The field of oncology offers varied career paths for healthcare professionals dedicated to cancer care and research. Job opportunities exist in hospitals, cancer centers, research institutions, and pharmaceutical companies. Professionals in this sector work to improve cancer treatment, prevention, and patient support. 220 Oncology jobs in Bahrain
Senior Clinical Pharmacist - Oncology
901 Al Muharraq
BHD105000 Annually
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Posted 19 days ago
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Job Description
Our client, a leading healthcare institution, is seeking a highly skilled Senior Clinical Pharmacist specializing in Oncology to join their dedicated pharmacy team. This is an on-site role, essential for providing expert pharmaceutical care to cancer patients. You will be responsible for managing and dispensing complex chemotherapy regimens, monitoring patient response to therapy, managing adverse drug reactions, and providing patient counseling. The ideal candidate possesses a deep understanding of oncology pharmacology, including various chemotherapy agents, targeted therapies, and immunotherapy. You will play a critical role in ensuring safe and effective medication use, collaborating closely with oncologists, nurses, and other healthcare professionals to optimize patient outcomes. This position requires strong clinical judgment, meticulous attention to detail, and excellent communication skills. You will also be involved in drug information services, formulary management, and potentially contributing to clinical research initiatives. The Senior Clinical Pharmacist will also mentor and precept pharmacy residents and students, contributing to the education and development of future pharmacists. Our client is committed to delivering compassionate and cutting-edge cancer care, and this role is central to achieving that mission within the **Sitra, Capital, BH** region.
Responsibilities:
Responsibilities:
- Provide comprehensive pharmaceutical care to oncology patients.
- Dispense and verify chemotherapy and other oncology medications.
- Monitor patient therapy for efficacy, toxicity, and drug interactions.
- Manage and counsel patients on their medication regimens and potential side effects.
- Collaborate with the multidisciplinary oncology team to develop and implement treatment plans.
- Participate in tumor board conferences and provide drug therapy recommendations.
- Respond to drug information requests from healthcare professionals.
- Ensure compliance with all relevant regulations and pharmacy standards.
- Mentor and precept pharmacy residents and students.
- Contribute to quality improvement initiatives within the pharmacy department.
- Doctor of Pharmacy (PharmD) degree from an accredited institution.
- Licensed Pharmacist in Bahrain.
- Completion of a PGY-1 Pharmacy Residency.
- PGY-2 Oncology Pharmacy Residency or equivalent experience is strongly preferred.
- Minimum of 5 years of clinical pharmacy experience, with a significant focus on oncology.
- Board Certified Pharmacotherapy Specialist (BCPS) or Board Certified Oncology Pharmacist (BCOP) is highly desirable.
- Extensive knowledge of cancer chemotherapy, supportive care medications, and emerging oncology therapeutics.
- Strong clinical skills, including patient assessment and medication therapy management.
- Excellent communication, interpersonal, and critical thinking skills.
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Clinical Research Associate - Oncology
702 Galali
BHD95000 Annually
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Posted today
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A globally recognized pharmaceutical leader is seeking a dedicated and meticulous Clinical Research Associate (CRA) to support groundbreaking oncology trials. This critical position is situated in the thriving city of Sitra, Capital, BH . As a CRA, you will play a vital role in the successful execution of clinical studies, ensuring data integrity, patient safety, and adherence to regulatory requirements. You will be responsible for site selection, initiation, monitoring, and close-out visits to clinical trial sites, ensuring all study-related activities are conducted in accordance with the protocol, Good Clinical Practice (GCP) guidelines, and applicable regulations. The ideal candidate will possess a strong understanding of clinical trial processes, therapeutic areas, and regulatory frameworks within the pharmaceutical industry. Your responsibilities will include verifying source documentation, monitoring patient recruitment, ensuring proper investigational product accountability, and resolving data queries. You will serve as the primary liaison between the sponsor and investigative sites, fostering strong working relationships and providing necessary training and support to study personnel. This role requires exceptional organizational skills, attention to detail, and the ability to manage multiple priorities effectively. A proactive approach to problem-solving and a commitment to excellence in clinical research are paramount. The successful candidate will contribute to the advancement of life-saving therapies by ensuring the highest quality standards in clinical trial conduct. We are looking for individuals who are passionate about making a difference in patients' lives and possess a robust scientific and ethical foundation. Excellent communication and interpersonal skills are essential for effective collaboration with investigators, site staff, and internal project teams.
