29 Clinical Research Associate Remote jobs in whatjobs
Clinical Research Associate (Remote)
Posted 19 days ago
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Job Description
Our client, a prominent pharmaceutical research organization, is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their fully remote team. This role is critical in ensuring the successful execution of clinical trials, adhering to strict regulatory guidelines and protocols. You will be responsible for monitoring study sites, ensuring data integrity, patient safety, and compliance with Good Clinical Practice (GCP) standards. This is an excellent opportunity for a skilled CRA to contribute to life-saving medical advancements while enjoying the flexibility of a remote work environment.
Key Responsibilities:
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with significant experience as a CRA. A thorough understanding of ICH-GCP guidelines and regulatory requirements is mandatory. Excellent organizational, time management, and communication skills are essential. The ability to work independently, manage multiple sites remotely, and travel occasionally as required is necessary. This fully remote position supports clinical research activities impacting healthcare in and around Nakuru, Nakuru, KE .
Key Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits to ensure adherence to protocol, regulations, and quality standards.
- Verify the accuracy, completeness, and integrity of clinical trial data by reviewing source documents and case report forms (CRFs).
- Ensure patient safety and well-being at study sites, reporting adverse events and deviations promptly.
- Train and provide ongoing support to site staff, including investigators and study coordinators, on protocol requirements and data collection procedures.
- Manage communication between study sites, the sponsor, and other relevant parties to ensure smooth trial progress.
- Resolve data discrepancies and ensure timely query resolution.
- Maintain comprehensive and accurate trial documentation, including monitoring visit reports and site files.
- Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA) and company SOPs.
- Participate in investigator meetings and other relevant training sessions.
- Contribute to the development and review of study-related documents, such as protocols and informed consent forms.
- Build strong working relationships with site personnel, fostering a collaborative approach to research.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with significant experience as a CRA. A thorough understanding of ICH-GCP guidelines and regulatory requirements is mandatory. Excellent organizational, time management, and communication skills are essential. The ability to work independently, manage multiple sites remotely, and travel occasionally as required is necessary. This fully remote position supports clinical research activities impacting healthcare in and around Nakuru, Nakuru, KE .
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Clinical Research Associate (Remote)
Posted 19 days ago
Job Viewed
Job Description
Our client is seeking a highly organized and detail-oriented Clinical Research Associate (CRA) to join their fully remote clinical operations team. This role is critical for ensuring the successful execution of clinical trials by monitoring study sites, ensuring compliance with protocols and regulations, and collecting accurate data. As a remote CRA, you will conduct site visits (virtual or in-person as required), verify data integrity, manage regulatory documentation, and serve as a key liaison between study sites, sponsors, and regulatory authorities. The ideal candidate possesses a strong understanding of Good Clinical Practice (GCP) guidelines, clinical trial processes, and medical terminology. Excellent communication, interpersonal, and problem-solving skills are essential for building rapport with site staff and addressing challenges effectively. You must be highly self-motivated, capable of managing your time and travel effectively (if applicable) in a remote setting, and committed to upholding the highest standards of research integrity. This position offers the flexibility of remote work, allowing you to contribute significantly to groundbreaking medical research from your chosen location. Join a dedicated team making a real impact on healthcare.
Responsibilities:
Responsibilities:
- Monitor clinical trial sites to ensure adherence to protocols, SOPs, and regulatory requirements.
- Verify accuracy and completeness of clinical trial data through source data verification.
- Manage and maintain regulatory documentation at study sites.
- Ensure patient safety and rights are protected throughout the trial.
- Act as a liaison between study sites, sponsors, and ethics committees/IRBs.
- Train and educate site staff on study procedures and requirements.
- Identify and resolve site-specific issues and deviations.
- Prepare site monitoring reports and communicate findings to management.
- Participate in site selection and initiation visits.
- Ensure timely drug/device accountability and investigational product management.
- Bachelor's degree in a life science, nursing, or a related healthcare field.
- Minimum of 3-5 years of experience as a Clinical Research Associate or similar role.
