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. 113 Oncology jobs in Bahrain
Senior Clinical Pharmacist - Oncology
901 Al Muharraq
BHD105000 Annually
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Posted 1 day ago
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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 Scientist - Oncology
30005 Galali
BHD9000 Monthly
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Our client, a leading biopharmaceutical company at the forefront of developing innovative therapies, is actively seeking a dedicated and accomplished Clinical Research Scientist specializing in Oncology. This full-time position is based at our state-of-the-art research facility in Sanad, Capital, BH . The successful candidate will play a crucial role in the design, execution, and interpretation of clinical trials for novel cancer treatments. You will collaborate closely with cross-functional teams, including R&D, regulatory affairs, medical affairs, and clinical operations, to ensure the successful progression of drug candidates through the development pipeline. Key responsibilities include developing clinical trial protocols, overseeing study conduct, analyzing trial data, and contributing to regulatory submissions. The ideal candidate will possess a strong scientific background in oncology, a deep understanding of clinical trial methodologies, and excellent analytical and critical thinking skills. Experience in drug development, specifically within the oncology therapeutic area, is essential. You will be expected to stay abreast of the latest scientific advancements and regulatory requirements in the field. This role offers a unique opportunity to contribute to life-saving innovations and make a significant impact on the lives of patients. We are looking for a proactive and detail-oriented individual who can manage multiple projects simultaneously and work effectively in a collaborative environment. Strong communication and presentation skills are vital for sharing research findings with internal stakeholders and the broader scientific community. Join our team of passionate scientists and contribute to the future of cancer treatment.
Responsibilities:
Qualifications:
Responsibilities:
- Design, develop, and implement clinical trial protocols for oncology drug candidates.
- Oversee the execution of clinical trials, ensuring adherence to Good Clinical Practice (GCP) and regulatory guidelines.
- Analyze and interpret clinical trial data, contributing to study reports and publications.
- Collaborate with internal and external stakeholders, including investigators, study coordinators, and regulatory agencies.
- Provide scientific and clinical expertise to cross-functional teams throughout the drug development process.
- Contribute to the preparation of regulatory submissions, such as Investigational New Drug (IND) applications and New Drug Applications (NDAs).
- Stay current with scientific literature, emerging technologies, and competitive landscape in oncology.
- Present research findings at scientific meetings and conferences.
- Manage relationships with key opinion leaders (KOLs) in the oncology field.
- Ensure ethical conduct of all clinical research activities.
Qualifications:
- Ph.D. or M.D. in a relevant life science discipline (e.g., Medicine, Biology, Pharmacology, Biochemistry).
- Minimum of 5-7 years of experience in clinical research and drug development, with a strong focus on oncology.
- In-depth knowledge of oncology, cancer biology, and therapeutic strategies.
- Extensive experience in clinical trial design, conduct, and data analysis.
- Familiarity with ICH-GCP guidelines and regulatory requirements (e.g., FDA, EMA).
- Excellent scientific writing and presentation skills.
- Strong analytical and problem-solving abilities.
- Ability to work effectively in a fast-paced, collaborative research environment.
- Proven track record of successful project management and leadership.
- Excellent interpersonal skills and ability to build relationships with stakeholders.
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Clinical Research Associate - Oncology
BH-114 Manama, Capital
BHD85000 Annually
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Posted 1 day ago
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Our client, a leading pharmaceutical company located in Manama, Capital, BH , is seeking a dedicated and experienced Clinical Research Associate (CRA) specializing in Oncology to join their dynamic clinical development team. This hybrid role offers a unique opportunity to contribute to life-saving cancer research and development. The CRA will be responsible for managing and monitoring clinical trials at investigative sites, ensuring adherence to protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulations. Key responsibilities include site initiation visits, routine monitoring visits, close-out visits, and ensuring the accuracy, completeness, and quality of data collected. You will serve as the primary point of contact for study sites, building strong relationships with investigators and site staff to facilitate trial progress. The ideal candidate will possess a strong understanding of oncology therapeutics, clinical trial design, and regulatory requirements within the pharmaceutical industry. Excellent communication, organizational, and time management skills are essential, along with the ability to work independently and manage multiple priorities. Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS) is required. Travel to investigative sites will be necessary, balanced with remote work for administrative tasks and reporting. This position requires a Bachelor's degree in a life science, nursing, or related field, with significant experience as a CRA, preferably with a focus on oncology trials. Join our client in their commitment to advancing cancer treatments and improving patient outcomes through rigorous and ethical clinical research.
