421 Nursing Research jobs in Bahrain
Clinical Research Associate
50000 Busaiteen, Muharraq
BHD2500 month
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Our client, a prominent pharmaceutical company with operations in **A'ali, Northern, BH**, is looking for a meticulous and dedicated Clinical Research Associate (CRA) to contribute to their groundbreaking drug development programs. As a CRA, you will play a vital role in ensuring the quality and integrity of clinical trials, adhering to strict protocols and regulatory guidelines. Your primary responsibilities will include monitoring clinical trial sites, ensuring accurate data collection and reporting, and verifying that trials are conducted in compliance with Good Clinical Practice (GCP) and other relevant regulations. You will be responsible for site initiation visits, routine monitoring visits, and close-out visits, as well as managing study documentation and resolving data queries. Building and maintaining strong relationships with investigators, site staff, and study sponsors is crucial for the success of the trials. The ideal candidate will possess a strong understanding of clinical trial processes, medical terminology, and regulatory requirements within the pharmaceutical industry. Excellent attention to detail, strong organizational and communication skills, and the ability to work independently and as part of a team are essential. A Bachelor's degree in a life science or healthcare-related field, along with previous experience as a CRA or in a related clinical research role, is highly preferred. This is an excellent opportunity for an experienced professional to make a significant contribution to advancing healthcare through rigorous clinical research.
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Clinical Research Associate
770 Southern, Southern
BHD65000 Annually
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Our client, a leading pharmaceutical company, is looking for a dedicated Clinical Research Associate (CRA) to contribute to groundbreaking medical advancements. This position is located in Nuwaidrat, Southern, BH , a hub of innovation. As a CRA, you will play a critical role in the planning, implementation, and execution of clinical trials. Your responsibilities will include site selection and initiation, monitoring clinical trial conduct to ensure compliance with protocols and Good Clinical Practice (GCP) guidelines, and managing data collection and verification. You will also liaise with investigators, study coordinators, and regulatory authorities, ensuring the safety and rights of trial participants are protected. The ideal candidate will have a Bachelor's degree in a life science, nursing, or a related field. A minimum of two years of experience in clinical research or as a CRA is mandatory. Strong knowledge of clinical trial processes, ICH-GCP, and regulatory requirements is essential. Excellent organizational skills, attention to detail, and the ability to work independently and as part of a team are crucial. Proficiency in clinical trial management software and a strong command of English, both written and verbal, are required. This role requires a proactive individual who is passionate about contributing to the development of new therapies. You will be working at the forefront of pharmaceutical research, making a tangible impact on patient health. Join a collaborative environment that values scientific rigor and employee growth.
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1
Clinical Research Associate
10001 Manama, Capital
BHD80000 Annually
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Our client, a distinguished pharmaceutical company, is actively seeking a meticulous and experienced Clinical Research Associate (CRA) to join their team based in **Manama, Capital, BH**. This role is crucial for the successful execution of clinical trials, ensuring adherence to protocols, regulatory guidelines, and ethical standards. The CRA will be responsible for monitoring clinical trial sites, verifying data accuracy, and ensuring patient safety throughout the trial process. This hybrid role requires a balance of on-site visits to study centers and remote data review and administrative tasks. You will play a key role in managing relationships with investigators, study coordinators, and other site personnel, providing training and support as needed. Key responsibilities include site selection, initiation, monitoring, and close-out visits. You will also review case report forms (CRFs), source documents, and investigational product accountability. The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) and relevant regulatory requirements. Excellent organizational skills, attention to detail, and the ability to travel regularly are essential for this position. This is an excellent opportunity for a dedicated professional to contribute to the development of life-saving medicines and advance their career in clinical research.
Responsibilities:
Responsibilities:
- Conduct pre-study, initiation, monitoring, and close-out visits for clinical trial sites.
- Ensure compliance with study protocols, SOPs, GCP, and regulatory requirements.
- Verify the accuracy and completeness of clinical data by reviewing case report forms (CRFs) and source documents.
- Monitor patient safety and report adverse events and serious adverse events in a timely manner.
- Train and support study site personnel on trial procedures and data collection.
- Build and maintain strong working relationships with investigators and study staff.
- Manage investigational product accountability and ensure proper storage and dispensing.
- Review and approve site-specific trial documents.
- Prepare and submit site monitoring reports and follow up on action items.
- Participate in team meetings and contribute to the overall success of clinical trial execution.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial role.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Experience in site monitoring, data verification, and adverse event reporting.
- Excellent understanding of clinical trial processes and documentation.
- Strong interpersonal, communication, and organizational skills.
- Ability to work independently and manage multiple tasks effectively.
