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Remote Clinical Research Coordinator
303, BH Al Ghurayfah
BHD65000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a prominent healthcare organization, is actively recruiting a Remote Clinical Research Coordinator to support their groundbreaking research initiatives. This position is fully remote, offering a flexible and dynamic work environment for individuals passionate about advancing medical science. As a Clinical Research Coordinator, you will play a vital role in the planning, execution, and administration of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. Your responsibilities will encompass recruiting and screening potential study participants, obtaining informed consent, managing study documentation, coordinating participant visits, collecting and processing data, and maintaining accurate and comprehensive study records. You will also liaise with investigators, sponsors, and regulatory agencies, providing timely updates and addressing any queries. The ideal candidate possesses a strong understanding of clinical trial phases, GCP guidelines, and relevant regulations. Excellent organizational, communication, and interpersonal skills are paramount, as is meticulous attention to detail. Proficiency in clinical trial management software and electronic data capture systems is highly desirable. A Bachelor's degree in a life science, nursing, or a related healthcare field is required, along with (X) years of experience in clinical research. This role requires individuals who are self-motivated, able to work autonomously, and proficient in virtual collaboration tools. The opportunity to contribute to life-changing medical advancements from the comfort of your home office makes this a truly exceptional prospect for dedicated research professionals.
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0
Senior Clinical Research Coordinator
730 Hamad Town, Northern
BHD75000 Annually
WhatJobs
Posted 7 days ago
Job Viewed
Job Description
Our client, a leading non-profit organization committed to improving community well-being, is seeking a highly organized and experienced Senior Clinical Research Coordinator to join their fully remote team. This critical role will support the planning, implementation, and execution of clinical research studies focused on community health initiatives. You will be instrumental in ensuring that research protocols are followed meticulously, data is collected accurately, and all regulatory requirements are met. The ideal candidate possesses a strong understanding of clinical research methodologies, excellent communication and interpersonal skills, and a passion for contributing to impactful community-based research. As a remote coordinator, you will leverage digital platforms to manage study documentation, communicate with participants and research sites, and oversee data integrity. Your proactive approach and meticulous attention to detail will be key to the success of these vital research endeavors. Responsibilities will include:
- Coordinating all aspects of clinical research studies, from initiation to closure, ensuring adherence to protocols and regulatory guidelines.
- Recruiting, screening, and enrolling eligible participants for research studies.
- Collecting, documenting, and managing research data accurately and efficiently using electronic data capture systems.
- Monitoring participant compliance with study protocols and reporting any adverse events or protocol deviations.
- Managing study supplies, equipment, and investigational products.
- Communicating effectively with principal investigators, research staff, participants, and regulatory bodies.
- Maintaining comprehensive and organized study documentation, including source documents, case report forms (CRFs), and consent forms.
- Assisting with study site visits, audits, and inspections.
- Contributing to the development of study protocols, informed consent forms, and other research-related documents.
- Ensuring compliance with all relevant ethical guidelines and institutional review board (IRB) requirements.
- Providing training and guidance to junior research staff as needed.
- Staying up-to-date with best practices and regulatory changes in clinical research.
- Bachelor's degree in Nursing, Public Health, Biology, or a related healthcare field. A Master's degree is a plus.
- Minimum of 5 years of experience in clinical research coordination, preferably in community or public health settings.
- Thorough understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements (e.g., FDA, ICH).
- Experience with various electronic data capture (EDC) systems and electronic health records (EHR).
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to interact professionally with diverse populations.
- Proficiency in Microsoft Office Suite and familiarity with research management software.
- Ability to work independently and manage workload effectively in a remote environment.
- Certification as a Certified Clinical Research Professional (CCRP) or similar is highly desirable.
- A compassionate and ethical approach to working with research participants.
