33 Oncology jobs in Bahrain
Clinical Pharmacist - Oncology
7701 Tubli, Central
BHD50000 Annually
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Posted 1 day ago
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Job Description
Our client, a leading healthcare provider, is seeking a highly qualified and dedicated Clinical Pharmacist specializing in Oncology to join their esteemed medical team. This crucial role, based in Nuwaidrat, Southern, BH , involves providing comprehensive pharmaceutical care to oncology patients, ensuring safe and effective medication management throughout their treatment journey. The ideal candidate will possess advanced knowledge of cancer therapies, pharmacotherapy, and patient counseling.
Responsibilities:
Qualifications:
Responsibilities:
- Provide direct patient care services to oncology patients, including medication therapy management, patient education, and monitoring for therapeutic outcomes and adverse drug reactions.
- Review and interpret physician orders, ensuring accurate and appropriate medication selection, dosing, and administration.
- Prepare and dispense chemotherapy, biotherapy, and supportive care medications following established protocols and safety standards.
- Collaborate closely with oncologists, nurses, and other healthcare professionals to develop and implement individualized patient treatment plans.
- Participate in multidisciplinary rounds and tumor boards to provide expert pharmaceutical input.
- Monitor patients for side effects, drug interactions, and treatment efficacy, making recommendations for adjustments as needed.
- Educate patients and their families about their medications, potential side effects, and proper administration techniques.
- Manage drug inventory, ensuring availability of critical medications and adherence to storage requirements.
- Stay abreast of the latest advancements in oncology pharmacotherapy, clinical guidelines, and research.
- Participate in quality improvement initiatives and research activities within the pharmacy and oncology departments.
- Maintain accurate and thorough patient records and documentation.
- Supervise and mentor pharmacy residents and technicians.
Qualifications:
- Doctor of Pharmacy (PharmD) degree from an accredited institution.
- Minimum of 3-5 years of clinical pharmacy experience, with a significant focus on oncology.
- Completion of a PGY-1 Pharmacy Practice Residency is required; PGY-2 Oncology Pharmacy Residency is highly preferred.
- Board Certification in Oncology Pharmacy (BCOP) is desirable.
- In-depth knowledge of cancer treatment modalities, chemotherapy regimens, and supportive care medications.
- Strong understanding of pharmacokinetics, pharmacodynamics, and drug interactions.
- Excellent patient assessment, communication, and interpersonal skills.
- Ability to work collaboratively in a team-oriented healthcare environment.
- Proficiency in electronic health record (EHR) systems and pharmacy information systems.
- Active pharmacy license in good standing.
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0
Clinical Research Scientist - Oncology
30685 Northern, Northern
BHD95000 Annually
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Posted 1 day ago
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Our client is searching for a highly qualified and dedicated Clinical Research Scientist specializing in Oncology to join their cutting-edge pharmaceutical research division in Shakhura, Northern, BH . This role is integral to the advancement of novel cancer therapies, contributing significantly to the drug development lifecycle. The successful candidate will be responsible for designing, executing, and analyzing clinical trials, with a primary focus on oncological treatments. Key responsibilities include developing clinical trial protocols, identifying and recruiting eligible patients, managing trial data, ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements, collaborating with cross-functional teams (including medical affairs, regulatory affairs, and data management), preparing scientific reports and publications, and presenting findings at internal and external meetings. A Ph.D. or M.D. in a relevant life science field (e.g., pharmacology, oncology, molecular biology) is required, along with substantial experience in clinical trial management, particularly in oncology. Excellent scientific knowledge, strong analytical skills, and a deep understanding of cancer biology and therapeutic approaches are essential. The ability to work effectively in a fast-paced, collaborative environment and to communicate complex scientific information clearly is paramount. This is an exceptional opportunity to contribute to life-saving medical advancements and grow your career within a leading pharmaceutical organization. If you are passionate about advancing cancer care through rigorous scientific research, we encourage you to apply.
