1 076 Cancer Research jobs in Bahrain
Clinical Research Scientist - Oncology
1110 Muharraq, Muharraq
BHD7800 Annually
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Our client, a leading pharmaceutical company dedicated to advancing healthcare, is seeking a highly skilled and motivated Clinical Research Scientist specializing in Oncology to join their esteemed research team in Muharraq, Muharraq, BH . This role is integral to the design, execution, and interpretation of clinical trials for novel oncology therapeutics. The Clinical Research Scientist will be responsible for contributing to the development of clinical trial protocols, selecting and managing clinical sites, ensuring compliance with regulatory guidelines (e.g., GCP), and analyzing clinical data. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, drug development, and statisticians, to advance drug candidates through the development pipeline. Key responsibilities include preparing clinical study reports, contributing to regulatory submissions, and staying abreast of the latest scientific advancements and competitive landscape in oncology. The ideal candidate will possess a strong scientific background, demonstrated experience in clinical trial management within the pharmaceutical industry, and a deep understanding of oncology drug development. Excellent analytical, problem-solving, and communication skills are essential. This hybrid role offers a combination of on-site work at our Muharraq facility and remote flexibility. We are seeking an individual with a rigorous scientific approach, a commitment to patient safety and data integrity, and the ability to work effectively in a collaborative, fast-paced environment. A PhD or MD with relevant post-doctoral or clinical research experience is highly preferred. If you are passionate about making a difference in the lives of cancer patients through cutting-edge research, we encourage you to apply.
Key Responsibilities:
Key Responsibilities:
- Contribute to the design and development of clinical trial protocols for oncology therapeutics.
- Oversee and manage the execution of clinical trials, ensuring adherence to protocols and timelines.
- Select, train, and manage clinical investigators and site staff.
- Ensure compliance with Good Clinical Practice (GCP) guidelines and relevant regulatory requirements.
- Monitor clinical trial data for safety and efficacy, and manage adverse event reporting.
- Collaborate with biostatisticians and data management teams for data analysis and interpretation.
- Prepare clinical study reports, manuscripts, and regulatory submission documents.
- Stay updated on scientific literature, emerging therapies, and the competitive landscape in oncology.
- Present clinical trial findings at scientific meetings and conferences.
- Provide scientific and medical input for drug development strategies.
- PhD or MD degree in a relevant life science discipline (e.g., Biology, Pharmacology, Medicine) required.
- Minimum of 5 years of experience in clinical research, preferably within the pharmaceutical industry and focused on oncology.
- Strong understanding of clinical trial design, execution, and data analysis.
- In-depth knowledge of oncology drug development and relevant therapeutic areas.
- Familiarity with GCP guidelines and regulatory submission processes (e.g., FDA, EMA).
- Excellent scientific writing, analytical, and problem-solving skills.
- Strong communication, presentation, and interpersonal skills.
- Ability to work effectively in a cross-functional team environment.
- Experience with hybrid work models and remote collaboration tools is a plus.
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0
Clinical Research Scientist - Oncology
790 Southern, Southern
BHD120000 Annually
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Our client, a leading pharmaceutical company dedicated to advancing healthcare, is seeking a highly specialized Clinical Research Scientist with expertise in Oncology. This role will play a crucial part in the design, execution, and interpretation of clinical trials for novel cancer therapies. You will be responsible for overseeing study protocols, analyzing data, and ensuring compliance with regulatory requirements. Collaboration with internal scientific teams, external investigators, and regulatory bodies will be a significant aspect of this position. The ideal candidate will possess a strong scientific background, a deep understanding of oncology, and extensive experience in clinical trial management. This position offers a hybrid work arrangement, requiring presence at our Nuwaidrat, Southern, BH facility for key meetings, laboratory work, and collaborative sessions, while allowing for remote work for data analysis and report writing.
Key Responsibilities:
Key Responsibilities:
- Contribute to the design and development of clinical trial protocols for oncology indications.
- Oversee the conduct of clinical trials, ensuring adherence to protocols, GCP, and regulatory guidelines.
- Analyze and interpret complex clinical trial data, including efficacy, safety, and pharmacokinetic data.
- Prepare clinical study reports, scientific publications, and regulatory submission documents.
- Collaborate with statisticians, data managers, and clinical operations teams.
- Provide scientific and medical expertise to support study activities.
- Stay current with scientific literature, industry trends, and advancements in oncology drug development.