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1
Senior Clinical Research Coordinator
20081 Northern, Northern
BHD72000 Annually
WhatJobs
Posted 8 days ago
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Job Description
Our client is seeking a highly motivated and experienced Senior Clinical Research Coordinator to join their dedicated team, contributing to groundbreaking research in community and social care settings. This hybrid role offers a blend of in-office collaboration and remote flexibility, allowing for optimal engagement with research participants and project stakeholders. You will play a crucial role in the successful execution of clinical trials, ensuring adherence to protocols, regulatory guidelines, and ethical standards. Responsibilities include recruiting and consenting participants, managing study documentation, administering study-related procedures, and meticulously collecting and entering data. You will also liaise with investigators, study sponsors, and regulatory authorities, serving as a key point of contact throughout the research process. The ideal candidate will possess a strong understanding of clinical trial methodologies, GCP (Good Clinical Practice) guidelines, and relevant ethical principles. Excellent organizational skills, attention to detail, and the ability to manage multiple tasks concurrently are essential. Strong interpersonal and communication skills are vital for effective interaction with diverse participant populations and multidisciplinary research teams. This role presents an exciting opportunity to contribute to vital research that impacts community well-being and social care practices. We are looking for an individual with a passion for improving healthcare outcomes and a commitment to scientific integrity. Qualifications include a Bachelor's degree in a relevant healthcare or life science field, along with a minimum of 4 years of direct experience as a Clinical Research Coordinator. Certification as a Certified Clinical Research Professional (CCRC) or similar is highly desirable. Experience with electronic data capture (EDC) systems and proficiency in data management are required. Familiarity with IRB/ethics committee submissions and regulatory compliance is also essential. The ability to work both independently and collaboratively within a team environment is a must. Prior experience in community or social care research settings will be a significant advantage. You will be expected to travel occasionally to different sites as required by the research protocols.
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2
Senior Clinical Research Coordinator
456 Busaiteen, Muharraq
BHD70000 Annually
WhatJobs
Posted 12 days ago
Job Viewed
Job Description
Our client, a renowned research institution, is seeking a dedicated and experienced Senior Clinical Research Coordinator to join their vibrant team in **Busaiteen, Muharraq, BH**. This role is crucial for the successful execution of clinical trials, contributing to the advancement of medical knowledge and patient care. The Senior Clinical Research Coordinator will manage all aspects of clinical research studies, ensuring compliance with protocols, regulatory requirements, and ethical guidelines. Responsibilities include participant recruitment and screening, obtaining informed consent, managing study visits, and collecting and documenting research data accurately. You will serve as a key liaison between investigators, study participants, regulatory authorities, and sponsors. The ideal candidate possesses a strong understanding of clinical trial phases, Good Clinical Practice (GCP) guidelines, and relevant medical terminology. Experience in managing multiple complex research protocols simultaneously is essential. This Hybrid position involves both on-site patient interaction and administrative tasks, offering a balanced work environment. The Senior Clinical Research Coordinator will also be involved in data quality assurance, regulatory submissions, and potentially contributing to study design and protocol development. Excellent organizational, communication, and interpersonal skills are paramount for success in this role. We are looking for a meticulous, proactive individual with a passion for advancing healthcare through rigorous clinical research. This is an excellent opportunity to grow your career in clinical research within a supportive and innovative setting in **Busaiteen, Muharraq, BH**. A Bachelor's degree in Nursing, Life Sciences, or a related field is required, along with significant experience as a Clinical Research Coordinator. Certification from a recognized professional body (e.g., ACRP, SoCRA) is highly desirable.
Responsibilities:
Responsibilities:
- Coordinate and manage all aspects of clinical research studies according to protocol.
- Recruit, screen, and enroll eligible participants into clinical trials.
- Obtain informed consent from participants and explain study procedures.
- Schedule and conduct study visits, administer study medications/interventions as required.
- Collect, manage, and document study data accurately and confidentially.
- Monitor participants for adverse events and report them according to regulatory guidelines.
- Liaise with investigators, sponsors, IRBs, and other stakeholders.
- Maintain study documentation and regulatory files.
- Ensure compliance with GCP, HIPAA, and other relevant regulations.
- Assist in the preparation of study reports and regulatory submissions.
- Bachelor's degree in Nursing, Life Sciences, or a related healthcare field.
