4 Clinical Oncology jobs in Bahrain
Senior Clinical Research Scientist - Oncology
23456 Southern, Southern
BHD110000 Annually
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Our client, a globally recognized pharmaceutical leader, is seeking an exceptional Senior Clinical Research Scientist specializing in Oncology to join their innovative research and development division in Nuwaidrat, Southern, BH . This pivotal role will involve the design, execution, and interpretation of clinical trials for novel oncology therapeutics. You will be at the forefront of advancing cancer treatment, working with cutting-edge investigational drugs and contributing to the development of life-saving therapies. The ideal candidate will possess a profound understanding of cancer biology, clinical trial methodologies, and regulatory requirements within the pharmaceutical industry. Responsibilities will include developing clinical trial protocols, overseeing patient recruitment and monitoring, analyzing clinical data, and preparing comprehensive study reports. You will collaborate closely with a multidisciplinary team of clinicians, statisticians, regulatory affairs specialists, and other scientists to ensure the successful progression of clinical programs. A strong scientific acumen, coupled with excellent analytical and problem-solving skills, is essential. The successful applicant will have a proven ability to interpret complex scientific data, translate research findings into actionable strategies, and contribute to the scientific literature through publications and presentations. We are looking for a motivated and results-oriented individual with a passion for improving patient outcomes in oncology. The ability to thrive in a fast-paced, collaborative environment and a commitment to scientific rigor are crucial. This position offers a unique opportunity to make a significant impact on cancer research and development within a highly respected organization. Embrace the challenge of transforming scientific discovery into tangible patient benefits.
Responsibilities:
Responsibilities:
- Design and develop clinical trial protocols for oncology drugs.
- Oversee the conduct of clinical trials, ensuring patient safety and data integrity.
- Analyze and interpret clinical trial data, including efficacy and safety endpoints.
- Prepare clinical study reports and regulatory submission documents.
- Collaborate with internal and external stakeholders, including investigators and regulatory agencies.
- Contribute to the scientific strategy for oncology drug development.
- Stay abreast of the latest advancements in oncology research and clinical practice.
- Mentor junior research staff and contribute to knowledge sharing.
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Biology).
- Minimum of 5 years of experience in clinical research within the pharmaceutical industry, with a focus on oncology.
- In-depth knowledge of cancer biology and therapeutic strategies.
- Strong understanding of clinical trial design, GCP, and regulatory guidelines.
- Excellent analytical, statistical interpretation, and written communication skills.
- Experience in data analysis software and statistical methods.
- Proven ability to manage multiple projects and timelines effectively.
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0
Senior Clinical Research Associate - Oncology
78720 Bilad Al Qadeem, Capital
BHD85000 Annually
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Our client, a leading pharmaceutical innovator, is seeking a highly skilled and dedicated Senior Clinical Research Associate (CRA) to join their dynamic team in **A'ali, Northern, BH**. This pivotal role will involve managing and overseeing clinical trial activities, ensuring compliance with all regulatory requirements and company protocols. The ideal candidate will have a strong background in oncology clinical trials, demonstrating a deep understanding of study protocols, data collection, and patient safety monitoring. You will be responsible for site selection, initiation, monitoring, and close-out activities, building and maintaining strong relationships with clinical investigators and site staff. Key responsibilities include ensuring the accuracy and integrity of clinical data, preparing site visit reports, and identifying potential risks and issues, developing and implementing mitigation strategies. You will also play a crucial role in training and mentoring junior CRAs, fostering a collaborative and high-performing team environment.
The successful candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree or higher is a plus. A minimum of 5 years of experience as a CRA, with a significant portion focused on oncology trials, is essential. You must have comprehensive knowledge of ICH-GCP guidelines and local regulatory requirements. Excellent organizational skills, attention to detail, and the ability to manage multiple priorities effectively are critical. Strong written and verbal communication skills are required, along with proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems. The ability to travel up to 60% of the time for site visits is expected. Join us in making a significant impact on advancing cancer research and improving patient outcomes.
Responsibilities:
The successful candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree or higher is a plus. A minimum of 5 years of experience as a CRA, with a significant portion focused on oncology trials, is essential. You must have comprehensive knowledge of ICH-GCP guidelines and local regulatory requirements. Excellent organizational skills, attention to detail, and the ability to manage multiple priorities effectively are critical. Strong written and verbal communication skills are required, along with proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems. The ability to travel up to 60% of the time for site visits is expected. Join us in making a significant impact on advancing cancer research and improving patient outcomes.
Responsibilities:
- Plan, execute, and manage clinical trial site activities in accordance with study protocols and regulatory guidelines.
- Conduct site visits (selection, initiation, monitoring, close-out) and ensure adherence to protocol and GCP.
- Verify the accuracy, completeness, and quality of clinical data through source data verification.
- Build and maintain positive relationships with investigative sites, ensuring effective communication and collaboration.
- Prepare and present site monitoring reports, addressing any findings or deviations promptly.
- Manage drug accountability and investigational product handling at clinical sites.
- Ensure timely resolution of site issues and escalate critical problems as needed.
- Contribute to the development and review of study-related documents, including protocols, informed consent forms, and case report forms.
- Mentor and train junior CRAs on best practices and study-specific requirements.