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1
Clinical Research Scientist - Oncology
20191 Seef, Capital
BHD75000 Annually
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Posted 1 day ago
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Our client, a leading pharmaceutical innovator, is actively recruiting a highly motivated Clinical Research Scientist specializing in Oncology for their facility in **Janabiyah, Northern, BH**. This senior-level position will play a critical role in the design, execution, and analysis of clinical trials for novel cancer therapies. The successful candidate will be responsible for developing study protocols, overseeing patient recruitment, managing data integrity, and ensuring compliance with regulatory guidelines (e.g., ICH-GCP). You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, and clinical operations, as well as external investigators and research sites. Key responsibilities include interpreting clinical data, preparing regulatory submissions, and contributing to scientific publications and presentations. A Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology) is mandatory, coupled with a minimum of 7 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry, with a strong focus on oncology. Excellent understanding of cancer biology, drug development processes, and regulatory requirements is essential. Demonstrated success in managing complex clinical trials and a strong publication record are highly desirable. This role requires exceptional analytical, problem-solving, and communication skills. The ability to lead and mentor junior staff is also important. Our client is committed to advancing cancer treatment and offers a stimulating research environment with state-of-the-art facilities. This is an outstanding opportunity to contribute to life-saving medical advancements in a key therapeutic area. The ideal candidate will be passionate about oncology research and possess a strategic mindset to drive successful trial outcomes.
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2
Clinical Research Scientist (Oncology)
20150 Amwaj Islands
BHD95000 Annually
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Posted 2 days ago
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Our client is seeking a dedicated and experienced Clinical Research Scientist specializing in Oncology to join their pioneering pharmaceutical research team in Isa Town, Southern, BH . This critical role will involve the design, execution, and analysis of clinical trials aimed at developing novel cancer therapies. The successful candidate will be instrumental in advancing our understanding of cancer biology and translating scientific discoveries into life-saving treatments. Responsibilities include developing clinical trial protocols, identifying and evaluating potential study sites and investigators, and overseeing patient recruitment and data collection. You will be responsible for ensuring that all clinical research activities are conducted in strict accordance with regulatory guidelines (e.g., ICH-GCP) and ethical standards. The Clinical Research Scientist will work closely with cross-functional teams, including medical affairs, regulatory affairs, and biostatistics, to ensure the successful progression of clinical programs. Strong scientific acumen, a deep understanding of oncology, and experience in clinical trial management are essential. The ability to critically evaluate scientific literature, interpret complex data, and contribute to the preparation of regulatory submission documents is also crucial. We are looking for a motivated individual with a passion for scientific innovation and a commitment to improving patient outcomes. This position offers a challenging and rewarding opportunity to contribute to the development of breakthrough cancer therapies.
Responsibilities:
Qualifications:
Responsibilities:
- Design and develop clinical trial protocols for oncology studies.
- Identify and assess potential clinical investigators and sites.
- Oversee the execution of clinical trials, ensuring compliance with GCP and regulations.
- Monitor study progress, data quality, and patient safety.
- Analyze clinical trial data and interpret study results.
- Prepare clinical study reports and contribute to regulatory submissions.
- Collaborate with internal and external stakeholders, including medical monitors and statisticians.
- Stay abreast of the latest advancements in oncology research and drug development.
- Manage budgets and timelines for clinical trials.
- Ensure effective communication among study teams and investigators.
Qualifications:
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Molecular Biology, Pharmacology, Medicine).
- Minimum of 5 years of experience in clinical research, preferably in oncology.
- Thorough understanding of clinical trial design and methodology.
- In-depth knowledge of oncology drug development and cancer biology.
- Familiarity with ICH-GCP guidelines and regulatory requirements.
- Strong analytical and data interpretation skills.
- Excellent written and verbal communication skills.
- Ability to manage complex projects and multiple tasks.
- Experience with data management systems and statistical analysis software.
- Strong problem-solving abilities and attention to detail.
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3
Clinical Research Associate - Oncology
211 Hamad Town, Northern
BHD70000 Annually
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Posted 6 days ago
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Our client, a leading global pharmaceutical company renowned for its innovation in oncology, is seeking a highly skilled and dedicated Clinical Research Associate (CRA) to join their team in **Hamad Town, Northern, BH**. This crucial role involves overseeing and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and regulatory requirements. The ideal candidate will have a strong background in clinical research, meticulous attention to detail, and a commitment to advancing cancer treatments. You will be responsible for site selection, initiation, monitoring, and close-out activities, ensuring data integrity and patient safety throughout the trial.