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Clinical Research Scientist - Oncology
2100 Shahrakan
BHD6000 Monthly
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Posted 1 day ago
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Our client is seeking a highly skilled and dedicated Clinical Research Scientist specializing in Oncology to join their cutting-edge pharmaceutical research facility in Budaiya, Northern, BH . This role is central to advancing novel cancer therapies from preclinical stages through to clinical trials. You will be responsible for designing, implementing, and managing complex research projects, ensuring adherence to Good Clinical Practice (GCP) and regulatory guidelines. This involves developing study protocols, selecting appropriate patient cohorts, overseeing data collection and analysis, and interpreting research findings. Collaboration with a multidisciplinary team of oncologists, pharmacologists, statisticians, and regulatory affairs specialists is essential. You will play a key role in preparing research reports, scientific publications, and presentations for internal and external stakeholders. The ideal candidate will possess a strong scientific background, a deep understanding of cancer biology and therapeutic modalities, and proven experience in clinical trial design and execution. Exceptional analytical, problem-solving, and critical thinking skills are required. Responsibilities:
- Designing and overseeing clinical trials for oncology therapeutics.
- Developing comprehensive study protocols and research plans.
- Identifying and recruiting eligible patient participants.
- Ensuring compliance with GCP, FDA, and other relevant regulatory standards.
- Managing and analyzing clinical trial data.
- Interpreting study results and drawing scientific conclusions.
- Preparing scientific manuscripts for publication and presenting findings.
- Collaborating with internal and external research teams.
- Managing research budgets and timelines effectively.
- Ph.D. or equivalent in Oncology, Molecular Biology, Pharmacology, or a related life science field.
- Significant experience in clinical research, specifically in oncology drug development.
- Proven track record in designing and managing Phase I, II, or III clinical trials.
- In-depth knowledge of cancer biology, immunology, and therapeutic mechanisms.
- Familiarity with regulatory requirements (e.g., ICH-GCP, FDA).
- Strong statistical analysis skills and experience with relevant software.
- Excellent written and verbal communication skills, with a strong publication record.
- Ability to lead and motivate research teams.
- Strong project management skills.
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2
Clinical Research Scientist - Oncology
101 Manama, Capital
BHD120000 Annually
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Posted 1 day ago
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Our client, a leading pharmaceutical innovator, is seeking a dedicated and experienced Clinical Research Scientist specializing in Oncology for a fully remote position. This role is crucial in advancing our oncology drug development pipeline, contributing to life-saving therapies for cancer patients. The successful candidate will be responsible for the design, execution, and interpretation of clinical trials, from early-phase studies to late-stage development. Key responsibilities include developing clinical trial protocols, overseeing study conduct, analyzing clinical data, preparing regulatory submissions, and collaborating with internal and external stakeholders, including investigators, ethics committees, and regulatory agencies. You will play a pivotal role in evaluating the safety and efficacy of novel oncology treatments. The ideal candidate will possess a strong scientific background in oncology or a related field, extensive experience in clinical trial management, and a deep understanding of pharmaceutical regulations and Good Clinical Practice (GCP). Excellent analytical, communication, and problem-solving skills are essential. This is a fully remote role, requiring exceptional self-discipline, organizational skills, and the ability to manage complex projects independently. You will be expected to stay abreast of the latest scientific advancements and therapeutic strategies in oncology. This is an exceptional opportunity to make a significant impact on cancer treatment and patient outcomes from a remote setting. Your scientific rigor and strategic thinking will drive progress in developing innovative cancer therapies. Collaboration with multidisciplinary teams, including medical affairs, biostatistics, and regulatory affairs, will be integral to your success.
