What Jobs are available for Drug Development in Bahrain?
Showing 5000+ Drug Development jobs in Bahrain
Senior Clinical Research Scientist - Drug Development
Posted 13 days ago
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Job Description
Key Responsibilities:
- Design and develop clinical trial protocols, including study objectives, endpoints, and statistical considerations.
- Oversee the execution of clinical trials, ensuring compliance with Good Clinical Practice (GCP) and regulatory guidelines.
- Analyze and interpret clinical trial data, preparing comprehensive study reports and publications.
- Collaborate with statisticians, clinicians, and other scientists to ensure scientific integrity and rigor.
- Manage relationships with Contract Research Organizations (CROs) and other external partners.
- Contribute to the preparation of regulatory submissions (e.g., IND, NDA).
- Provide scientific and technical guidance to project teams and junior researchers.
- Stay updated on scientific advancements and competitive intelligence in relevant therapeutic areas.
- Present study results and strategic recommendations to senior management and stakeholders.
- Identify and evaluate potential new drug candidates and therapeutic strategies.
- Ph.D. or M.D. in a relevant life science discipline (e.g., Pharmacology, Biology, Medicine).
- Minimum of 7 years of experience in clinical research and drug development within the pharmaceutical or biotechnology industry.
- Proven track record of successfully designing and executing Phase I-III clinical trials.
- Deep understanding of regulatory affairs, including FDA, EMA, and other international guidelines.
- Strong knowledge of biostatistics and data analysis methodologies relevant to clinical trials.
- Excellent scientific writing and presentation skills.
- Demonstrated leadership and project management capabilities.
- Ability to work effectively in a fast-paced, team-oriented environment.
- Experience in a specific therapeutic area (e.g., oncology, cardiology, immunology) is highly desirable.
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Senior Medicinal Chemist - Drug Discovery & Development
Posted 7 days ago
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Job Description
- Designing and synthesizing novel chemical entities for drug discovery programs across various therapeutic areas.
- Developing efficient and robust synthetic routes for target molecules and intermediates.
- Conducting structure-activity relationship (SAR) studies to optimize lead compounds for potency, selectivity, and pharmacokinetic properties.
- Collaborating closely with biologists, pharmacologists, and DMPK scientists to guide compound design and testing.
- Utilizing computational chemistry tools and techniques to aid in molecular design and property prediction.
- Troubleshooting synthetic challenges and developing innovative solutions.
- Characterizing synthesized compounds using analytical techniques such as NMR, LC-MS, and HPLC.
- Managing external synthesis collaborations and contract research organizations (CROs).
- Staying abreast of the latest advancements in medicinal chemistry, synthetic methodology, and relevant therapeutic areas.
- Authoring scientific reports, publications, and contributing to patent applications.
- Ensuring strict adherence to laboratory safety protocols and good laboratory practices (GLP).
- Mentoring junior chemists and providing technical guidance.
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Clinical Research Associate (Drug Development)
Posted 23 days ago
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Job Description
As a CRA, you will be responsible for monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements (e.g., GCP, FDA regulations), and company policies. This involves conducting site visits (pre-study, initiation, interim monitoring, and close-out), assessing the quality of trial conduct, and verifying the accuracy and completeness of source data and case report forms (CRFs). You will serve as the primary point of contact for study sites, providing training to investigators and site staff on study-related matters, and resolving any site-level issues that may arise. Data management is a key component, ensuring that all data is collected, reviewed, and reported in a timely and accurate manner. You will also be involved in regulatory document review, study budget management, and liaising with various internal departments, including data management, biostatistics, and regulatory affairs. The successful candidate will possess a strong understanding of clinical trial processes, excellent communication and interpersonal skills, and the ability to travel to clinical sites as needed. A meticulous approach to work and a commitment to maintaining the highest standards of research ethics are essential.
Key Responsibilities:
- Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory guidelines.
- Conduct site initiation visits, routine monitoring visits, and close-out visits.
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Ensure proper documentation and maintenance of site regulatory files.
