What Jobs are available for Clinical Trial in Bahrain?
Showing 5000+ Clinical Trial jobs in Bahrain
Clinical Trial Specialist
26501 Muharraq, Muharraq
BHD80000 Annually
WhatJobs
Posted 11 days ago
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Job Description
Our client, a rapidly expanding pharmaceutical company, is actively recruiting a meticulous and experienced Clinical Trial Specialist to join their dedicated Clinical Operations team. This role is instrumental in the successful planning, execution, and monitoring of clinical trials, ensuring adherence to global regulatory standards and company protocols. You will be responsible for managing all aspects of assigned clinical trials, including site selection, investigator recruitment, protocol development support, and budget management. Key responsibilities include developing and finalizing clinical trial protocols, Case Report Forms (CRFs), and other essential trial documentation. You will serve as the primary point of contact for investigative sites, providing ongoing training and support to study coordinators and investigators to ensure proper trial conduct. Monitoring trial progress, ensuring data integrity, and resolving site-level issues are critical components of this role. You will also collaborate closely with internal departments such as regulatory affairs, data management, and biostatistics, as well as external vendors and partners, to ensure efficient trial execution. Adherence to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements is paramount. This position is based at our state-of-the-art facility in Muharraq, Muharraq, BH . Candidates must possess a Bachelor's degree in a life science, nursing, or related field; a Master's degree is preferred. A minimum of 5 years of progressive experience in clinical trial management within the pharmaceutical or biotechnology industry is required. Demonstrated knowledge of GCP, ICH guidelines, and clinical trial phases is essential. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is mandatory. Excellent organizational, project management, and communication skills, with the ability to manage multiple priorities and work effectively in a cross-functional team environment, are crucial. Strong attention to detail and a commitment to ensuring patient safety and data accuracy are imperative. This is an exceptional opportunity to contribute to groundbreaking medical advancements.
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0
Remote Pharmaceutical Clinical Trial Manager
2800 Southern, Southern
BHD110000 Annually
WhatJobs
Posted 19 days ago
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Job Description
Our client, a pioneering company in the Pharmaceutical sector, is seeking an experienced and highly organized Remote Pharmaceutical Clinical Trial Manager to lead critical research initiatives. This is a fully remote position, offering the flexibility to work from your home office anywhere within the designated operational regions. The Clinical Trial Manager will be responsible for the planning, execution, and oversight of clinical trials, ensuring compliance with regulatory requirements, protocols, and company standards. Key responsibilities include developing trial protocols, managing budgets, timelines, and resources. You will also oversee site selection and management, data collection, and monitoring activities.
The ideal candidate will possess a strong background in clinical research and pharmaceutical development, with a minimum of 5 years of experience managing clinical trials. A comprehensive understanding of Good Clinical Practice (GCP), regulatory guidelines (e.g., FDA, EMA), and clinical trial methodologies is essential. Proven experience in therapeutic areas relevant to the company's pipeline is highly desirable. Excellent project management skills, with the ability to manage complex, multi-center trials, are required. Strong leadership and team management capabilities, particularly in a remote setting, are crucial. Exceptional communication, negotiation, and problem-solving skills are vital for effectively collaborating with investigators, clinical research associates, and other stakeholders.
This role requires a detail-oriented, proactive, and results-driven professional who can ensure the integrity and success of clinical trials. You will be responsible for identifying and mitigating trial-related risks, managing vendor relationships, and ensuring timely submission of regulatory documents. Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a must. A bachelor's degree in a life science, nursing, or a related field is required; an advanced degree (M.S., Ph.D., Pharm.D.) is a significant asset. This is a challenging and rewarding opportunity for a seasoned Clinical Trial Manager to contribute to the development of life-changing pharmaceuticals.
The ideal candidate will possess a strong background in clinical research and pharmaceutical development, with a minimum of 5 years of experience managing clinical trials. A comprehensive understanding of Good Clinical Practice (GCP), regulatory guidelines (e.g., FDA, EMA), and clinical trial methodologies is essential. Proven experience in therapeutic areas relevant to the company's pipeline is highly desirable. Excellent project management skills, with the ability to manage complex, multi-center trials, are required. Strong leadership and team management capabilities, particularly in a remote setting, are crucial. Exceptional communication, negotiation, and problem-solving skills are vital for effectively collaborating with investigators, clinical research associates, and other stakeholders.
