424 Clinical Trial Manager jobs in Bahrain
Clinical Trial Manager
701 Saar, Northern
BHD90000 Annually
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Posted 3 days ago
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Our client is seeking a dedicated and experienced Clinical Trial Manager to oversee the execution of Phase II and Phase III clinical trials within the pharmaceutical sector. This hybrid role offers the flexibility to work both remotely and from our state-of-the-art facility located in Saar. The Clinical Trial Manager will be responsible for the planning, implementation, and successful completion of clinical studies in compliance with Good Clinical Practice (GCP), FDA regulations, and other relevant guidelines. Your core duties will include site selection and initiation, budget management, vendor oversight, and ensuring the timely recruitment of patients. You will lead and mentor a team of clinical research associates (CRAs) and other study personnel, fostering a collaborative and high-performance work environment. Key responsibilities involve developing and managing clinical trial protocols, monitoring trial progress, ensuring data integrity, and identifying and resolving study-related issues. The role demands strong communication skills for effective interaction with investigators, site staff, regulatory authorities, and internal stakeholders. A comprehensive understanding of clinical trial management software, electronic data capture (EDC) systems, and clinical trial databases is essential. The successful candidate will play a crucial role in bringing innovative pharmaceutical products to market, ensuring patient safety and data accuracy throughout the trial lifecycle. This position requires a meticulous approach to detail, exceptional organizational abilities, and the capacity to manage multiple complex projects simultaneously. Join our team and contribute to groundbreaking medical advancements.
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Clinical Trial Manager
206 Al Jasra
BHD95000 Annually
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Posted 4 days ago
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Our client is looking for a dedicated and meticulous Clinical Trial Manager to oversee and execute clinical trials within **Hidd, Muharraq, BH**. This role is crucial for ensuring the successful and compliant management of clinical studies from initiation through to completion. You will be responsible for developing study protocols, managing site selection and initiation, ensuring subject recruitment targets are met, and monitoring study progress. Key responsibilities include ensuring adherence to Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements. You will manage budgets, timelines, and resources effectively, and build strong relationships with investigators, study coordinators, and regulatory authorities. This position requires a comprehensive understanding of clinical trial operations, data management, and risk assessment. The ability to troubleshoot and resolve issues promptly is vital. You will also be involved in preparing study documentation, analyzing trial data, and contributing to regulatory submissions. This is a challenging yet rewarding role for an experienced professional looking to advance their career in clinical research management and contribute to bringing innovative treatments to patients. We are seeking a proactive individual with exceptional organizational and communication skills.
Qualifications: Bachelor's degree in a scientific or healthcare-related field; advanced degree preferred. Minimum of 7 years of experience in clinical research, with at least 3 years in a trial management capacity. Proven experience managing Phase I-IV clinical trials. In-depth knowledge of ICH-GCP and regulatory requirements. Strong project management skills and budget management experience. Excellent communication, interpersonal, and leadership abilities.
Qualifications: Bachelor's degree in a scientific or healthcare-related field; advanced degree preferred. Minimum of 7 years of experience in clinical research, with at least 3 years in a trial management capacity. Proven experience managing Phase I-IV clinical trials. In-depth knowledge of ICH-GCP and regulatory requirements. Strong project management skills and budget management experience. Excellent communication, interpersonal, and leadership abilities.
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1
Clinical Trial Manager (Oncology)
00974 Al Jasra
BHD95000 Annually
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Posted 4 days ago
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Our client, a global leader in pharmaceutical research and development, is seeking a highly skilled and experienced Clinical Trial Manager to oversee oncology-focused clinical trials from initiation to closure. This critical role will be based in Hidd, Muharraq, BH , with hybrid work flexibility. You will be responsible for the planning, execution, and monitoring of complex clinical studies, ensuring adherence to Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. This includes site selection and initiation, investigator training, patient recruitment strategies, data monitoring, and ensuring the timely completion of study milestones.
Key responsibilities encompass managing budgets, timelines, and resources for multiple clinical trials. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, data management, and study statisticians, as well as external vendors and research sites. The successful candidate will proactively identify and mitigate risks, resolve issues that arise during trial conduct, and ensure the integrity and quality of collected data. Strong communication and interpersonal skills are essential for building and maintaining effective relationships with investigators, study coordinators, and regulatory authorities. This position demands exceptional organizational skills and the ability to manage complex projects in a demanding environment.
Qualifications required include a Bachelor's or Master's degree in a life science, nursing, or related field, with a minimum of 5 years of direct experience in clinical trial management, specifically within the oncology therapeutic area. A deep understanding of clinical trial design, ICH-GCP, FDA regulations, and relevant drug development processes is mandatory. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is essential. The ability to travel to clinical sites as needed is required. This is an exceptional opportunity to join a forward-thinking company making significant contributions to cancer treatment. If you are passionate about driving medical advancements and have a proven track record in clinical trial management, we encourage you to apply.
Key responsibilities encompass managing budgets, timelines, and resources for multiple clinical trials. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, data management, and study statisticians, as well as external vendors and research sites. The successful candidate will proactively identify and mitigate risks, resolve issues that arise during trial conduct, and ensure the integrity and quality of collected data. Strong communication and interpersonal skills are essential for building and maintaining effective relationships with investigators, study coordinators, and regulatory authorities. This position demands exceptional organizational skills and the ability to manage complex projects in a demanding environment.
Qualifications required include a Bachelor's or Master's degree in a life science, nursing, or related field, with a minimum of 5 years of direct experience in clinical trial management, specifically within the oncology therapeutic area. A deep understanding of clinical trial design, ICH-GCP, FDA regulations, and relevant drug development processes is mandatory. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is essential. The ability to travel to clinical sites as needed is required. This is an exceptional opportunity to join a forward-thinking company making significant contributions to cancer treatment. If you are passionate about driving medical advancements and have a proven track record in clinical trial management, we encourage you to apply.
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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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4
Clinical Research Associate
10001 Manama, Capital
BHD80000 Annually
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Posted 1 day ago
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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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5
Clinical Research Associate
1011 Riffa, Southern
BHD70000 Annually
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Posted 1 day ago
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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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Clinical Research Associate
34567 Riffa, Southern
BHD70000 Annually
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Posted 1 day ago
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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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7
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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8
Clinical Research Associate
600 Riffa, Southern
BHD80000 Annually
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Posted 1 day ago
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Job Description
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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