Key Responsibilities:
Qualifications:
This is an exciting opportunity to contribute to cutting-edge research and make a meaningful impact on the lives of cancer patients. If you are a meticulous and motivated CRA, we invite you to apply.
Key Responsibilities:
- Perform site selection, qualification, and initiation visits to ensure study sites meet the necessary criteria.
- Monitor clinical trial conduct at assigned sites to ensure adherence to protocol, SOPs, and regulatory guidelines (e.g., GCP, FDA, EMA).
- Verify the accuracy and completeness of clinical trial data through source data verification (SDV).
- Manage and maintain essential regulatory documents for assigned study sites.
- Identify and report potential adverse events and product complaints in a timely manner.
- Ensure investigational product is managed correctly and securely at the study sites.
- Build and maintain positive relationships with investigators and site staff.
- Conduct site close-out visits and ensure all study-related activities are completed.
- Prepare and submit monitoring reports and follow up on action items.
- Participate in Investigator Meetings and internal team meetings.
- Ensure timely enrollment and completion of study milestones at assigned sites.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline.
- Minimum of 3-5 years of experience as a Clinical Research Associate, preferably with a focus on oncology trials.
- In-depth knowledge of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements.
- Experience in site management, monitoring, and data verification.
- Strong understanding of clinical trial processes and documentation.
- Excellent organizational, analytical, and problem-solving skills.
- Exceptional communication and interpersonal abilities.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel frequently to study sites (up to 60%).
- Fluency in English; Arabic language skills are beneficial.
This is an exciting opportunity to contribute to cutting-edge research and make a meaningful impact on the lives of cancer patients. If you are a meticulous and motivated CRA, we invite you to apply.
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4
Clinical Research Associate - Oncology
2030 Zallaq, Southern
BHD80000 Annually
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Posted 6 days ago
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Job Description
Our client, a prominent pharmaceutical company, is seeking an experienced Clinical Research Associate (CRA) with a specialization in Oncology to join their dedicated team in **Zallaq, Southern, BH**. This critical role involves monitoring clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The ideal candidate will have a strong background in clinical research, particularly within the oncology therapeutic area, and possess excellent organizational, communication, and problem-solving skills. This position offers an exceptional opportunity to contribute to the development of life-saving medications.
Key Responsibilities:
Key Responsibilities:
- Initiate, monitor, and close-out clinical trial sites in accordance with study protocols and regulatory requirements.
- Ensure the quality, integrity, and accuracy of clinical trial data collected at study sites.
- Verify that investigational product is dispensed, administered, and accounted for correctly.
- Perform site visits (pre-study, initiation, interim monitoring, and close-out) as required.
- Train and support site staff on protocol requirements, data collection, and regulatory compliance.
- Act as the primary liaison between the sponsor and the investigative sites.
- Identify, track, and resolve site-level issues and deviations.
- Prepare and present monitoring visit reports in a timely manner.
- Ensure all documentation is maintained in accordance with GCP and regulatory standards.
- Participate in Investigator Meetings and other study-related meetings.
- Contribute to the development of study protocols, informed consent forms, and other trial-related documents.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific field. A Master's degree is a plus.
- Minimum of 3-5 years of experience as a Clinical Research Associate.
- Demonstrated experience in oncology clinical trials is essential.
- In-depth knowledge of ICH-GCP guidelines and other relevant regulatory requirements.
- Experience with various Electronic Data Capture (EDC) systems.
- Strong understanding of clinical trial processes and documentation.
- Excellent organizational, time management, and problem-solving skills.
- Exceptional communication and interpersonal skills.
- Ability to travel up to 60% of the time.
- Proficiency in Microsoft Office Suite.