- In-depth knowledge of ICH-GCP guidelines and other relevant regulatory requirements.
- Experience with various therapeutic areas is a plus.
- Strong understanding of clinical trial operations and methodologies.
- Excellent analytical, problem-solving, and organizational skills.
- Exceptional communication, interpersonal, and negotiation skills.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently, manage multiple priorities, and meet deadlines in a remote setting.
- Willingness to travel as required for site visits.
This advertiser has chosen not to accept applicants from your region.
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Clinical Research Associate (Remote)
Posted 20 days ago
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Job Description
Our client is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join our fully remote team. As a CRA, you will play a vital role in ensuring the quality and integrity of clinical trials conducted across various therapeutic areas. You will be responsible for monitoring study sites, ensuring compliance with protocols and regulations, and maintaining accurate documentation. This position offers the flexibility of remote work, allowing you to contribute significantly to groundbreaking pharmaceutical research without the need for a physical office. You will remotely support sites that may include those in **Nakuru, Nakuru, KE**.
Responsibilities:
Responsibilities:
- Monitor clinical trial sites to ensure adherence to study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements.
- Verify the accuracy, completeness, and timeliness of data collected at study sites.
- Conduct site initiation visits, routine monitoring visits, and close-out visits.
- Train study site personnel on study procedures, data collection, and regulatory compliance.
- Identify, document, and track deviations from protocols and regulations, working with sites to implement corrective actions.
- Communicate effectively with investigators, study coordinators, and other site staff.
- Prepare and submit monitoring visit reports in a timely manner.
- Ensure that all essential regulatory documents are maintained at the study sites and are up-to-date.
- Assist in the resolution of data discrepancies and queries.
- Liaise with internal study teams, including project managers, data managers, and medical monitors.
- Contribute to the development of study-related documents, such as protocols and case report forms (CRFs).
- Ensure the safety of study participants by monitoring adverse event reporting.
- Manage multiple study sites remotely, ensuring consistent oversight and support.
- Maintain a strong understanding of the therapeutic area under investigation.
- Provide remote guidance and support to site staff, fostering a strong working relationship crucial for operations in **Nakuru, Nakuru, KE** and other monitored locations.
- 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 monitoring role.
- Thorough understanding of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Proven experience in site monitoring and data verification.
- Excellent verbal and written communication skills.
- Strong organizational and time management abilities, with the capacity to manage multiple priorities in a remote setting.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently with minimal supervision and as part of a remote team.
- Willingness to travel occasionally to study sites if required (though the role is primarily remote).
- Detail-oriented with a high level of accuracy.
- Experience in pharmaceutical or biotechnology industry preferred.
- Familiarity with the Kenyan healthcare system and regulatory environment, particularly concerning clinical research in **Nakuru, Nakuru, KE**, is a plus.
This advertiser has chosen not to accept applicants from your region.
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Clinical Research Associate (Remote)
Posted 21 days ago
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Job Description
Our client is seeking a dedicated and meticulous Clinical Research Associate to join their fully remote clinical operations team. In this vital role, you will be instrumental in ensuring the smooth and compliant execution of clinical trials. Your primary responsibilities will include site selection, initiation, monitoring, and close-out activities for clinical trial sites, all conducted virtually. You will serve as the key liaison between the clinical trial sites, the project team, and regulatory authorities, facilitating seamless communication and problem-solving. This is a remote-first position, requiring you to manage your workload and interactions effectively from a home-based office. You will be responsible for verifying the accuracy and completeness of clinical trial data, ensuring adherence to protocols, Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP) guidelines. Proactive identification and resolution of issues are critical. The ideal candidate will possess excellent organizational skills, a keen eye for detail, and strong interpersonal abilities to build and maintain positive relationships with site personnel, investigators, and internal study teams. Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems is essential. Your expertise will help accelerate the development of new and innovative pharmaceutical products, ultimately benefiting patient health worldwide. This role demands a deep understanding of the clinical trial lifecycle and a commitment to maintaining the highest standards of quality and integrity. You will be empowered to manage multiple protocols and sites concurrently, demonstrating strong time management and prioritization skills. The specific therapeutic areas may vary but will likely include cardiovascular and metabolic diseases. Our client values a proactive approach to problem-solving and fosters a supportive remote working culture.