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3
Clinical Research Associate - Oncology
BH-418 Sanad
BHD68000 Annually
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Posted 2 days ago
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Our client, a leading pharmaceutical innovator, is seeking a dedicated Clinical Research Associate (CRA) to join their team. This role involves a hybrid work model, combining remote flexibility with essential on-site responsibilities in Janabiyah, Northern, BH . The CRA will play a vital role in ensuring the successful execution of clinical trials, adhering to strict regulatory guidelines and company protocols. You will be responsible for monitoring clinical trial sites, verifying data accuracy, and ensuring subject safety and rights are protected.
The successful candidate will conduct site visits (remote and in-person) to assess trial progress, review source documentation, and verify case report form (CRF) completion. You will manage site initiation, interim monitoring, and close-out visits. This position requires a thorough understanding of Good Clinical Practice (GCP) guidelines, FDA regulations, and other applicable regulatory requirements. You will be the primary point of contact for assigned clinical trial sites, providing training and ongoing support to site staff. Effective communication and problem-solving skills are paramount as you address any issues that arise during the trial.
Responsibilities include maintaining accurate and organized trial documentation, ensuring compliance with protocol amendments, and reporting adverse events promptly. You will collaborate closely with investigators, study coordinators, and internal project teams to ensure the smooth operation of the trial. The ability to manage multiple sites and priorities simultaneously is essential. A strong commitment to quality and ethical conduct in clinical research is expected. This is an excellent opportunity for a driven CRA to contribute to groundbreaking research in oncology and advance their career within a reputable pharmaceutical organization. The hybrid nature of this role allows for a balance between focused remote work and critical on-site engagement with research professionals. The company invests heavily in professional development, offering continuous learning opportunities to its employees. Our client is committed to fostering a diverse and inclusive workplace, where all employees feel valued and respected.
Responsibilities:
The successful candidate will conduct site visits (remote and in-person) to assess trial progress, review source documentation, and verify case report form (CRF) completion. You will manage site initiation, interim monitoring, and close-out visits. This position requires a thorough understanding of Good Clinical Practice (GCP) guidelines, FDA regulations, and other applicable regulatory requirements. You will be the primary point of contact for assigned clinical trial sites, providing training and ongoing support to site staff. Effective communication and problem-solving skills are paramount as you address any issues that arise during the trial.
Responsibilities include maintaining accurate and organized trial documentation, ensuring compliance with protocol amendments, and reporting adverse events promptly. You will collaborate closely with investigators, study coordinators, and internal project teams to ensure the smooth operation of the trial. The ability to manage multiple sites and priorities simultaneously is essential. A strong commitment to quality and ethical conduct in clinical research is expected. This is an excellent opportunity for a driven CRA to contribute to groundbreaking research in oncology and advance their career within a reputable pharmaceutical organization. The hybrid nature of this role allows for a balance between focused remote work and critical on-site engagement with research professionals. The company invests heavily in professional development, offering continuous learning opportunities to its employees. Our client is committed to fostering a diverse and inclusive workplace, where all employees feel valued and respected.
Responsibilities:
- Conduct on-site and remote monitoring visits to clinical trial sites.
- Ensure adherence to study protocols, GCP, and regulatory requirements.
- Verify the accuracy and completeness of clinical trial data.
- Manage site initiation, monitoring, and close-out activities.
- Provide training and ongoing support to site personnel.
- Maintain accurate and up-to-date trial documentation.
- Report and track adverse events and safety issues.
- Collaborate with investigators, study coordinators, and internal teams.
- Ensure subject rights, safety, and well-being are protected.
- Contribute to the overall success of clinical trial execution.
- Bachelor's degree in a life science or healthcare-related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- Strong knowledge of GCP and regulatory guidelines.
- Experience in oncology trials is highly preferred.
- Excellent monitoring, organizational, and time management skills.
- Proficiency in electronic data capture (EDC) systems.
- Effective communication and interpersonal skills.
- Ability to travel for on-site visits as required.
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4
Clinical Research Scientist - Oncology
303 Muharraq, Muharraq
BHD9200 Annually
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Posted 4 days ago
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Our client, a leading innovator in the pharmaceutical sector, is looking for a dedicated and brilliant Clinical Research Scientist to spearhead groundbreaking oncology research. This is a fully remote position, offering a unique opportunity to contribute to life-saving advancements from anywhere. You will be at the forefront of designing, implementing, and analyzing clinical trials for novel cancer therapies. Your expertise will be crucial in evaluating drug efficacy, safety profiles, and therapeutic potential, contributing to the development of next-generation treatments.