- Interact with investigators, site personnel, and key opinion leaders.
- Contribute to the development of regulatory strategies and submissions.
- Present research findings at scientific meetings and conferences.
- Ph.D. or M.D. in a relevant scientific or medical field (e.g., Oncology, Pharmacology, Biology).
- Minimum of 5 years of experience in clinical research, with a strong focus on oncology drug development.
- In-depth knowledge of oncology, cancer biology, and treatment modalities.
- Proven experience in clinical trial design, execution, and data analysis.
- Familiarity with regulatory requirements (e.g., FDA, EMA) and Good Clinical Practice (GCP).
- Excellent scientific writing and presentation skills.
- Strong analytical and problem-solving abilities.
- Ability to work effectively in a cross-functional team environment.
- Experience in a hybrid work setting, balancing remote responsibilities with on-site collaboration.
- Strong understanding of biostatistics and data interpretation.
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1
Clinical Research Scientist - Oncology
508 Northern, Northern
BHD90000 Annually
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Our client, a prominent global pharmaceutical company, is searching for a talented and dedicated Clinical Research Scientist with a focus on Oncology to join their esteemed research and development department, located in Shakhura, Northern, BH . This role is critical in driving innovation and advancing the development of novel cancer therapies. You will be instrumental in designing, executing, and analyzing clinical trials, ensuring adherence to regulatory guidelines and scientific rigor. Responsibilities include developing clinical trial protocols, selecting investigative sites, overseeing study conduct, and interpreting complex data sets. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and data management, to ensure the successful progression of clinical programs. The ideal candidate will possess extensive knowledge of oncology, disease mechanisms, and current therapeutic strategies. A strong background in clinical trial design and management, with a proven ability to manage multiple projects simultaneously, is required. You will be responsible for preparing scientific documents, including study reports, manuscripts for publication, and regulatory submissions. Strong analytical and problem-solving skills, coupled with excellent written and verbal communication abilities, are essential. Experience with Good Clinical Practice (GCP) guidelines and other relevant regulatory requirements is mandatory. You will contribute to the scientific strategy for the oncology pipeline, providing critical insights and recommendations. This role demands a high level of scientific curiosity, meticulous attention to detail, and a commitment to improving patient outcomes through groundbreaking research. The successful applicant will have a Ph.D. or M.D. in a relevant scientific discipline, with several years of post-doctoral or industry experience in clinical research. Prior experience in pharmaceutical R&D or a Contract Research Organization (CRO) is highly preferred. This position offers a unique opportunity to contribute to life-saving treatments within a supportive and collaborative research environment.
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2
Clinical Research Scientist - Oncology
2650 Saar, Northern
BHD95000 Annually
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Our client, a pioneering pharmaceutical company at the forefront of medical innovation, is seeking a highly qualified Clinical Research Scientist specializing in Oncology to join their esteemed research and development team in Saar, Northern, BH . This role offers a hybrid work model, blending essential in-office collaboration with the flexibility of remote work. The Clinical Research Scientist will play a pivotal role in the design, execution, and analysis of clinical trials for novel oncology therapeutics. Your responsibilities will encompass developing clinical trial protocols, selecting investigational sites, and managing relationships with principal investigators and clinical research coordinators. You will ensure that all clinical trial activities comply with regulatory requirements, Good Clinical Practice (GCP) guidelines, and company SOPs. Data integrity and patient safety are paramount, and you will be involved in monitoring trial progress, reviewing adverse event reports, and contributing to the interpretation of clinical data. The successful candidate will collaborate closely with cross-functional teams, including biostatistics, data management, regulatory affairs, and medical affairs, to achieve project milestones. This position requires a strong scientific background, a deep understanding of cancer biology and treatment modalities, and proven experience in clinical trial management. You will contribute to the scientific communication of study results through presentations, publications, and regulatory submissions. A proactive approach to problem-solving, excellent analytical skills, and the ability to manage complex projects in a fast-paced environment are essential. This is an exceptional opportunity to contribute to the development of life-saving cancer treatments and advance your career in clinical research within a globally recognized pharmaceutical organization.