- Willingness to travel to clinical trial sites as required.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
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2
Clinical Research Associate
1011 Riffa, Southern
BHD70000 Annually
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Our client, a reputable pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their expanding operations in **Riffa, Southern, BH**. As a CRA, you will be instrumental in ensuring the smooth and compliant execution of clinical trials. Your primary responsibility will be to monitor study sites, verify the accuracy and completeness of clinical data, and ensure adherence to protocols, regulatory requirements (ICH-GCP), and ethical standards. This role involves extensive travel to investigational sites, building strong relationships with Principal Investigators and site staff, and providing essential support throughout the trial process. Key duties include pre-study visits, initiation visits, routine monitoring visits, and close-out visits. You will be responsible for source data verification, reviewing regulatory documents, and ensuring that all trial-related activities are conducted and documented appropriately. The successful candidate will possess excellent communication, interpersonal, and organizational skills. A strong understanding of clinical trial phases, study design, and regulatory guidelines is essential. We are looking for someone with a keen eye for detail, problem-solving capabilities, and the ability to manage multiple tasks effectively. A bachelor's degree in a life science, nursing, or a related field is required, along with a minimum of 2-3 years of direct experience as a CRA or in a similar clinical research role. Proficiency in clinical trial management software and electronic data capture systems is also a requirement. This is an on-site position offering a stimulating environment within the pharmaceutical industry, contributing to the development of life-saving medications. Join a team committed to scientific excellence and patient well-being.
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3
Clinical Research Associate
34567 Riffa, Southern
BHD70000 Annually
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Our client, a prominent pharmaceutical company, is seeking an experienced Clinical Research Associate (CRA) to join their dedicated team in Riffa, Southern, BH . This critical role involves ensuring the smooth and efficient execution of clinical trials according to protocol, Good Clinical Practice (GCP) guidelines, and all applicable regulations. You will be responsible for monitoring clinical trial sites, ensuring data accuracy and integrity, and verifying patient safety. Key responsibilities include site initiation visits, routine monitoring visits (on-site and remote), and site closure visits. You will manage all aspects of trial documentation, review case report forms (CRFs), and resolve data queries. Building and maintaining strong relationships with investigators and site staff is essential for successful trial conduct. You will also be responsible for identifying and reporting adverse events and ensuring protocol compliance at all times. The CRA will work closely with internal project teams, including project managers, data managers, and medical monitors, to ensure the overall success of the trial. Travel to clinical sites within the designated region will be a significant part of the role.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field. A minimum of 2-3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role is required. Strong knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials is essential. Excellent organizational, time management, and communication skills are paramount. The ability to travel frequently (up to 60% of the time) is a must. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is expected. Candidates should demonstrate a high level of attention to detail, problem-solving abilities, and the capacity to work independently and as part of a team. Prior experience in pharmaceutical or biotechnology industry research is highly preferred.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field. A minimum of 2-3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role is required. Strong knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials is essential. Excellent organizational, time management, and communication skills are paramount. The ability to travel frequently (up to 60% of the time) is a must. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is expected. Candidates should demonstrate a high level of attention to detail, problem-solving abilities, and the capacity to work independently and as part of a team. Prior experience in pharmaceutical or biotechnology industry research is highly preferred.
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4
Clinical Research Associate
903 Askar, Southern
BHD75000 Annually
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Posted 1 day ago
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Our client is seeking a diligent and motivated Clinical Research Associate (CRA) to contribute to groundbreaking pharmaceutical research, based in Tubli, Capital, BH . This role involves a hybrid work arrangement, balancing on-site clinical trial monitoring with remote data review and reporting. You will be responsible for ensuring the quality and integrity of clinical trials, adhering strictly to Good Clinical Practice (GCP) guidelines and regulatory requirements. Key responsibilities include site selection, initiation, monitoring, and close-out visits. You will manage investigational product accountability, review patient records for accuracy and completeness, and ensure protocol compliance. Communication with clinical sites, investigators, and study sponsors will be a core part of your duties. The ideal candidate will have a Bachelor's degree in a life science, nursing, or a related field, with at least 2-3 years of experience as a CRA or in a similar clinical research role. Strong knowledge of clinical trial processes, ICH-GCP, and regulatory requirements is essential. Excellent organizational, problem-solving, and communication skills are required. The ability to travel to clinical sites as needed is also a requirement. This position offers a challenging yet rewarding career path, contributing to the development of life-saving therapies and offering a flexible work environment.
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5
Clinical Research Associate
600 Riffa, Southern
BHD80000 Annually
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Posted 1 day ago
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Our client is looking for a dedicated Clinical Research Associate to join their expanding pharmaceutical team. This role offers a hybrid work arrangement, blending remote flexibility with essential on-site collaboration. You will play a critical role in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Responsibilities include site initiation visits, routine monitoring visits (both remote and on-site), data review, and ensuring accurate and timely submission of regulatory documents. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with a minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial role. Strong understanding of clinical trial processes, ICH-GCP, and relevant regulatory guidelines (e.g., FDA, EMA) is essential. Excellent communication, interpersonal, and organizational skills are required, along with the ability to manage multiple projects and priorities effectively. You will be responsible for building and maintaining strong relationships with clinical investigators and site staff, ensuring the smooth progression of studies. Proficiency in clinical trial management software and data management systems is highly beneficial. This position requires a meticulous approach to detail, a commitment to data integrity, and the ability to adapt to evolving project needs. Join our client's team and contribute to the development of life-changing pharmaceutical products. This is an excellent opportunity to advance your career in clinical research within a supportive and dynamic environment.
