adherence to regulatory guidelines, and preparing scientific reports. Key duties include collaborating with investigators and site staff, monitoring trial progress, interpreting clinical data, and contributing to the publication of research findings. The ideal candidate will possess a strong scientific background in a relevant therapeutic area, extensive knowledge of Good Clinical Practice (GCP) and regulatory requirements (FDA, EMA), and excellent analytical and statistical skills. A PhD or Master's degree in a life science field is typically required. This position is based in our client's state-of-the-art facility and requires regular on-site presence to effectively manage and oversee clinical research activities in the **Hamad Town, Northern, BH** area. We seek a highly motivated individual with a passion for advancing medical science and a commitment to patient safety. The ability to work effectively in a team, manage multiple projects, and communicate complex scientific information clearly is essential. This role offers an exceptional opportunity to be at the forefront of pharmaceutical innovation, working with cutting-edge research and contributing to life-changing therapies. Continuous learning and professional development are encouraged, ensuring you remain at the pinnacle of your field. Your expertise will directly impact the success of critical drug development programs, making a tangible difference in healthcare.
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0
Clinical Research Scientist
221 Busaiteen, Muharraq
BHD85000 Annually
WhatJobs
Posted 10 days ago
Job Viewed
Job Description
Our client is a rapidly expanding pharmaceutical company situated in Busaiteen, Muharraq, BH , actively seeking a highly motivated and experienced Clinical Research Scientist to spearhead critical research initiatives. This role is integral to our drug development pipeline, focusing on the design, execution, and analysis of clinical trials that adhere to the highest scientific and ethical standards. The Clinical Research Scientist will be instrumental in advancing our understanding of therapeutic interventions and ensuring the safety and efficacy of new pharmaceutical products. You will play a key role in protocol development, data interpretation, and the preparation of regulatory submission documents. This position offers a unique opportunity to contribute to groundbreaking medical advancements within a supportive and innovative research environment.
The core responsibilities include planning and overseeing the conduct of clinical studies, ensuring compliance with Good Clinical Practice (GCP) guidelines and relevant regulatory requirements. You will collaborate closely with investigators, study coordinators, and internal teams to manage study timelines, budgets, and resources effectively. A significant aspect of this role involves in-depth analysis of clinical data, statistical interpretation, and the generation of comprehensive study reports. You will also be involved in identifying potential research collaborators and key opinion leaders in relevant therapeutic areas. Furthermore, the Clinical Research Scientist will contribute to the scientific strategy of the company, identifying new research opportunities and staying abreast of the latest scientific literature and technological advancements in pharmaceutical research. Excellent problem-solving skills and a meticulous attention to detail are essential for success in this demanding yet rewarding position. The ability to effectively communicate complex scientific information to both technical and non-technical audiences is crucial.
Qualifications:
This is an exceptional chance to join a forward-thinking organization and make a tangible difference in patient lives through cutting-edge pharmaceutical research.
The core responsibilities include planning and overseeing the conduct of clinical studies, ensuring compliance with Good Clinical Practice (GCP) guidelines and relevant regulatory requirements. You will collaborate closely with investigators, study coordinators, and internal teams to manage study timelines, budgets, and resources effectively. A significant aspect of this role involves in-depth analysis of clinical data, statistical interpretation, and the generation of comprehensive study reports. You will also be involved in identifying potential research collaborators and key opinion leaders in relevant therapeutic areas. Furthermore, the Clinical Research Scientist will contribute to the scientific strategy of the company, identifying new research opportunities and staying abreast of the latest scientific literature and technological advancements in pharmaceutical research. Excellent problem-solving skills and a meticulous attention to detail are essential for success in this demanding yet rewarding position. The ability to effectively communicate complex scientific information to both technical and non-technical audiences is crucial.
Qualifications:
- PhD or equivalent doctoral degree in Pharmacology, Biomedical Sciences, Pharmacy, or a related life science discipline.
- Minimum of 5 years of hands-on experience in clinical research within the pharmaceutical industry or a contract research organization (CRO).