Responsibilities:
Responsibilities:
- Conduct remote site monitoring visits to ensure protocol adherence and data integrity.
- Perform site selection, initiation, and close-out activities.
- Verify source data against case report forms (CRFs) and electronic data capture (EDC) systems.
- Manage and resolve site-level issues and deviations.
- Ensure compliance with GCP, SOPs, and regulatory requirements.
- Serve as the primary point of contact for assigned clinical sites.
- Train site personnel on study protocols and procedures.
- Track study progress and provide regular updates to the project team.
- Review and approve monitoring reports.
- Participate in Investigator Meetings and other study-related meetings.
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- Thorough understanding of GCP, ICH guidelines, and regulatory requirements.
- Proficiency in CTMS and EDC systems.
- Excellent monitoring and site management skills.
- Strong analytical and problem-solving abilities.
- Exceptional written and verbal communication skills.
- Ability to work independently and manage time effectively in a remote setting.
- Willingness to travel occasionally for essential site visits (if required, though the role is primarily remote).
- Experience in cardiovascular or metabolic disease trials is a plus.
This advertiser has chosen not to accept applicants from your region.
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Clinical Research Associate (Remote)
Posted 22 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join their fully remote global clinical operations team. This pivotal role involves overseeing and managing clinical trials from initiation to close-out, ensuring compliance with regulatory requirements and study protocols. The CRA will be responsible for site selection, monitoring clinical trial conduct, data verification, and ensuring the safety and rights of study participants. The ideal candidate will possess a strong background in clinical research, exceptional organizational skills, and a thorough understanding of Good Clinical Practice (GCP) guidelines. This position requires a self-starter who can manage multiple priorities effectively in a remote setting. Key Responsibilities:
- Conduct remote site monitoring visits (and potentially occasional on-site visits as required) to assess protocol compliance, data integrity, and subject safety.
- Ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
- Verify the accuracy, completeness, and quality of data collected at clinical trial sites.
- Manage and train site personnel on study-specific procedures and regulatory requirements.
- Serve as the primary point of contact between the sponsor and the investigative sites.
- Resolve data discrepancies and ensure timely query resolution.
- Prepare and present monitoring visit reports.
- Oversee site activation, initiation, and close-out processes.
- Maintain all required documentation and regulatory compliance for assigned sites.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate, with experience in remote monitoring.
- In-depth knowledge of GCP, FDA regulations, and other relevant regulatory guidelines.
- Proven ability to effectively monitor clinical trials and manage multiple study sites.
- Excellent interpersonal, communication, and problem-solving skills.
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Ability to work independently, prioritize tasks, and meet deadlines in a remote environment.
- Strong attention to detail and commitment to data accuracy.
- Experience in specific therapeutic areas is a plus.
This advertiser has chosen not to accept applicants from your region.
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Clinical Research Associate (Remote)
Posted 22 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to improving global health outcomes, is seeking a diligent and meticulous Clinical Research Associate (CRA) to join their innovative team. This is a fully remote position, offering flexibility while ensuring the critical oversight of clinical trials. You will play a vital role in ensuring the safety and integrity of research data, adhering strictly to study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. Your responsibilities will encompass site selection, initiation, monitoring, and close-out visits for clinical trial sites. This involves verifying data accuracy, ensuring proper source documentation, managing investigational product, and resolving site-level issues. The ideal candidate will possess a strong understanding of clinical trial processes, regulatory affairs, and medical terminology. Excellent communication and interpersonal skills are essential for building and maintaining effective relationships with investigators, site staff, and internal project teams. You will be responsible for tracking study progress, identifying and mitigating risks, and ensuring compliance with all relevant ethical and regulatory standards. This role demands exceptional organizational skills, attention to detail, and the ability to work autonomously in a remote setting. While the role is remote, the insights gained from working with healthcare professionals and understanding patient populations in areas like **Malindi, Kilifi, KE** can be invaluable for context and contributing to broader research initiatives.