- Minimum of 4 years of experience as a Clinical Research Coordinator.
- In-depth knowledge of clinical trial processes and GCP guidelines.
- Experience with electronic data capture (EDC) systems.
- Strong understanding of medical terminology and research methodologies.
- Excellent organizational, time management, and problem-solving skills.
- Outstanding written and verbal communication skills.
- Ability to build rapport with patients and maintain confidentiality.
- Professional certification (e.g., Certified Clinical Research Coordinator - CRC) is a plus.
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3
Clinical Research Coordinator (Remote)
500 Saar, Northern
BHD65000 Annually
WhatJobs
Posted 22 days ago
Job Viewed
Job Description
Our client, a leading organization in community and social care research, is seeking a dedicated and organized Clinical Research Coordinator to join their team on a fully remote basis. This crucial role supports the execution of vital research studies aimed at improving community well-being and social care practices. You will be responsible for managing study protocols, coordinating participant recruitment and data collection, and ensuring compliance with all ethical and regulatory guidelines. The ideal candidate will have a strong understanding of clinical research methodologies, excellent organizational skills, and the ability to manage multiple tasks efficiently. Experience with electronic data capture (EDC) systems and familiarity with Good Clinical Practice (GCP) guidelines are essential. You will work closely with principal investigators, study sponsors, and research participants, facilitating effective communication and smooth study operations. This remote position requires a high level of self-motivation, attention to detail, and strong interpersonal skills to engage with participants and team members virtually. You will play a key role in advancing research that makes a positive impact on society. This is an exciting opportunity for a motivated individual to contribute to meaningful research from a remote setting.
Responsibilities:
Qualifications:
Responsibilities:
- Coordinate the daily operations of assigned clinical research studies.
- Recruit, screen, and enroll study participants according to protocol requirements.
- Collect, process, and manage study data using electronic data capture systems.
- Ensure all research activities comply with ethical standards and regulatory guidelines (e.g., GCP, IRB).
- Maintain accurate and complete study documentation, including case report forms and source documents.
- Schedule participant visits and communicate study requirements to participants.
- Liaise with principal investigators, study sponsors, and other stakeholders.
- Monitor participant safety and report adverse events as required.
- Assist with study-related audits and regulatory inspections.
- Contribute to the development of study protocols and data management plans.
Qualifications:
- Bachelor's degree in a health science, life science, or related field.
- Minimum of 3 years of experience as a Clinical Research Coordinator or in a similar research support role.
- Thorough understanding of clinical research principles, GCP, and regulatory requirements.
- Experience with electronic data capture (EDC) systems.
- Excellent organizational skills and attention to detail.
- Strong communication, interpersonal, and problem-solving abilities.
- Ability to work independently and manage time effectively in a remote environment.
- Proficiency in standard office software (e.g., Microsoft Office Suite).
- Certification such as Certified Clinical Research Coordinator (CCRC) is a plus.
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4
Clinical Research Coordinator - Oncology
54321 Ghuraifa, Capital
BHD65000 Annually
WhatJobs
Posted 25 days ago
Job Viewed
Job Description
Our client is actively seeking a dedicated and highly organized Clinical Research Coordinator specializing in Oncology to join their innovative research team. This is a critical role focused on advancing cancer treatments through meticulously managed clinical trials. As a remote-first position, you will play a pivotal role in the day-to-day management and implementation of research protocols, working from the comfort of your own home office. Your primary responsibilities will include patient recruitment and screening, ensuring participants meet eligibility criteria for various oncology trials. You will be responsible for obtaining informed consent, meticulously collecting and managing study data, ensuring its accuracy and completeness according to regulatory guidelines (GCP, FDA). This involves diligent data entry into electronic data capture (EDC) systems and preparing comprehensive reports. You will serve as a key liaison between investigators, study participants, sponsors, and regulatory bodies, maintaining clear and consistent communication. This role requires a profound understanding of cancer biology and current therapeutic strategies, alongside a deep commitment to ethical research conduct. You will manage study supplies, track patient visits, and coordinate with diagnostic laboratories and imaging centers as required by the study protocols. The ability to navigate complex electronic health records (EHR) and clinical trial management systems (CTMS) is essential. We are looking for an individual with exceptional attention to detail, strong organizational skills, and the ability to manage multiple priorities in a fast-paced, remote environment. A compassionate demeanor and excellent interpersonal skills are crucial for interacting with study participants and their families. Experience in oncology research is highly preferred, demonstrating a solid grasp of the unique challenges and nuances of cancer clinical trials. This position operates entirely remotely, serving the research initiatives in Jidhafs, Capital, BH , and offers the flexibility to work from anywhere.