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3
Clinical Research Coordinator
100 Muharraq, Muharraq
BHD65000 Annually
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Our client, a leading healthcare provider in Muharraq, Muharraq, BH , is seeking a meticulous and organized Clinical Research Coordinator to join their dedicated research department. This role is essential in supporting the successful execution of clinical trials, ensuring adherence to protocols, ethical standards, and regulatory requirements. The Clinical Research Coordinator will be responsible for managing all aspects of participant recruitment, screening, enrollment, and follow-up. This includes educating potential participants about study procedures, obtaining informed consent, and ensuring all necessary documentation is accurately completed and maintained. You will meticulously collect and record patient data, manage study supplies, and coordinate with investigators, study sponsors, and regulatory agencies. A key part of this role involves ensuring the safety and well-being of participants by monitoring for adverse events and reporting them promptly. The ideal candidate will possess a strong understanding of medical terminology, research ethics, and Good Clinical Practice (GCP) guidelines. Excellent interpersonal and communication skills are vital for building rapport with patients and collaborating effectively with the healthcare team. If you are passionate about advancing medical knowledge and improving patient outcomes through research, and possess exceptional organizational skills, we encourage you to apply for this critical position. This role offers a chance to be at the forefront of medical innovation within a supportive and professional environment.
Key Responsibilities:
Key Responsibilities:
- Recruit, screen, and enroll eligible participants into clinical trials.
- Obtain informed consent from participants, ensuring they fully understand study procedures and risks.
- Collect, process, and manage study-related data and specimens accurately and efficiently.
- Maintain comprehensive and organized study documentation, adhering to regulatory requirements.
- Monitor participants' progress throughout the study, including vital signs and adverse event reporting.
- Coordinate study visits, ensuring all necessary procedures are completed on schedule.
- Liaise with investigators, study sponsors, ethics committees, and regulatory bodies.
- Manage study supplies, medications, and equipment.
- Ensure compliance with Good Clinical Practice (GCP) and other relevant regulations.
- Assist in the preparation of study reports and regulatory submissions.
- Bachelor's degree in Nursing, Life Sciences, or a related healthcare field.
- Minimum of 3 years of experience as a Clinical Research Coordinator or in a similar research role.
- Strong knowledge of clinical trial processes, research ethics, and GCP guidelines.
- Proficiency in electronic data capture (EDC) systems and clinical trial management software.
- Excellent organizational, time management, and multitasking skills.
- Strong interpersonal and communication skills, with the ability to interact professionally with diverse populations.
- Attention to detail and a commitment to accuracy.
- Ability to work independently and as part of a team.
- Current certification (e.g., SoCRA, ACRP) is a plus.
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4
Clinical Research Associate
10001 Al Seef
BHD75000 Annually
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Our client, a prominent pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their team in **Salmabad, Northern, BH**. This role is integral to the successful execution of clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. The CRA will be responsible for monitoring trial sites, verifying data accuracy, and ensuring the safety and well-being of study participants. This position offers the chance to contribute to the development of life-saving medications and therapies.
Key responsibilities include initiating, monitoring, and closing out clinical trial sites. This involves conducting site visits, reviewing essential documents, ensuring proper drug accountability, and verifying source data against case report forms. The CRA will serve as the primary liaison between the study sponsor and the clinical sites, facilitating communication and resolving any issues that arise. Ensuring compliance with safety reporting requirements and timely reporting of adverse events is paramount. The successful candidate will play a vital role in maintaining the integrity and quality of clinical trial data, which is essential for regulatory submissions.
The ideal candidate will possess a Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related field. A minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical research role is required. Thorough knowledge of GCP, FDA regulations, and clinical trial methodologies is essential. Excellent organizational, communication, and interpersonal skills are necessary for effective site management and sponsor interaction. The ability to travel to trial sites periodically is required. Proficiency in clinical trial management software and electronic data capture (EDC) systems is highly desirable. This is an excellent opportunity for a motivated professional to advance their career in pharmaceutical research and development.
Key responsibilities include initiating, monitoring, and closing out clinical trial sites. This involves conducting site visits, reviewing essential documents, ensuring proper drug accountability, and verifying source data against case report forms. The CRA will serve as the primary liaison between the study sponsor and the clinical sites, facilitating communication and resolving any issues that arise. Ensuring compliance with safety reporting requirements and timely reporting of adverse events is paramount. The successful candidate will play a vital role in maintaining the integrity and quality of clinical trial data, which is essential for regulatory submissions.
