What Jobs are available for Study Coordinator in Bahrain?
Showing 548 Study Coordinator jobs in Bahrain
Remote Clinical Trials Manager
2520 Isa Town, Northern
BHD100000 Annually
WhatJobs
Posted 23 days ago
Job Viewed
Job Description
Our client is a leading innovator in developing novel therapeutic treatments and is seeking an experienced and motivated Remote Clinical Trials Manager to oversee critical clinical research studies. This fully remote position allows you to manage and coordinate all aspects of clinical trials from initiation through to completion, ensuring adherence to protocols, regulatory requirements, and timelines. You will collaborate with investigators, site staff, and internal teams to drive successful trial execution and contribute to bringing life-changing medicines to patients.
Key Responsibilities:
Key Responsibilities:
- Plan, manage, and execute clinical trials according to study protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Oversee the selection, initiation, monitoring, and close-out of clinical trial sites.
- Develop and manage trial budgets, ensuring cost-effectiveness and timely resource allocation.
- Create and maintain essential study documents, including clinical protocols, case report forms (CRFs), and investigator brochures.
- Ensure timely data collection, query resolution, and database lock.
- Manage relationships with investigators, site staff, contract research organizations (CROs), and other vendors.
- Monitor trial progress, identify potential risks, and implement mitigation strategies to ensure study timelines are met.
- Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA) and company SOPs.
- Conduct regular site monitoring visits (remotely or on-site as required) to ensure protocol adherence and data integrity.
- Prepare study reports, including interim and final study reports.
- Contribute to the development of clinical development plans and regulatory submission documents.
- Mentor and train junior clinical research staff.
- Bachelor's degree in a life science, nursing, or related field; advanced degree (MSc, PhD) is preferred.
- Minimum of 5 years of experience in clinical trial management, with a proven track record of successfully managing Phase II and/or Phase III trials.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Experience with various therapeutic areas is desirable.
- Strong project management skills, including budgeting, scheduling, and resource allocation.
- Excellent understanding of clinical trial operations and site management.
- Proficiency with clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Exceptional communication, interpersonal, and leadership skills.
- Ability to work autonomously, manage multiple priorities, and thrive in a remote work environment.
- Strong problem-solving and decision-making abilities.
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0
Senior Biostatistician - Clinical Trials
650 Tubli
BHD8800 Annually
WhatJobs
Posted 24 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical research organization, is seeking a highly experienced Senior Biostatistician to join their dynamic, fully remote team focused on clinical trials. This critical role involves applying advanced statistical methodologies to the design, analysis, and reporting of clinical studies. You will collaborate closely with clinical researchers, data managers, and medical writers to ensure the integrity and validity of trial outcomes. The ideal candidate possesses a strong academic background in statistics or biostatistics, extensive experience with statistical software, and a deep understanding of clinical trial phases and regulatory requirements. This remote position offers a significant opportunity to contribute to the development of life-saving therapies.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Provide statistical expertise for the design of clinical trials, including sample size calculations and randomization schemes.
- Develop and review Statistical Analysis Plans (SAPs) for clinical studies.
- Perform statistical analyses of clinical trial data using appropriate software (e.g., SAS, R, SPSS).
- Interpret statistical results and contribute to the preparation of clinical study reports, manuscripts, and regulatory submissions.
- Collaborate with cross-functional teams, including clinical operations, data management, and medical affairs.
- Ensure adherence to statistical principles, regulatory guidelines (e.g., ICH), and company SOPs.
- Mentor and provide guidance to junior biostatisticians and statistical programmers.
- Contribute to the development and implementation of statistical methodologies and tools.
- Participate in scientific and technical discussions with regulatory agencies.
- Maintain up-to-date knowledge of statistical advancements and their applications in clinical research.
Qualifications:
- Ph.D. or Master's degree in Biostatistics, Statistics, or a related quantitative field.
- Minimum of 5 years of experience in biostatistics, with a focus on clinical trial design and analysis.
- Proficiency in statistical software such as SAS (highly preferred), R, or SPSS.
- In-depth knowledge of clinical trial phases, endpoints, and regulatory requirements (e.g., FDA, EMA).
- Strong understanding of statistical modeling techniques relevant to clinical research.
- Excellent analytical, problem-solving, and critical-thinking skills.
