933 Remote Clinical Research Associate jobs in Kenya
Remote Pharmaceutical Quality Control Analyst (Trainee)
Posted 15 days ago
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Job Description
Our client, a leading pharmaceutical entity, is seeking a driven and detail-oriented individual for a fully remote Pharmaceutical Quality Control Analyst Trainee position. This is a groundbreaking opportunity to enter the pharmaceutical industry and develop critical skills in quality assurance and control from a remote setting. You will be trained on rigorous testing procedures, data analysis, and regulatory compliance standards that govern pharmaceutical product development and manufacturing. Responsibilities will include reviewing batch records, analyzing laboratory data (virtually), preparing reports on quality testing outcomes, and assisting in the implementation of quality improvement initiatives. The ideal candidate will possess a strong scientific aptitude, meticulous attention to detail, and a solid understanding of basic chemistry and biology principles. Familiarity with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is advantageous, though not required as comprehensive training will be provided. You must be able to work independently, manage your time effectively in a remote environment, and communicate clearly and concisely with team members and supervisors. This role requires a proactive approach to learning and a commitment to maintaining the highest standards of quality and safety. The successful candidate will gain invaluable experience in a highly regulated industry, contributing to the development of life-saving medications. While the position is fully remote, we are looking for individuals based in or with a strong connection to **Naivasha, Nakuru, KE**, and surrounding regions who are ready to embark on a challenging yet rewarding career path. This is an excellent opportunity for aspiring professionals to gain specialized knowledge and contribute to pharmaceutical excellence from a distance.
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Remote Clinical Research Associate
Posted 22 days ago
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Job Description
Our client, a leading innovator in pharmaceutical research and development, is seeking a dedicated and meticulous Remote Clinical Research Associate to join their global team. This fully remote position allows you to contribute to life-changing medical advancements from the comfort of your home office, with primary responsibilities centered around the **Eldoret, Uasin Gishu, KE** region. You will play a crucial role in the planning, execution, and monitoring of clinical trials, ensuring data integrity and adherence to regulatory standards (GCP, FDA, EMA). Key responsibilities include site selection and initiation visits, ongoing monitoring of study sites, and ensuring all study-related documentation is accurate and up-to-date. You will act as a liaison between the sponsor, investigators, and study personnel, providing essential support and training. This role requires excellent organizational skills, strong attention to detail, and the ability to manage multiple tasks effectively in a virtual environment. Proficiency in clinical trial management systems and electronic data capture (EDC) is essential. You will be responsible for reviewing and resolving data queries, verifying source documents, and ensuring the safety and rights of study participants are protected. The ability to work independently, communicate effectively through digital channels, and adapt to evolving project needs is paramount. We are looking for a proactive individual with a solid understanding of pharmaceutical drug development processes. A Bachelor's degree in a life science, nursing, or related field is required, along with significant experience in clinical research. Excellent written and verbal communication skills, along with strong interpersonal abilities to foster positive working relationships with study sites and internal teams, are essential. The ideal candidate will demonstrate a commitment to ethical research practices and a passion for advancing healthcare. This is an exceptional opportunity to make a significant impact on patient well-being from a flexible, remote setting. Your expertise will directly contribute to bringing innovative therapies to market.
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Senior Data Analyst - Healthcare Analytics
Posted 22 days ago
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Job Description
Our client is seeking a highly analytical and experienced Senior Data Analyst to join their Healthcare Analytics team. This role offers a hybrid work model, combining the flexibility of remote work with essential in-person collaboration at our offices. You will be instrumental in transforming complex healthcare data into actionable insights that improve patient care, operational efficiency, and strategic decision-making. This position demands a deep understanding of healthcare systems, strong statistical analysis skills, and the ability to communicate findings effectively to both technical and non-technical stakeholders.
Responsibilities:
Responsibilities:
- Analyze large and complex healthcare datasets, including patient demographics, clinical outcomes, claims data, and operational metrics.
- Develop and implement advanced analytical models to identify trends, patterns, and correlations in healthcare data.
- Design and create comprehensive reports, dashboards, and visualizations to present findings to key stakeholders, including clinicians, administrators, and executives.
- Collaborate with cross-functional teams to define data requirements and analytical objectives.
