What Jobs are available for Drug Development in Bahrain?
Showing 5000+ Drug Development jobs in Bahrain
Senior Clinical Research Scientist - Drug Development
511 Arad
BHD110000 Annually
WhatJobs
Posted 13 days ago
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Job Description
Our client, a prominent pharmaceutical company located in **Salmabad, Northern, BH**, is seeking an accomplished Senior Clinical Research Scientist to spearhead critical aspects of drug development. This role is based in our state-of-the-art facilities and requires an on-site presence. You will play a pivotal role in designing, executing, and analyzing clinical trials for novel therapeutics, contributing significantly to bringing life-changing medicines to patients. The ideal candidate possesses a strong scientific background, extensive experience in clinical trial management, and a thorough understanding of regulatory requirements within the pharmaceutical industry. You will be expected to lead cross-functional teams, manage external collaborations, and contribute to the strategic direction of drug development programs.
Key Responsibilities:
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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0
Senior Medicinal Chemist - Drug Discovery & Development
2045 Seef, Capital
BHD115000 Annually
WhatJobs
Posted 7 days ago
Job Viewed
Job Description
Our client is seeking a highly accomplished Senior Medicinal Chemist to drive forward their innovative drug discovery programs. This pivotal role involves the design, synthesis, and optimization of novel small molecules with therapeutic potential. The successful candidate will be an integral part of a multidisciplinary research team, contributing expertise in organic synthesis, structure-activity relationships (SAR), and drug metabolism and pharmacokinetics (DMPK). This position requires a strong background in synthetic organic chemistry and a proven track record of contributing to drug candidate progression. Key responsibilities include:
- 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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1
Clinical Research Associate (Drug Development)
78901 Al Muharraq
BHD85000 Annually
WhatJobs
Posted 23 days ago
Job Viewed
Job Description
Our client, a dynamic pharmaceutical company at the forefront of medical innovation, is actively seeking a skilled Clinical Research Associate (CRA) to join their team. This role is critical to the successful execution of clinical trials, ensuring the safety of participants and the integrity of data for novel drug development programs. The position is based at our state-of-the-art facility in Sitra, Capital, BH .
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:
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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2
Lead Clinical Pharmacologist, Drug Development
911 Tubli
BHD130000 Annually
WhatJobs
Posted 1 day ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking an experienced Lead Clinical Pharmacologist to join their innovative drug development team. This critical role is fully remote, offering the chance to shape the pharmacological profile of novel therapeutics from early-stage research through to clinical application. You will be responsible for designing and overseeing clinical pharmacology studies, analyzing pharmacokinetic (PK) and pharmacodynamic (PD) data, and developing robust dose selection strategies.
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:
Qualifications:
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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3
Senior Formulation Scientist - Drug Development
12353 Zallaq, Southern
BHD100000 Annually
WhatJobs
Posted 8 days ago
Job Viewed
Job Description
Our client, a cutting-edge pharmaceutical company dedicated to advancing human health, is seeking a highly experienced Senior Formulation Scientist to join their innovative remote research and development team. This vital role will focus on the design, development, and optimization of novel drug formulations to ensure efficacy, stability, and patient compliance. The ideal candidate will possess a profound understanding of pharmaceutical science, advanced drug delivery systems, and regulatory requirements. You will be a key driver in bringing life-changing medicines from concept to clinical trials. This position is fully remote, enabling you to contribute your expertise within a flexible and dynamic work setting.
Responsibilities:
Qualifications:
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.
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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4
Senior Formulation Scientist - Drug Development
10001 Galali
BHD95000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking a highly skilled Senior Formulation Scientist to join their innovative research and development team based in Jidhafs, Capital, BH . This role is crucial for the development of novel drug delivery systems and the optimization of existing formulations. You will be responsible for designing, executing, and analyzing pre-formulation and formulation development studies for various dosage forms. The ideal candidate will possess a strong understanding of pharmaceutics, physical chemistry, and drug delivery technologies. Experience with different dosage forms (e.g., oral solids, injectables, topicals) and a proven ability to troubleshoot formulation challenges are essential. This hybrid position will involve laboratory work and collaborative meetings, requiring flexibility and excellent communication skills. Responsibilities include:
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.