- Superior written and verbal communication skills, with the ability to present complex statistical concepts clearly.
- Proven ability to work independently and collaboratively within a remote team environment.
- Experience with data management systems and concepts related to clinical data collection.
- Demonstrated ability to manage multiple projects and meet deadlines effectively.
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1
Senior Data Scientist - Clinical Trials Analysis
220 Hamad Town, Northern
BHD140000 Annually
WhatJobs Direct
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading scientific research organization, is seeking a highly skilled Senior Data Scientist to focus on the analysis of clinical trials data. This role is based in our facility in **Hamad Town, Northern, BH**, and requires an on-site presence to leverage our advanced computational resources and collaborate closely with our research teams. You will be responsible for applying sophisticated statistical and machine learning techniques to complex clinical trial datasets, extracting actionable insights, and contributing to the design and interpretation of studies. This position demands a deep understanding of biostatistics, statistical modeling, and data science methodologies within the pharmaceutical and healthcare sectors. You will play a crucial role in advancing scientific understanding and supporting the development of new treatments.
Key Responsibilities:
Qualifications:
This is an exceptional opportunity for a talented data scientist to contribute to cutting-edge clinical research and impact the development of innovative therapies. Join a dynamic scientific organization dedicated to pushing the boundaries of medical science.
Key Responsibilities:
- Design and implement statistical analysis plans for clinical trials.
- Develop and apply advanced statistical and machine learning models to analyze clinical trial data.
- Perform exploratory data analysis to identify trends, patterns, and potential biomarkers.
- Collaborate with clinicians, statisticians, and researchers to interpret study results and generate insights.
- Develop data visualization tools and dashboards to communicate findings effectively.
- Ensure the integrity, accuracy, and validity of data analysis.
- Contribute to the design of future clinical trials based on previous findings.
- Stay current with the latest advancements in data science, biostatistics, and clinical research methodologies.
- Present findings to internal teams and external stakeholders, including regulatory bodies.
- Mentor junior data scientists and contribute to the team's technical expertise.
Qualifications:
- Master's degree or Ph.D. in Biostatistics, Statistics, Data Science, Computer Science, or a related quantitative field.
- Minimum of 5 years of experience in data analysis, with a significant focus on clinical trials data in the pharmaceutical or biotech industry.
- Proven expertise in statistical modeling, hypothesis testing, and experimental design.
- Proficiency in statistical programming languages such as R or SAS, and data science libraries (e.g., Python, scikit-learn).
- Experience with clinical data management systems and relevant data standards (e.g., CDISC).
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent communication and presentation skills, with the ability to explain complex technical concepts to non-technical audiences.
- Experience with data visualization tools (e.g., Tableau, Power BI).
- Ability to work effectively in a collaborative, research-oriented environment.
This is an exceptional opportunity for a talented data scientist to contribute to cutting-edge clinical research and impact the development of innovative therapies. Join a dynamic scientific organization dedicated to pushing the boundaries of medical science.
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2
Remote Pharmaceutical Data Scientist - Clinical Trials
711 Amwaj Islands
BHD110000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical research company, is seeking a highly analytical and innovative Remote Pharmaceutical Data Scientist to join their Biostatistics and Data Management team. This is a fully remote position, allowing you to contribute to critical clinical trial data analysis from anywhere. You will leverage advanced statistical techniques and machine learning algorithms to interpret complex clinical trial data, identify trends, and support evidence-based decision-making. This role is crucial for accelerating drug development and ensuring the safety and efficacy of new therapies.
Responsibilities:
Responsibilities:
- Design and implement statistical analysis plans for clinical trials across various therapeutic areas.
- Analyze large, complex datasets generated from clinical trials, including real-world data.
- Develop and apply predictive models and machine learning algorithms to identify patient cohorts, predict treatment outcomes, and optimize trial design.
- Collaborate closely with clinical researchers, biostatisticians, and medical professionals to interpret findings and provide actionable insights.
- Develop data visualization tools and dashboards to communicate complex data effectively to diverse audiences.
- Ensure the integrity, accuracy, and quality of clinical trial data analysis in compliance with regulatory standards (e.g., FDA, EMA).
- Contribute to the development of innovative data analysis methodologies and approaches.
- Stay current with the latest advancements in data science, machine learning, and pharmaceutical statistics.