This role requires a detail-oriented, proactive, and results-driven professional who can ensure the integrity and success of clinical trials. You will be responsible for identifying and mitigating trial-related risks, managing vendor relationships, and ensuring timely submission of regulatory documents. Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a must. A bachelor's degree in a life science, nursing, or a related field is required; an advanced degree (M.S., Ph.D., Pharm.D.) is a significant asset. This is a challenging and rewarding opportunity for a seasoned Clinical Trial Manager to contribute to the development of life-changing pharmaceuticals.
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1
Clinical Research Associate
BH30 1AN Tubli
BHD65000 Annually
WhatJobs Direct
Posted today
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Job Description
Our client is a leading pharmaceutical company seeking a dedicated and experienced Clinical Research Associate to join their innovative team. This role will involve a mix of on-site responsibilities and remote work, providing flexibility while ensuring critical project milestones are met. You will be instrumental in overseeing the execution of clinical trials, ensuring compliance with protocols and regulatory standards.
Responsibilities:
Qualifications:
This hybrid role is based in Sitra, Capital, BH , offering a dynamic work environment for professionals passionate about advancing pharmaceutical research and development.
Responsibilities:
- Monitor clinical trial sites to ensure adherence to study protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Verify accuracy, completeness, and quality of data recorded by study sites.
- Conduct site initiation, interim monitoring, and close-out visits.
- Manage and resolve data queries and discrepancies.
- Ensure investigational product accountability and proper handling at study sites.
- Build and maintain strong relationships with investigators and site staff.
- Prepare monitoring reports and follow up on action items.
- Facilitate communication between study sites, the clinical operations team, and other departments.
- Ensure all study-related documentation is maintained accurately and securely.
- Participate in study team meetings and contribute to study planning and execution.
- Identify potential risks and implement mitigation strategies.
- Ensure compliance with safety reporting requirements.
Qualifications:
- Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
- Minimum of 2-3 years of experience as a Clinical Research Associate or in a similar role.
- In-depth knowledge of ICH-GCP guidelines and local regulatory requirements.
- Proven experience in monitoring clinical trials across various therapeutic areas.
- Excellent understanding of clinical trial processes from start-up to close-out.
- Strong organizational and time management skills.
- Exceptional written and verbal communication skills.
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Ability to travel to study sites as required.
- Critical thinking and problem-solving abilities.
- Team player with the ability to work effectively in a cross-functional environment.
This hybrid role is based in Sitra, Capital, BH , offering a dynamic work environment for professionals passionate about advancing pharmaceutical research and development.
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2
Clinical Research Associate
100 MAN Arad
BHD70000 Annually
WhatJobs Direct
Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join their team based in **Manama, Capital, BH**. This role is integral to the successful execution of clinical trials, ensuring compliance with study protocols, regulatory requirements, and ethical standards. The CRA will be responsible for monitoring clinical trial sites, ensuring the quality and integrity of data collected, and managing relationships with investigators and site staff.
Key responsibilities include conducting site visits (initiation, routine monitoring, and close-out) to verify trial conduct. You will review and verify source documents, case report forms (CRFs), and other trial-related records for accuracy and completeness. The CRA will ensure that investigational products are dispensed, stored, and accounted for correctly. You will also be responsible for identifying and resolving site-level issues, reporting deviations, and ensuring adherence to Good Clinical Practice (GCP) guidelines. Maintaining effective communication with study teams, investigators, and regulatory authorities is essential. This role requires a thorough understanding of clinical trial processes, regulatory landscapes, and ethical considerations in pharmaceutical research.
The ideal candidate will hold a Bachelor's degree in a life science, nursing, or a related field. A minimum of 2-3 years of direct experience as a Clinical Research Associate is required. Demonstrated knowledge of GCP, ICH guidelines, and relevant regulatory requirements is essential. Strong organizational, analytical, and problem-solving skills are necessary, along with excellent interpersonal and communication abilities. The ability to work independently and travel to clinical trial sites as required is a key component of this role. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is highly desirable. This position offers a competitive salary and benefits package, with opportunities for professional growth within a respected pharmaceutical organization.