- Proven track record in designing and managing Phase II/III clinical trials.
- In-depth knowledge of GCP, ICH guidelines, and regulatory submission processes.
- Strong statistical analysis and data interpretation skills.
- Excellent written and verbal communication abilities.
- Experience in the pharmaceutical sector in Muharraq, BH is highly desirable.
- Ability to travel as required for study monitoring and investigator meetings.
This is an exceptional chance to join a forward-thinking organization and make a tangible difference in patient lives through cutting-edge pharmaceutical research.
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1
Clinical Research Scientist
30005 Gudaibiya, Capital
BHD105000 Annually
WhatJobs
Posted 12 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is looking for a highly skilled Clinical Research Scientist to contribute to groundbreaking drug development programs. This position is based in our state-of-the-art facility in **Tubli, Capital, BH**, and requires a hands-on approach to clinical trial design, execution, and data analysis. You will play a pivotal role in translating scientific discoveries into viable therapeutic solutions, working closely with a multidisciplinary team of researchers, clinicians, and regulatory experts. Your expertise will be crucial in ensuring the integrity, safety, and efficacy of our client's investigational products throughout the clinical trial lifecycle.
Key responsibilities include:
The ideal candidate will possess a Ph.D. or M.D. in a relevant scientific discipline (e.g., pharmacology, molecular biology, medicine) with a minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry. Demonstrated experience in designing and managing Phase II/III clinical trials is essential. Strong understanding of regulatory requirements (FDA, EMA, etc.) and GCP is mandatory. Excellent analytical, critical thinking, and problem-solving skills are required, along with strong written and verbal communication abilities. Experience with statistical analysis software and data visualization tools is preferred. You must be detail-oriented, organized, and capable of working effectively in a collaborative team environment. This is an exceptional opportunity to contribute to the advancement of novel therapies in **Tubli, Capital, BH**.
Key responsibilities include:
- Designing and developing clinical trial protocols in accordance with regulatory guidelines and scientific objectives.
- Overseeing the planning and execution of clinical studies, ensuring adherence to Good Clinical Practice (GCP) and other relevant standards.
- Managing relationships with investigational sites, principal investigators, and clinical research organizations (CROs).
- Monitoring study progress, data collection, and safety reporting, identifying and mitigating potential risks.
- Analyzing clinical trial data, interpreting results, and contributing to scientific publications and regulatory submissions.
- Collaborating with statisticians and data management teams to ensure data quality and integrity.
- Providing scientific and technical expertise to cross-functional teams involved in drug development.
- Keeping abreast of the latest scientific literature, therapeutic advancements, and regulatory changes.
- Contributing to the preparation of Investigator Brochures, Clinical Study Reports, and other essential study documents.
- Participating in internal and external scientific meetings and conferences.
The ideal candidate will possess a Ph.D. or M.D. in a relevant scientific discipline (e.g., pharmacology, molecular biology, medicine) with a minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry. Demonstrated experience in designing and managing Phase II/III clinical trials is essential. Strong understanding of regulatory requirements (FDA, EMA, etc.) and GCP is mandatory. Excellent analytical, critical thinking, and problem-solving skills are required, along with strong written and verbal communication abilities. Experience with statistical analysis software and data visualization tools is preferred. You must be detail-oriented, organized, and capable of working effectively in a collaborative team environment. This is an exceptional opportunity to contribute to the advancement of novel therapies in **Tubli, Capital, BH**.
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2
Clinical Research Scientist
78901 Seef, Capital
BHD160000 Annually
WhatJobs
Posted 20 days ago
Job Viewed
Job Description
Our client, a leading innovator in the pharmaceutical industry, is seeking a highly skilled and dedicated Clinical Research Scientist to join their world-class research and development team. This is a remote position, allowing you to contribute significantly to groundbreaking clinical trials from anywhere. The successful candidate will be responsible for the design, implementation, and interpretation of clinical studies, contributing to the development of novel therapeutics. You will collaborate with cross-functional teams, including medical affairs, regulatory affairs, data management, and statistics, to ensure the highest standards of scientific rigor and ethical conduct. A deep understanding of clinical trial methodologies, regulatory requirements, and data analysis is essential. This is an exceptional opportunity to advance your career in pharmaceutical research and contribute to improving patient outcomes.