- Prepare technical reports, research papers, and presentations for scientific conferences and regulatory submissions.
- Manage multiple projects simultaneously and work effectively in a remote, cross-functional team environment.
- Validate and document analytical processes and results.
- Contribute to the strategic direction of data science applications within drug development.
- Ph.D. or Master's degree in Data Science, Biostatistics, Statistics, Computer Science, or a related quantitative field.
- Minimum of 5 years of experience in data science, with a focus on pharmaceutical or clinical trial data analysis.
- Strong proficiency in statistical modeling, machine learning techniques (e.g., regression, classification, clustering, deep learning), and experimental design.
- Expertise in programming languages such as R, Python, and SQL.
- Experience with clinical trial data standards (e.g., CDISC) and regulatory requirements.
- Familiarity with clinical trial phases and drug development processes.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong communication and presentation skills, with the ability to explain complex technical concepts to non-technical stakeholders.
- Proven ability to work independently and collaboratively in a remote setting.
- Experience with data visualization tools (e.g., Tableau, Power BI) is a plus.
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3
Clinical Research Associate - Pharmaceutical Trials
223, Capital Governorate Al Muharraq
BHD78000 Annually
WhatJobs
Posted 9 days ago
Job Viewed
Job Description
Our client, a globally recognized pharmaceutical company committed to advancing healthcare, is seeking a diligent and detail-oriented Clinical Research Associate (CRA) to join their team. This hybrid role, based in Tubli, Capital, Bahrain , offers the opportunity to contribute to critical clinical trials that bring life-changing medications to patients. As a CRA, you will play a vital role in monitoring clinical trial sites, ensuring data integrity, patient safety, and adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements. You will be responsible for site selection, initiation, monitoring, and close-out activities, acting as the key liaison between the sponsor and the clinical investigators. This position requires strong organizational skills, excellent communication abilities, and a thorough understanding of the clinical trial process.
Key Responsibilities:
Qualifications:
This is a critical role within our research and development division, offering the chance to impact patient care and contribute to the development of innovative pharmaceuticals. This hybrid position requires regular presence at our Tubli, Capital, Bahrain office.
Key Responsibilities:
- Conduct pre-study, initiation, routine, and close-out monitoring visits at clinical trial sites.
- Verify the accuracy, completeness, and compliance of clinical trial data by reviewing source documents and electronic case report forms (eCRFs).
- Ensure adherence to the study protocol, investigational plan, and all applicable regulatory requirements (e.g., GCP, FDA, EMA).
- Assess patient safety and ensure adverse events are appropriately reported and managed.
- Verify the qualification and training of site staff involved in the clinical trial.
- Manage site supplies, including investigational product, and ensure proper storage and accountability.
- Build and maintain effective working relationships with investigators, study coordinators, and other site personnel.
- Identify site issues and develop corrective and preventive action plans (CAPAs) in collaboration with site staff and the study team.
- Prepare detailed monitoring visit reports and communicate findings and recommendations promptly.
- Assist in resolving data discrepancies and queries from the data management team.
- Ensure timely submission of essential study documents.
- Stay updated on regulatory guidelines and company policies related to clinical research.
Qualifications:
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related scientific discipline.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- In-depth knowledge of ICH-GCP guidelines and other relevant regulatory requirements.
- Experience in site management, including site selection, initiation, monitoring, and close-out.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent monitoring skills, including source data verification and query resolution.
- Strong written and verbal communication skills, with the ability to communicate effectively with healthcare professionals.
- Highly organized with strong attention to detail and ability to manage multiple priorities.
- Ability to work independently and travel to clinical sites as required by the hybrid model.
- Knowledge of specific therapeutic areas is an advantage.
This is a critical role within our research and development division, offering the chance to impact patient care and contribute to the development of innovative pharmaceuticals. This hybrid position requires regular presence at our Tubli, Capital, Bahrain office.
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4
Clinical Research Associate - Pharmaceutical Trials
304 Riffa, Southern
BHD60000 Annually
WhatJobs
Posted 19 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to improving global health, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their esteemed team. This hybrid role offers a blend of remote flexibility and essential on-site collaboration, ensuring efficient oversight of clinical trials. You will play a pivotal role in ensuring the quality, integrity, and accuracy of data collected during clinical studies, adhering strictly to ethical standards and regulatory guidelines.