- Train and support investigators and site staff on study procedures and requirements.
- Identify and resolve site-level issues and escalate as necessary.
- Liaise with study participants, investigators, and other stakeholders.
- Oversee drug accountability at trial sites.
- Contribute to the development of study protocols and case report forms.
- Ensure timely data entry and query resolution.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Experience in site monitoring and management.
- Strong understanding of clinical trial processes and documentation.
- Excellent written and verbal communication skills.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as required.
- Strong organizational skills and attention to detail.
- Ability to work independently and as part of a team.
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Lead Clinical Pharmacologist, Drug Development
Posted 1 day ago
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Job Description
The ideal candidate will possess deep expertise in drug metabolism, pharmacokinetics, drug interactions, and population PK/PD modeling. You will play a pivotal role in contributing to regulatory submissions by preparing comprehensive pharmacological documentation and interacting with health authorities. Collaboration is paramount; you will work closely with preclinical scientists, clinical investigators, biostatisticians, and regulatory affairs professionals to ensure a cohesive and efficient drug development process. This position requires a highly analytical and detail-oriented individual with excellent scientific communication skills. The ability to interpret complex data, translate findings into actionable insights, and effectively present results to diverse audiences is essential. As a lead, you will also provide scientific guidance and mentorship to junior pharmacologists and contribute to the strategic direction of the company's drug development pipeline. A strong understanding of GxP regulations and experience with relevant software tools (e.g., NONMEM, Phoenix WinNonlin) is required. This role is ideal for a seasoned professional seeking to make a significant impact in a fully remote, intellectually stimulating environment.
Location: Budaiya, Northern, BH
Responsibilities:
- Design and execute clinical pharmacology studies to assess PK, PD, and drug interactions.
- Develop and validate PK/PD models, including population PK analysis.
- Lead dose selection recommendations for clinical development.
- Analyze and interpret clinical pharmacology data.
- Author clinical pharmacology sections of regulatory submissions (e.g., IND, NDA).
- Collaborate with cross-functional teams, including preclinical, clinical, biostatistics, and regulatory affairs.
- Provide scientific expertise on drug metabolism and disposition.
- Mentor and train junior members of the pharmacology team.
- Stay abreast of regulatory guidelines and scientific advancements in clinical pharmacology.
- Present findings at scientific conferences and publish in peer-reviewed journals.
Qualifications:
- M.D. or Ph.D. in Pharmacology, Pharmaceutical Sciences, or a related field.
- Minimum of 7 years of experience in clinical pharmacology within the pharmaceutical industry.
- Extensive experience in PK/PD analysis and modeling.
- Proven track record of successful contributions to drug development programs.
- Strong understanding of regulatory requirements (FDA, EMA).
- Excellent written and verbal communication skills, with experience in authoring regulatory documents.
- Proficiency in specialized software such as NONMEM, Phoenix WinNonlin, or similar.
- Ability to work independently and lead scientific discussions in a remote setting.
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Senior Formulation Scientist - Drug Development
Posted 8 days ago
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Job Description
Responsibilities:
- Lead the formulation development of small molecule and/or biologic drug candidates across various dosage forms (e.g., oral, injectable, topical).
- Design and execute experimental studies to investigate drug solubility, stability, and compatibility with excipients.
- Develop and optimize pre-formulation and formulation processes, including screening of excipients and technologies.
- Characterize formulated drug products using analytical techniques (e.g., HPLC, dissolution testing, particle size analysis).
- Scale-up formulation processes from laboratory to pilot and manufacturing scales.
- Prepare comprehensive technical reports, development summaries, and regulatory submission documents.
- Collaborate effectively with analytical development, CMC, and project management teams.
- Troubleshoot formulation-related issues and implement effective solutions.
- Stay current with industry trends, new technologies, and regulatory guidelines in pharmaceutical formulation.
- Mentor junior scientists and contribute to the scientific growth of the team.
- Manage outsourced formulation development activities as needed.
