What Jobs are available for Clinical Trial Methodologies in Bahrain?
Showing 5000+ Clinical Trial Methodologies jobs in Bahrain
Clinical Trial Specialist
Posted 11 days ago
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Research Scientist
Posted today
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Remote Pharmaceutical Clinical Trial Manager
Posted 19 days ago
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The ideal candidate will possess a strong background in clinical research and pharmaceutical development, with a minimum of 5 years of experience managing clinical trials. A comprehensive understanding of Good Clinical Practice (GCP), regulatory guidelines (e.g., FDA, EMA), and clinical trial methodologies is essential. Proven experience in therapeutic areas relevant to the company's pipeline is highly desirable. Excellent project management skills, with the ability to manage complex, multi-center trials, are required. Strong leadership and team management capabilities, particularly in a remote setting, are crucial. Exceptional communication, negotiation, and problem-solving skills are vital for effectively collaborating with investigators, clinical research associates, and other stakeholders.
This role requires a detail-oriented, proactive, and results-driven professional who can ensure the integrity and success of clinical trials. You will be responsible for identifying and mitigating trial-related risks, managing vendor relationships, and ensuring timely submission of regulatory documents. Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a must. A bachelor's degree in a life science, nursing, or a related field is required; an advanced degree (M.S., Ph.D., Pharm.D.) is a significant asset. This is a challenging and rewarding opportunity for a seasoned Clinical Trial Manager to contribute to the development of life-changing pharmaceuticals.
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Clinical Research Scientist
Posted 8 days ago
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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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Clinical Research Scientist
Posted 10 days ago
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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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Clinical Research Scientist
Posted 18 days ago
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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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Pharmaceutical Research Scientist
Posted today
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Primary responsibilities include:
- Designing and conducting in vitro and in vivo experiments to evaluate the efficacy and safety of potential drug candidates.
- Developing and optimizing assays for high-throughput screening and lead optimization.
- Analyzing experimental data, interpreting results, and presenting findings to internal teams and stakeholders.
- Collaborating with medicinal chemists, biologists, and pharmacologists to advance drug discovery programs.
- Contributing to the preparation of research reports, publications, and patent applications.
- Staying current with scientific literature and emerging trends in pharmaceutical research.
- Maintaining accurate and detailed laboratory records in accordance with GLP standards.
- Managing laboratory resources and ensuring compliance with safety regulations.
- Identifying new research opportunities and contributing to the strategic direction of the R&D department.
Qualifications:
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- A minimum of 3 years of postdoctoral or industry research experience in drug discovery.
- Hands-on experience with a variety of biological and biochemical techniques, including cell culture, molecular biology methods, and protein analysis.
- Proficiency in data analysis software and statistical methods.
- Excellent written and verbal communication skills, with a track record of scientific publications.
- Strong problem-solving abilities and critical thinking skills.
- Ability to work effectively in a collaborative, fast-paced research environment.
- Experience with specific therapeutic areas (e.g., oncology, immunology) is a plus.
- Demonstrated ability to independently design, execute, and interpret complex experiments.
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Research Scientist (Biotechnology)
Posted today
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Key Responsibilities:
- Design, plan, and execute complex experiments in the field of biotechnology.
- Develop and optimize new methodologies and protocols for research.
- Collect, analyze, and interpret experimental data using statistical software and bioinformatics tools.
- Maintain detailed and accurate laboratory notebooks and research records.
- Prepare scientific reports, manuscripts for publication, and presentations for conferences.
- Collaborate effectively with other researchers, technicians, and principal investigators.
- Troubleshoot experimental issues and propose solutions.
- Stay current with the latest scientific literature and advancements in biotechnology.
- Manage laboratory equipment and supplies, ensuring a safe and organized work environment.
- Contribute to grant writing and funding applications as needed.
- Adhere to all safety protocols and ethical guidelines for research.
Qualifications:
- Ph.D. in Biotechnology, Molecular Biology, Biochemistry, or a related life science discipline.
- Minimum of 3-5 years of post-doctoral research experience or equivalent industry experience.
- Demonstrated expertise in specific areas of biotechnology relevant to the company's research focus (e.g., gene editing, protein engineering, immunology).
- Proficiency in a range of molecular biology techniques, cell culture, and assay development.
- Experience with data analysis software (e.g., R, Python for scientific computing) and bioinformatics tools.
- Excellent written and verbal communication skills, with a strong publication record.
- Ability to work independently and as part of a collaborative research team.
- Strong problem-solving skills and attention to detail.
- Experience with microscopy, flow cytometry, or other relevant advanced techniques is a plus.
This research-intensive role is based at our client's state-of-the-art facility in Sitra, Capital, BH .
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AI Research Scientist
Posted today
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Key Responsibilities:
- Conduct advanced research in artificial intelligence, machine learning, and related fields.
- Develop, implement, and evaluate novel AI algorithms and models.
- Design and execute experiments to validate research hypotheses and model performance.
- Collaborate with software engineers to integrate research prototypes into scalable solutions.
- Stay current with the latest academic research and industry trends in AI.
- Publish research findings in leading academic journals and present at conferences.
- Contribute to intellectual property development through patents and publications.
- Mentor junior researchers and contribute to a collaborative research environment.
- Explore and define new research directions and opportunities.
- Contribute to the strategic vision for AI development within the organization.
Qualifications:
- Ph.D. or Master's degree in Computer Science, Artificial Intelligence, Machine Learning, or a related quantitative field.
- Strong publication record in top-tier AI conferences and journals.
- Proven experience in developing and implementing machine learning and deep learning models.
- Proficiency in programming languages such as Python, and ML frameworks like TensorFlow, PyTorch, or Keras.
- Expertise in at least one AI subfield (e.g., NLP, computer vision, reinforcement learning, recommender systems).
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong communication and presentation skills.
- Ability to work independently and collaboratively in a research-intensive environment.
- Experience with large-scale data processing and distributed computing is a plus.
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AI Research Scientist
Posted today
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Job Description
Key Responsibilities:
- Conduct advanced research in areas such as machine learning, deep learning, natural language processing, computer vision, and reinforcement learning.
- Design, develop, and implement state-of-the-art AI algorithms and models.
- Process, clean, and analyze large datasets to extract meaningful insights and train models.
- Collaborate with engineering teams to integrate AI models into production systems and applications.
- Stay current with the latest advancements in AI research and literature, and identify opportunities for innovation.
- Publish research findings in top-tier conferences and journals.
- Develop and present prototypes and proof-of-concepts to demonstrate the potential of new AI technologies.
- Evaluate and benchmark the performance of AI models, identifying areas for improvement.
- Contribute to the intellectual property portfolio of the company through patent filings.
- Work closely with product managers and domain experts to understand business needs and translate them into research objectives.
- Ph.D. or Master's degree in Computer Science, Artificial Intelligence, Machine Learning, or a related quantitative field.
- A strong publication record in leading AI conferences (e.g., NeurIPS, ICML, CVPR, ACL) or journals.
- Proven experience in developing and deploying machine learning models using frameworks like TensorFlow, PyTorch, or JAX.
- Expertise in at least one of the following areas: deep learning, NLP, computer vision, reinforcement learning, or generative models.
- Proficiency in programming languages such as Python, R, or C++.
- Experience with big data technologies and cloud platforms (e.g., AWS, Azure, GCP) is a plus.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong communication and collaboration abilities, with the capacity to explain complex technical concepts to diverse audiences.
- Ability to work independently and as part of a research-driven team.
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