1 153 Oncology Research Scientist jobs in Bahrain
Principal Research Scientist - Oncology
Posted 2 days ago
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Job Description
Key Responsibilities:
- Lead and manage independent research projects focused on identifying and validating novel drug targets in oncology.
- Design, optimize, and execute in vitro and in vivo preclinical studies to evaluate therapeutic candidates.
- Interpret complex experimental data, draw meaningful conclusions, and communicate findings effectively to internal and external stakeholders.
- Develop and implement innovative assays and methodologies to support drug discovery efforts.
- Mentor and guide junior scientists, fostering a collaborative and high-performing research environment.
- Collaborate closely with cross-functional teams, including medicinal chemistry, pharmacology, and clinical development.
- Prepare scientific manuscripts for publication in peer-reviewed journals and present research at international conferences.
- Contribute to the strategic direction of the oncology pipeline and identify new opportunities for scientific advancement.
- Ensure compliance with all relevant regulatory guidelines and ethical standards.
- Ph.D. in Molecular Biology, Immunology, Pharmacology, or a related life science discipline.
- A minimum of 8 years of post-doctoral research experience in oncology drug discovery, with a strong publication record.
- Demonstrated expertise in cancer biology, signaling pathways, and therapeutic modalities.
- Proven experience in designing and leading complex research projects and managing scientific staff.
- Hands-on experience with a variety of molecular and cellular biology techniques, including CRISPR, NGS, and flow cytometry.
- Excellent understanding of drug discovery and development processes.
- Strong written and oral communication skills, with the ability to present complex scientific information clearly and concisely.
- Ability to work effectively in a collaborative, multidisciplinary team setting, both on-site and remotely.
Clinical Research Scientist - Oncology
Posted 3 days ago
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Job Description
Key responsibilities include contributing to the development of clinical trial protocols, Investigator's Brochures, and other essential regulatory documents. You will play a vital role in site selection and initiation, providing scientific and operational support to clinical trial investigators and site staff. The Clinical Research Scientist will also be responsible for monitoring trial progress, analyzing data, and preparing scientific reports and publications. You will stay abreast of the latest scientific advancements and clinical developments in oncology, ensuring our research remains at the cutting edge.
The ideal candidate will possess a Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology) with a strong understanding of cancer biology and clinical oncology. A minimum of 3-5 years of experience in clinical research within the pharmaceutical industry or a contract research organization (CRO) is required. Demonstrated experience in designing and managing oncology clinical trials is essential. Excellent written and verbal communication skills are necessary for interacting with internal teams, external investigators, and regulatory agencies. The ability to critically evaluate scientific data and translate complex findings into actionable insights is crucial. Proficiency in statistical analysis and interpretation is expected. This hybrid role requires regular attendance in the Seef, Capital, BH office, with flexibility for remote work. Join us in our mission to accelerate the development of groundbreaking cancer therapies.
Senior Pharmaceutical Research Scientist - Oncology
Posted 1 day ago
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Job Description
Responsibilities:
- Design and execute in vitro and in vivo studies to evaluate the efficacy and safety of novel oncology drug candidates.
- Develop and optimize assays for target identification and validation.
- Analyze complex biological data, interpret results, and generate actionable insights for drug development strategies.
- Lead research projects from early discovery through preclinical development.
- Stay abreast of the latest scientific literature and emerging trends in oncology and drug discovery.
- Collaborate closely with cross-functional teams, including medicinal chemistry, pharmacology, toxicology, and clinical development.
- Present research findings at internal meetings and external scientific conferences.
- Contribute to the preparation of regulatory submission documents.
- Mentor junior scientists and provide technical guidance.
- Manage external collaborations with academic institutions and contract research organizations (CROs).
- Contribute to the intellectual property portfolio of the company.
- Ph.D. in Cancer Biology, Pharmacology, Molecular Biology, or a related life science field.
- Minimum of 5 years of postdoctoral and/or industry experience in oncology research.
- Proven track record of independent research and publication in peer-reviewed journals.
- Extensive experience with various cancer models (cell-based assays, xenografts, genetically engineered mouse models).
- Deep understanding of cancer biology, signaling pathways, and therapeutic mechanisms.
- Hands-on experience with molecular and cellular biology techniques (e.g., Western blotting, ELISA, qPCR, flow cytometry, immunohistochemistry).
- Experience with drug discovery principles and the drug development process.
- Strong analytical, problem-solving, and critical-thinking skills.
- Excellent written and verbal communication skills, with the ability to present complex scientific data effectively.
- Ability to work independently and collaboratively in a fast-paced research environment.
- Experience with bioinformatics tools and data analysis is a plus.
Senior Pharmaceutical Research Scientist - Oncology
Posted 1 day ago
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Job Description
Responsibilities:
- Lead and conduct innovative research projects in oncology drug discovery.
