Explore exciting opportunities in clinical research. This field is at the forefront of medical advancements, offering roles for skilled professionals eager to contribute to 4 054 Clinical Research jobs in Bahrain
Clinical Research Scientist - Oncology
4567 Northern, Northern
BHD110000 Annually
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Our client, a leading pharmaceutical innovator, is seeking a highly skilled and dedicated Clinical Research Scientist specializing in Oncology. This is a crucial, fully remote position that will contribute significantly to the advancement of novel cancer therapies. You will be at the forefront of designing, implementing, and managing clinical trials, from protocol development through to data analysis and reporting. Your expertise will guide the scientific integrity of our oncology research programs. You will collaborate closely with internal R&D teams, clinical operations, regulatory affairs, and external investigators to ensure the successful execution of clinical studies. Responsibilities include identifying research opportunities, developing scientifically sound protocols, selecting investigational sites, and overseeing data collection and analysis. You will play a key role in interpreting trial results and communicating findings to regulatory agencies, scientific communities, and internal stakeholders.
Key responsibilities include:
The ideal candidate will hold a PhD or MD in a relevant scientific discipline, with a minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry, specifically focused on oncology. A deep understanding of cancer biology, therapeutic targets, and clinical trial methodologies is essential. Proven experience in protocol development, clinical data analysis, and regulatory submissions is required. Excellent written and verbal communication skills, strong analytical abilities, and the capacity to work effectively in a fully remote, collaborative environment are critical for success. If you are driven by a passion for advancing cancer care through cutting-edge research, this remote opportunity is an excellent fit for your expertise.
Key responsibilities include:
- Designing and developing clinical trial protocols for oncology therapeutics.
- Overseeing the scientific and medical aspects of clinical trials from initiation to closure.
- Collaborating with biostatisticians and data managers on data analysis and interpretation.
- Writing clinical study reports, regulatory submissions, and manuscripts for publication.
- Identifying and evaluating potential clinical investigators and trial sites.
- Providing scientific and medical guidance to cross-functional teams.
- Staying current with scientific literature, competitive landscape, and regulatory guidelines in oncology.
- Presenting trial progress and results at internal meetings and external scientific conferences.
- Ensuring compliance with Good Clinical Practice (GCP) and other relevant regulations.
The ideal candidate will hold a PhD or MD in a relevant scientific discipline, with a minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry, specifically focused on oncology. A deep understanding of cancer biology, therapeutic targets, and clinical trial methodologies is essential. Proven experience in protocol development, clinical data analysis, and regulatory submissions is required. Excellent written and verbal communication skills, strong analytical abilities, and the capacity to work effectively in a fully remote, collaborative environment are critical for success. If you are driven by a passion for advancing cancer care through cutting-edge research, this remote opportunity is an excellent fit for your expertise.
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Senior Clinical Research Scientist
2208 Hamala, Northern
BHD110000 Annually
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Our client is seeking a highly accomplished Senior Clinical Research Scientist to lead groundbreaking research initiatives in a fully remote capacity. This role is central to designing, executing, and analyzing complex clinical trials, contributing to significant advancements in healthcare and scientific understanding. You will be responsible for developing study protocols, managing data integrity, interpreting results, and preparing comprehensive scientific reports. The ideal candidate possesses a deep understanding of clinical research methodologies, regulatory requirements, and statistical analysis. This remote-first position demands exceptional scientific acumen, strong project management skills, and the ability to collaborate effectively with global research teams. Key responsibilities include:
- Designing and developing clinical trial protocols, ensuring alignment with scientific objectives and regulatory guidelines.
- Overseeing the planning and execution of clinical studies, from site selection to data analysis.
- Managing and ensuring the quality and integrity of clinical trial data.
- Conducting statistical analysis of clinical trial data and interpreting findings.
- Preparing comprehensive scientific reports, publications, and presentations for internal and external audiences.
- Collaborating with Principal Investigators, study site personnel, and internal teams to ensure smooth trial operations.
- Monitoring study progress, identifying potential risks, and implementing mitigation strategies.
- Ensuring compliance with Good Clinical Practice (GCP) and other relevant regulatory standards.
- Mentoring junior research staff and contributing to the scientific development of the team.
- Evaluating new research technologies and methodologies to enhance study design and execution.