- Identify opportunities for improving healthcare quality, patient safety, and cost-effectiveness through data-driven insights.
- Develop predictive models for patient risk stratification, disease forecasting, and resource allocation.
- Ensure data accuracy, integrity, and compliance with healthcare regulations (e.g., HIPAA).
- Mentor junior data analysts and provide technical guidance.
- Stay current with the latest trends and technologies in healthcare analytics and data science.
- Translate business requirements into technical specifications for data extraction and analysis.
- Perform ad-hoc data analysis to support urgent business needs and research initiatives.
- Contribute to the development of data governance policies and best practices.
- Evaluate and recommend new analytical tools and methodologies.
- Communicate complex analytical findings in a clear and understandable manner to diverse audiences.
- Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, Health Informatics, or a related quantitative field.
- Minimum of 5 years of experience in data analysis, with a significant focus on the healthcare industry.
- Proven experience with SQL for data extraction and manipulation from relational databases.
- Proficiency in statistical programming languages such as R or Python.
- Experience with data visualization tools (e.g., Tableau, Power BI, QlikView).
- Strong understanding of healthcare data sources, terminology, and common analytical challenges.
- Knowledge of healthcare regulations and data privacy standards (e.g., HIPAA).
- Excellent analytical, critical thinking, and problem-solving skills.
- Strong communication and presentation skills, with the ability to explain complex findings to non-technical audiences.
- Experience with predictive modeling and machine learning techniques is a plus.
- Ability to work effectively both independently and collaboratively in a hybrid team environment.
- Familiarity with electronic health records (EHR) systems is advantageous.
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Remote Clinical Research Associate (CRA)
Posted 22 days ago
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Job Description
Our client is actively seeking an experienced and meticulous Clinical Research Associate (CRA) for a fully remote position. This role is integral to ensuring the successful execution and integrity of clinical trials, contributing to the development of life-saving pharmaceuticals. As a remote CRA, you will be responsible for monitoring clinical trial sites, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your primary focus will be on data quality, patient safety, and study integrity, all managed through virtual interactions and site visits as required, though the role is primarily remote. You will conduct site initiation, interim monitoring, and close-out visits (virtually or in person as needed), review source documents, verify data accuracy, and manage investigational product accountability. The ideal candidate possesses a strong understanding of clinical trial processes, excellent communication skills, and the ability to build rapport with investigators and site staff from a distance. Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS) is crucial. This fully remote role demands a high degree of organization, independence, and proactivity. You will be a key liaison between the sponsor and clinical trial sites, ensuring seamless study conduct. We are looking for individuals who are passionate about clinical research, committed to patient well-being, and possess the skills to manage complex projects remotely. Your ability to adapt to evolving trial needs and maintain rigorous standards in a decentralized setting will be paramount. This opportunity, while connected to **Kericho, Kericho, KE**, offers the flexibility of a fully remote work arrangement, making it accessible to qualified professionals across the region. Our client values scientific integrity and efficiency, providing a supportive environment for professionals dedicated to advancing healthcare.
Key Responsibilities:
Key Responsibilities:
- Monitor clinical trial sites remotely and conduct necessary on-site visits as required.
- Ensure compliance with study protocols, SOPs, and regulatory guidelines (e.g., GCP).
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Manage investigational product accountability and site supplies.
- Serve as the primary point of contact for assigned clinical trial sites.
- Facilitate communication between sites, sponsor, and relevant stakeholders.
- Conduct site initiation, interim, and close-out monitoring activities.
- Identify and report potential issues, deviations, and adverse events.
- Prepare monitoring visit reports and track action items.
- Support site staff with study-related queries and training.
- Bachelor's degree in a life science, nursing, or a related healthcare field.
- Minimum of 2-3 years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Proficiency with EDC systems and CTMS software.
- Excellent monitoring and auditing skills.
- Strong written and verbal communication and interpersonal skills.
- Proven ability to work independently, manage time effectively, and meet deadlines.
- High level of organization, attention to detail, and problem-solving abilities.
- Ability to travel as needed for on-site monitoring visits.
- Commitment to patient safety and data integrity.
