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. 35 Oncology jobs in Bahrain
Clinical Research Scientist - Oncology
345 Seef, Capital
BHD110000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical innovator dedicated to developing life-changing therapies, is seeking a highly motivated Clinical Research Scientist specializing in Oncology to join their team in Seef, Capital, BH . This role is integral to the design, execution, and interpretation of clinical trials aimed at bringing novel cancer treatments to patients. You will work closely with cross-functional teams, including R&D, regulatory affairs, medical affairs, and data management, to ensure the successful progression of clinical programs.
Key responsibilities include contributing to the development of clinical trial protocols, Investigator's Brochures, and other essential regulatory documents. You will play a vital role in site selection and initiation, providing scientific and operational support to clinical trial investigators and site staff. The Clinical Research Scientist will also be responsible for monitoring trial progress, analyzing data, and preparing scientific reports and publications. You will stay abreast of the latest scientific advancements and clinical developments in oncology, ensuring our research remains at the cutting edge.
The ideal candidate will possess a Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology) with a strong understanding of cancer biology and clinical oncology. A minimum of 3-5 years of experience in clinical research within the pharmaceutical industry or a contract research organization (CRO) is required. Demonstrated experience in designing and managing oncology clinical trials is essential. Excellent written and verbal communication skills are necessary for interacting with internal teams, external investigators, and regulatory agencies. The ability to critically evaluate scientific data and translate complex findings into actionable insights is crucial. Proficiency in statistical analysis and interpretation is expected. This hybrid role requires regular attendance in the Seef, Capital, BH office, with flexibility for remote work. Join us in our mission to accelerate the development of groundbreaking cancer therapies.
Key responsibilities include contributing to the development of clinical trial protocols, Investigator's Brochures, and other essential regulatory documents. You will play a vital role in site selection and initiation, providing scientific and operational support to clinical trial investigators and site staff. The Clinical Research Scientist will also be responsible for monitoring trial progress, analyzing data, and preparing scientific reports and publications. You will stay abreast of the latest scientific advancements and clinical developments in oncology, ensuring our research remains at the cutting edge.
The ideal candidate will possess a Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology) with a strong understanding of cancer biology and clinical oncology. A minimum of 3-5 years of experience in clinical research within the pharmaceutical industry or a contract research organization (CRO) is required. Demonstrated experience in designing and managing oncology clinical trials is essential. Excellent written and verbal communication skills are necessary for interacting with internal teams, external investigators, and regulatory agencies. The ability to critically evaluate scientific data and translate complex findings into actionable insights is crucial. Proficiency in statistical analysis and interpretation is expected. This hybrid role requires regular attendance in the Seef, Capital, BH office, with flexibility for remote work. Join us in our mission to accelerate the development of groundbreaking cancer therapies.
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Clinical Research Associate - Oncology
0000 Jaww, Southern
BHD60000 Annually
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Posted 5 days ago
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Our client is seeking a diligent and experienced Clinical Research Associate (CRA) with a specialization in Oncology to join their pharmaceutical research team based in **A'ali, Northern, BH**. This crucial role involves monitoring and managing clinical trials, ensuring adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. The CRA will be responsible for site selection, initiation, monitoring, and close-out visits for investigational sites, verifying the accuracy and completeness of clinical data. You will work closely with investigators, site staff, and internal project teams to facilitate the smooth execution of trials, ensuring patient safety and data integrity. Key responsibilities include reviewing source documents, source data verification (SDV), monitoring patient eligibility, and managing study supplies. The ideal candidate will possess strong organizational skills, excellent attention to detail, and the ability to manage multiple priorities in a dynamic environment. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is essential. A background in oncology research is highly preferred, along with a solid understanding of cancer treatments and clinical trial methodologies in this field. This position offers the opportunity to contribute to life-saving therapies and work within a collaborative and supportive pharmaceutical environment. Our client is dedicated to advancing medical treatments and provides ample opportunities for professional development. The role involves travel to clinical sites as needed, combined with remote administrative tasks.
Key Responsibilities:
Key Responsibilities:
- Conduct site initiation, interim, and close-out monitoring visits.
- Ensure study conduct is in compliance with protocol, SOPs, and GCP guidelines.
- Verify the accuracy, completeness, and consistency of clinical data.
- Manage site communications and provide training to site personnel.
- Oversee patient recruitment and enrollment efforts.
- Monitor drug accountability and investigational product management.
- Prepare and present monitoring visit reports.
- Identify and escalate site issues and risks to the project team.
- Ensure regulatory documentation is complete and maintained.