Responsibilities:
Responsibilities:
- Recruit, screen, and enroll participants for oncology clinical trials.
- Obtain informed consent from study participants.
- Collect, manage, and accurately record research data using EDC systems.
- Monitor patient safety and adherence to study protocols.
- Serve as a primary point of contact for investigators, participants, and sponsors.
- Manage study documentation and regulatory compliance (GCP, FDA).
- Coordinate study-related procedures and specimen collection.
- Prepare and present study progress reports.
- Maintain up-to-date knowledge of oncology and clinical trial methodologies.
- Bachelor's degree in a relevant scientific or healthcare field.
- Minimum of 3-5 years of experience as a Clinical Research Coordinator.
- Specific experience in oncology clinical trials is highly desirable.
- Proficiency with EDC systems, EHR, and CTMS.
- Strong understanding of Good Clinical Practice (GCP) guidelines.
- Excellent organizational, communication, and interpersonal skills.
- Ability to work independently and manage time effectively in a remote setting.
- Certification as a Certified Clinical Research Professional (CCRP) or similar is a plus.
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5
Senior Clinical Research Coordinator (Remote)
2011 Al Ghurayfah
BHD70000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a leading organization in health innovation, is seeking a highly dedicated and experienced Senior Clinical Research Coordinator to join their fully remote team. This vital role will be instrumental in the successful execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. You will manage all aspects of study coordination, from patient recruitment and screening to data collection, documentation, and follow-up.
The ideal candidate will possess a comprehensive understanding of clinical trial phases, Good Clinical Practice (GCP) guidelines, and regulatory affairs. Your responsibilities will include recruiting and consenting participants, scheduling study visits, performing study-related procedures (e.g., vital signs, sample collection), and managing study data accurately and efficiently. You will maintain meticulous study records, ensuring data integrity and compliance with all institutional and regulatory policies.
This role requires exceptional organizational, communication, and interpersonal skills, with the ability to build rapport with patients and effectively communicate with investigators, study sponsors, and regulatory agencies. You will be responsible for identifying potential challenges, developing solutions, and ensuring the smooth progression of clinical trials. Experience with electronic data capture (EDC) systems and electronic trial master files (eTMF) is essential. As a senior member of the team, you may also be involved in training and mentoring junior coordinators, contributing to the development of research protocols, and improving study processes. This fully remote position demands self-discipline, excellent time management, and the ability to work autonomously while collaborating effectively with a distributed team.
Responsibilities:
The ideal candidate will possess a comprehensive understanding of clinical trial phases, Good Clinical Practice (GCP) guidelines, and regulatory affairs. Your responsibilities will include recruiting and consenting participants, scheduling study visits, performing study-related procedures (e.g., vital signs, sample collection), and managing study data accurately and efficiently. You will maintain meticulous study records, ensuring data integrity and compliance with all institutional and regulatory policies.
This role requires exceptional organizational, communication, and interpersonal skills, with the ability to build rapport with patients and effectively communicate with investigators, study sponsors, and regulatory agencies. You will be responsible for identifying potential challenges, developing solutions, and ensuring the smooth progression of clinical trials. Experience with electronic data capture (EDC) systems and electronic trial master files (eTMF) is essential. As a senior member of the team, you may also be involved in training and mentoring junior coordinators, contributing to the development of research protocols, and improving study processes. This fully remote position demands self-discipline, excellent time management, and the ability to work autonomously while collaborating effectively with a distributed team.
Responsibilities:
- Coordinate and manage clinical trials according to study protocols.