The ideal candidate will possess a Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related field. A minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical research role is required. Thorough knowledge of GCP, FDA regulations, and clinical trial methodologies is essential. Excellent organizational, communication, and interpersonal skills are necessary for effective site management and sponsor interaction. The ability to travel to trial sites periodically is required. Proficiency in clinical trial management software and electronic data capture (EDC) systems is highly desirable. This is an excellent opportunity for a motivated professional to advance their career in pharmaceutical research and development.
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5
Clinical Research Associate
23556 Al Muharraq
BHD75000 Annually
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Posted 2 days ago
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Our client, a leading pharmaceutical company, is seeking a diligent and experienced Clinical Research Associate (CRA) to join their team. This position, based in Sitra, Capital, BH , offers a hybrid work arrangement, allowing for a blend of site visits and remote administrative duties. You will be responsible for monitoring clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your role will involve conducting site initiation visits, routine monitoring visits, and close-out visits, ensuring accurate and complete data collection. The ideal candidate will possess a strong understanding of clinical trial processes, pharmaceutical drug development, and relevant regulatory frameworks. Excellent attention to detail, organizational skills, and the ability to travel to study sites are crucial. You will serve as the primary liaison between the sponsor and the investigational sites, addressing any issues or concerns that may arise. The ability to communicate effectively with investigators, site staff, and internal team members is essential. You will review essential documents, monitor subject safety, and ensure the integrity of the clinical trial data. This role requires a proactive approach to problem-solving and a commitment to ethical research practices. A bachelor's degree in a life science or healthcare-related field is typically required, along with prior experience as a CRA or in a related clinical research role. Join us in contributing to the advancement of medical science and patient care.
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6
Clinical Research Associate
1001 Hamad Town, Northern
BHD70000 Annually
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Our client, a prominent pharmaceutical company, is seeking an experienced Clinical Research Associate (CRA) to join their dedicated team based in **Hamad Town, Northern, BH**. This role is crucial for the successful execution of clinical trials, ensuring compliance with protocols, regulatory standards, and ethical guidelines. The CRA will be responsible for monitoring trial sites, collecting data, and ensuring the safety and well-being of study participants.
Key Responsibilities:
Key Responsibilities:
- Conduct site initiation, monitoring, and close-out visits for clinical trial sites.
- Verify the accuracy, completeness, and integrity of clinical trial data through source data verification.
- Ensure compliance with Good Clinical Practice (GCP) guidelines, FDA regulations, and protocol requirements.
- Train and support site staff on study protocols, procedures, and regulatory requirements.
- Manage communication between study sites, the sponsor, and other stakeholders.
- Monitor patient safety and report adverse events as per protocol.
- Review and approve site essential documents and investigational product accountability.
- Identify potential risks and issues at clinical sites and develop mitigation strategies.
- Prepare and present monitoring visit reports to the clinical trial team.
- Assist in the selection and qualification of clinical trial sites.
- Contribute to the development of clinical trial protocols and case report forms (CRFs).
- Ensure timely data entry and query resolution.
- Maintain detailed and accurate records of all monitoring activities.
- Participate in Investigator Meetings and internal team meetings.
- Stay abreast of advancements in clinical research methodologies and regulatory affairs.
- Bachelor's degree in a life science, nursing, or related healthcare field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial management role.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Proven experience in monitoring clinical trial sites and conducting source data verification.
- Excellent understanding of clinical trial processes and documentation.
- Strong analytical, problem-solving, and organizational skills.
- Exceptional communication, interpersonal, and negotiation skills.
- Ability to travel to clinical sites as required (up to 50%).
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Detail-oriented with a commitment to accuracy and quality.
- Ability to work independently and manage multiple projects effectively.
- Relevant certifications (e.g., ACRP, SoCRA) are a plus.
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7
Senior Clinical Research Scientist
806 Jbeil
BHD120000 Annually
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Our client, a cutting-edge pharmaceutical company at the forefront of medical innovation, is seeking a highly skilled and motivated Senior Clinical Research Scientist to join their dynamic, fully remote team. This position is integral to the design, execution, and analysis of groundbreaking clinical trials aimed at developing novel therapeutics. The ideal candidate will possess a deep understanding of pharmaceutical research, clinical trial methodologies, and regulatory requirements. You will be responsible for developing study protocols, overseeing data collection and integrity, and collaborating with cross-functional teams, including statisticians, medical monitors, and regulatory affairs specialists. This role demands a rigorous scientific approach, exceptional analytical skills, and the ability to interpret complex data sets to draw meaningful conclusions. The successful applicant will play a key role in advancing drug development pipelines, contributing to regulatory submissions, and ultimately improving patient outcomes. Strong communication and presentation skills are essential for disseminating research findings to internal and external stakeholders. This is a remote-first opportunity, offering significant flexibility while requiring a high degree of self-discipline and proactivity. Responsibilities include:
- Designing and managing complex clinical trials in accordance with GCP and regulatory guidelines.