- Ensure compliance with all applicable regulations, including FDA, EMA, and local health authority requirements.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 5 years of clinical trial monitoring experience, with a strong emphasis on oncology.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Experience with CTMS and EDC systems.
- Excellent communication, interpersonal, and problem-solving skills.
- Ability to travel domestically and internationally as required.
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1
Senior Clinical Research Associate - Oncology
23100 Manama, Capital
BHD120000 Annually
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Our client, a leading global pharmaceutical company renowned for its innovation in oncology therapeutics, is seeking a highly qualified Senior Clinical Research Associate (CRA) to support critical clinical trials in Manama, Capital, BH . This role is essential for ensuring the quality, integrity, and compliance of our clinical studies, adhering strictly to Good Clinical Practice (GCP) guidelines and regulatory requirements. The ideal candidate will have a strong background in clinical trial monitoring and a passion for advancing cancer treatment.
Responsibilities:
Qualifications:
This is an exceptional career opportunity for a dedicated CRA to contribute to life-saving cancer research and development in Manama, Capital, BH .
Responsibilities:
- Manage and monitor clinical trial sites to ensure adherence to protocol, GCP, and regulatory requirements.
- Conduct pre-study, initiation, interim, and close-out visits at clinical sites.
- Verify the accuracy, completeness, and integrity of source documents and clinical trial data.
- Ensure proper investigational product accountability at study sites.
- Identify and report adverse events and protocol deviations promptly.
- Train and support site staff on trial-related matters, including study procedures and data entry.
- Build and maintain strong working relationships with investigators, site staff, and study sponsors.
- Prepare monitoring reports and follow up on action items with study sites.
- Ensure timely submission of study-related documents and regulatory filings.
- Contribute to the development of study protocols, informed consent forms, and other essential trial documents.
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 ICH-GCP guidelines and regulatory requirements (e.g., FDA, EMA).
- Proven experience in monitoring clinical trials across multiple sites.
- Excellent understanding of clinical trial processes and documentation.
- Strong attention to detail and organizational skills.
- Exceptional communication, interpersonal, and problem-solving abilities.
- Ability to travel as required to clinical sites.
- Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Demonstrated ability to work independently and manage multiple priorities effectively.
This is an exceptional career opportunity for a dedicated CRA to contribute to life-saving cancer research and development in Manama, Capital, BH .
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2
Senior Clinical Research Associate - Oncology
25152 Riffa, Southern
BHD85000 Annually
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Our client, a leading biopharmaceutical research organization, is seeking a highly motivated and experienced Senior Clinical Research Associate (CRA) to join their dynamic team. This pivotal role will be based in the thriving city of Riffa, Southern, BH . The Senior CRA will be responsible for overseeing and managing all phases of clinical trials, ensuring compliance with Good Clinical Practice (GCP) guidelines, protocols, and regulatory requirements.
Key responsibilities include site selection, initiation, monitoring, and close-out visits to ensure data integrity and patient safety. The successful candidate will act as the primary point of contact for study sites, providing guidance and support to investigators and study staff. You will be instrumental in protocol adherence, patient recruitment, and resolving site-level issues to maintain trial timelines.
This position requires a deep understanding of oncology drug development, therapeutic areas, and clinical trial processes. The ideal candidate will possess excellent communication, negotiation, and problem-solving skills, with a proven ability to work independently and collaboratively within a multidisciplinary team. You will meticulously document trial activities, review case report forms (CRFs), and manage essential study documents.
Qualifications should include a Bachelor's degree in a life science, nursing, or related field. A Master's degree or PhD is a plus. A minimum of 5 years of direct experience as a Clinical Research Associate, with a significant portion focused on oncology trials, is essential. Knowledge of Bahrain's healthcare system and regulatory environment is highly desirable. Strong understanding of ICH-GCP and local regulatory requirements is mandatory. Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS) is expected. This is an exceptional opportunity to contribute to groundbreaking research and advance your career in a supportive and innovative environment.
Key responsibilities include site selection, initiation, monitoring, and close-out visits to ensure data integrity and patient safety. The successful candidate will act as the primary point of contact for study sites, providing guidance and support to investigators and study staff. You will be instrumental in protocol adherence, patient recruitment, and resolving site-level issues to maintain trial timelines.
This position requires a deep understanding of oncology drug development, therapeutic areas, and clinical trial processes. The ideal candidate will possess excellent communication, negotiation, and problem-solving skills, with a proven ability to work independently and collaboratively within a multidisciplinary team. You will meticulously document trial activities, review case report forms (CRFs), and manage essential study documents.
Qualifications should include a Bachelor's degree in a life science, nursing, or related field. A Master's degree or PhD is a plus. A minimum of 5 years of direct experience as a Clinical Research Associate, with a significant portion focused on oncology trials, is essential. Knowledge of Bahrain's healthcare system and regulatory environment is highly desirable. Strong understanding of ICH-GCP and local regulatory requirements is mandatory. Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS) is expected. This is an exceptional opportunity to contribute to groundbreaking research and advance your career in a supportive and innovative environment.
- Monitor clinical trial activities at assigned sites.
- Ensure protocol and regulatory compliance.
- Maintain strong relationships with study investigators and staff.
- Oversee data collection and ensure accuracy.
- Prepare and present study progress reports.
- Contribute to the development of clinical study protocols and documentation.
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