756 Medical Research jobs in Bahrain
Senior Bio-Medical Research Scientist
Posted today
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Responsibilities will include:
- Conceptualizing and developing innovative research protocols and methodologies.
- Conducting in-depth literature reviews to stay abreast of the latest scientific advancements.
- Designing and executing experiments related to molecular biology, cell culture, protein expression, and purification.
- Analyzing experimental data using advanced statistical methods and presenting findings to cross-functional teams.
- Troubleshooting experimental issues and optimizing protocols to ensure data integrity and reproducibility.
- Mentoring junior researchers and providing technical guidance.
- Collaborating with external partners and academic institutions to foster innovation and knowledge sharing.
- Ensuring compliance with all laboratory safety regulations and ethical guidelines.
- Contributing to the preparation of grant proposals and scientific publications.
- Managing laboratory resources and maintaining detailed experimental records.
The ideal candidate will possess a Ph.D. in Molecular Biology, Biochemistry, or a related life science discipline, with a minimum of 5 years of post-doctoral research experience in a relevant field. Demonstrated expertise in CRISPR-Cas9 gene editing, mammalian cell culture techniques, and protein-ligand binding assays is essential. Strong analytical and problem-solving skills, coupled with excellent written and verbal communication abilities, are required. The ability to work independently as well as part of a dynamic team is crucial. Experience with bioinformatics tools and data analysis software is a significant advantage. Familiarity with regulatory affairs pertaining to drug development is also desirable. This is an exceptional opportunity for a dedicated scientist eager to make a significant impact on human health.
Senior Scientific Research Scientist - Biotechnology
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Key Responsibilities:
- Design, conduct, and optimize experiments related to molecular biology, cell biology, protein engineering, or related biotechnological fields.
- Develop and validate new research methodologies and techniques.
- Analyze and interpret complex scientific data using statistical software and bioinformatics tools.
- Write and present research findings at scientific conferences and in peer-reviewed publications.
- Collaborate with cross-functional teams, including other scientists, engineers, and project managers, to advance research projects.
- Oversee laboratory operations, ensuring compliance with safety protocols and regulatory standards.
- Manage research projects, including planning, resource allocation, and timeline management.
- Mentor and guide junior research associates and scientists.
- Identify and pursue new research opportunities and funding avenues.
- Maintain comprehensive and accurate laboratory notebooks and documentation.
- Ph.D. in Biotechnology, Molecular Biology, Biochemistry, Genetics, or a related life science discipline.
- Minimum of 5 years of post-doctoral research experience in a relevant biotechnology field.
- Demonstrated expertise in experimental design, data analysis, and scientific interpretation.
- Proficiency in a range of laboratory techniques relevant to biotechnology (e.g., PCR, Western blotting, ELISA, flow cytometry, CRISPR, recombinant protein expression).
- Experience with bioinformatics tools and databases is highly desirable.
- Strong publication record in reputable scientific journals.
- Excellent written and verbal communication skills, with the ability to articulate complex scientific concepts clearly.
- Proven leadership and project management skills.
- Ability to work independently and collaboratively in a team-oriented research environment.
- Strong critical thinking and problem-solving abilities.
Senior Research Scientist, Medical Devices
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Clinical Research Scientist
Posted 1 day ago
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Responsibilities:
- Design and develop clinical trial protocols, ensuring scientific validity and alignment with regulatory requirements.
- Oversee the operational aspects of clinical trials, including site selection, initiation, monitoring, and close-out.
- Collaborate with cross-functional teams, including medical affairs, regulatory affairs, data management, and biostatistics.
- Analyze clinical trial data, interpret results, and prepare comprehensive study reports.
- Contribute to the writing of regulatory submission documents (e.g., INDs, NDAs) and scientific publications.
- Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and other relevant guidelines.
- Manage external collaborations with clinical sites, investigators, and contract research organizations (CROs).
- Develop and present scientific findings at internal meetings and external conferences.
- Stay current with scientific literature, emerging technologies, and therapeutic area advancements.
- Contribute to the strategy and planning of future clinical development programs.
- Ensure the safety and well-being of study participants throughout the trial lifecycle.