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Senior Clinical Research Scientist
78901 Tubli, Central
BHD100000 Annually
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Our client, a pioneering biopharmaceutical company at the forefront of medical innovation, is searching for a highly accomplished Senior Clinical Research Scientist to lead groundbreaking research initiatives from their state-of-the-art facility in **Janabiyah, Northern, BH**. This role is critical for advancing our understanding of complex diseases and developing novel therapeutic solutions. The Senior Clinical Research Scientist will be responsible for designing, conducting, and analyzing clinical trials, from Phase I through Phase IV. Key duties include developing study protocols, overseeing data collection and analysis, interpreting results, and preparing scientific publications and presentations. You will collaborate with cross-functional teams, including medical affairs, regulatory affairs, and R&D, to ensure the successful execution of research programs. The ideal candidate will possess a Ph.D. in a relevant scientific discipline (e.g., Pharmacology, Biology, Biochemistry, Medicine) and have extensive experience in clinical trial design, execution, and data analysis within the pharmaceutical or biotechnology industry. Strong leadership skills, exceptional analytical and problem-solving abilities, and a deep understanding of scientific methodologies and regulatory requirements are essential. We are seeking an individual with a proven track record of scientific achievement and a passion for driving medical advancements. This position offers a competitive salary, comprehensive benefits package, and exceptional opportunities for professional development and career progression. You will have the opportunity to work on cutting-edge research and contribute to improving patient outcomes globally. Join a team dedicated to making a difference in healthcare. Qualifications include a Ph.D. in a relevant life science or medical field, a minimum of 7 years of experience in clinical research, preferably within drug development. Demonstrable experience in designing and managing clinical trials, including protocol development, statistical analysis planning, and regulatory submissions, is required. Excellent scientific writing and communication skills are paramount.
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Principal Clinical Research Scientist
234 Manama, Capital
BHD135000 Annually
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Our client, a leading biopharmaceutical company with a robust pipeline, is seeking an exceptional Principal Clinical Research Scientist to be based in Manama, Capital, BH . This senior role will be instrumental in designing, executing, and analyzing clinical trials that advance the development of innovative pharmaceutical products. The successful candidate will bring a wealth of experience in clinical trial methodology, data interpretation, and regulatory compliance within the pharmaceutical sector.
Key Responsibilities:
Key Responsibilities:
- Lead the scientific and operational aspects of clinical trial design, protocol development, and scientific interpretation of data.
- Oversee the execution of clinical trials, ensuring adherence to Good Clinical Practice (GCP), regulatory requirements, and company standards.
- Collaborate with cross-functional teams, including R&D, medical affairs, regulatory affairs, and project management, to ensure successful trial implementation.
- Analyze and interpret complex clinical data, contributing to scientific publications, presentations, and regulatory submissions.
- Develop and maintain strong relationships with key opinion leaders (KOLs), investigators, and clinical sites.
- Provide scientific and technical expertise to internal teams and external partners regarding drug development and clinical research.
- Contribute to the strategic direction of the company's clinical development programs.
- Prepare clinical study reports, investigator brochures, and other essential study documents.
- Identify and evaluate potential new research opportunities and technologies.
- Mentor and guide junior research scientists and clinical team members.
- Ph.D. or M.D. in a relevant life science discipline (e.g., pharmacology, biology, medicine).
- Minimum of 8-12 years of experience in clinical research and development within the pharmaceutical or biotechnology industry.
- Extensive experience in designing and managing Phase I-IV clinical trials.
- In-depth knowledge of pharmaceutical drug development processes, regulatory guidelines (e.g., FDA, EMA, SFDA), and ICH-GCP.
- Proven ability to analyze and interpret complex clinical datasets and translate findings into actionable insights.
- Excellent scientific writing and presentation skills.
- Strong leadership, project management, and problem-solving abilities.
- Demonstrated experience in collaborating with external scientific experts and clinical investigators.
- Experience in therapeutic areas such as oncology, immunology, or cardiovascular diseases is highly preferred.
- Fluency in English; proficiency in Arabic is an advantage.
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3
Senior Clinical Research Scientist
321, Muharraq, Muharraq, BH Muharraq, Muharraq
BHD75000 Annually
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Our client, a highly respected biotechnology firm, is actively recruiting a Senior Clinical Research Scientist to lead critical aspects of their drug development programs in Muharraq, Muharraq, BH . This role demands extensive expertise in clinical trial design, execution, and data analysis, with a strong focus on scientific rigor and regulatory compliance. The Senior Clinical Research Scientist will be responsible for translating scientific insights into actionable clinical strategies, collaborating with cross-functional teams, and ensuring the successful progression of research studies from initiation to completion. Responsibilities include:
Qualifications:
- Designing and developing comprehensive clinical trial protocols in alignment with therapeutic area strategies and regulatory requirements.