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Remote Clinical Research Associate (CR-A)
Posted 18 days ago
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Job Description
Our client, a pioneering biopharmaceutical company at the forefront of scientific discovery, is seeking an experienced and meticulous Clinical Research Associate (CR-A) to join their fully remote research and development division. This critical role will involve overseeing and managing various aspects of clinical trials to ensure data integrity, patient safety, and adherence to regulatory standards. As a remote CR-A, you will be responsible for site selection and initiation, monitoring trial progress, ensuring compliance with study protocols and Good Clinical Practice (GCP) guidelines, and managing source data verification. You will also play a key part in training site staff, resolving data discrepancies, and communicating effectively with investigators, site personnel, and internal study teams. This position requires a deep understanding of clinical trial processes, regulatory requirements (FDA, EMA), and therapeutic areas relevant to the company's research pipeline. Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS) is essential. The ideal candidate will possess strong organizational skills, excellent attention to detail, and the ability to work autonomously and manage time effectively in a remote setting. You will be expected to travel periodically for essential site visits and audits, as required by the study. This is an outstanding opportunity to contribute to groundbreaking medical research and drug development while benefiting from a flexible remote work environment. We are looking for a dedicated professional with a passion for advancing healthcare through rigorous scientific investigation and a commitment to maintaining the highest ethical standards in clinical research. Your expertise will be invaluable in bringing life-changing therapies to patients.
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Remote Clinical Research Associate (CRC)
Posted 22 days ago
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Job Description
Our client, a prominent pharmaceutical research organization, is seeking a dedicated and experienced Remote Clinical Research Associate (CRC) to support their groundbreaking clinical trials. This is a fully remote position, allowing you to contribute to vital medical research from the convenience of your home office. As a CRC, you will play a crucial role in ensuring the integrity and quality of clinical trials by monitoring study sites, verifying data accuracy, and ensuring compliance with protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The ideal candidate will possess a strong understanding of clinical trial processes, excellent attention to detail, and exceptional communication and organizational skills. You will serve as a key liaison between study sites, sponsors, and regulatory authorities. This role requires the ability to work independently, manage time effectively, and travel occasionally for on-site monitoring visits if required (though the primary role is remote). You will be responsible for site selection, initiation, monitoring, and close-out activities, ensuring participant safety and data integrity throughout the trial lifecycle. Key responsibilities include:
Qualifications:
- Performing remote site monitoring activities, including source data verification and source document review.
- Ensuring adherence to study protocols, GCP, and applicable regulatory requirements.
- Monitoring patient safety and reporting adverse events in a timely manner.
- Training site personnel on study procedures and documentation.
- Conducting remote pre-study, initiation, interim, and close-out visits.
- Reviewing and ensuring the accuracy and completeness of clinical trial data.
- Maintaining effective communication with investigators, site staff, and study sponsors.
- Resolving data queries and ensuring timely resolution of site issues.
- Preparing monitoring reports and providing regular updates to study management.
- Assisting with regulatory submissions and audits.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 4 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- In-depth knowledge of GCP guidelines, FDA regulations, and clinical trial methodologies.
- Proven experience in conducting remote monitoring activities.
- Experience with various clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent analytical and problem-solving skills.
- Strong written and verbal communication skills, with the ability to communicate effectively with diverse stakeholders.
- Exceptional organizational skills and meticulous attention to detail.
- Ability to work independently with minimal supervision and manage time effectively in a remote setting.
- Willingness to travel occasionally for necessary on-site monitoring as per project needs.
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Remote Clinical Research Associate (Pharmacology)
Posted 22 days ago
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Job Description
Our client, a prominent pharmaceutical company, is seeking a highly qualified Clinical Research Associate (CRA) to join their innovative research team on a fully remote basis. This critical role involves managing and overseeing clinical trials to ensure the safety of participants and the integrity of data collected. You will be responsible for site selection, initiation, monitoring, and close-out activities for assigned clinical trial sites. This includes verifying the accuracy and completeness of case report forms, ensuring compliance with protocols, and adhering to Good Clinical Practice (GCP) guidelines and regulatory requirements. The successful candidate will maintain effective communication with investigators, site staff, and internal project teams, addressing any study-related issues promptly. Responsibilities encompass conducting site visits (virtually or in-person as required by specific project needs), reviewing essential documents, and ensuring timely query resolution. You will also be involved in preparing monitoring reports and contributing to study documentation. A strong understanding of drug development processes, clinical trial methodologies, and relevant regulations (e.g., FDA, EMA) is essential. The ideal candidate will possess excellent organizational skills, meticulous attention to detail, and the ability to work independently and manage multiple priorities in a remote setting. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is required. This is a fantastic opportunity to contribute to the development of life-saving medications while enjoying the flexibility of a remote work arrangement. We are committed to advancing healthcare and seek individuals who share our passion for scientific discovery and patient well-being.