Key Responsibilities:
Qualifications:
This remote role offers a competitive compensation package and the opportunity to significantly impact the development of life-saving medicines.
Key Responsibilities:
- Design and develop clinical trial protocols, including study objectives, endpoints, methodology, and statistical considerations.
- Oversee the execution of clinical studies, ensuring adherence to protocols, good clinical practice (GCP) guidelines, and regulatory requirements.
- Collaborate with investigative sites to ensure proper study conduct, data collection, and patient safety monitoring.
- Interpret clinical study data, analyze results, and prepare comprehensive study reports, publications, and presentations.
- Provide scientific and medical expertise to internal teams, including regulatory affairs, marketing, and project management.
- Stay abreast of the latest scientific literature, clinical trends, and regulatory updates relevant to the company's therapeutic areas.
- Contribute to the strategic planning of the clinical development pipeline.
- Liaise with external stakeholders, including key opinion leaders (KOLs), regulatory agencies (e.g., FDA, EMA), and ethical committees.
- Manage and mentor junior research staff and provide scientific guidance.
- Ensure compliance with all company policies, SOPs, and ethical standards.
- Participate in the preparation of regulatory submission documents.
- Develop and manage relationships with clinical research organizations (CROs) and other external vendors.
- Contribute to the identification and evaluation of new drug candidates and therapeutic opportunities.
- Present scientific data at national and international conferences.
- Ensure data integrity and accuracy throughout the clinical trial lifecycle.
Qualifications:
- Ph.D. or M.D. in a relevant scientific discipline (e.g., pharmacology, medicine, biology).
- Minimum of 7 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry.
- Demonstrated experience in designing, conducting, and analyzing Phase I, II, III, or IV clinical trials.
- In-depth knowledge of GCP guidelines, regulatory requirements, and clinical trial methodologies.
- Excellent scientific writing, communication, and presentation skills.
- Proven ability to interpret complex data and translate scientific findings into actionable insights.
- Strong analytical and problem-solving skills.
- Experience working effectively in a remote, cross-functional team environment.
- Proficiency in statistical software and data analysis techniques is desirable.
- Ability to manage multiple projects and meet deadlines in a dynamic environment.
- Experience in a specific therapeutic area relevant to the company's pipeline is a significant advantage.
This remote role offers a competitive compensation package and the opportunity to significantly impact the development of life-saving medicines.
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3
Clinical Research Scientist - Oncology
25004 Amwaj Islands
BHD115000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to advancing human health, is seeking a highly qualified Clinical Research Scientist specializing in Oncology to join their innovative team in Isa Town, Southern, BH . This role is integral to the design, execution, and interpretation of clinical trials for novel cancer therapies. The ideal candidate will possess a deep understanding of oncology, clinical trial methodologies, and regulatory requirements. You will be responsible for developing clinical protocols, managing study timelines, and collaborating with investigators and clinical sites to ensure the successful conduct of trials. Key responsibilities include analyzing clinical data, preparing study reports, and contributing to regulatory submissions. You will also play a crucial role in staying abreast of the latest scientific advancements and translating them into effective clinical research strategies. Strong scientific acumen, excellent analytical and problem-solving skills, and the ability to work effectively in a cross-functional team are essential. Experience in drug development, particularly in the oncology therapeutic area, is a significant asset. A Ph.D. or Master's degree in Life Sciences, Medicine, Pharmacy, or a related field is required, along with a minimum of 5 years of experience in clinical research. Experience with Good Clinical Practice (GCP) guidelines and regulatory affairs is mandatory. This position offers a hybrid work model, blending essential on-site laboratory and clinical engagement with the flexibility of remote work, based in Isa Town, Southern, BH . The opportunity to contribute to life-saving treatments makes this a highly rewarding career path.