Key Responsibilities:
Key Responsibilities:
- Design and oversee Phase I-III clinical trials in oncology, ensuring adherence to scientific protocols and regulatory guidelines (FDA, EMA, etc.).
- Develop clinical trial protocols, investigator brochures, and study reports.
- Analyze complex clinical data, interpret results, and provide insights for further research and development.
- Collaborate with cross-functional teams, including statisticians, medical monitors, regulatory affairs, and drug development scientists.
- Stay abreast of the latest scientific literature, emerging trends, and advancements in oncology and drug development.
- Manage relationships with external investigators, research sites, and Key Opinion Leaders (KOLs).
- Prepare and present research findings at scientific conferences and in peer-reviewed publications.
- Ensure compliance with all Good Clinical Practice (GCP) guidelines and ethical standards.
- Contribute to the strategic planning of the drug development pipeline.
- Mentor junior research staff and contribute to a culture of scientific excellence.
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5
Clinical Research Scientist - Oncology
BH24 Zallaq, Southern
BHD95000 Annually
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Posted 6 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is actively recruiting a highly skilled and dedicated Clinical Research Scientist specializing in Oncology to join their fully remote R&D team. This role is crucial in advancing innovative cancer therapies through the design, execution, and analysis of clinical trials. You will be at the forefront of drug development, contributing to groundbreaking research that aims to improve patient outcomes. Responsibilities include developing clinical trial protocols, identifying and selecting investigational sites, and overseeing trial conduct from initiation to closure. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and clinical operations, to ensure the successful progression of clinical development programs. The ideal candidate will possess a deep understanding of oncology, clinical trial methodologies, and regulatory requirements (e.g., FDA, EMA). Strong data analysis and interpretation skills are essential, along with the ability to effectively communicate complex scientific information. Proficiency in relevant scientific literature and research databases is expected. A Ph.D. or M.D. in a relevant life science discipline (e.g., Oncology, Pharmacology, Molecular Biology) is required, coupled with significant post-doctoral or industry experience in clinical research. This is a remote-first position, providing an exceptional opportunity to contribute to life-saving research from anywhere. Our client is committed to fostering a collaborative and supportive virtual work environment, empowering scientists to achieve their best work. We offer a competitive compensation and benefits package, along with ample opportunities for professional development and career advancement within a leading pharmaceutical organization. Join us in making a tangible difference in the lives of cancer patients worldwide.
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6
Clinical Research Scientist - Oncology
3002 Manama, Capital
BHD95000 Annually
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Posted 6 days ago
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Job Description
Our client, a leading pharmaceutical company at the forefront of medical innovation, is seeking a highly skilled and dedicated Clinical Research Scientist specializing in Oncology. This critical role is based in Manama, Capital, BH . The Clinical Research Scientist will be instrumental in designing, implementing, and managing clinical trials for novel cancer therapies. You will contribute to the entire lifecycle of drug development, from early-stage research to post-market surveillance, ensuring scientific integrity and regulatory compliance. Responsibilities include protocol development, data analysis and interpretation, investigator recruitment and site management, and authoring scientific publications and regulatory submissions. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management, as well as external investigators and key opinion leaders. The ideal candidate will possess a strong scientific background in oncology, a deep understanding of clinical trial methodologies, and a passion for advancing cancer treatment. Excellent analytical, critical thinking, and problem-solving skills are essential. This role requires a proactive and detail-oriented individual with strong communication and interpersonal abilities to effectively engage with diverse stakeholders. This hybrid position offers a balanced approach to work, combining essential in-office collaboration with the flexibility of remote work for specific tasks and periods. We are looking for a motivated scientist eager to make a tangible difference in the lives of cancer patients.
Responsibilities:
Responsibilities:
- Design and develop clinical trial protocols for oncology drug development.
- Oversee the execution of clinical trials, ensuring adherence to protocols and regulatory guidelines.
- Analyze and interpret clinical trial data, providing scientific insights and recommendations.