- Developing and refining clinical trial protocols and study documents.
- Overseeing the collection, management, and analysis of clinical trial data.
- Collaborating with principal investigators, site staff, and research teams globally.
- Interpreting trial results and contributing to the preparation of clinical study reports.
- Providing scientific and technical expertise to support drug development.
- Identifying and evaluating new research opportunities and technologies.
- Preparing scientific publications and presentations for conferences.
- Ensuring compliance with all ethical and regulatory standards in research.
- Mentoring junior research scientists and contributing to team development.
- Ph.D. or M.D. in a relevant life science discipline (e.g., Pharmacology, Biology, Medicine).
- Minimum of 7 years of progressive experience in clinical research within the pharmaceutical or biotech industry.
- Extensive experience in designing, conducting, and analyzing Phase I-IV clinical trials.
- In-depth knowledge of ICH-GCP guidelines and regulatory submission processes (e.g., FDA, EMA).
- Proven ability to interpret complex scientific and statistical data.
- Excellent written and verbal communication skills, with a strong publication record.
- Demonstrated ability to work independently and collaboratively in a remote environment.
- Strong project management and problem-solving skills.
- Experience with clinical data management systems and statistical software is a plus.
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8
Clinical Research Scientist (Remote)
1002 Busaiteen, Muharraq
BHD90000 Annually
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Our client, a rapidly growing pharmaceutical company focused on innovative therapies, is seeking a highly motivated and experienced Clinical Research Scientist to join their expanding team. This is a fully remote position, offering flexibility and the opportunity to contribute to groundbreaking medical advancements from anywhere. You will play a critical role in the design, execution, and analysis of clinical trials, ensuring the highest standards of scientific rigor and regulatory compliance. Your expertise will be instrumental in advancing our drug development pipeline and bringing life-changing treatments to patients. Key responsibilities include:
The ideal candidate will possess a PhD or MD in a relevant scientific discipline (e.g., pharmacology, toxicology, biomedical sciences) and a minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry. Demonstrated experience in designing and managing Phase I-IV clinical trials is essential. You must have a strong understanding of drug development processes, clinical pharmacology, and regulatory affairs. Excellent written and verbal communication skills, with the ability to clearly articulate complex scientific information, are critical. Proven ability to work independently, manage multiple projects simultaneously, and collaborate effectively in a remote team environment is required. A strong publication record and experience with statistical analysis are advantageous.
- Contributing to the development of clinical trial protocols, ensuring scientific integrity and alignment with regulatory requirements.
- Providing scientific and clinical input into study design, data collection, and analysis plans.
- Collaborating with internal teams (e.g., biostatistics, data management, regulatory affairs) and external partners (e.g., investigators, CROs) to ensure successful trial execution.
- Monitoring study progress, identifying potential risks or issues, and implementing mitigation strategies.
- Interpreting clinical trial data, preparing comprehensive study reports, and presenting findings to stakeholders.
- Ensuring adherence to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements (e.g., FDA, EMA).
- Contributing to the scientific and medical review of clinical trial documents, including Investigator's Brochures and informed consent forms.
- Evaluating and selecting investigational sites and investigators for participation in clinical trials.
- Staying abreast of the latest scientific literature, therapeutic areas, and competitive landscape in assigned drug development programs.
- Supporting the development of regulatory submissions by providing scientific and clinical expertise.
- Participating in scientific meetings and conferences to present study results and network with the research community.
The ideal candidate will possess a PhD or MD in a relevant scientific discipline (e.g., pharmacology, toxicology, biomedical sciences) and a minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry. Demonstrated experience in designing and managing Phase I-IV clinical trials is essential. You must have a strong understanding of drug development processes, clinical pharmacology, and regulatory affairs. Excellent written and verbal communication skills, with the ability to clearly articulate complex scientific information, are critical. Proven ability to work independently, manage multiple projects simultaneously, and collaborate effectively in a remote team environment is required. A strong publication record and experience with statistical analysis are advantageous.
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