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2
Clinical Research Associate (Oncology)
991 Al Muharraq
BHD80000 Annually
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Posted 3 days ago
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Our client, a leading pharmaceutical company at the forefront of innovative cancer therapies, is seeking a dedicated and meticulous Clinical Research Associate (CRA) specializing in Oncology to join their team in Sitra, Capital, BH . This role offers a hybrid work model, combining essential on-site monitoring of clinical trial sites with remote data review, analysis, and reporting. You will be responsible for ensuring the quality, integrity, and compliance of clinical trials, adhering to strict regulatory standards (GCP, FDA, EMA). Your expertise will be critical in advancing groundbreaking treatments from preclinical stages through to regulatory approval.
Key Responsibilities:
Qualifications:
This hybrid position provides a critical link between our research facilities and the sites conducting vital clinical studies. You will contribute directly to bringing life-saving therapies to patients while benefiting from a flexible work arrangement.
Key Responsibilities:
- Conduct site initiation, interim monitoring, and site closure visits for clinical trials in accordance with study protocols and standard operating procedures.
- Verify the accuracy and completeness of clinical data, ensuring compliance with GCP and regulatory requirements.
- Manage communication between study sites, investigators, and the study team, addressing any queries or issues promptly.
- Ensure the proper training of site personnel on study protocols, investigational products, and data collection procedures.
- Review and track essential study documents, including regulatory binders, informed consent forms, and source documents.
- Oversee the investigational product accountability and ensure its proper storage and dispensing.
- Identify and report adverse events and serious adverse events in a timely manner.
- Prepare and submit site monitoring reports, detailing findings, action items, and resolutions.
- Collaborate with data management, regulatory affairs, and project management teams to ensure successful trial execution.
- Contribute to the development of study protocols and clinical trial plans.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree is a plus.
- Minimum of 3-5 years of experience as a Clinical Research Associate, with a strong emphasis on oncology trials.
- Thorough understanding of ICH-Good Clinical Practice (GCP) guidelines and other relevant regulatory requirements.
- Proven experience in site monitoring, data review, and regulatory compliance.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication abilities, with the capacity to build rapport with investigators and site staff.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as required for monitoring visits (up to 40-60%).
- High level of attention to detail and commitment to data integrity.
This hybrid position provides a critical link between our research facilities and the sites conducting vital clinical studies. You will contribute directly to bringing life-saving therapies to patients while benefiting from a flexible work arrangement.
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3
Clinical Research Scientist - Oncology
701 Zallaq, Southern
BHD9500 Annually
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Posted 3 days ago
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Our client, a leading pharmaceutical innovator, is seeking a dedicated and experienced Clinical Research Scientist specializing in Oncology. This critical role will be instrumental in designing, implementing, and monitoring clinical trials that advance cancer therapies. The successful candidate will possess a deep understanding of oncology, clinical trial methodologies, and regulatory requirements (e.g., ICH-GCP). Responsibilities include protocol development, site selection and initiation, data analysis and interpretation, and contributing to regulatory submissions. You will collaborate closely with internal teams, including R&D, regulatory affairs, and medical affairs, as well as external stakeholders such as investigators, clinical research organizations (CROs), and ethics committees. The Clinical Research Scientist will be responsible for ensuring the scientific integrity and operational excellence of assigned clinical studies. This involves meticulous attention to detail in data review, safety monitoring, and overall trial management. A strong ability to critically evaluate scientific literature and translate research findings into actionable strategies is essential. You will also contribute to the preparation of manuscripts for publication and presentations at scientific conferences. The ideal candidate will have a Ph.D. or Master's degree in a relevant life science discipline, with a proven track record in oncology clinical research. Excellent communication, interpersonal, and project management skills are required. This role is based at our state-of-the-art facilities in Zallaq, Southern, BH , offering a collaborative and intellectually stimulating work environment.
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4
Clinical Research Scientist - Oncology
23005 Hamad Town, Northern
BHD110000 Annually
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Posted 3 days ago
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Job Description
Our client, a prestigious pharmaceutical company, is looking for a dedicated and innovative Clinical Research Scientist to focus on oncology therapeutics. This role is integral to the advancement of novel cancer treatments, contributing to life-saving discoveries. The successful candidate will play a key role in designing, executing, and analyzing clinical trials, working closely with cross-functional teams including R&D, medical affairs, and regulatory. Responsibilities include developing study protocols, identifying and liaising with clinical investigators, overseeing data collection and interpretation, and preparing comprehensive scientific reports. A deep understanding of oncology, clinical trial methodologies, and regulatory guidelines is paramount. You will be expected to stay at the forefront of scientific literature, identify emerging trends, and translate scientific insights into actionable research strategies. This hybrid position requires a commitment to on-site collaboration at least two days a week at our Hamad Town, Northern, BH facility, while offering flexibility for remote work. Essential qualifications include a Ph.D. in a relevant life science discipline, a proven track record in clinical research within the pharmaceutical industry, and excellent communication and analytical skills. You will contribute to critical decision-making processes and present findings at scientific conferences. This is an exceptional opportunity to make a significant impact in the fight against cancer and grow your career within a leading global pharmaceutical organization.