Key Responsibilities:
Key Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits for clinical trial sites.
- Ensure compliance with study protocols, SOPs, and regulatory requirements (e.g., GCP, FDA).
- Verify the accuracy and completeness of clinical trial data through source document verification.
- Manage investigational product at clinical sites.
- Identify, track, and resolve site-level issues and action items.
- Train and mentor site staff on study-specific procedures.
- Prepare visit reports and communicate findings to internal teams.
- Ensure timely reporting of adverse events and safety concerns.
- Build and maintain strong relationships with investigators and site staff.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate (CRA) or equivalent role.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements.
- Experience with various clinical trial phases and therapeutic areas.
- Excellent monitoring skills, including source data verification.
- Strong organizational, time management, and problem-solving abilities.
- Exceptional written and verbal communication skills.
- Ability to work independently and manage multiple priorities in a remote environment.
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Must be able to travel occasionally as needed for specific site visits if required, though the role is primarily remote.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate (Remote)
Posted 22 days ago
Job Viewed
Job Description
Our esteemed pharmaceutical client is actively recruiting a dedicated and experienced Clinical Research Associate (CRA) to join their fully remote global team. This critical role will involve overseeing and managing clinical trials in compliance with Good Clinical Practice (GCP), local regulations, and study protocols. The successful candidate will be responsible for site selection, initiation, monitoring, and close-out activities, ensuring the quality and integrity of data collected. You will serve as the primary liaison between the sponsor and the investigational sites, providing training and support to site personnel. This is a remote-first position, offering significant autonomy and the flexibility to manage your workload effectively from your home office. We are looking for an individual with exceptional organizational skills, a keen eye for detail, and a strong understanding of clinical trial processes. Your responsibilities will include conducting site visits (virtual and potentially on-site as needed), reviewing essential documents, verifying data accuracy, resolving data queries, and ensuring timely reporting of adverse events. You will also be instrumental in identifying and escalating site issues to management. This role requires a proactive and self-driven individual who can work independently while maintaining strong collaborative relationships with research teams and stakeholders. The pharmaceutical industry demands rigorous adherence to standards, and this role is central to ensuring the safety and efficacy of new treatments. Your expertise in pharmaceutical development and clinical research methodologies will be highly valued. This position offers a unique opportunity to contribute to groundbreaking medical advancements while enjoying the benefits of a remote work arrangement. The position is based in Mombasa, Mombasa, KE , but is a fully remote role.
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Clinical Research Associate (Remote)
Posted 14 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly motivated and experienced Clinical Research Associate (CRA) to join our team. This hybrid role offers the flexibility of remote work with occasional on-site requirements. You will be responsible for monitoring clinical trials at investigational sites, ensuring compliance with protocols, regulations, and Good Clinical Practice (GCP) guidelines. Your duties will include site selection and initiation, routine monitoring visits (both remote and on-site), and site closure activities. You will review and assess patient records, verify data accuracy, and ensure the safety and integrity of trial participants. This role requires strong analytical and organizational skills, with the ability to manage multiple sites and studies simultaneously. Excellent communication and interpersonal skills are essential for building and maintaining effective relationships with investigators, study coordinators, and internal stakeholders. The ideal candidate will possess a Bachelor's degree in a life science or related field, with significant experience in clinical trial monitoring. Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS) is required. A thorough understanding of pharmaceutical industry regulations and clinical research processes is paramount. This position, associated with **Garissa, Kenya**, offers a flexible work arrangement, allowing for effective performance and contribution to critical pharmaceutical research initiatives. You will play a vital role in advancing medical treatments and ensuring the successful execution of our clinical development programs, contributing significantly to the pharmaceutical landscape.