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Remote Clinical Research Associate - Pharmaceutical
Posted 22 days ago
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Job Description
Our client, a rapidly growing biopharmaceutical company dedicated to developing life-changing therapies, is seeking a highly motivated and experienced Clinical Research Associate (CRA) to join their remote-first clinical operations team. This pivotal role involves overseeing and managing clinical trial sites to ensure compliance with study protocols, regulatory requirements, and good clinical practice (GCP) guidelines. The ideal candidate will possess a strong understanding of clinical trial processes, excellent organizational skills, and a keen eye for detail, all while operating effectively in a distributed work environment.
As a remote CRA, your primary responsibilities will include remote monitoring of clinical trial sites, which may involve reviewing electronic trial master files (eTMF), source data verification (SDV) via remote access, and analyzing site performance data. You will conduct remote site initiation visits, interim monitoring visits, and remote close-out visits, ensuring sites are adequately prepared, well-managed, and compliant throughout the trial lifecycle. You will be responsible for training site staff on study protocols and procedures, addressing protocol deviations, and ensuring the timely resolution of data queries. Building and maintaining strong relationships with investigators and site staff is crucial for successful trial execution. You will also be tasked with ensuring the accurate and timely submission of essential documents and reports. The ability to travel occasionally for essential on-site visits (if required by specific project needs) should be considered, though the role is fundamentally remote. We are looking for a proactive, self-disciplined individual with excellent communication and problem-solving skills, committed to maintaining the highest standards of data integrity and patient safety. This is an excellent opportunity to contribute to groundbreaking pharmaceutical research from **Ruiru, Kiambu, KE**, with the flexibility and autonomy of a remote position.
Key Responsibilities:
As a remote CRA, your primary responsibilities will include remote monitoring of clinical trial sites, which may involve reviewing electronic trial master files (eTMF), source data verification (SDV) via remote access, and analyzing site performance data. You will conduct remote site initiation visits, interim monitoring visits, and remote close-out visits, ensuring sites are adequately prepared, well-managed, and compliant throughout the trial lifecycle. You will be responsible for training site staff on study protocols and procedures, addressing protocol deviations, and ensuring the timely resolution of data queries. Building and maintaining strong relationships with investigators and site staff is crucial for successful trial execution. You will also be tasked with ensuring the accurate and timely submission of essential documents and reports. The ability to travel occasionally for essential on-site visits (if required by specific project needs) should be considered, though the role is fundamentally remote. We are looking for a proactive, self-disciplined individual with excellent communication and problem-solving skills, committed to maintaining the highest standards of data integrity and patient safety. This is an excellent opportunity to contribute to groundbreaking pharmaceutical research from **Ruiru, Kiambu, KE**, with the flexibility and autonomy of a remote position.
Key Responsibilities:
- Perform remote monitoring of clinical trial sites to ensure compliance with protocols, SOPs, and GCP.
- Conduct remote site initiation, interim, and close-out visits via virtual platforms.
- Verify source data against electronic case report forms (eCRFs) through remote access methods.
- Train and support site staff on study conduct, regulatory requirements, and data management.
- Monitor site progress, identify potential risks, and implement corrective and preventive actions (CAPAs).
- Ensure the timely resolution of data queries and protocol deviations.
- Manage the trial master file (TMF) remotely, ensuring all essential documents are current and complete.
- Build and maintain strong working relationships with investigators, study coordinators, and other site personnel.
- Prepare and submit monitoring visit reports promptly.
- Ensure subject safety and data integrity throughout the trial.
- Stay current with relevant regulations, guidelines, and industry best practices.
- 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 management role.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with remote monitoring techniques and electronic data capture (EDC) systems.
- Proficiency in using clinical trial management software (CTMS) and electronic trial master file (eTMF) systems.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills.