- Contribute to the intellectual property strategy through patentable inventions.
Qualifications:
- Ph.D. or M.S. in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
- Minimum of 6 years of progressive experience in pharmaceutical formulation development.
- Demonstrated expertise in various dosage forms and drug delivery systems.
- Strong knowledge of pre-formulation, formulation design, and process development.
- Proficiency in analytical techniques relevant to pharmaceutical characterization.
- Familiarity with Good Manufacturing Practices (GMP) and regulatory requirements (e.g., FDA, EMA).
- Excellent problem-solving, critical thinking, and experimental design skills.
- Strong written and verbal communication skills, with the ability to present scientific data clearly.
- Ability to work independently and manage multiple projects in a remote setting.
- Experience with biologics formulation is a plus.
- Proven track record of contributing to successful drug development programs.
This role is based in Zallaq, Southern, BH but is offered as a fully remote position. Our client is committed to building a high-performing, collaborative remote team focused on scientific excellence. We are looking for a visionary scientist eager to contribute to the development of novel therapies and improve patient outcomes. This is an outstanding opportunity to leverage your formulation expertise within a world-class pharmaceutical organization, making a real difference in global health.
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Senior Formulation Scientist - Drug Development
Posted 14 days ago
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Job Description
- Designing and conducting pre-formulation studies to characterize active pharmaceutical ingredients (APIs).
- Developing and optimizing formulations for various dosage forms, ensuring desired release profiles and stability.
- Performing experiments related to solubility enhancement, bioavailability, and drug stability.
- Utilizing analytical techniques (e.g., HPLC, dissolution testing) to characterize formulations.
- Troubleshooting formulation-related issues and developing innovative solutions.
- Documenting experimental procedures, results, and conclusions in detailed reports.
- Collaborating with analytical, process development, and regulatory affairs teams.
- Staying current with scientific literature, new technologies, and industry best practices in pharmaceutical formulation.
- Contributing to the development of intellectual property through invention disclosures.
- Preparing materials for regulatory submissions.
A Ph.D. or Master's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related discipline is required. A minimum of 5 years of relevant experience in pharmaceutical formulation development is mandatory. Strong knowledge of solid dosage form development, including granulation, blending, tableting, and coating, is essential. Experience with parenteral formulations or other advanced drug delivery systems is a significant plus. Excellent analytical, problem-solving, and experimental design skills are vital. Proficiency in laboratory techniques and instrumentation is expected. Strong written and verbal communication skills are necessary for effective team collaboration and reporting.
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Senior Formulation Scientist - Drug Development
Posted 20 days ago
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Job Description
Responsibilities:
- Design, develop, and optimize pharmaceutical formulations for various dosage forms.
- Conduct pre-formulation studies, including physicochemical characterization of drug substances.
- Select appropriate excipients and optimize formulation composition.
- Prepare and test prototype formulations (e.g., tablets, capsules, injectables, topicals).
- Perform analytical testing to evaluate formulation stability, dissolution, and performance.
- Troubleshoot formulation challenges and identify solutions.
- Collaborate with analytical development and process chemistry teams.
- Maintain accurate and detailed laboratory notebooks and reports.
- Ensure compliance with Good Manufacturing Practices (GMP) and regulatory guidelines.
- Stay updated on industry trends and new formulation technologies.
- Master's or Ph.D. in Pharmaceutics, Pharmaceutical Sciences, Chemistry, or a related field.
- Minimum of 5 years of experience in pharmaceutical formulation development.
- Proven experience with various dosage forms (oral solids, liquids, injectables, etc.).
- Proficiency in analytical techniques relevant to formulation characterization (e.g., HPLC, dissolution, spectroscopy).
- Knowledge of GMP requirements and regulatory guidelines.
- Strong understanding of material science and drug delivery principles.
- Excellent problem-solving, organizational, and documentation skills.
- Ability to work effectively in a collaborative team environment and a hybrid setting.