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4
Clinical Research Scientist - Oncology
88722 Muharraq, Muharraq
BHD85000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly skilled and dedicated Clinical Research Scientist specializing in Oncology to join their fully remote team. This critical role will contribute to the advancement of groundbreaking cancer therapies by designing, implementing, and overseeing clinical trials. You will play a key part in translating scientific discoveries into life-saving treatments for patients.
Key Responsibilities:
This is a fully remote position, requiring exceptional scientific acumen, excellent communication skills, and the ability to work independently and collaboratively. The ideal candidate will possess a Ph.D. or M.D. in a relevant scientific discipline, with a strong background in oncology research and a minimum of 5 years of experience in clinical trial design and execution within the pharmaceutical or biotechnology industry. Thorough understanding of oncology drug development, clinical pharmacology, and regulatory affairs is essential. Experience with biostatistics and data analysis is also required. This role offers a unique opportunity to make a significant impact on cancer treatment. The position is based in Muharraq, Muharraq, BH , but operates entirely remotely.
Key Responsibilities:
- Design and develop clinical trial protocols for oncology studies, ensuring scientific rigor and regulatory compliance.
- Provide scientific and medical expertise throughout the clinical development process, from Phase I to Phase IV studies.
- Collaborate with investigators, site staff, and internal teams (regulatory, biostatistics, data management) to ensure successful trial execution.
- Analyze and interpret clinical trial data, preparing study reports and regulatory submissions.
- Stay current with the latest scientific advancements, clinical practice, and regulatory guidelines in oncology.
- Contribute to the development of scientific publications and presentations.
- Manage relationships with key opinion leaders (KOLs) and external scientific advisors.
- Ensure adherence to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements.
- Participate in protocol review meetings and provide scientific input.
- Contribute to the strategic planning and pipeline development within the oncology therapeutic area.
This is a fully remote position, requiring exceptional scientific acumen, excellent communication skills, and the ability to work independently and collaboratively. The ideal candidate will possess a Ph.D. or M.D. in a relevant scientific discipline, with a strong background in oncology research and a minimum of 5 years of experience in clinical trial design and execution within the pharmaceutical or biotechnology industry. Thorough understanding of oncology drug development, clinical pharmacology, and regulatory affairs is essential. Experience with biostatistics and data analysis is also required. This role offers a unique opportunity to make a significant impact on cancer treatment. The position is based in Muharraq, Muharraq, BH , but operates entirely remotely.
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5
Clinical Research Scientist - Oncology
7031 Tubli
BHD85000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly skilled and motivated Clinical Research Scientist specializing in Oncology. This hybrid role requires a candidate who can contribute significantly both remotely and from our facility in **Sitra, Capital, BH**. You will play a crucial role in the design, execution, and interpretation of clinical trials for novel oncology therapeutics. Your responsibilities will include developing clinical trial protocols, selecting investigational sites, managing data integrity, and ensuring compliance with regulatory guidelines. This position offers a unique opportunity to work at the forefront of cancer research, contributing to the development of life-saving treatments.
Key Responsibilities:
The ideal candidate will have a Ph.D. or M.D. in a relevant scientific discipline, with substantial experience in clinical research, particularly in oncology. A strong understanding of drug development processes, clinical trial methodologies, and regulatory affairs is essential. Excellent analytical, communication, and project management skills are required. This role offers a compelling opportunity to make a significant impact in the fight against cancer, blending remote work flexibility with essential on-site collaboration in **Sitra, Capital, BH**.
Key Responsibilities:
- Design and develop clinical trial protocols for oncology drugs, including study objectives, endpoints, and statistical considerations.
- Collaborate with cross-functional teams (e.g., R&D, regulatory affairs, medical affairs) to ensure successful trial implementation.
- Identify and evaluate potential clinical trial sites and investigators.
- Oversee the conduct of clinical trials, ensuring adherence to Good Clinical Practice (GCP) and regulatory requirements.
- Monitor trial progress, analyze data, and interpret results to support drug development decisions.
- Prepare study reports, manuscripts, and presentations for scientific and regulatory audiences.