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6
Clinical Research Associate
401 Zallaq, Southern
BHD70000 Annually
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Our client is seeking a meticulous and dedicated Clinical Research Associate (CRA) to join their expanding pharmaceutical research division. This is a full-time, office-based position requiring presence in **Zallaq, Southern, BH**. You will be responsible for monitoring and managing clinical trials at investigative sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your duties will include site initiation, routine monitoring visits, source data verification, patient safety monitoring, and trial close-out activities. You will act as the primary liaison between the sponsor and investigative sites, ensuring clear communication and timely resolution of issues. The ideal candidate will have a strong understanding of clinical trial phases, study design, and regulatory affairs within the pharmaceutical industry. Excellent organizational, problem-solving, and communication skills are essential. A Bachelor's degree in a life science, nursing, pharmacy, or a related field is required. Prior experience as a CRA or in a similar clinical research role is highly preferred. You should be proficient in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems. This role demands a commitment to data integrity and patient safety, with the ability to travel to various research sites as needed. Join a leading pharmaceutical company dedicated to advancing healthcare through cutting-edge research and development.
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7
Clinical Research Associate
2110 Manama, Capital
BHD85000 Annually
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Posted 1 day ago
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Our client, a reputable pharmaceutical company dedicated to advancing healthcare through groundbreaking research, is seeking a meticulous and driven Clinical Research Associate (CRA) to join their clinical development team in Manama, Capital, BH . This position involves a hybrid work schedule, balancing remote monitoring and data review with essential on-site site initiation, monitoring, and close-out visits. The CRA will play a crucial role in ensuring the quality and integrity of clinical trials by monitoring study conduct at investigational sites, verifying compliance with protocols, and ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements. Key responsibilities include site selection and qualification, initiating and monitoring clinical trial sites, training site personnel, reviewing case report forms (CRFs) and source documentation, resolving data discrepancies, and facilitating communication between study sites and the sponsor. The ideal candidate will possess strong knowledge of clinical trial processes, ICH-GCP guidelines, and regulatory affairs within the pharmaceutical industry. Excellent organizational, communication, and interpersonal skills are paramount. The ability to travel to clinical sites as needed is required. A Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline, along with at least 3 years of experience as a CRA or in a similar clinical research role, is essential. Data management skills and familiarity with Electronic Data Capture (EDC) systems are highly valued. Join a leading pharmaceutical company and contribute to the development of life-saving medicines.
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8
Clinical Research Associate
4005 Zallaq, Southern
BHD60000 Annually
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Our client, a pioneering pharmaceutical company, is actively seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their operations in **Zallaq, Southern, BH**. This critical role involves overseeing and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with the study protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and all applicable regulatory requirements. The CRA will be responsible for site selection, initiation, monitoring, and close-out visits. You will liaise with investigators and study staff to ensure protocol compliance, data accuracy, and patient safety throughout the trial.
Key responsibilities include verifying patient eligibility, reviewing case report forms (CRFs) for completeness and accuracy, and ensuring proper drug accountability. The CRA will also manage study supplies and documentation, identify and report adverse events, and work to resolve any site-level issues that may arise. A strong understanding of pharmaceutical development, regulatory affairs, and clinical trial methodologies is essential. We are looking for individuals with exceptional organizational skills, attention to detail, and the ability to build rapport with healthcare professionals. This is an excellent opportunity to contribute to groundbreaking medical research and advance patient care in a supportive and professional environment. The role requires regular travel to clinical sites. A competitive remuneration package, comprehensive benefits, and ample opportunities for professional growth and development are offered. Join us and be a part of a team that is committed to improving health outcomes worldwide.
Responsibilities:
Key responsibilities include verifying patient eligibility, reviewing case report forms (CRFs) for completeness and accuracy, and ensuring proper drug accountability. The CRA will also manage study supplies and documentation, identify and report adverse events, and work to resolve any site-level issues that may arise. A strong understanding of pharmaceutical development, regulatory affairs, and clinical trial methodologies is essential. We are looking for individuals with exceptional organizational skills, attention to detail, and the ability to build rapport with healthcare professionals. This is an excellent opportunity to contribute to groundbreaking medical research and advance patient care in a supportive and professional environment. The role requires regular travel to clinical sites. A competitive remuneration package, comprehensive benefits, and ample opportunities for professional growth and development are offered. Join us and be a part of a team that is committed to improving health outcomes worldwide.
Responsibilities:
- Conduct pre-study, initiation, interim, and close-out monitoring visits.
- Ensure protocol compliance and data integrity at clinical sites.
- Verify source data and document case report forms (CRFs).
- Monitor patient safety and report adverse events.
- Manage study-related materials and documentation.
- Provide training and support to site staff.
- Collaborate with study teams and investigators.
- Ensure compliance with GCP and regulatory guidelines.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a CRA or in a similar clinical research role.
- Thorough knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with clinical trial monitoring and data management.
- Strong organizational and time management skills.
- Excellent interpersonal and communication skills.
- Ability to travel to clinical sites as required.
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