- Contribute to the development of study protocols and other study documents.
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- Proven experience in oncology clinical trials is highly desirable.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Proficiency with EDC and CTMS systems.
- Excellent monitoring and data verification skills.
- Strong interpersonal and communication abilities.
- Ability to work independently and manage time effectively.
- Willingness to travel to clinical sites as required.
- Valid driver's license and passport.
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1
Senior Clinical Research Associate - Oncology
21103 Shahrakan
BHD105000 Annually
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Posted 2 days ago
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Job Description
Our client is seeking an experienced Senior Clinical Research Associate (CRA) specializing in oncology to join their pharmaceutical research division. This role operates on a hybrid model, combining remote work flexibility with essential on-site visits to clinical trial sites. You will be responsible for the overall management and monitoring of clinical trials, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your expertise in oncology clinical research will be crucial in driving trial success and patient safety. Responsibilities include: conducting site initiation, routine monitoring, and close-out visits to ensure study compliance; managing and overseeing a portfolio of oncology clinical trials; ensuring data accuracy and integrity through source data verification; identifying and resolving site-level issues and escalating as necessary; training and mentoring site staff on study procedures and regulatory requirements; preparing and presenting trial status reports to project teams and management; ensuring adherence to timelines and budgets for assigned sites; maintaining effective communication with investigators, site staff, and internal project teams; contributing to the development of study protocols and clinical trial documents; staying current with advancements in oncology research and clinical trial methodologies. The ideal candidate will hold a Bachelor's degree in Life Sciences, Nursing, or a related field, with a minimum of 5 years of experience as a Clinical Research Associate, including dedicated experience in oncology studies. Strong knowledge of GCP, ICH guidelines, and regulatory requirements is essential. Excellent monitoring skills, a keen eye for detail, and strong problem-solving abilities are required. Proficiency in clinical trial management software and electronic data capture systems is a must. Outstanding communication, interpersonal, and organizational skills are necessary. The ability to travel to clinical sites as required is mandatory. This is a challenging and rewarding opportunity to contribute to life-saving cancer treatments and advance your career in pharmaceutical research.
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2
Senior Clinical Research Associate - Oncology
BH3 Jaww, Southern
BHD105000 Annually
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Posted 2 days ago
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Job Description
Our client, a rapidly growing pharmaceutical company dedicated to improving patient outcomes through innovative therapies, is seeking a highly motivated and experienced Senior Clinical Research Associate (CRA) specializing in Oncology. This hybrid role offers a compelling opportunity to play a pivotal part in the advancement of life-saving cancer treatments. You will be responsible for overseeing and managing clinical trial sites, ensuring data integrity, compliance with regulatory standards, and adherence to study protocols. This position demands a strong understanding of oncology, clinical trial management, and GCP guidelines, along with exceptional organizational and communication skills. You will be a key contributor to bringing groundbreaking pharmaceutical solutions to patients in need.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Site selection, initiation, monitoring, and close-out visits for clinical trials in oncology.
- Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, FDA regulations, and study protocols.
- Verify the accuracy, completeness, and consistency of clinical data through source data verification.
- Manage investigational product accountability and drug release at study sites.
- Identify, evaluate, and resolve site-level issues and risks promptly.
- Build and maintain strong working relationships with investigators, site staff, and other stakeholders.
- Prepare and present monitoring reports, detailing site performance, findings, and action plans.
- Ensure timely submission of regulatory documents and study-related materials.
- Participate in study team meetings and contribute to the development of clinical trial protocols and study plans.
- Provide training and guidance to site personnel on study conduct and data collection.
- Contribute to the development and improvement of clinical operations processes.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 5 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 for clinical trials.
- Proven experience in monitoring clinical trial sites and managing data integrity.
- Excellent understanding of oncology disease states and therapeutic areas.
- Strong analytical, problem-solving, and organizational skills.
- Exceptional written and verbal communication skills.
- Ability to work independently and manage multiple priorities effectively.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel to clinical sites as required for monitoring activities.
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3
Senior Clinical Research Scientist - Oncology
124 Tubli
BHD8500 Annually
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Posted 2 days ago
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Job Description
Our client is a leading pharmaceutical company seeking a highly accomplished Senior Clinical Research Scientist specializing in Oncology to join their cutting-edge research and development team. This fully remote position offers a unique opportunity to contribute to the advancement of life-saving cancer therapies from the comfort of your home office. You will play a pivotal role in the design, execution, and interpretation of clinical trials, working collaboratively with cross-functional teams to bring innovative treatments to patients.