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5
Senior Clinical Research Scientist (Oncology)
BH12 Saar, Northern
BHD95000 Annually
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Posted today
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Our client, a leading pharmaceutical innovator, is seeking a highly skilled and experienced Senior Clinical Research Scientist specializing in Oncology to join their dynamic team in **Saar, Northern, BH**. This pivotal role will be instrumental in the design, execution, and interpretation of clinical trials for novel cancer therapies. The successful candidate will possess a profound understanding of oncology drug development, from preclinical research through to Phase III trials. You will be responsible for developing clinical trial protocols, investigator brochures, and other regulatory submission documents. This position involves close collaboration with cross-functional teams, including R&D, regulatory affairs, medical affairs, and clinical operations, to ensure the successful and timely completion of clinical studies. You will also play a key role in analyzing clinical data, contributing to scientific publications, and presenting findings at international conferences. The ideal candidate will have a strong scientific background, excellent analytical skills, and a proven ability to manage complex projects. A PhD or MD in a relevant life science discipline is required, along with a minimum of 7 years of experience in clinical development within the pharmaceutical industry, specifically focused on oncology. Knowledge of Good Clinical Practice (GCP) and relevant regulatory guidelines is essential. You will also contribute to the strategic direction of the company's oncology pipeline, identifying new opportunities and innovative approaches. This role offers the chance to make a significant impact on patient lives by advancing cutting-edge cancer treatments. If you are a passionate and driven scientist looking to contribute to groundbreaking research in a collaborative environment, we encourage you to apply.
Responsibilities:
Responsibilities:
- Design and develop clinical trial protocols and associated documents.
- Oversee the execution of clinical trials, ensuring adherence to protocols and regulatory requirements.
- Analyze and interpret clinical data, collaborating with biostatisticians and data management teams.
- Contribute to the preparation of clinical study reports, regulatory submissions, and scientific publications.
- Collaborate with internal and external stakeholders, including investigators, research sites, and regulatory authorities.
- Provide scientific and clinical expertise to cross-functional teams.
- Stay abreast of the latest advancements in oncology research and drug development.
- Contribute to the strategic planning of the oncology pipeline.
- PhD or MD in a relevant life science discipline.
- Minimum 7 years of clinical development experience in the pharmaceutical industry, with a focus on oncology.
- In-depth knowledge of oncology drug development and clinical trial design.
- Strong understanding of regulatory requirements and GCP guidelines.
- Excellent analytical, scientific, and communication skills.
- Proven project management and leadership abilities.
- Ability to work effectively in a matrixed team environment.
- Experience in statistical analysis interpretation and data review.
- Strong publication record and presentation skills.
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6
Senior Clinical Research Scientist, Oncology
456 Hamad Town, Northern
BHD95000 Annually
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Posted today
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Job Description
Our client, a leading pharmaceutical innovator, is looking for a highly motivated and experienced Senior Clinical Research Scientist specializing in Oncology to join their esteemed team in **Hamad Town, Northern, BH**. This critical role will involve designing, implementing, and managing cutting-edge clinical trials focused on developing novel cancer therapies. You will be instrumental in the end-to-end process of clinical research, from protocol development and site selection to data analysis and regulatory submissions.
The Senior Clinical Research Scientist will work closely with internal teams, including R&D, regulatory affairs, and medical affairs, as well as external collaborators such as principal investigators, clinical research organizations (CROs), and regulatory agencies. Responsibilities include ensuring adherence to Good Clinical Practice (GCP) guidelines, ethical standards, and all applicable regulatory requirements. You will be responsible for reviewing and interpreting complex clinical data, identifying trends, and contributing to scientific publications and presentations. Strong statistical knowledge and experience with clinical trial management software are essential.
This position requires a Ph.D. or Master's degree in a relevant life science field (e.g., Pharmacology, Biology, Medicine) with a minimum of 5-8 years of hands-on experience in clinical research, specifically within the oncology therapeutic area. A proven ability to manage multiple clinical studies simultaneously, robust scientific writing skills, and excellent problem-solving abilities are necessary. The ideal candidate will possess strong leadership qualities and the capacity to mentor junior research staff. This is a unique opportunity to contribute to life-saving advancements in cancer treatment from our base in **Hamad Town, Northern, BH**.
The Senior Clinical Research Scientist will work closely with internal teams, including R&D, regulatory affairs, and medical affairs, as well as external collaborators such as principal investigators, clinical research organizations (CROs), and regulatory agencies. Responsibilities include ensuring adherence to Good Clinical Practice (GCP) guidelines, ethical standards, and all applicable regulatory requirements. You will be responsible for reviewing and interpreting complex clinical data, identifying trends, and contributing to scientific publications and presentations. Strong statistical knowledge and experience with clinical trial management software are essential.