- Design, optimize, and execute in vitro and in vivo experiments.
- Analyze and interpret complex biological data using statistical methods.
- Develop and validate new assays for target identification and validation.
- Mentor and guide junior research scientists and technicians.
- Collaborate with cross-functional teams and external partners.
- Prepare scientific reports, presentations, and manuscripts for publication.
- Contribute to intellectual property generation through patent filings.
- Maintain up-to-date knowledge of cancer biology and therapeutic strategies.
- PhD in Molecular Biology, Biochemistry, Pharmacology, or a related field.
- Minimum of 5 years of relevant post-doctoral or industry research experience in oncology.
- Proven track record of successfully designing and executing complex biological experiments.
- Expertise in cancer cell biology, molecular mechanisms of cancer, and drug discovery.
- Hands-on experience with various biochemical and cell-based assays.
- Experience with animal models for cancer research is a plus.
- Excellent written and oral communication skills.
- Strong leadership and team collaboration abilities.
Senior Pharmaceutical Research Scientist - Oncology
Posted 2 days ago
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Job Description
Key Responsibilities:
- Design and execute complex in vitro and in vivo experiments to identify and validate novel drug targets for oncology indications.
- Develop and optimize cell-based assays to assess drug efficacy and mechanisms of action.
- Manage and conduct preclinical studies, including PK/PD analysis and toxicology assessments.
- Analyze and interpret experimental data, drawing robust conclusions and making recommendations for future research directions.
- Prepare scientific reports, manuscripts for publication, and presentations for internal and external stakeholders.
- Collaborate with medicinal chemists, pharmacologists, and clinical development teams to advance drug candidates through the development pipeline.
- Stay current with the latest advancements in oncology research, drug discovery technologies, and relevant scientific literature.
- Supervise and mentor junior research scientists and laboratory technicians.
- Contribute to the strategic planning and direction of the oncology research program.
- Ensure adherence to all laboratory safety protocols and regulatory guidelines (e.g., GLP).
- Manage external collaborations with academic institutions and contract research organizations (CROs).
- Maintain accurate and detailed laboratory notebooks and research records.
- Ph.D. in Molecular Biology, Cell Biology, Pharmacology, Biochemistry, or a related life science discipline.
- Minimum of 5 years of post-doctoral or industry research experience in oncology drug discovery.
- Demonstrated expertise in cancer biology, signal transduction pathways, and tumor immunology.
- Proven experience in designing, optimizing, and executing a variety of in vitro (e.g., cell culture, Western blot, ELISA, flow cytometry) and in vivo models.
- Strong track record of scientific achievement, evidenced by peer-reviewed publications and presentations.
- Excellent data analysis and interpretation skills, with proficiency in relevant statistical software.
- Experience with preclinical drug development processes and regulatory requirements is highly desirable.
- Strong leadership, project management, and team collaboration skills.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a multidisciplinary team.
Senior Pharmaceutical Research Scientist - Oncology
Posted 2 days ago
Job Viewed
Job Description
- Designing and executing complex in vitro and in vivo experiments to evaluate the efficacy and safety of novel oncology drug candidates.
- Developing and validating new assays for drug screening and target engagement studies.
- Analyzing and interpreting experimental data, and communicating findings to project teams and management.
- Contributing to the preparation of regulatory documents and scientific publications.
- Staying abreast of the latest scientific literature and technological advancements in oncology and drug discovery.
- Mentoring junior scientists and contributing to a positive and productive lab culture.
Qualifications:
- PhD in Pharmacology, Molecular Biology, Biochemistry, or a related field.
- Minimum of 5 years of post-doctoral or industry experience in oncology drug discovery.
- Strong understanding of cancer biology, signaling pathways, and tumor microenvironment.
- Proficiency in various laboratory techniques, including cell culture, molecular biology techniques (PCR, Western blotting), flow cytometry, and ELISA.
- Experience with in vivo models of cancer is highly desirable.
- Excellent written and verbal communication skills.
- Ability to work effectively in a fast-paced, team-oriented environment.
Senior Clinical Research Scientist - Oncology
Posted 2 days ago
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Job Description
Key responsibilities include:
- Designing and developing clinical trial protocols for oncology studies, ensuring scientific rigor and regulatory compliance.
- Overseeing the operational aspects of clinical trials, including site selection, patient recruitment, and data collection.
- Analyzing and interpreting complex clinical trial data, generating comprehensive reports and scientific publications.
- Collaborating closely with medical affairs, regulatory affairs, biostatistics, and other internal teams.
- Providing scientific expertise and guidance to study teams, investigators, and external stakeholders.
- Ensuring adherence to Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements.
- Managing relationships with Contract Research Organizations (CROs) and other external vendors.
- Identifying and evaluating new scientific opportunities and technologies in oncology drug development.
- Presenting research findings at scientific conferences and internal meetings.