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5
Clinical Research Scientist - Oncology
2002 BH Al Daih, Northern
BHD120000 Annually
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Posted 4 days ago
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Our client, a cutting-edge pharmaceutical company dedicated to advancing human health, is looking for a talented and innovative Clinical Research Scientist specializing in Oncology. This role is integral to our drug discovery and development pipeline, focusing on bringing life-saving therapies to patients. You will be responsible for designing, executing, and analyzing preclinical and early-phase clinical studies, contributing to the strategic direction of oncology research programs. The ideal candidate will possess a strong scientific background in oncology, extensive experience in clinical trial design and management, and a deep understanding of regulatory requirements. You will collaborate closely with a multidisciplinary team of researchers, clinicians, statisticians, and regulatory affairs professionals to translate scientific insights into viable therapeutic strategies. Responsibilities include literature review, protocol development, data interpretation, manuscript preparation, and presentation of research findings. The ability to critically evaluate scientific data, identify potential risks and opportunities, and communicate complex scientific information clearly and concisely is essential. This position offers a stimulating environment for professional growth and the opportunity to make a significant impact in the fight against cancer. The role will involve a hybrid work model, combining remote work flexibility with necessary on-site presence for laboratory work and team collaboration in Budaiya, Northern, BH .
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Clinical Research Associate - Oncology
1201 Ghuraifa, Capital
BHD75000 Annually
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Posted 5 days ago
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Job Description
Our client, a prominent pharmaceutical company, is seeking a diligent and experienced Clinical Research Associate (CRA) to support their cutting-edge oncology clinical trials. This role plays a vital part in ensuring the successful execution of research studies, adhering to strict protocols, and upholding the highest standards of data integrity and patient safety. You will be responsible for monitoring clinical trial sites, ensuring compliance with Good Clinical Practice (GCP) guidelines, and managing all aspects of study conduct. The ideal candidate possesses a strong understanding of pharmaceutical research processes, excellent organizational skills, and a passion for advancing cancer treatments.
Responsibilities:
This position requires a Bachelor's degree in a life science, nursing, or a related healthcare field. A minimum of 3-5 years of experience as a Clinical Research Associate, with specific experience in oncology trials, is mandatory. Strong knowledge of GCP, ICH guidelines, and regulatory submission processes is essential. Excellent communication, interpersonal, and problem-solving skills are required. The ability to travel to clinical sites as needed is a requirement of this role, which offers a hybrid work arrangement based in **Jidhafs, Capital, BH**. Our client provides a stimulating work environment, competitive compensation, comprehensive benefits, and opportunities for professional development within the pharmaceutical industry.
Responsibilities:
- Conduct site initiation, monitoring, and close-out visits in accordance with study protocols and company SOPs.
- Ensure the quality and integrity of clinical trial data by verifying source documents and case report forms (CRFs).
- Monitor subject safety and protocol compliance at assigned clinical trial sites.
- Train and support investigators and study site staff on study procedures and regulatory requirements.
- Manage study supplies and investigational product accountability.
- Facilitate communication between the sponsor, study sites, and ethics committees.
- Identify and report deviations, adverse events, and safety concerns in a timely manner.
- Prepare and submit regulatory documents and correspondence.
- Maintain accurate and organized study documentation and files.
- Contribute to the development of clinical study protocols and reports.
- Ensure adherence to all applicable regulatory requirements (e.g., FDA, EMA, ICH-GCP).
This position requires a Bachelor's degree in a life science, nursing, or a related healthcare field. A minimum of 3-5 years of experience as a Clinical Research Associate, with specific experience in oncology trials, is mandatory. Strong knowledge of GCP, ICH guidelines, and regulatory submission processes is essential. Excellent communication, interpersonal, and problem-solving skills are required. The ability to travel to clinical sites as needed is a requirement of this role, which offers a hybrid work arrangement based in **Jidhafs, Capital, BH**. Our client provides a stimulating work environment, competitive compensation, comprehensive benefits, and opportunities for professional development within the pharmaceutical industry.
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7
Clinical Research Associate - Oncology
453 Al Malikiyah, Northern
BHD90000 Annually
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Posted 6 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly motivated and detail-oriented Clinical Research Associate (CRA) specializing in oncology to join their dedicated research team. This role is pivotal in ensuring the successful execution of clinical trials, from site initiation to study close-out, adhering strictly to Good Clinical Practice (GCP) guidelines and regulatory requirements. You will be responsible for monitoring clinical trial sites, ensuring data accuracy and integrity, and verifying patient safety throughout the trial.