- Stay abreast of the latest scientific advancements and clinical research trends in oncology.
- Contribute to the strategic planning of the clinical development pipeline.
- Manage relationships with external investigators, key opinion leaders, and contract research organizations (CROs).
- Ensure timely submission of regulatory documents and adherence to timelines.
The ideal candidate will have a Ph.D. or M.D. in a relevant scientific discipline, with substantial experience in clinical research, particularly in oncology. A strong understanding of drug development processes, clinical trial methodologies, and regulatory affairs is essential. Excellent analytical, communication, and project management skills are required. This role offers a compelling opportunity to make a significant impact in the fight against cancer, blending remote work flexibility with essential on-site collaboration in **Sitra, Capital, BH**.
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6
Clinical Research Scientist - Oncology
4001 Zallaq, Southern
BHD4500 Monthly
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a pioneering pharmaceutical company, is seeking a dedicated and innovative Clinical Research Scientist to join their esteemed R&D department. This critical role will be based in Zallaq, Southern, BH , and will focus on the design, execution, and analysis of clinical trials for novel oncology therapeutics. You will play a key part in advancing groundbreaking treatments from preclinical stages through to regulatory submission, contributing significantly to patient care and the future of medicine.
Primary Responsibilities:
Primary Responsibilities:
- Design and develop clinical trial protocols in alignment with regulatory requirements, scientific objectives, and company strategy for oncology indications.
- Oversee the operational aspects of clinical trials, ensuring adherence to Good Clinical Practice (GCP) guidelines and ethical standards.
- Collaborate with internal and external stakeholders, including investigators, ethics committees, regulatory authorities, and contract research organizations (CROs).
- Analyze and interpret complex clinical data, including safety, efficacy, and pharmacokinetic data, to assess the performance of investigational drugs.
- Prepare comprehensive clinical study reports, regulatory submission documents (e.g., IND, NDA), and scientific publications.
- Contribute to the identification and evaluation of new drug targets and therapeutic strategies in oncology.
- Provide scientific and technical expertise to cross-functional teams, including medical affairs, regulatory affairs, and marketing.
- Manage clinical trial budgets and timelines, ensuring efficient resource allocation.
- Stay abreast of the latest scientific advancements, clinical trends, and regulatory changes in oncology drug development.
- Present research findings at scientific conferences and meetings.
- Contribute to the strategic planning and lifecycle management of the oncology pipeline.
- Ensure data integrity and quality throughout the clinical trial process.
- Participate in the selection and training of clinical investigators and site staff.
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology, Medicine).
- Minimum of 5 years of experience in clinical drug development, with a strong focus on oncology.
- Proven track record in designing, implementing, and managing clinical trials from Phase I to Phase IV.
- In-depth understanding of oncology, cancer biology, and relevant therapeutic areas.
- Expertise in regulatory requirements (FDA, EMA, etc.) and GCP guidelines.
- Strong analytical, statistical interpretation, and data management skills.
- Excellent written and verbal communication skills, with the ability to present complex scientific information clearly.
- Demonstrated ability to lead and collaborate effectively within a multidisciplinary team environment.
- Experience working with CROs and managing external vendors.
- Proficiency in clinical data review and interpretation.
- Strong project management and organizational skills.
- Ability to work independently and drive projects to completion.
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7
Clinical Research Scientist - Oncology
105, BH Arad
BHD90000 Annually
WhatJobs
Posted 7 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology to join our innovative and fully remote research team. This role is crucial for driving forward groundbreaking cancer therapies from concept to clinical application. You will be responsible for the design, execution, and interpretation of clinical trials, contributing to the development of novel treatments that improve patient outcomes.
Key responsibilities include developing clinical trial protocols, selecting appropriate study endpoints, and identifying suitable clinical sites and investigators. You will manage the day-to-day operations of clinical studies, ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements. This involves close collaboration with cross-functional teams, including R&D, regulatory affairs, data management, and biostatistics. The Clinical Research Scientist will also be involved in analyzing clinical trial data, preparing regulatory submissions (e.g., IND, NDA), and disseminating research findings through publications and presentations.