Key responsibilities include:
Qualifications:
Key responsibilities include:
- Designing and developing clinical trial protocols for oncology studies, ensuring scientific rigor and regulatory compliance.
- Overseeing the operational aspects of clinical trials, including site selection, patient recruitment, and data collection.
- Analyzing and interpreting complex clinical trial data, generating comprehensive reports and scientific publications.
- Collaborating closely with medical affairs, regulatory affairs, biostatistics, and other internal teams.
- Providing scientific expertise and guidance to study teams, investigators, and external stakeholders.
- Ensuring adherence to Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements.
- Managing relationships with Contract Research Organizations (CROs) and other external vendors.
- Identifying and evaluating new scientific opportunities and technologies in oncology drug development.
- Presenting research findings at scientific conferences and internal meetings.
- Contributing to the development of regulatory submissions (e.g., IND, NDA).
- Mentoring junior scientists and contributing to the overall scientific strategy of the R&D department.
- Staying abreast of the latest advancements in oncology research and clinical trial methodologies.
Qualifications:
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Biology, Medicine).
- Minimum of 7 years of experience in clinical research, specifically within the pharmaceutical industry and with a strong focus on oncology.
- Demonstrated experience in designing and managing Phase I-IV clinical trials.
- In-depth understanding of oncology disease areas, therapeutic strategies, and drug development processes.
- Excellent knowledge of GCP, regulatory affairs, and clinical trial methodologies.
- Strong analytical and data interpretation skills, with experience in statistical analysis concepts.
- Exceptional written and verbal communication skills, with a proven ability to publish scientific findings.
- Demonstrated ability to lead cross-functional teams and manage projects effectively in a remote setting.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
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4
Senior Clinical Research Scientist - Oncology
245 Durrat Al Bahrain
BHD85000 Annually
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Posted 2 days ago
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Job Description
Our client, a leading innovator in pharmaceutical research and development, is seeking a highly motivated and experienced Senior Clinical Research Scientist to join their dynamic team in **Sitra, Capital, BH**. This pivotal role will focus on advancing oncology treatments from bench to bedside. You will be instrumental in designing, implementing, and overseeing clinical trials, ensuring adherence to regulatory standards and ethical guidelines. Key responsibilities include developing study protocols, managing data collection and analysis, collaborating with cross-functional teams (including medical affairs, regulatory, and data management), and interpreting complex scientific data. The ideal candidate will possess a deep understanding of oncology, clinical trial methodologies, and statistical principles. You will also be responsible for preparing scientific publications and presentations for key opinion leaders and regulatory bodies. This is an exciting opportunity to contribute to life-saving therapies and shape the future of cancer treatment. The successful applicant will have a strong track record in pharmaceutical research, excellent analytical and problem-solving skills, and the ability to thrive in a fast-paced, collaborative environment. We are looking for individuals who are passionate about scientific discovery and dedicated to improving patient outcomes. The role involves a hybrid work model, offering a balance between collaborative on-site work and focused remote execution. Extensive experience with GCP, ICH, and other relevant regulatory frameworks is essential. A Ph.D. or Master's degree in a life science discipline is preferred, coupled with at least 5 years of relevant industry experience. Excellent written and verbal communication skills are paramount. Your expertise will be crucial in driving forward our client's pipeline of groundbreaking oncology drugs.
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5
Senior Clinical Research Scientist - Oncology
78870 Southern, Southern
BHD110000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing cancer treatments, is seeking a highly qualified Senior Clinical Research Scientist specializing in Oncology to join their research and development team in Nuwaidrat, Southern, BH . This hybrid role offers a blend of on-site laboratory work and remote data analysis and reporting, providing a dynamic and flexible work environment. You will play a crucial role in the design, execution, and interpretation of clinical trials for novel oncology therapies. This position requires a strong scientific background, extensive experience in oncology drug development, and a deep understanding of clinical trial methodologies, regulatory requirements, and data analysis.
Key Responsibilities:
Key Responsibilities:
- Lead the design and development of clinical trial protocols for oncology studies, ensuring scientific rigor and alignment with regulatory guidelines.
- Oversee the execution of clinical trials, from site initiation to study close-out, ensuring data integrity and patient safety.
- Collaborate closely with cross-functional teams, including R&D, regulatory affairs, medical affairs, and clinical operations.
- Analyze and interpret complex clinical trial data, identifying key findings and implications for drug development.
- Prepare scientific reports, manuscripts, and presentations for internal stakeholders, regulatory agencies, and scientific publications.
- Contribute to the development of regulatory submission documents (e.g., IND, NDA).