Key Responsibilities:
Required Qualifications:
This position is located in Riffa, Southern, BH , with a hybrid work arrangement. If you are passionate about advancing medical research and possess the required expertise, we encourage you to apply.
Key Responsibilities:
- Conduct site visits (initiation, monitoring, and close-out) to ensure compliance with protocols, SOPs, and GCP.
- Verify the accuracy, completeness, and consistency of clinical trial data through source document verification.
- Manage and maintain trial master files (TMF) and site regulatory documents.
- Oversee drug accountability and ensure proper handling and storage of investigational products.
- Train and support site staff on study-related procedures and regulatory requirements.
- Identify and resolve site-specific issues, escalating as necessary.
- Communicate effectively with investigators, study coordinators, and internal project teams.
- Prepare monitoring reports and ensure timely submission of study-related documentation.
- Participate in study team meetings and contribute to protocol development and amendments.
Required Qualifications:
- Bachelor's degree in a life science, nursing, or a related field.
- Minimum of 3-5 years of direct experience as a Clinical Research Associate.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Demonstrated experience in site monitoring and data verification.
- Excellent organizational skills and attention to detail.
- Strong verbal and written communication abilities.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as required (estimated 30-50% travel).
- A proactive approach to problem-solving and a commitment to ethical research practices.
This position is located in Riffa, Southern, BH , with a hybrid work arrangement. If you are passionate about advancing medical research and possess the required expertise, we encourage you to apply.
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5
Remote Clinical Research Associate - Pharmaceutical Trials
601 Arad
BHD90000 Annually
WhatJobs Direct
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company at the forefront of medical innovation, is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their fully remote clinical operations team. This role is crucial for the successful execution of clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. You will play a key part in monitoring trial progress, managing investigator sites, and ensuring the safety and well-being of study participants. The ideal candidate will possess a strong understanding of clinical trial phases, data management, and regulatory affairs within the pharmaceutical industry. This remote position offers the flexibility to contribute significantly to groundbreaking research from anywhere, while collaborating with a team of highly skilled professionals.
Key Responsibilities:
Location: This role is based in **Hidd, Muharraq, BH**, but is a fully remote position.
Key Responsibilities:
- Monitor clinical trial sites to ensure adherence to protocols, SOPs, and regulatory requirements (e.g., FDA, EMA, GCP).
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Conduct site initiation visits, interim monitoring visits, and close-out visits, both virtually and in-person as needed (though role is primarily remote).
- Manage communication with investigators and site staff, providing support and addressing queries.
- Ensure proper documentation and maintenance of essential trial documents (e.g., Trial Master File).
- Oversee drug accountability and investigational product management at trial sites.
- Identify and report adverse events and serious adverse events according to regulatory guidelines.
- Prepare monitoring visit reports and follow up on action items with study sites.
- Collaborate with internal project teams, including clinical project managers, data managers, and biostatisticians.
- Contribute to the development and review of clinical trial protocols and other study-related documents.
Location: This role is based in **Hidd, Muharraq, BH**, but is a fully remote position.
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6
Clinical Research Associate - Pharmaceutical Trials (Remote)
410 Saar, Northern
BHD85000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is actively seeking a diligent and experienced Clinical Research Associate (CRA) to join their dynamic team. This is a fully remote role, focused on the meticulous oversight and management of clinical trials. The CRA will be responsible for ensuring that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and good clinical practices (GCP). Key responsibilities include site initiation, monitoring, and close-out visits, as well as ensuring the quality and integrity of study data. You will act as the primary point of contact for clinical investigative sites, providing support and guidance to study personnel. The role involves verifying the accuracy and completeness of source documents, patient records, and study investigational product accountability. The Clinical Research Associate will also be responsible for identifying, evaluating, and recommending new clinical investigators. Ensuring regulatory compliance and maintaining accurate trial documentation are paramount. Excellent communication, organizational, and problem-solving skills are essential for success in this demanding, remote role. The ability to travel occasionally to sites may be required, but the primary work environment is remote, supporting trials impacting the Saar, Northern, BH region and beyond. This is an excellent opportunity for a motivated CRA to contribute to life-saving pharmaceutical research.