- Collaborate with statisticians and data management teams to ensure data accuracy and integrity.
- Author clinical study reports, scientific manuscripts, and regulatory submission documents.
- Manage relationships with clinical investigators, sites, and external experts.
- Contribute to the development of regulatory strategies and submissions.
- Stay updated on the latest scientific advancements and research in oncology.
- Participate in internal and external scientific meetings and conferences.
- Provide scientific expertise and support to cross-functional teams.
- Ph.D. or M.D. in a relevant life science field (e.g., Oncology, Pharmacology, Biology).
- Minimum of 5 years of experience in clinical research within the pharmaceutical industry or academia, with a focus on oncology.
- Proven experience in clinical trial design, execution, and data analysis.
- Strong understanding of ICH-GCP guidelines and regulatory requirements.
- Excellent scientific writing and presentation skills.
- Proficiency in statistical analysis and interpretation of clinical data.
- Strong project management and organizational skills.
- Ability to work effectively in a multidisciplinary team environment.
- Excellent problem-solving and critical thinking abilities.
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7
Clinical Research Scientist - Oncology
777 Zallaq, Southern
BHD110000 Annually
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Posted 7 days ago
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Job Description
Our client is a leading pharmaceutical company looking for a dedicated Clinical Research Scientist with a specialization in Oncology to join their pioneering team. This role is 100% remote, allowing you to contribute your expertise from anywhere. You will play a crucial role in the design, execution, and interpretation of clinical trials for novel cancer therapies. Responsibilities include developing clinical trial protocols, selecting investigational sites, managing data collection and analysis, and ensuring compliance with regulatory guidelines (FDA, EMA, etc.). You will collaborate closely with internal and external stakeholders, including medical affairs, regulatory affairs, biostatistics, and key opinion leaders in the oncology field. The ideal candidate will possess a strong scientific background, deep understanding of oncology, and extensive experience in clinical trial management. You should be adept at scientific writing, data interpretation, and presenting complex scientific information. A Ph.D. or MD in a relevant life sciences field is required, along with a minimum of 5 years of experience in clinical drug development, specifically within oncology. Experience with early-phase (Phase I/II) and late-phase (Phase III/IV) trials is highly advantageous. This fully remote position requires exceptional organizational skills, a meticulous approach to detail, and the ability to work independently and effectively within a global team. Proficiency in scientific literature review and critical evaluation of research findings is essential. Our client is committed to advancing cancer treatment through rigorous scientific research and offers a dynamic environment for professionals passionate about making a difference in patient lives. You will be at the forefront of discovering and developing life-saving medications, contributing to a healthier future.
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8
Clinical Research Scientist - Oncology
13579 Markh, Northern
BHD95000 Annually
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Posted 8 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is searching for a highly skilled and dedicated Clinical Research Scientist specializing in Oncology to join their esteemed team in A'ali, Northern, BH . This challenging position involves contributing significantly to the design, execution, and analysis of cutting-edge clinical trials focused on developing novel cancer therapies. The ideal candidate will possess a strong scientific background, a thorough understanding of clinical trial methodologies, and expertise in cancer biology and pharmacology. Your responsibilities will include protocol development, investigator site support, data interpretation, and contributing to regulatory submissions. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, and statistics, to ensure the successful progression of research programs. The ability to critically evaluate scientific literature, identify research opportunities, and translate scientific findings into clinical strategies is essential. A Ph.D. or M.D. in a relevant life science discipline (e.g., Molecular Biology, Pharmacology, Oncology) is required. Postdoctoral experience or equivalent research experience in a pharmaceutical or biotechnology setting is strongly preferred. Proven experience in oncology drug development and clinical trial management is a must. Excellent written and verbal communication skills are vital for preparing scientific reports, presentations, and publications. This role offers the chance to work on groundbreaking research that has the potential to profoundly impact patient lives. You will be at the forefront of scientific discovery, contributing to the development of life-saving treatments. The successful applicant will demonstrate a high level of scientific rigor, ethical conduct, and a commitment to achieving project goals. A keen eye for detail and the ability to manage multiple complex projects simultaneously are critical. Join us and be part of a collaborative and intellectually stimulating environment dedicated to advancing cancer care.
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