- Stay abreast of the latest advancements in oncology research, clinical trial design, and therapeutic approaches.
- Manage relationships with external investigators, key opinion leaders (KOLs), and clinical research organizations (CROs).
- Ensure compliance with all relevant ethical and regulatory standards (e.g., GCP, ICH).
- Provide scientific and technical expertise to guide study design and problem-solving.
- Mentor junior scientists and contribute to the overall scientific growth of the team.
- Ph.D. or M.D. in a relevant life science discipline (e.g., Oncology, Pharmacology, Biology, Medicine).
- Minimum of 7 years of progressive experience in clinical research, with a significant focus on oncology drug development.
- Proven track record in designing and conducting Phase I, II, and III clinical trials.
- In-depth knowledge of oncology pathways, mechanisms of action, and therapeutic strategies.
- Strong understanding of clinical trial methodologies, statistical analysis, and data interpretation.
- Familiarity with regulatory requirements and guidelines (FDA, EMA, ICH GCP).
- Excellent scientific writing and presentation skills.
- Demonstrated ability to collaborate effectively in a cross-functional, matrixed organization.
- Experience in managing external partnerships with CROs and academic institutions.
- Strong analytical and problem-solving skills.
- Ability to work effectively in a hybrid work model, balancing on-site and remote responsibilities.
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6
Senior Clinical Research Scientist - Oncology
710 Askar, Southern
BHD110000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly skilled and dedicated Senior Clinical Research Scientist specializing in Oncology. This position requires a deep understanding of clinical trial design, execution, and data analysis within the oncology therapeutic area. You will play a crucial role in advancing novel cancer treatments from early-phase development through to regulatory submission.
Responsibilities include designing and overseeing complex clinical trials, ensuring adherence to regulatory guidelines (FDA, EMA) and Good Clinical Practice (GCP). You will collaborate closely with internal teams, including R&D, medical affairs, regulatory affairs, and project management, as well as external investigators and clinical sites. Developing clinical protocols, investigator brochures, and other essential study documents will be a key duty. You will be responsible for data interpretation, statistical analysis oversight, and preparing comprehensive clinical study reports.
Furthermore, you will contribute to the scientific strategy for oncology drug development, identifying new research opportunities and therapeutic targets. Staying updated on the latest scientific literature, clinical advancements, and competitive landscape in oncology is essential. You will also be involved in preparing regulatory submissions and responding to queries from health authorities. The ideal candidate will possess strong analytical, problem-solving, and communication skills. Experience in oncology clinical research, including hands-on involvement in trial design and management, is mandatory. Proficiency in statistical software and data analysis techniques is required. A Ph.D. or M.D. in a relevant scientific or medical field is required. Postdoctoral research experience or equivalent in oncology is highly desirable. This is a critical role for an experienced scientist looking to make a significant impact on cancer patient care. This role is based in Sanad, Capital, BH .
Responsibilities include designing and overseeing complex clinical trials, ensuring adherence to regulatory guidelines (FDA, EMA) and Good Clinical Practice (GCP). You will collaborate closely with internal teams, including R&D, medical affairs, regulatory affairs, and project management, as well as external investigators and clinical sites. Developing clinical protocols, investigator brochures, and other essential study documents will be a key duty. You will be responsible for data interpretation, statistical analysis oversight, and preparing comprehensive clinical study reports.
Furthermore, you will contribute to the scientific strategy for oncology drug development, identifying new research opportunities and therapeutic targets. Staying updated on the latest scientific literature, clinical advancements, and competitive landscape in oncology is essential. You will also be involved in preparing regulatory submissions and responding to queries from health authorities. The ideal candidate will possess strong analytical, problem-solving, and communication skills. Experience in oncology clinical research, including hands-on involvement in trial design and management, is mandatory. Proficiency in statistical software and data analysis techniques is required. A Ph.D. or M.D. in a relevant scientific or medical field is required. Postdoctoral research experience or equivalent in oncology is highly desirable. This is a critical role for an experienced scientist looking to make a significant impact on cancer patient care. This role is based in Sanad, Capital, BH .
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7
Senior Clinical Research Associate - Oncology
99227 Zallaq, Southern
BHD75000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly experienced and motivated Senior Clinical Research Associate (CRA) to join their dynamic team. This pivotal role will focus on the oncology therapeutic area, contributing to groundbreaking research and drug development. The position is based in the vibrant area of Zallaq, Southern, BH .