- Recruit, screen, and consent study participants.
- Schedule participant visits and conduct study-related procedures.
- Collect, manage, and document study data accurately.
- Maintain regulatory documentation and study files.
- Ensure compliance with GCP and regulatory requirements.
- Communicate effectively with investigators, sponsors, and regulatory bodies.
- Monitor participant adherence to study protocols.
- Assist with study close-out activities.
- Train and mentor junior clinical research staff.
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 5 years of experience as a Clinical Research Coordinator.
- In-depth knowledge of clinical trial phases and GCP guidelines.
- Proficiency with EDC systems and eTMF.
- Excellent organizational and time management skills.
- Strong interpersonal and communication skills.
- Ability to work independently and manage multiple priorities in a remote setting.
- Attention to detail and commitment to data integrity.
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6
Senior Clinical Research Coordinator - Remote
221 Zallaq, Southern
BHD85000 Annually
WhatJobs
Posted 9 days ago
Job Viewed
Job Description
Our client is seeking a dedicated and experienced Senior Clinical Research Coordinator to join their growing remote team. This role is crucial for managing and coordinating various aspects of clinical trials, ensuring adherence to protocols, regulations, and ethical standards. The successful candidate will work from a remote location, collaborating with research sites, principal investigators, and study sponsors to facilitate the successful execution of research studies.
Responsibilities:
Qualifications:
This fully remote position offers a unique opportunity to contribute significantly to critical research initiatives from the comfort of your own home.
Responsibilities:
- Coordinate all phases of clinical trials, from study initiation to close-out, ensuring timely and efficient completion of tasks.
- Recruit, screen, and enroll participants according to study protocols, obtaining informed consent.
- Manage study documentation, including regulatory binders, case report forms (CRFs), and source documents, ensuring accuracy and completeness.
- Administer study-related procedures, collect and process biological samples, and conduct patient assessments as required.
- Monitor participant adherence to study protocols and provide ongoing participant education and support.
- Liaise with investigators, study sponsors, contract research organizations (CROs), and regulatory agencies.
- Track study progress, identify and resolve potential issues, and maintain accurate study databases.
- Ensure compliance with Good Clinical Practice (GCP) guidelines, FDA regulations, and other applicable ethical and legal standards.
- Prepare and submit study-related reports and communications.
- Participate in remote site visits and audits as necessary.
Qualifications:
- Bachelor's degree in a life science, nursing, or a related field. A Master's degree is a plus.
- Minimum of 5 years of progressive experience as a Clinical Research Coordinator.
- In-depth knowledge of clinical trial processes, GCP, and regulatory requirements (e.g., FDA, ICH).
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Strong organizational, time management, and problem-solving skills.
- Excellent communication, interpersonal, and active listening skills.
- Ability to work independently and proactively in a remote setting, demonstrating strong self-discipline and initiative.
- Proficiency in standard office software (Microsoft Office Suite).
- Certifications such as Certified Clinical Research Professional (CCRC) or Certified Clinical Research Associate (CCRA) are highly desirable.
- Previous experience working remotely in a clinical research capacity is advantageous.
This fully remote position offers a unique opportunity to contribute significantly to critical research initiatives from the comfort of your own home.
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7
Senior Clinical Research Coordinator (Remote)
456 Southern, Southern
BHD75000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client, a prominent healthcare research organization, is seeking a dedicated Senior Clinical Research Coordinator to join their expanding remote team. This vital role involves managing and coordinating all aspects of clinical trials, ensuring compliance with study protocols, and maintaining high standards of data integrity. You will be a key liaison between research sites, investigators, participants, and regulatory authorities, all performed from your home office. The ideal candidate will possess extensive experience in clinical research, exceptional organizational skills, and a deep commitment to advancing medical knowledge. This is a fully remote position, offering flexibility and the opportunity to contribute to groundbreaking research without geographic constraints.
Responsibilities:
Qualifications:
Responsibilities:
- Coordinate and manage multiple clinical trials simultaneously, from initiation to close-out.