- Contributing to the development of regulatory submissions (e.g., IND, NDA).
- Mentoring junior scientists and contributing to the overall scientific strategy of the R&D department.
- Staying abreast of the latest advancements in oncology research and clinical trial methodologies.
Qualifications:
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Biology, Medicine).
- Minimum of 7 years of experience in clinical research, specifically within the pharmaceutical industry and with a strong focus on oncology.
- Demonstrated experience in designing and managing Phase I-IV clinical trials.
- In-depth understanding of oncology disease areas, therapeutic strategies, and drug development processes.
- Excellent knowledge of GCP, regulatory affairs, and clinical trial methodologies.
- Strong analytical and data interpretation skills, with experience in statistical analysis concepts.
- Exceptional written and verbal communication skills, with a proven ability to publish scientific findings.
- Demonstrated ability to lead cross-functional teams and manage projects effectively in a remote setting.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
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Senior Pharmaceutical Research Scientist - Oncology
Posted 2 days ago
Job Viewed
Job Description
Key Responsibilities:
- Leading independent research projects focused on oncology drug discovery and development.
- Designing, performing, and interpreting in vitro and in vivo experiments to evaluate novel therapeutic candidates.
- Developing and validating innovative assays and experimental models relevant to cancer biology.
- Analyzing complex biological data using statistical methods and bioinformatics tools.
- Troubleshooting experimental challenges and proposing creative solutions.
- Preparing and presenting research findings at internal meetings and external scientific conferences.
- Contributing to the writing of research protocols, scientific publications, and regulatory documents.
- Mentoring and guiding junior scientists and research associates.
- Collaborating effectively with cross-functional teams to advance projects towards IND filing.
- Staying current with the latest advancements in oncology research and drug discovery.
- Contributing to the intellectual property strategy through invention disclosures and patent applications.
Qualifications:
- Ph.D. in Molecular Biology, Cancer Biology, Immunology, Pharmacology, or a related field.
- 5+ years of postdoctoral or industry experience in pharmaceutical research, with a strong focus on oncology.
- Proven expertise in cancer cell biology, immunology, or molecular targeted therapies.
- Hands-on experience with a variety of molecular and cellular biology techniques (e.g., qPCR, Western blotting, flow cytometry, ELISA, cell culture, primary cell isolation).
- Experience with in vivo pharmacology models in oncology is highly desirable.
- Proficiency in data analysis software and bioinformatics tools.
- Demonstrated ability to lead research projects and mentor junior staff.
- Excellent scientific writing and presentation skills.
- Strong problem-solving abilities and a collaborative mindset.
- Willingness to work in a hybrid model, balancing remote research analysis and planning with essential on-site laboratory work in Seef, Capital, BH .
Senior Clinical Research Scientist - Oncology
Posted 2 days ago
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Job Description
Senior Clinical Research Scientist - Oncology
Posted 3 days ago
Job Viewed
Job Description
Key Responsibilities:
- Lead the design and development of clinical trial protocols for oncology studies, ensuring scientific rigor and alignment with regulatory guidelines.
- Oversee the execution of clinical trials, from site initiation to study close-out, ensuring data integrity and patient safety.
- Collaborate closely with cross-functional teams, including R&D, regulatory affairs, medical affairs, and clinical operations.
- Analyze and interpret complex clinical trial data, identifying key findings and implications for drug development.
- Prepare scientific reports, manuscripts, and presentations for internal stakeholders, regulatory agencies, and scientific publications.
- Contribute to the development of regulatory submission documents (e.g., IND, NDA).
- Stay abreast of the latest advancements in oncology research, clinical trial design, and therapeutic approaches.
- Manage relationships with external investigators, key opinion leaders (KOLs), and clinical research organizations (CROs).
- Ensure compliance with all relevant ethical and regulatory standards (e.g., GCP, ICH).
- Provide scientific and technical expertise to guide study design and problem-solving.
- Mentor junior scientists and contribute to the overall scientific growth of the team.
- Ph.D. or M.D. in a relevant life science discipline (e.g., Oncology, Pharmacology, Biology, Medicine).
- Minimum of 7 years of progressive experience in clinical research, with a significant focus on oncology drug development.
- Proven track record in designing and conducting Phase I, II, and III clinical trials.
- In-depth knowledge of oncology pathways, mechanisms of action, and therapeutic strategies.
- Strong understanding of clinical trial methodologies, statistical analysis, and data interpretation.
- Familiarity with regulatory requirements and guidelines (FDA, EMA, ICH GCP).
- Excellent scientific writing and presentation skills.
- Demonstrated ability to collaborate effectively in a cross-functional, matrixed organization.
- Experience in managing external partnerships with CROs and academic institutions.
- Strong analytical and problem-solving skills.
- Ability to work effectively in a hybrid work model, balancing on-site and remote responsibilities.