Key responsibilities include conducting site visits (initiation, routine monitoring, and close-out) to verify trial conduct. You will review and verify source documents, case report forms (CRFs), and other trial-related records for accuracy and completeness. The CRA will ensure that investigational products are dispensed, stored, and accounted for correctly. You will also be responsible for identifying and resolving site-level issues, reporting deviations, and ensuring adherence to Good Clinical Practice (GCP) guidelines. Maintaining effective communication with study teams, investigators, and regulatory authorities is essential. This role requires a thorough understanding of clinical trial processes, regulatory landscapes, and ethical considerations in pharmaceutical research.
The ideal candidate will hold a Bachelor's degree in a life science, nursing, or a related field. A minimum of 2-3 years of direct experience as a Clinical Research Associate is required. Demonstrated knowledge of GCP, ICH guidelines, and relevant regulatory requirements is essential. Strong organizational, analytical, and problem-solving skills are necessary, along with excellent interpersonal and communication abilities. The ability to work independently and travel to clinical trial sites as required is a key component of this role. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is highly desirable. This position offers a competitive salary and benefits package, with opportunities for professional growth within a respected pharmaceutical organization.
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3
Clinical Research Associate
109 Al Muharraq, Muharraq
BHD80000 Annually
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is looking for a dedicated Clinical Research Associate to join their expanding team. This role offers a hybrid work arrangement, balancing remote flexibility with essential in-person collaboration. You will play a pivotal role in the execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your responsibilities will encompass site initiation, monitoring, and close-out visits, as well as managing study documentation, data collection, and source data verification. You will serve as a key liaison between investigative sites, internal study teams, and regulatory authorities, ensuring effective communication and problem resolution. The ideal candidate will possess a strong scientific background, meticulous attention to detail, and exceptional organizational skills. Experience in managing Phase II and Phase III clinical trials across various therapeutic areas is highly valued. Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems is essential. You must be adept at identifying and mitigating risks, troubleshooting site issues, and ensuring data integrity and patient safety. A Bachelor's degree in a life science, nursing, or a related healthcare field is required; a Master's degree or equivalent experience is a plus. Excellent interpersonal and communication skills are necessary to build strong relationships with site personnel and internal stakeholders. Travel to clinical sites will be required periodically. You should be proactive, resourceful, and committed to the successful and ethical conduct of clinical research. Your work will directly contribute to the development of life-saving therapies and improving patient outcomes. We seek individuals with a proven track record in clinical monitoring and a passion for advancing medical science. The ability to work independently while remaining a strong team player is crucial. Understanding of regulatory submissions and pharmacovigilance processes is beneficial.
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4
Clinical Research Associate
10048 Manama, Capital
BHD70000 Annually
WhatJobs
Posted 2 days ago
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Job Description
Our client is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their dedicated pharmaceutical team. This role is integral to ensuring the successful execution of clinical trials in compliance with regulatory standards and protocol requirements. The CRA will be responsible for site selection, initiation, monitoring, and close-out activities. This includes conducting site visits to assess the quality and integrity of trial data, verifying patient eligibility, ensuring adherence to Good Clinical Practice (GCP) guidelines, and managing investigational product accountability. You will serve as the primary liaison between the investigative sites and the sponsor, addressing any queries or issues that may arise during the trial. Strong communication and interpersonal skills are essential for building effective relationships with investigators, site staff, and internal project teams. The ideal candidate will possess a strong understanding of pharmaceutical drug development processes and regulatory affairs. A bachelor's degree in a life science, nursing, or a related field is required, along with a minimum of 2 years of experience as a CRA. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is highly desirable. This position is based in **Manama, Capital, BH**, and requires a commitment to on-site monitoring and collaboration. We are looking for an individual with exceptional organizational skills, a keen eye for detail, and the ability to work independently while meeting strict deadlines. Your dedication to patient safety and data integrity will be paramount. This is an excellent opportunity for a professional looking to advance their career in clinical research within a leading pharmaceutical organization. The role demands a high level of ethical conduct and a commitment to scientific excellence.