The ideal candidate will have a strong background in clinical research, specifically within the oncology therapeutic area. You will conduct site visits (pre-study, initiation, monitoring, and close-out), assess protocol compliance, and train site staff on study procedures. Your role will involve managing communication between clinical trial sites, the sponsor, and regulatory authorities. Excellent organizational skills and the ability to manage multiple priorities are essential. You must be proficient in clinical data management systems and have a thorough understanding of the drug development process.
Key Responsibilities:
The ideal candidate will have a strong background in clinical research, specifically within the oncology therapeutic area. You will conduct site visits (pre-study, initiation, monitoring, and close-out), assess protocol compliance, and train site staff on study procedures. Your role will involve managing communication between clinical trial sites, the sponsor, and regulatory authorities. Excellent organizational skills and the ability to manage multiple priorities are essential. You must be proficient in clinical data management systems and have a thorough understanding of the drug development process.
Key Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits in accordance with clinical trial protocols and SOPs.
- Ensure compliance with GCP, FDA regulations, and other applicable guidelines.
- Verify accuracy, completeness, and validity of clinical data collected at study sites.
- Monitor patient safety and report adverse events promptly.
- Train and support site staff on study-related procedures and documentation.
- Build and maintain strong working relationships with investigators and site personnel.
- Manage and resolve site-specific issues and deviations.
- Prepare monitoring reports and communicate findings to the clinical trial team.
- Ensure timely retrieval and review of essential study documents.
- Contribute to the development of clinical trial protocols and other study-related documents.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 3 years of experience as a Clinical Research Associate, with a significant focus on oncology trials.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with various phases of clinical trials (Phase I-IV).
- Strong understanding of medical terminology and oncology treatments.
- Proficiency in clinical data management software and EDC systems.
- Excellent communication, interpersonal, and problem-solving skills.
- Ability to travel to clinical sites as required.
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8
Clinical Research Scientist - Oncology
1020 Ghuraifa, Capital
BHD110000 Annually
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Posted 10 days ago
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Our client, a globally recognized pharmaceutical innovator, is looking for a highly motivated and skilled Clinical Research Scientist specializing in Oncology to join their dedicated team. This vital role, based in the vicinity of Jidhafs, Capital, BH , will involve the design, execution, and monitoring of clinical trials aimed at developing novel therapies for cancer. The successful candidate will play a crucial part in advancing our oncology pipeline, from early-phase studies to late-stage clinical development.
Key responsibilities include developing clinical trial protocols, Investigator's Brochures, and other essential study documents. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and data management, to ensure the successful conduct of clinical trials. The role requires rigorous data analysis, interpretation of results, and contribution to scientific publications and regulatory submissions. You will also be responsible for staying abreast of the latest advancements in oncology research and clinical practice.
The ideal candidate will hold a Ph.D. or M.D. in a relevant life science discipline, with a strong background in oncology research. A minimum of 5 years of experience in clinical research within the pharmaceutical industry or a contract research organization (CRO) is essential. Demonstrated expertise in oncology drug development, clinical trial design, and relevant regulatory guidelines (e.g., ICH-GCP) is required. Excellent scientific writing, presentation, and communication skills are critical. The ability to work independently and collaboratively in a fast-paced environment is also necessary.
This position offers a competitive compensation package, excellent benefits, and the opportunity to contribute to groundbreaking research that has the potential to improve and save lives. You will be part of a passionate and collaborative team dedicated to making a significant impact in the fight against cancer. If you are driven by scientific curiosity and a commitment to patient care, this role presents an exceptional career opportunity.
Key responsibilities include developing clinical trial protocols, Investigator's Brochures, and other essential study documents. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and data management, to ensure the successful conduct of clinical trials. The role requires rigorous data analysis, interpretation of results, and contribution to scientific publications and regulatory submissions. You will also be responsible for staying abreast of the latest advancements in oncology research and clinical practice.
The ideal candidate will hold a Ph.D. or M.D. in a relevant life science discipline, with a strong background in oncology research. A minimum of 5 years of experience in clinical research within the pharmaceutical industry or a contract research organization (CRO) is essential. Demonstrated expertise in oncology drug development, clinical trial design, and relevant regulatory guidelines (e.g., ICH-GCP) is required. Excellent scientific writing, presentation, and communication skills are critical. The ability to work independently and collaboratively in a fast-paced environment is also necessary.
This position offers a competitive compensation package, excellent benefits, and the opportunity to contribute to groundbreaking research that has the potential to improve and save lives. You will be part of a passionate and collaborative team dedicated to making a significant impact in the fight against cancer. If you are driven by scientific curiosity and a commitment to patient care, this role presents an exceptional career opportunity.
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