- Recruit, screen, and enroll eligible participants according to protocol requirements.
- Educate participants on study procedures, potential risks, and benefits.
- Administer study medications and collect biological samples as per protocol.
- Maintain accurate and complete source documentation and case report forms (CRFs).
- Monitor patient safety and report adverse events promptly to the principal investigator and sponsor.
- Ensure compliance with Good Clinical Practice (GCP) guidelines, FDA regulations, and IRB requirements.
- Manage study supplies, equipment, and investigational product.
- Liaise with sponsors, contract research organizations (CROs), and site personnel.
- Prepare for and participate in monitoring visits and audits.
- Contribute to protocol development and study design discussions.
- Train and mentor junior research staff remotely.
- Maintain effective communication channels with all stakeholders in a virtual environment.
Qualifications:
- Bachelor's degree in a science-related field or equivalent combination of education and experience.
- Minimum of 4 years of experience as a Clinical Research Coordinator.
- Extensive knowledge of clinical trial phases, ICH-GCP guidelines, and relevant regulatory requirements.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Strong organizational, time management, and multitasking skills.
- Excellent verbal and written communication skills, adept at virtual interactions.
- Ability to work independently and proactively in a remote setting.
- Proficiency in Microsoft Office Suite and virtual collaboration tools.
- Certified Clinical Research Professional (CCRC) or similar certification is highly desirable.
- Demonstrated understanding of ethical principles in research.
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8
Senior Clinical Research Coordinator - Remote
15001 Muharraq, Muharraq
BHD80000 Annually
WhatJobs
Posted 17 days ago
Job Viewed
Job Description
Our client, a leading healthcare research organization, is seeking a dedicated and experienced Senior Clinical Research Coordinator to join their fully remote team. This pivotal role involves overseeing the execution of clinical trials, ensuring adherence to protocols, and maintaining meticulous patient records. You will play a crucial part in advancing medical research by coordinating study activities, managing data, and liaising with investigators, participants, and regulatory bodies. The ideal candidate possesses a strong understanding of clinical trial processes, excellent organizational skills, and a commitment to patient welfare and data integrity.
Key Responsibilities:
Key Responsibilities:
- Coordinate and manage all aspects of clinical trial activities according to study protocols and regulatory guidelines (e.g., GCP, FDA).
- Recruit, screen, and enroll eligible participants into clinical trials.
- Obtain informed consent from study participants, ensuring they understand the trial procedures and risks.
- Collect, document, and manage study data accurately and efficiently using electronic data capture (EDC) systems.
- Perform study-related procedures as trained and delegated by the investigator, such as vital signs measurement, specimen collection, and drug administration.
- Monitor participants' progress and safety throughout the trial, reporting any adverse events promptly.
- Schedule participant visits and manage study timelines to ensure adherence to the protocol.
- Maintain accurate and organized study files, including source documents and case report forms (CRFs).
- Liaise effectively with investigators, study sponsors, contract research organizations (CROs), and Institutional Review Boards (IRBs).
- Participate in study initiation visits, monitoring visits, and close-out visits.
- Provide ongoing training and support to study staff on trial-specific procedures.
- Ensure compliance with all applicable regulatory requirements and institutional policies.
- Assist in the preparation of regulatory submissions and study-related documentation.
- Contribute to the development and refinement of study protocols and operational procedures.
- Serve as a primary point of contact for participants and their families, providing clear communication and support.
- Bachelor's degree in Nursing, Life Sciences, or a related healthcare field.
- Minimum of 5 years of experience as a Clinical Research Coordinator.
- Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Experience with various EDC systems and clinical trial management software.
- Excellent organizational, time management, and multitasking skills.
- Proficiency in medical terminology and understanding of disease processes.
- Exceptional communication, interpersonal, and patient management skills.
- Ability to work independently and manage workload effectively in a remote setting.
- Attention to detail and commitment to data accuracy and integrity.
- Current RN license or relevant certification (e.g., CCRP, CCRA) is highly desirable.
- Experience with specific therapeutic areas (e.g., oncology, cardiology) is a plus.
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9