The ideal candidate will possess a Ph.D. or M.D. in a life science or medical field, with a strong background in oncology research. A minimum of 5-7 years of experience in clinical research within the pharmaceutical or biotechnology industry is required. Demonstrated experience in designing and managing Phase I-III clinical trials is essential. Excellent understanding of oncology, clinical trial methodology, biostatistics, and regulatory affairs (FDA, EMA) is mandatory. Strong analytical, problem-solving, and written/verbal communication skills are crucial. This remote position allows you to contribute significantly to cancer research advancements while enjoying the flexibility of working from home, supporting our efforts in developing life-saving treatments impacting patients in Jidhafs, Capital, BH and globally.
Key responsibilities include developing clinical trial protocols, selecting appropriate study endpoints, and identifying suitable clinical sites and investigators. You will manage the day-to-day operations of clinical studies, ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements. This involves close collaboration with cross-functional teams, including R&D, regulatory affairs, data management, and biostatistics. The Clinical Research Scientist will also be involved in analyzing clinical trial data, preparing regulatory submissions (e.g., IND, NDA), and disseminating research findings through publications and presentations.
The ideal candidate will possess a Ph.D. or M.D. in a life science or medical field, with a strong background in oncology research. A minimum of 5-7 years of experience in clinical research within the pharmaceutical or biotechnology industry is required. Demonstrated experience in designing and managing Phase I-III clinical trials is essential. Excellent understanding of oncology, clinical trial methodology, biostatistics, and regulatory affairs (FDA, EMA) is mandatory. Strong analytical, problem-solving, and written/verbal communication skills are crucial. This remote position allows you to contribute significantly to cancer research advancements while enjoying the flexibility of working from home, supporting our efforts in developing life-saving treatments impacting patients in Jidhafs, Capital, BH and globally.
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8
Clinical Research Scientist - Oncology
2100 Shahrakan
BHD6000 Monthly
WhatJobs
Posted 10 days ago
Job Viewed
Job Description
Our client is seeking a highly skilled and dedicated Clinical Research Scientist specializing in Oncology to join their cutting-edge pharmaceutical research facility in Budaiya, Northern, BH . This role is central to advancing novel cancer therapies from preclinical stages through to clinical trials. You will be responsible for designing, implementing, and managing complex research projects, ensuring adherence to Good Clinical Practice (GCP) and regulatory guidelines. This involves developing study protocols, selecting appropriate patient cohorts, overseeing data collection and analysis, and interpreting research findings. Collaboration with a multidisciplinary team of oncologists, pharmacologists, statisticians, and regulatory affairs specialists is essential. You will play a key role in preparing research reports, scientific publications, and presentations for internal and external stakeholders. The ideal candidate will possess a strong scientific background, a deep understanding of cancer biology and therapeutic modalities, and proven experience in clinical trial design and execution. Exceptional analytical, problem-solving, and critical thinking skills are required. Responsibilities:
- Designing and overseeing clinical trials for oncology therapeutics.
- Developing comprehensive study protocols and research plans.
- Identifying and recruiting eligible patient participants.
- Ensuring compliance with GCP, FDA, and other relevant regulatory standards.
- Managing and analyzing clinical trial data.
- Interpreting study results and drawing scientific conclusions.
- Preparing scientific manuscripts for publication and presenting findings.
- Collaborating with internal and external research teams.
- Managing research budgets and timelines effectively.
- Ph.D. or equivalent in Oncology, Molecular Biology, Pharmacology, or a related life science field.
- Significant experience in clinical research, specifically in oncology drug development.
- Proven track record in designing and managing Phase I, II, or III clinical trials.
- In-depth knowledge of cancer biology, immunology, and therapeutic mechanisms.
- Familiarity with regulatory requirements (e.g., ICH-GCP, FDA).
- Strong statistical analysis skills and experience with relevant software.
- Excellent written and verbal communication skills, with a strong publication record.
- Ability to lead and motivate research teams.
- Strong project management skills.
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9