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5
Clinical Research Associate
2025 Al Budayyi, Northern
BHD4000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical company, is actively seeking a skilled Clinical Research Associate (CRA) to join their team in A'ali, Northern, BH . This role is critical in supporting the conduct of clinical trials, ensuring adherence to protocols, and maintaining data integrity. The CRA will be responsible for site selection, initiation, monitoring, and close-out activities. This includes conducting site visits to assess compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements, verifying data accuracy, and ensuring patient safety throughout the trial. The ideal candidate will possess a strong understanding of clinical trial processes, excellent analytical skills, and meticulous attention to detail. You will work closely with investigators, site staff, and internal project teams to ensure trials are conducted efficiently and ethically. Key responsibilities include managing study timelines, resolving site issues, and preparing monitoring reports. This position requires extensive travel to study sites. The successful applicant will be adept at managing multiple priorities and communicating effectively with a diverse range of stakeholders. This is a challenging yet rewarding opportunity for a dedicated professional passionate about advancing medical research. We are looking for an individual who is committed to scientific rigor and ethical conduct in clinical research. The role involves close collaboration with regulatory authorities and ethical committees, ensuring all necessary documentation is meticulously maintained and submitted on time. You will also be responsible for identifying and mitigating risks associated with clinical trial conduct, ensuring the highest standards of patient care and data quality are upheld. The ability to interpret complex study protocols and translate them into actionable site-level instructions is essential. Responsibilities include, but are not limited to: monitoring clinical trial sites, ensuring protocol compliance, verifying data accuracy, protecting patient safety, preparing monitoring reports, managing study timelines, facilitating communication between sites and the sponsor, and ensuring regulatory compliance. Qualifications: Bachelor's degree in a life science, nursing, or related field; Master's degree is a plus. Proven experience as a Clinical Research Associate. In-depth knowledge of GCP, ICH guidelines, and local regulations. Excellent monitoring and auditing skills. Strong analytical and problem-solving abilities. Exceptional communication and interpersonal skills. Ability to travel extensively.
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6
Clinical Research Associate
BH24 Southern, Southern
BHD70000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical research organization, is seeking a meticulous and proactive Clinical Research Associate to contribute to groundbreaking studies in Nuwaidrat, Southern, BH . This role offers a flexible hybrid work model, combining essential on-site activities with remote responsibilities. The Clinical Research Associate will be instrumental in ensuring the quality and integrity of clinical trials by monitoring trial sites, verifying data, and ensuring compliance with study protocols and regulatory guidelines. Responsibilities include site initiation visits, routine monitoring visits, and close-out visits; ensuring adherence to Good Clinical Practice (GCP) and all applicable regulations; managing and reviewing study documentation; and acting as a liaison between the sponsor and study sites. The ideal candidate will possess strong analytical and problem-solving skills, with an exceptional ability to manage multiple tasks and prioritize effectively. You will be required to travel to various research sites as needed. A Bachelor's degree in a life science, nursing, or a related field is essential, along with demonstrable experience in clinical trial monitoring. Proficiency with clinical trial management systems and electronic data capture (EDC) systems is highly desirable. Excellent written and verbal communication skills are a must, as is the ability to build and maintain strong working relationships with healthcare professionals and site staff. This is a challenging and rewarding opportunity for a dedicated professional looking to advance their career in pharmaceutical research and development, contributing to the advancement of new therapies and treatments from our key location in Nuwaidrat.
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7
Clinical Research Associate
BH455 Saar, Northern
BHD70000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a globally recognized pharmaceutical company at the forefront of medical innovation, is seeking a meticulous and dedicated Clinical Research Associate (CRA) to join their expanding clinical operations team. This role is essential for the successful execution of clinical trials, ensuring adherence to strict protocols, regulatory guidelines, and ethical standards. The CRA will be responsible for monitoring investigational sites, verifying data accuracy, and ensuring the safety and well-being of trial participants. Based in or frequently visiting the **Saar, Northern, BH** area, this position requires a proactive approach to trial management and a keen eye for detail. You will play a critical part in bringing new therapies to patients by ensuring the integrity and quality of clinical data.