- Overseeing the execution of clinical trials, ensuring adherence to protocol, GCP, and all relevant guidelines.
- Collaborating with principal investigators, clinical research coordinators, and site staff to ensure high-quality data collection and patient care.
- Analyzing and interpreting clinical trial data, including safety and efficacy endpoints.
- Preparing clinical study reports, regulatory submissions, and scientific publications.
- Providing scientific and clinical expertise to internal teams, including regulatory affairs, medical affairs, and project management.
- Identifying and mitigating risks associated with clinical trial conduct.
- Contributing to the development of target product profiles and strategic decision-making for drug development programs.
- Staying abreast of the latest scientific advancements, clinical trends, and regulatory changes in the pharmaceutical industry.
- Managing budgets and timelines for clinical research activities.
Qualifications:
- Ph.D. or M.D. in a life science, medical, or related field.
- Minimum 6 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry.
- Proven experience in designing, conducting, and managing clinical trials (Phase I-IV).
- In-depth knowledge of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements.
- Strong understanding of statistical principles for clinical data analysis.
- Excellent written and verbal communication skills, with a track record of scientific publications.
- Ability to work independently and lead cross-functional teams.
- Project management skills and experience are highly desirable.
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4
Clinical Research Scientist - Pharmaceutical
23415 Askar, Southern
BHD90000 Annually
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Our client, a progressive pharmaceutical company, is looking for a highly skilled Clinical Research Scientist to join their R&D team in **Tubli, Capital, BH**. This role is integral to the successful design, execution, and analysis of clinical trials for novel drug development. You will be responsible for contributing to study protocols, overseeing data collection and analysis, and ensuring compliance with regulatory guidelines throughout the clinical development process.
Key responsibilities include developing clinical study protocols and investigator brochures, collaborating with clinical investigators and site staff, and monitoring study progress to ensure adherence to scientific rigor and ethical standards. You will be involved in data analysis, interpretation of results, and preparation of reports for regulatory submissions and scientific publications. A strong understanding of Good Clinical Practice (GCP), regulatory affairs, and statistical analysis methodologies is essential. You will also contribute to the strategic planning of clinical development programs.
The ideal candidate will possess a Ph.D. or Master's degree in a relevant life science field (e.g., Pharmacology, Biotechnology, Medicine). A minimum of 5-7 years of experience in clinical research within the pharmaceutical or biotechnology industry is required. Proven experience in designing and managing clinical trials, analyzing clinical data, and preparing regulatory documentation is mandatory. Excellent scientific acumen, critical thinking, problem-solving, and communication skills are crucial. Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is beneficial. This is a compelling opportunity to contribute to groundbreaking pharmaceutical research and development in **Tubli, Capital, BH**.
Key responsibilities include developing clinical study protocols and investigator brochures, collaborating with clinical investigators and site staff, and monitoring study progress to ensure adherence to scientific rigor and ethical standards. You will be involved in data analysis, interpretation of results, and preparation of reports for regulatory submissions and scientific publications. A strong understanding of Good Clinical Practice (GCP), regulatory affairs, and statistical analysis methodologies is essential. You will also contribute to the strategic planning of clinical development programs.
The ideal candidate will possess a Ph.D. or Master's degree in a relevant life science field (e.g., Pharmacology, Biotechnology, Medicine). A minimum of 5-7 years of experience in clinical research within the pharmaceutical or biotechnology industry is required. Proven experience in designing and managing clinical trials, analyzing clinical data, and preparing regulatory documentation is mandatory. Excellent scientific acumen, critical thinking, problem-solving, and communication skills are crucial. Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is beneficial. This is a compelling opportunity to contribute to groundbreaking pharmaceutical research and development in **Tubli, Capital, BH**.