- 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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5
Senior Formulation Scientist - Drug Development
40004 Riffa, Southern
BHD100000 Annually
WhatJobs
Posted 20 days ago
Job Viewed
Job Description
Our client, a leader in the pharmaceutical industry, is seeking a highly skilled Senior Formulation Scientist to join their Research & Development team. This role, based in Riffa, Southern, BH , will focus on the development and optimization of novel drug formulations. You will play a pivotal role in designing, preparing, and characterizing various dosage forms, ensuring product stability, bioavailability, and efficacy. Key responsibilities include conducting pre-formulation studies, selecting appropriate excipients, developing liquid, semi-solid, and solid dosage forms, and performing analytical testing to assess formulation performance. You will collaborate closely with analytical chemists, process engineers, and regulatory affairs specialists throughout the drug development lifecycle. The ideal candidate will possess a strong understanding of pharmaceutical sciences, formulation development principles, and GMP guidelines. Experience with various analytical techniques (e.g., HPLC, dissolution testing, particle size analysis) is essential. This position offers a hybrid work arrangement, allowing for a balance between laboratory-based research and flexible remote work. We are looking for a creative problem-solver with excellent attention to detail and strong documentation skills. If you are passionate about advancing pharmaceutical innovation and contributing to the development of life-changing medicines in Riffa, Southern, BH , we encourage you to apply.
Responsibilities:
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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6
Senior Pre-clinical Drug Development Scientist
30003 Northern, Northern
BHD135000 Annually
WhatJobs
Posted 15 days ago
Job Viewed
Job Description
Our client, a pioneering biopharmaceutical company, is seeking an experienced Senior Pre-clinical Drug Development Scientist to join their innovative team. This is a fully remote position, allowing you to contribute to groundbreaking drug development from anywhere. The role focuses on the critical stage of pre-clinical testing and evaluation of new drug candidates, with a strong emphasis on pharmacokinetics (PK), pharmacodynamics (PD), and toxicology studies. You will be instrumental in designing, executing, and interpreting complex pre-clinical studies to assess the safety and efficacy of novel therapeutic agents. This involves developing and validating analytical methods, managing CRO relationships, and ensuring compliance with regulatory guidelines (e.g., GLP). The ideal candidate will possess a strong scientific background in pharmacology, toxicology, or a related field, with a proven track record of successful pre-clinical program management. You will collaborate closely with medicinal chemists, biologists, and clinical development teams to define optimal development strategies. Excellent written and verbal communication skills are essential for preparing study reports, regulatory submissions, and presenting findings to internal and external stakeholders. This remote role requires a high degree of self-discipline, organization, and the ability to work independently while maintaining seamless communication with colleagues. Our client is dedicated to advancing healthcare through innovative science and offers a challenging yet rewarding career path. This position is physically associated with Shakhura, Northern, BH , but is structured as a fully remote opportunity.
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7
Research Scientist - Drug Discovery
555 Manama, Capital
BHD7200 Monthly
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client is a pioneering pharmaceutical research company seeking a dedicated and innovative Research Scientist specializing in Drug Discovery to join our state-of-the-art laboratories in Manama, Capital, BH . This role is fundamental to our mission of developing life-saving therapies. You will be instrumental in identifying and validating novel drug targets, designing and synthesizing potential therapeutic compounds, and conducting preclinical studies. The ideal candidate possesses a strong background in medicinal chemistry, pharmacology, or a related discipline, coupled with hands-on experience in small molecule discovery and optimization.
Key Responsibilities:
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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8
Pharmaceutical Research Scientist - Drug Discovery
10021 Galali
BHD110000 Annually
WhatJobs Direct
Posted today
Job Viewed
Job Description
Our client, a cutting-edge pharmaceutical company, is seeking a highly skilled Pharmaceutical Research Scientist to join their innovative drug discovery team. This is a fully remote position, offering a unique opportunity to contribute to the development of novel therapeutics from early-stage research through to preclinical evaluation. The scientist will be responsible for designing and executing experiments to identify and validate new drug targets, synthesize and characterize potential drug candidates, and perform in vitro and in vivo studies. You will leverage your expertise in medicinal chemistry, pharmacology, or a related discipline to drive research programs forward.
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:
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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