Key responsibilities include initiating, monitoring, and closing out investigational sites participating in clinical trials. You will conduct site visits to verify source documentation, review case report forms (CRFs), and ensure compliance with the study protocol, Good Clinical Practice (GCP) guidelines, and applicable regulations. The CRA will be responsible for identifying, evaluating, and resolving site-specific issues and deviations. You will manage communication between the sponsor and the investigational sites, providing training and support to site staff as needed. Ensuring accurate and timely data entry and query resolution is paramount. The role involves maintaining trial master files (TMF) and ensuring all required documentation is complete and up-to-date. You will also be involved in safety reporting, including the timely reporting of adverse events. Regular reporting on site performance and trial progress to the project manager is required.
Required qualifications include a Bachelor's degree in a life science, nursing, pharmacy, or a related field. A Master's degree or equivalent advanced degree is a plus. A minimum of 3 years of direct experience as a Clinical Research Associate monitoring clinical trials is essential. In-depth knowledge of ICH-GCP guidelines, clinical trial regulations, and drug development processes is mandatory. Proven experience in site management, data verification, and regulatory compliance is required. Excellent interpersonal, communication, and presentation skills are necessary. Strong organizational and time management abilities, with the capacity to manage multiple priorities in a fast-paced environment, are crucial. Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS) is expected. Willingness to travel extensively (up to 60%) to investigational sites, predominantly within the **Saar, Northern, BH** region and potentially beyond, is a requirement. This hybrid role offers flexibility in managing your work schedule and location, balancing essential on-site visits with remote administrative tasks.
Key responsibilities include initiating, monitoring, and closing out investigational sites participating in clinical trials. You will conduct site visits to verify source documentation, review case report forms (CRFs), and ensure compliance with the study protocol, Good Clinical Practice (GCP) guidelines, and applicable regulations. The CRA will be responsible for identifying, evaluating, and resolving site-specific issues and deviations. You will manage communication between the sponsor and the investigational sites, providing training and support to site staff as needed. Ensuring accurate and timely data entry and query resolution is paramount. The role involves maintaining trial master files (TMF) and ensuring all required documentation is complete and up-to-date. You will also be involved in safety reporting, including the timely reporting of adverse events. Regular reporting on site performance and trial progress to the project manager is required.
Required qualifications include a Bachelor's degree in a life science, nursing, pharmacy, or a related field. A Master's degree or equivalent advanced degree is a plus. A minimum of 3 years of direct experience as a Clinical Research Associate monitoring clinical trials is essential. In-depth knowledge of ICH-GCP guidelines, clinical trial regulations, and drug development processes is mandatory. Proven experience in site management, data verification, and regulatory compliance is required. Excellent interpersonal, communication, and presentation skills are necessary. Strong organizational and time management abilities, with the capacity to manage multiple priorities in a fast-paced environment, are crucial. Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS) is expected. Willingness to travel extensively (up to 60%) to investigational sites, predominantly within the **Saar, Northern, BH** region and potentially beyond, is a requirement. This hybrid role offers flexibility in managing your work schedule and location, balancing essential on-site visits with remote administrative tasks.
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8
Clinical Research Associate
10108 Arad
BHD78000 Annually
WhatJobs
Posted 4 days ago
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing healthcare, is looking for a meticulous and experienced Clinical Research Associate to join their team in Riffa, Southern, BH . This hybrid role allows for a balance between on-site responsibilities and remote flexibility. You will play a critical role in the execution of clinical trials, ensuring compliance with protocols, regulations, and Good Clinical Practice (GCP) guidelines. The ideal candidate will have a strong background in clinical trial management and a keen eye for detail. Responsibilities include site selection and initiation, monitoring trial progress, ensuring accurate data collection and source document verification, and managing investigational product accountability. You will serve as the primary point of contact between the study sites and the sponsor, fostering strong relationships with investigators and study staff. The ability to identify and resolve site-level issues, ensuring data integrity and patient safety, is paramount. You will also be responsible for preparing regulatory submissions, tracking trial milestones, and contributing to study close-out activities. Excellent organizational skills, strong communication and interpersonal abilities, and a thorough understanding of the drug development process are essential. This is an exciting opportunity to contribute to life-saving medical advancements within a supportive and collaborative environment.
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