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Senior Pre-clinical Drug Development Scientist
Posted 15 days ago
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Research Scientist - Drug Discovery
Posted 2 days ago
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Job Description
Key Responsibilities:
- Design and execute experiments to identify and validate novel drug targets and pathways.
- Synthesize and characterize small molecules with potential therapeutic activity using organic chemistry techniques.
- Conduct in vitro and in vivo assays to evaluate the efficacy and safety of candidate compounds.
- Collaborate with computational chemists, biologists, and pharmacologists to drive drug discovery programs forward.
- Analyze and interpret complex experimental data, drawing conclusions and proposing next steps.
- Stay abreast of the latest scientific advancements, methodologies, and emerging trends in drug discovery and relevant therapeutic areas.
- Contribute to the development of intellectual property through invention disclosures and patent filings.
- Prepare scientific reports, presentations, and publications.
- Manage external research collaborations and CROs.
- Ensure adherence to all laboratory safety protocols and regulatory guidelines.
- Contribute to strategic planning for drug discovery initiatives.
- Ph.D. in Medicinal Chemistry, Pharmacology, Organic Chemistry, Biochemistry, or a related field.
- Minimum of 5 years of experience in drug discovery research, preferably within the pharmaceutical or biotechnology industry.
- Proven experience in small molecule synthesis, structure-activity relationship (SAR) studies, and lead optimization.
- Hands-on experience with a variety of in vitro and in vivo assay formats.
- Proficiency in modern analytical techniques (e.g., NMR, Mass Spectrometry, HPLC).
- Strong understanding of pharmacokinetic and pharmacodynamic principles.
- Excellent experimental design, data analysis, and problem-solving skills.
- Exceptional written and verbal communication skills, with a track record of scientific publications.
- Ability to work independently and collaboratively in a fast-paced, team-oriented environment.
- Experience in specific therapeutic areas (e.g., oncology, immunology, infectious diseases) is a plus.
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Pharmaceutical Research Scientist - Drug Discovery
Posted today
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Job Description
This remote role requires a strong background in experimental design, data analysis, and scientific interpretation. You will collaborate closely with a global, multidisciplinary team of scientists, clinicians, and project managers, utilizing virtual communication tools and platforms to foster seamless collaboration. Responsibilities include literature review, development of research hypotheses, optimization of lead compounds, and preparation of scientific reports and publications. Experience with molecular biology techniques, high-throughput screening (HTS), and assay development is highly desirable. The ideal candidate is a self-motivated, results-oriented individual with a passion for scientific discovery and a deep understanding of the drug development process. Excellent written and verbal communication skills are essential for effectively disseminating research findings and contributing to project strategy discussions. This is an exceptional opportunity to make a significant impact on patient health by advancing innovative pharmaceutical research in a flexible, remote work environment. The company is committed to fostering a culture of scientific excellence and professional growth.
Key Responsibilities:
- Design and conduct experiments for drug discovery and target validation.
- Synthesize and characterize novel chemical entities for therapeutic development.
- Perform in vitro and in vivo assays to evaluate drug efficacy and safety.
- Analyze experimental data and interpret results in the context of project goals.
- Collaborate with cross-functional teams in a remote research setting.
- Contribute to the development of research strategies and project plans.
- Prepare detailed scientific reports, presentations, and publications.
- Stay current with advancements in pharmaceutical research and relevant scientific literature.
- Ensure compliance with laboratory safety standards and regulatory guidelines.
- Ph.D. in Pharmacology, Medicinal Chemistry, Biochemistry, or a related life science field.
- Minimum of 3-5 years of postdoctoral or industry experience in drug discovery.
- Proven track record in experimental design and execution.
- Strong knowledge of medicinal chemistry principles and synthetic organic chemistry.
- Experience with various biological assays and pharmacology techniques.
- Proficiency in data analysis and scientific software.
- Excellent written and verbal communication skills for remote collaboration.
- Ability to work independently, manage multiple priorities, and meet deadlines in a remote setting.
- Demonstrated ability to contribute to scientific publications and presentations.
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