This position requires a Ph.D. or Master's degree in a relevant life science field (e.g., Pharmacology, Biology, Medicine) with a minimum of 5-8 years of hands-on experience in clinical research, specifically within the oncology therapeutic area. A proven ability to manage multiple clinical studies simultaneously, robust scientific writing skills, and excellent problem-solving abilities are necessary. The ideal candidate will possess strong leadership qualities and the capacity to mentor junior research staff. This is a unique opportunity to contribute to life-saving advancements in cancer treatment from our base in **Hamad Town, Northern, BH**.
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7
Senior Clinical Research Associate - Oncology
4567 Zallaq, Southern
BHD105000 Annually
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Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing cancer treatments, is looking for a highly experienced Senior Clinical Research Associate (CRA) to contribute to groundbreaking oncology trials in Zallaq, Southern, BH . This vital role involves overseeing and managing all aspects of clinical trial conduct at investigational sites, ensuring compliance with protocols, GCP, and regulatory requirements. You will be responsible for site selection, initiation, monitoring, and close-out activities, ensuring data integrity and patient safety. Key duties include building strong relationships with investigators and site staff, providing training on study procedures, and resolving any issues that arise during the trial. You will also be responsible for reviewing regulatory documents, monitoring trial progress, and reporting findings to the clinical trial manager. A Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field is required; an advanced degree is preferred. A minimum of 5 years of experience as a CRA, with a significant focus on oncology clinical trials, is essential. In-depth knowledge of ICH-GCP guidelines and regulatory requirements (e.g., FDA, EMA) is mandatory. Excellent monitoring skills, strong data management capabilities, and exceptional attention to detail are required. Outstanding interpersonal, communication, and organizational skills are paramount. The ability to travel periodically to sites is also a requirement. Join our mission to develop life-saving medicines.
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8
Senior Clinical Research Associate - Oncology
0301 Tubli, Central
BHD6500 Annually
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Posted 1 day ago
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Our client, a pioneering pharmaceutical company, is looking for a dedicated Senior Clinical Research Associate (CRA) with expertise in Oncology to join their dynamic clinical development team in **Budaiya, Northern, BH**. This role is instrumental in advancing life-saving cancer therapies through rigorous clinical trials. The Senior CRA will be responsible for managing and monitoring clinical trial sites, ensuring data integrity, and maintaining compliance with all relevant regulatory standards.
Key responsibilities include site selection, initiation, monitoring, and close-out activities for Phase I-IV oncology clinical trials. You will ensure adherence to the study protocol, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. The Senior CRA will train and mentor site staff, review case report forms (CRFs), and manage data queries to ensure accuracy and completeness. Furthermore, you will collaborate with internal study teams, including data management, safety, and regulatory affairs departments, to ensure the smooth progression of clinical trials.
A Bachelor's degree in a life science or healthcare-related field is required. A Master's degree or a nursing qualification is a plus. Candidates must possess a minimum of 4-6 years of experience as a Clinical Research Associate, with a significant portion of this experience focused on oncology trials. Thorough knowledge of ICH-GCP guidelines and regulatory requirements is essential.
Excellent organizational, time management, and communication skills are critical. The ability to travel to clinical trial sites, both domestically and internationally, as needed, is a requirement. Strong analytical and problem-solving skills, along with proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems, are highly desirable. The successful candidate will demonstrate a strong commitment to patient safety and data quality.
Key responsibilities include site selection, initiation, monitoring, and close-out activities for Phase I-IV oncology clinical trials. You will ensure adherence to the study protocol, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. The Senior CRA will train and mentor site staff, review case report forms (CRFs), and manage data queries to ensure accuracy and completeness. Furthermore, you will collaborate with internal study teams, including data management, safety, and regulatory affairs departments, to ensure the smooth progression of clinical trials.
A Bachelor's degree in a life science or healthcare-related field is required. A Master's degree or a nursing qualification is a plus. Candidates must possess a minimum of 4-6 years of experience as a Clinical Research Associate, with a significant portion of this experience focused on oncology trials. Thorough knowledge of ICH-GCP guidelines and regulatory requirements is essential.
Excellent organizational, time management, and communication skills are critical. The ability to travel to clinical trial sites, both domestically and internationally, as needed, is a requirement. Strong analytical and problem-solving skills, along with proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems, are highly desirable. The successful candidate will demonstrate a strong commitment to patient safety and data quality.
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