- Ability to work independently, manage multiple priorities, and meet strict deadlines in a remote setting.
- Willingness to travel occasionally as required for essential on-site activities.
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Senior Remote Clinical Research Associate
Posted 21 days ago
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Job Description
Our client, a leading pharmaceutical entity, is seeking an experienced Senior Remote Clinical Research Associate (CRA) to contribute to groundbreaking drug development initiatives. This fully remote position allows you to conduct critical clinical trial monitoring from anywhere, ensuring adherence to protocols, regulations, and quality standards. The ideal candidate will possess a strong understanding of clinical trial processes, excellent analytical skills, and meticulous attention to detail. You will be responsible for site selection, initiation, monitoring, and close-out activities, ensuring the integrity and accuracy of trial data. Key Responsibilities include:
- Conducting remote site visits and monitoring to ensure compliance with protocols, SOPs, and GCP guidelines.
- Evaluating site performance and identifying potential issues or risks.
- Ensuring accurate and timely data collection, source document verification, and query resolution.
- Training and mentoring site staff on study procedures and regulatory requirements.
- Managing study timelines and ensuring sites meet recruitment and data quality targets.
- Preparing and submitting monitoring reports and communicating findings to study teams and management.
- Overseeing the investigational product management at study sites.
- Facilitating communication between study sites, investigators, and the sponsor.
- Participating in the development and review of study-related documents.
- Ensuring all regulatory requirements are met at the study sites.
- Bachelor's degree in a life science, nursing, or related field; Master's degree preferred.
- Proven experience as a Clinical Research Associate, with a significant portion of experience in remote monitoring.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with various clinical trial phases and therapeutic areas.
- Strong understanding of medical terminology and clinical trial documentation.
- Excellent communication, interpersonal, and organizational skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently, manage time effectively, and travel occasionally as needed for essential on-site visits.
- A meticulous approach to data management and quality assurance.
- Certification as a Clinical Research Professional is a plus.
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Remote Clinical Research Associate (Pharma)
Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a dedicated and experienced Remote Clinical Research Associate (CRA) to support groundbreaking drug development. This position is fully remote, offering flexibility and the opportunity to contribute to critical clinical trials from the comfort of your home office. As a Remote CRA, you will play a vital role in monitoring study conduct, ensuring data integrity, and upholding regulatory compliance across multiple research sites. The ideal candidate will possess a strong understanding of clinical trial processes, GCP guidelines, and excellent analytical and interpersonal skills. You will be responsible for conducting remote site visits, reviewing study documentation, and communicating effectively with investigators, site staff, and internal teams.
Key Responsibilities:
This role is based in Nakuru, Nakuru, KE , but operates as a fully remote position. We are looking for a self-motivated individual with a keen eye for detail and a commitment to advancing pharmaceutical research. Strong organizational skills and the ability to manage multiple tasks effectively in a remote setting are essential. If you are passionate about clinical research and seeking a challenging yet rewarding remote opportunity, we encourage you to apply.
Key Responsibilities:
- Conduct remote monitoring activities for clinical trials, including source data verification, regulatory document review, and protocol adherence assessment.
- Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and other applicable guidelines.
- Initiate, monitor, and close-out clinical trial sites remotely, performing necessary virtual visits and evaluations.
- Build and maintain strong relationships with investigators and site staff, providing guidance and support.
- Review and reconcile essential documents, ensuring accuracy and completeness.
- Identify and report adverse events and protocol deviations promptly.
- Prepare and present monitoring visit reports, documenting findings and action plans.
- Collaborate with internal study teams, including data management, regulatory affairs, and project management.
- Participate in site qualification, initiation, and close-out visits (potentially some on-site travel may be required as per project needs, though the role is primarily remote).
- Contribute to the development and review of study protocols and other clinical trial documents.
This role is based in Nakuru, Nakuru, KE , but operates as a fully remote position. We are looking for a self-motivated individual with a keen eye for detail and a commitment to advancing pharmaceutical research. Strong organizational skills and the ability to manage multiple tasks effectively in a remote setting are essential. If you are passionate about clinical research and seeking a challenging yet rewarding remote opportunity, we encourage you to apply.
This advertiser has chosen not to accept applicants from your region.
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