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Clinical Research Scientist - Oncology
910 Bilad Al Qadeem, Capital
BHD7000 Annually
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Our client, a leading pharmaceutical company situated in Sitra, Capital, BH , is looking for a dedicated and highly skilled Clinical Research Scientist specializing in Oncology. This role is critical in advancing our oncology drug development pipeline from pre-clinical research through clinical trials to market approval. The successful candidate will play a key role in designing, executing, and analyzing complex clinical studies, ensuring adherence to all regulatory guidelines (e.g., GCP, ICH). Responsibilities include protocol development, site selection and monitoring, data interpretation, and reporting on trial outcomes. You will collaborate with cross-functional teams including R&D, regulatory affairs, medical affairs, and marketing to ensure seamless project progression. A strong understanding of cancer biology, therapeutic targets, and current treatment modalities is essential. The ideal candidate will have a proven track record in clinical trial management and a deep knowledge of statistical analysis in clinical research. You will be expected to contribute to the scientific literature through publications and presentations at international conferences. This position offers the chance to work on groundbreaking therapies and make a significant impact on patient lives. Strong analytical, problem-solving, and communication skills are paramount. The ability to manage multiple projects simultaneously in a fast-paced environment is also crucial. We are looking for a motivated individual with a passion for scientific innovation and a commitment to improving cancer treatment.
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Lead Clinical Research Scientist
43521 Southern, Southern
BHD110000 Annually
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We are looking for a highly motivated and innovative Lead Clinical Research Scientist to join our cutting-edge research and development team in Nuwaidrat, Southern, BH . This senior position requires a deep understanding of scientific methodologies, experimental design, and data analysis within a clinical research setting. You will be instrumental in designing, executing, and overseeing groundbreaking research projects focused on developing novel therapeutic interventions. Your responsibilities will include leading a team of researchers, managing project timelines, securing necessary approvals, and ensuring compliance with all relevant ethical and regulatory guidelines. A significant part of your role will involve analyzing complex clinical trial data, interpreting results, and preparing high-impact publications and presentations for scientific conferences. Collaboration with cross-functional teams, including R&D, clinical operations, and regulatory affairs, will be essential for project success. The ideal candidate will possess a Ph.D. in a relevant life science discipline, coupled with a substantial track record of successful clinical research and project leadership. A strong publication record and experience in grant writing are highly desirable. You will contribute significantly to the company's innovation pipeline and scientific reputation. This role offers an exceptional opportunity to shape the future of healthcare through pioneering research in a stimulating and collaborative environment. Bring your expertise and passion for discovery to our team and make a tangible impact on patient outcomes. We value scientific rigor, intellectual curiosity, and a commitment to ethical research practices.
Key Responsibilities:
Key Responsibilities:
- Design and implement complex clinical research protocols.
- Lead and mentor a team of research scientists and technicians.
- Oversee all phases of clinical trial execution, from initiation to closure.
- Analyze and interpret complex scientific data using advanced statistical methods.
- Prepare manuscripts for publication in peer-reviewed journals and present findings at conferences.
- Ensure strict adherence to Good Clinical Practice (GCP) and other regulatory requirements.
- Collaborate with internal departments and external partners on research initiatives.
- Manage project budgets and resources effectively.
- Contribute to the development of research strategies and grant proposals.
- Identify and evaluate new research technologies and methodologies.
- Ph.D. in Biology, Pharmacology, Medicine, or a related life science field.
- Minimum of 7 years of post-doctoral experience in clinical research or drug development.
- Proven experience in leading research teams and managing complex projects.
- Extensive knowledge of clinical trial design, statistical analysis, and regulatory affairs.
- Excellent scientific writing and presentation skills.
- Demonstrated ability to secure research funding and publish in high-impact journals.
- Strong understanding of ethical principles in research.
- Proficiency in statistical software (e.g., SAS, R) and data management systems.
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7
Clinical Research Scientist - Oncology
751 Bilad Al Qadeem, Capital
BHD7500 Annually
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Our client, a leading pharmaceutical company, is seeking a dedicated and highly qualified Clinical Research Scientist specializing in Oncology to join their R&D team in Sitra, Capital, BH . This pivotal role involves the design, execution, and oversight of clinical trials for novel cancer therapies. The Clinical Research Scientist will be responsible for developing study protocols, identifying and assessing potential clinical trial sites, and collaborating with investigators and clinical research staff to ensure the smooth and efficient conduct of studies. You will play a key role in data analysis, interpretation, and reporting of study results, ensuring compliance with regulatory requirements and ethical standards.