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7
Senior Clinical Research Associate - Oncology Trials
1041 Amwaj Islands
BHD75000 Annually
WhatJobs
Posted 16 days ago
Job Viewed
Job Description
Our client, a leading innovator in pharmaceutical research, is seeking a highly motivated and experienced Senior Clinical Research Associate (CRA) to join their dynamic team. This pivotal role will focus on the successful execution of oncology clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. The ideal candidate will be instrumental in managing all site-specific trial activities, from initiation to closure.
Responsibilities:
Responsibilities:
- Conduct pre-study, initiation, routine monitoring, and close-out visits for clinical trial sites in and around Hamad Town, Northern, BH .
- Ensure compliance with Good Clinical Practice (GCP), protocol requirements, and all applicable regulatory guidelines.
- Manage investigational product accountability at study sites.
- Act as the primary liaison between study sites and the clinical trial team, fostering strong working relationships.
- Review and reconcile essential study documents, including regulatory binders, source documents, and case report forms (CRFs).
- Identify and report adverse events and serious adverse events according to protocol and regulatory requirements.
- Train and mentor site staff on study procedures, protocol amendments, and data collection.
- Participate in investigator meetings and site initiation meetings.
- Contribute to the development of study-related documents, such as protocols and monitoring plans.
- Identify potential risks and issues at study sites and develop mitigation strategies.
- Ensure timely data entry and query resolution.
- Communicate effectively with internal stakeholders, including project managers, data managers, and medical monitors.
- Bachelor's degree in a life science, nursing, or a related field. Master's degree or PhD is a plus.
- Minimum of 5 years of experience as a Clinical Research Associate, with a strong emphasis on oncology trials.
- In-depth knowledge of ICH-GCP guidelines and local regulatory requirements in Bahrain.
- Proven ability to manage multiple sites and complex trials simultaneously.
- Excellent communication, interpersonal, and organizational skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to study sites within the region as required for monitoring activities.
- Demonstrated ability to work independently and as part of a collaborative team.
- Strong problem-solving skills and attention to detail.
- Fluency in English is essential; knowledge of Arabic is advantageous.
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8
Senior Clinical Research Associate - Oncology Trials
201 Saar, Northern
BHD90000 Annually
WhatJobs
Posted 18 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company at the forefront of medical innovation, is seeking an accomplished Senior Clinical Research Associate (CRA) to join their esteemed team in **Saar, Northern, BH**. This pivotal role will involve overseeing and managing clinical trials, with a particular emphasis on groundbreaking oncology research. The successful candidate will be instrumental in ensuring the integrity, accuracy, and timely completion of clinical studies by adhering strictly to Good Clinical Practice (GCP) guidelines and regulatory requirements. Responsibilities will encompass site selection and initiation, regular monitoring visits to clinical sites, data verification, and ensuring patient safety throughout the trial duration. You will serve as the primary liaison between the sponsor and the clinical sites, fostering strong working relationships and facilitating effective communication. This position demands a meticulous attention to detail, exceptional organizational skills, and the ability to manage multiple complex projects simultaneously. A thorough understanding of oncology protocols, patient populations, and the challenges inherent in cancer research is essential. The ideal candidate will possess strong analytical skills for identifying potential risks and implementing mitigation strategies. Opportunities for professional development and contributing to life-saving therapies make this a highly rewarding role.
Key responsibilities include:
Key responsibilities include:
- Performing site initiation, interim, and close-out visits to ensure compliance with study protocols and regulatory requirements.
- Monitoring study conduct, including patient recruitment, data collection, and source document verification.
- Ensuring adherence to Good Clinical Practice (GCP) and all applicable local and international regulations.
- Identifying, assessing, and escalating potential study risks and issues to the Clinical Trial Manager.
- Training and supporting site staff on study procedures and protocol requirements.
- Maintaining accurate and complete study documentation and site files.
- Building and maintaining strong relationships with investigators, site staff, and internal stakeholders.
- Contributing to the development and review of study protocols, informed consent forms, and other study-related documents.
- Bachelor's degree in a life science, nursing, or a related discipline; advanced degree preferred.
- Minimum of 5 years of direct experience as a Clinical Research Associate, with significant experience in oncology trials.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements in Bahrain and internationally.
- Proven ability to manage multiple clinical trials and sites efficiently.
- Excellent verbal and written communication skills.
- Strong problem-solving and decision-making abilities.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as required.
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