220 Oncology jobs in Bahrain
Senior Clinical Pharmacist - Oncology
Posted 19 days ago
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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.
Clinical Research Associate - Oncology
Posted today
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Clinical Research Scientist - Oncology
Posted 1 day ago
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- 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.
Clinical Research Scientist - Oncology
Posted 1 day ago
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Clinical Research Associate - Oncology
Posted 2 days ago
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Job Description
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.
Clinical Research Scientist - Oncology
Posted 4 days ago
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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.
Clinical Research Scientist - Oncology
Posted 6 days ago
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Clinical Research Scientist - Oncology
Posted 6 days ago
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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.
Clinical Research Scientist - Oncology
Posted 7 days ago
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Clinical Research Scientist - Oncology
Posted 8 days ago
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