Responsibilities include managing trial budgets, timelines, and resources effectively. The Scientist will be involved in the preparation of regulatory submissions, including Investigational New Drug (IND) applications and New Drug Applications (NDA). Building and maintaining strong relationships with key opinion leaders (KOLs) in the oncology field, regulatory agencies, and internal stakeholders is crucial. You will contribute to the strategic planning of the oncology pipeline, identifying new research opportunities and therapeutic areas. Staying abreast of the latest advancements in oncology research, clinical trial methodologies, and regulatory guidelines is essential. This position requires excellent scientific acumen, critical thinking, and strong project management skills.
Qualifications:
Responsibilities include managing trial budgets, timelines, and resources effectively. The Scientist will be involved in the preparation of regulatory submissions, including Investigational New Drug (IND) applications and New Drug Applications (NDA). Building and maintaining strong relationships with key opinion leaders (KOLs) in the oncology field, regulatory agencies, and internal stakeholders is crucial. You will contribute to the strategic planning of the oncology pipeline, identifying new research opportunities and therapeutic areas. Staying abreast of the latest advancements in oncology research, clinical trial methodologies, and regulatory guidelines is essential. This position requires excellent scientific acumen, critical thinking, and strong project management skills.
Qualifications:
- Ph.D. or M.D. in a relevant life science field (e.g., Oncology, Pharmacology, Biology, Medicine).
- Minimum 5 years of experience in clinical research, specifically within the oncology therapeutic area.
- Proven experience in designing and managing Phase I-IV clinical trials.
- In-depth knowledge of GCP, ICH guidelines, and regulatory submission processes (FDA, EMA).
- Strong understanding of cancer biology, therapeutic strategies, and drug development.
- Excellent data analysis, interpretation, and scientific writing skills.
- Demonstrated ability to lead cross-functional teams and manage complex projects.
- Exceptional communication, presentation, and interpersonal skills.
- Ability to travel as required.
- Experience in biostatistics or epidemiology is a plus.
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Lead Clinical Research Scientist
10650 Seef, Capital
BHD110000 Annually
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Our client, a pioneering scientific research organization, is seeking a highly motivated and experienced Lead Clinical Research Scientist to contribute to groundbreaking studies in Jidhafs, Capital, BH . This pivotal role involves designing, conducting, and analyzing clinical trials, with a focus on translating scientific discoveries into practical applications. The Lead Clinical Research Scientist will guide research protocols, manage data integrity, and collaborate with a multidisciplinary team to advance medical knowledge.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and develop comprehensive clinical trial protocols, ensuring scientific rigor and compliance with regulatory requirements.
- Oversee the execution of clinical studies, including patient recruitment, data collection, and sample management.
- Analyze and interpret complex clinical data using statistical software and methodologies.
- Prepare scientific reports, publications, and presentations for internal and external stakeholders, including regulatory agencies.
- Collaborate with investigators, clinicians, statisticians, and other research personnel to ensure the successful conduct of trials.
- Ensure adherence to Good Clinical Practice (GCP) guidelines, ethical principles, and all applicable regulations.
- Manage research budgets, track project timelines, and ensure resource allocation is optimized.
- Evaluate new research technologies and methodologies to enhance study design and data quality.
- Mentor and provide scientific guidance to junior research staff and study teams.
- Contribute to the identification and prioritization of new research opportunities and potential therapeutic targets.
- Actively participate in scientific conferences and stay updated with the latest advancements in the field.
- Ensure the highest standards of data integrity, accuracy, and confidentiality.
- Manage interactions with regulatory authorities and ethics committees.
Qualifications:
- Ph.D. or equivalent in a relevant scientific discipline (e.g., Biomedical Sciences, Pharmacology, Biology, Statistics).
- Minimum of 8 years of experience in clinical research, with a significant focus on scientific study design and data analysis.
- Proven expertise in a specific therapeutic area (mention an area like: oncology, cardiology, infectious diseases, neurology).
- Strong understanding of clinical trial methodologies, statistical analysis, and regulatory affairs (e.g., FDA, EMA).
- Experience with electronic data capture (EDC) systems and statistical software (e.g., SAS, R).
- Excellent scientific writing, communication, and presentation skills.
- Demonstrated leadership abilities and experience managing research projects and teams.
- Ability to critically evaluate scientific literature and data.
- Strong problem-solving and critical thinking skills.
- Detail-oriented with a commitment to quality and ethical conduct.
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