As a Senior CRA, you will be instrumental in overseeing and managing clinical trial activities across multiple sites. Your responsibilities will include ensuring adherence to Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. You will conduct site selection, initiation, monitoring, and closure activities. This involves building strong relationships with investigators and site staff, providing training, and ensuring timely data collection and quality. You will also be responsible for identifying and resolving site-level issues, managing study supplies, and ensuring the safety of study participants. The role requires meticulous attention to detail, excellent organizational skills, and the ability to work independently as well as part of a collaborative team. You will play a crucial role in the successful execution of clinical trials, from early-phase research to late-stage studies, ultimately contributing to the advancement of new cancer therapies.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field. A Master's degree is a plus. A minimum of 5 years of progressive experience as a Clinical Research Associate is essential, with a significant portion dedicated to oncology trials. Demonstrable knowledge of ICH-GCP, FDA regulations, and clinical trial processes is mandatory. Excellent communication, interpersonal, and problem-solving skills are paramount. The ability to travel to study sites (approximately 50%) is required. Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems is expected. This is an exciting opportunity to make a tangible impact in a challenging and rewarding field, working with a company committed to improving patient outcomes.
As a Senior CRA, you will be instrumental in overseeing and managing clinical trial activities across multiple sites. Your responsibilities will include ensuring adherence to Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. You will conduct site selection, initiation, monitoring, and closure activities. This involves building strong relationships with investigators and site staff, providing training, and ensuring timely data collection and quality. You will also be responsible for identifying and resolving site-level issues, managing study supplies, and ensuring the safety of study participants. The role requires meticulous attention to detail, excellent organizational skills, and the ability to work independently as well as part of a collaborative team. You will play a crucial role in the successful execution of clinical trials, from early-phase research to late-stage studies, ultimately contributing to the advancement of new cancer therapies.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field. A Master's degree is a plus. A minimum of 5 years of progressive experience as a Clinical Research Associate is essential, with a significant portion dedicated to oncology trials. Demonstrable knowledge of ICH-GCP, FDA regulations, and clinical trial processes is mandatory. Excellent communication, interpersonal, and problem-solving skills are paramount. The ability to travel to study sites (approximately 50%) is required. Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems is expected. This is an exciting opportunity to make a tangible impact in a challenging and rewarding field, working with a company committed to improving patient outcomes.
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8
Senior Clinical Research Scientist - Oncology
201 Shahrakan
BHD6000 month
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking an experienced Senior Clinical Research Scientist specializing in Oncology. This critical role will involve the design, execution, and analysis of groundbreaking clinical trials aimed at developing novel cancer therapies. The ideal candidate will possess a strong scientific background in oncology, extensive experience in clinical trial management, and a deep understanding of drug development processes. You will be responsible for leading cross-functional teams, developing clinical protocols, managing study timelines, interpreting complex data, and ensuring compliance with regulatory guidelines. The Senior Clinical Research Scientist will contribute significantly to advancing our pipeline of innovative treatments and improving patient outcomes. A passion for scientific discovery and a commitment to ethical research practices are essential.
Responsibilities:
Responsibilities:
- Design and develop clinical trial protocols for oncology drug candidates, ensuring scientific rigor and regulatory compliance.
- Oversee the execution of clinical trials, from site selection and initiation to data analysis and final reporting.
- Collaborate with investigators, study coordinators, and other clinical site personnel to ensure proper study conduct.
- Interpret complex clinical data, including safety and efficacy endpoints, and contribute to the preparation of study reports and publications.
- Ensure adherence to Good Clinical Practice (GCP), regulatory requirements, and company policies.
- Work closely with regulatory affairs, preclinical development, and manufacturing teams to support drug development programs.
- Provide scientific and technical expertise to internal teams and external partners.
- Analyze emerging scientific literature and research trends in oncology.
- Manage budgets and timelines for clinical trial activities.
- Contribute to the strategic planning of the oncology pipeline and the development of new drug candidates.
- Ph.D. or M.D. in a relevant life science discipline (e.g., Oncology, Pharmacology, Biology).
- Minimum of 7 years of experience in clinical research, with a significant focus on oncology trials.
- Demonstrated experience in clinical trial design, protocol development, and data analysis.
- In-depth knowledge of oncology, cancer biology, and therapeutic approaches.
- Familiarity with global regulatory requirements for drug development (e.g., FDA, EMA).
- Excellent scientific writing, communication, and presentation skills.
- Experience working with cross-functional teams and managing external collaborations.
- Strong analytical and problem-solving abilities.
- Ability to travel as needed for site visits and scientific conferences.
- Proven ability to manage multiple projects and meet challenging deadlines.
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