- Ph.D. or equivalent doctoral degree in a relevant life science, biomedical science, or related field.
- Minimum of 5 years of experience in clinical research, with a focus on clinical trial design and execution within the pharmaceutical industry.
- Strong understanding of drug development processes, clinical trial phases, and regulatory pathways.
- Proven experience in data analysis, interpretation, and scientific writing.
- Excellent knowledge of GCP, ICH guidelines, and regulatory submission requirements.
- Demonstrated ability to manage complex projects and cross-functional teams.
- Strong analytical, problem-solving, and critical thinking skills.
- Effective communication and presentation skills, with the ability to convey complex scientific information clearly.
- Experience in therapeutic areas such as oncology, immunology, or cardiovascular diseases is highly desirable.
- Ability to work independently and as part of a collaborative team in a fast-paced environment.
Clinical Research Scientist
Posted 5 days ago
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Clinical Research Scientist - Oncology
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Clinical Research Scientist - Oncology
Posted today
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Senior Clinical Research Scientist
Posted 1 day ago
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- Lead the design and development of clinical trial protocols.
- Oversee the execution of clinical trials, ensuring adherence to timelines and budgets.
- Analyze and interpret complex clinical trial data to assess drug efficacy and safety.
- Collaborate with regulatory affairs and health authorities to ensure compliance.
- Prepare clinical study reports, manuscripts for publication, and regulatory submissions.
- Manage relationships with investigators, study coordinators, and clinical research organizations (CROs).
- Provide scientific expertise and guidance to clinical development teams.
- Evaluate and interpret safety data and implement risk management strategies.
We are looking for a passionate scientist eager to contribute to cutting-edge pharmaceutical research.
Clinical Research Scientist (Oncology)
Posted 1 day ago
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Responsibilities:
- Design and develop clinical trial protocols for oncology studies.
- Identify and assess potential clinical investigators and sites.
- Oversee the execution of clinical trials, ensuring compliance with GCP and regulations.
- Monitor study progress, data quality, and patient safety.
- Analyze clinical trial data and interpret study results.
- Prepare clinical study reports and contribute to regulatory submissions.
- Collaborate with internal and external stakeholders, including medical monitors and statisticians.
- Stay abreast of the latest advancements in oncology research and drug development.
- Manage budgets and timelines for clinical trials.
- Ensure effective communication among study teams and investigators.
Qualifications:
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Molecular Biology, Pharmacology, Medicine).
- Minimum of 5 years of experience in clinical research, preferably in oncology.
- Thorough understanding of clinical trial design and methodology.
- In-depth knowledge of oncology drug development and cancer biology.
- Familiarity with ICH-GCP guidelines and regulatory requirements.
- Strong analytical and data interpretation skills.
- Excellent written and verbal communication skills.
- Ability to manage complex projects and multiple tasks.
- Experience with data management systems and statistical analysis software.
- Strong problem-solving abilities and attention to detail.
Senior Clinical Research Scientist
Posted 5 days ago
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Job Description
- Designing and developing clinical trial protocols and associated documents.
- Overseeing the operational aspects of clinical trials, ensuring adherence to protocols and timelines.
- Monitoring study progress, data quality, and patient safety.
- Analyzing clinical data and contributing to the interpretation of results.
- Preparing study reports, manuscripts for publication, and regulatory submission documents.
- Ensuring compliance with all applicable regulatory requirements and ethical standards.
- Collaborating with external investigators and study sites to ensure efficient trial conduct.
- Providing scientific and technical expertise to the clinical development team.
- Staying abreast of scientific literature and advancements in relevant therapeutic areas.
- Ph.D. or Master's degree in a relevant scientific discipline (e.g., Pharmacology, Biomedical Sciences, Pharmacy).
- Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry.
- In-depth knowledge of clinical trial design, execution, and data analysis.
- Familiarity with ICH-GCP guidelines and other relevant regulatory requirements.
- Strong critical thinking and problem-solving abilities.
- Excellent written and verbal communication skills.
- Ability to manage multiple projects simultaneously and meet deadlines.
- Experience in specific therapeutic areas is a plus.