383 Research Associate 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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Pharmaceutical Research Associate
10010 Seef, Capital
BHD60000 Annually
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Our client, a reputable pharmaceutical company, is seeking a dedicated Pharmaceutical Research Associate to join their innovative R&D department in Seef, Capital, BH . This hybrid role requires a meticulous individual with a strong background in pharmaceutical sciences to contribute to drug discovery and development processes. You will conduct experiments, analyze data, and support research projects under the guidance of senior scientists. Responsibilities include performing laboratory assays, maintaining accurate research records, preparing technical reports, and collaborating with team members to achieve research objectives. You will also assist in the validation of analytical methods and ensure compliance with Good Laboratory Practices (GLP) and regulatory standards. The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline. Experience in pharmaceutical research, particularly in areas like formulation development, analytical chemistry, or drug metabolism, is highly desirable. Strong laboratory skills, proficiency in scientific instrumentation, and a keen attention to detail are essential. Excellent organizational, problem-solving, and communication skills are required. This position offers a hybrid work model, providing flexibility while ensuring essential hands-on laboratory work.
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2
Biotechnology Research Associate
4050 Askar, Southern
BHD6500 Annually
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Our client is a pioneering biotechnology research firm seeking a dedicated and skilled Biotechnology Research Associate to join their innovative laboratory in Tubli, Capital, BH . This role offers a fantastic opportunity to contribute to cutting-edge research in areas such as molecular biology, genetic engineering, and cell culture. The ideal candidate will hold a Bachelor's or Master's degree in Biotechnology, Molecular Biology, Biochemistry, or a related life science discipline, with practical laboratory experience. You will be responsible for supporting ongoing research projects, performing a variety of laboratory techniques, and meticulously documenting experimental results. Key responsibilities include preparing reagents and media, performing DNA/RNA extractions, PCR, cloning, cell culture, and various biochemical assays. The successful applicant will work closely with senior scientists, assisting in experimental design, data analysis, and troubleshooting. Meticulous attention to detail, strong organizational skills, and proficiency in sterile techniques are paramount. Familiarity with standard laboratory equipment and safety procedures is essential. This position requires a passionate individual with a commitment to scientific advancement and the ability to thrive in a collaborative research environment.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Perform molecular biology techniques, including PCR, gel electrophoresis, and DNA/RNA isolation.
- Conduct cell culture experiments using aseptic techniques.
- Assist in the development and execution of experimental protocols.
- Operate and maintain laboratory equipment.
- Accurately record and analyze experimental data.
- Collaborate with research teams to achieve project goals.
- Maintain laboratory inventory and order supplies as needed.
- Adhere to all safety and ethical guidelines in research.
Qualifications:
- Bachelor's or Master's degree in Biotechnology, Molecular Biology, Biochemistry, or a related field.
- Hands-on laboratory experience in molecular biology techniques.
- Proficiency in cell culture and aseptic techniques.
- Strong understanding of scientific principles and research methodologies.
- Excellent data recording and analytical skills.
- Ability to work independently and as part of a team.
- Good communication skills.
- Experience with bioinformatics tools is a plus.
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Research Associate - Biomedical
09220 Riffa, Southern
BHD3200 month
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Our client, a leading biomedical research institution, is actively seeking a dedicated and skilled Research Associate to contribute to their vital studies in **Riffa, Southern, BH**. This role is integral to advancing our understanding of complex diseases and developing innovative therapeutic strategies. The Research Associate will support senior scientists in designing and executing experiments, collecting and analyzing data, and maintaining laboratory operations. This position requires meticulous attention to detail, a strong foundation in biomedical sciences, and a passion for contributing to scientific progress.
Key responsibilities include:
Qualifications:
This is an excellent opportunity for an aspiring scientist to gain valuable experience and contribute to impactful biomedical research. If you are detail-oriented, scientifically curious, and eager to make a difference, we encourage you to apply.
Key responsibilities include:
- Assisting senior researchers in the design and execution of laboratory experiments, following established protocols.
- Performing a variety of molecular and cellular biology techniques, including cell culture, DNA/RNA extraction, PCR, Western blotting, and ELISA.
- Accurately recording experimental procedures, observations, and results in laboratory notebooks and databases.
- Collecting, organizing, and analyzing scientific data using statistical software and relevant tools.
- Preparing reagents, solutions, and culture media according to specific protocols.
- Maintaining laboratory equipment, ensuring it is calibrated and functioning correctly.
- Assisting with the ordering and inventory management of laboratory supplies and consumables.
- Ensuring adherence to all laboratory safety procedures and guidelines.
- Contributing to the preparation of research reports, presentations, and manuscripts.
- Collaborating with team members to troubleshoot experiments and achieve research objectives.
- Staying updated on relevant scientific literature and techniques.
- Maintaining a clean and organized laboratory workspace.
Qualifications:
- Bachelor's degree in Biomedical Science, Biology, Biochemistry, or a related field. A Master's degree is preferred.
- Minimum of 2-4 years of hands-on laboratory experience in a research setting.
- Proficiency in common molecular and cell biology techniques.
- Experience with data analysis software (e.g., SPSS, GraphPad Prism) is desirable.
- Strong organizational skills and exceptional attention to detail.
- Ability to follow complex protocols accurately and consistently.
- Good written and verbal communication skills.
- Ability to work effectively both independently and as part of a research team.
- A strong work ethic and a commitment to scientific accuracy.
- Familiarity with laboratory safety practices.
This is an excellent opportunity for an aspiring scientist to gain valuable experience and contribute to impactful biomedical research. If you are detail-oriented, scientifically curious, and eager to make a difference, we encourage you to apply.
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4
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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5
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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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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7
Clinical Research Associate
903 Askar, Southern
BHD75000 Annually
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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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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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