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7
Clinical Research Associate - Remote
Posted 13 days ago
Job Viewed
Job Description
Our client, a cutting-edge pharmaceutical company committed to advancing medical treatments, is looking for a highly skilled and experienced Clinical Research Associate (CRA). This position is fully remote, allowing you to contribute to groundbreaking research from your home office. You will be responsible for monitoring and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with the study protocol, standard operating procedures (SOPs), and applicable regulations. This includes site selection, initiation, monitoring, and close-out visits. You will ensure data accuracy and integrity by reviewing source documents and verifying case report forms (CRFs). Building and maintaining strong relationships with investigators, site staff, and internal project teams is crucial. The role requires excellent organizational skills, attention to detail, and the ability to work independently. You will be expected to ensure compliance with Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements. This position offers a unique opportunity to be part of developing life-saving medications and therapies.
Responsibilities:
Responsibilities:
- Conducts all necessary site visits (selection, initiation, interim monitoring, and close-out).
- Assesses protocol and related regulatory requirements on-site.
- Manages all aspects of study site monitoring and progress, including communication with investigators.
- Ensures that investigational sites are properly managed and maintained.
- Ensures compliance with protocol and applicable regulations.
- Reviews and verifies case report forms (CRFs) and source documents.
- Monitors study data for accuracy and completeness.
- Manages communication between study sites and the clinical trial team.
- Prepares and presents study-related information to investigators and site staff.
- Ensures timely submission of site reports and documentation.
- Bachelor's degree in a life science, nursing, pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Experience with various phases of clinical trials.
- Strong understanding of medical terminology and research protocols.
- Excellent organizational and time management skills.
- Exceptional attention to detail and accuracy.
- Strong communication, interpersonal, and problem-solving skills.
- Ability to work independently and manage a remote workload effectively.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Associate (Remote)
Posted 11 days ago
Job Viewed
Job Description
Our client is seeking a dedicated and detail-oriented Clinical Research Associate to join their fully remote pharmaceutical research team. In this role, you will be instrumental in ensuring the integrity and quality of clinical trials by monitoring study sites, verifying data, and ensuring compliance with protocols and regulatory guidelines. You will work closely with investigators, site staff, and internal project teams to facilitate the smooth execution of studies, all while maintaining a remote work setup. This is a fantastic opportunity to contribute to life-saving medical advancements from the convenience of your home office, connecting with study sites digitally and effectively.
Key Responsibilities:
Key Responsibilities:
- Conduct remote site monitoring visits to assess trial progress, data accuracy, and regulatory compliance.
- Verify source documentation against case report forms (CRFs) for accuracy and completeness.
- Ensure adherence to Good Clinical Practice (GCP) guidelines, ICH guidelines, and applicable regulations.
- Manage investigational product accountability and distribution records.
- Serve as a liaison between study sites, the sponsor, and internal project teams.
- Identify and report adverse events and protocol deviations in a timely manner.
- Train site staff on study protocols, procedures, and data entry requirements.
- Assist with site selection, initiation, and close-out activities, leveraging remote communication tools.
- Troubleshoot and resolve site-specific issues to ensure data integrity and patient safety.
- Prepare monitoring visit reports and follow-up action items.
- Maintain accurate and up-to-date trial documentation in electronic trial master files (eTMFs).
- Collaborate with data management and statistical teams to ensure data quality.
- Participate in remote team meetings and contribute to study strategy discussions.
- Proactively identify risks and implement mitigation strategies for assigned studies.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or equivalent role in pharmaceutical or biotech industry.
- Thorough understanding of clinical trial processes, GCP, ICH guidelines, and regulatory requirements.
- Proven experience in performing remote monitoring activities and virtual site engagement.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to communicate effectively with medical professionals and research staff.
- Proficiency in electronic data capture (EDC) systems and electronic trial master file (eTMF) systems.
- Ability to work independently with minimal supervision and manage multiple priorities in a remote setting.
- Detail-oriented with a commitment to data quality and patient safety.
- Experience in therapeutic areas such as oncology, cardiology, or neurology is a plus.
- Familiarity with virtual collaboration tools and platforms.
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