2,092 Clinical Research Associate Pharmaceutical jobs in Kenya
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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Clinical Research Associate - Pharmaceutical Development
Posted 7 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join our innovative, fully remote team. This position is vital to the successful execution of clinical trials, ensuring adherence to protocols, regulations, and ethical standards. As a remote-first role, you will have the flexibility to manage your responsibilities from anywhere, contributing to groundbreaking pharmaceutical research. You will be responsible for monitoring clinical trial sites, ensuring data integrity, and verifying patient safety. The ideal candidate has a solid understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements. Responsibilities include initiating, monitoring, and closing out clinical study sites, conducting source data verification, resolving data queries, and ensuring timely reporting of adverse events. You will also serve as a key liaison between the sponsor, investigators, and study staff. Strong organizational skills, excellent attention to detail, and the ability to work independently are essential. This role requires effective communication and interpersonal skills to build strong relationships with site personnel. The opportunity to contribute to the development of life-saving medications is significant. This is a remote position, with the **Nyeri, Nyeri, KE** location serving as the administrative base. Our client is committed to supporting its remote workforce and ensuring high standards of operational excellence.
Key Responsibilities:
Key Responsibilities:
- Initiate, monitor, and close-out clinical investigator sites.
- Ensure clinical trials are conducted, recorded, and reported in accordance with protocol, standard operating procedures (SOPs), and applicable regulations.
- Verify the accuracy and completeness of clinical trial data through source data verification.
- Ensure patient safety and rights are protected.
- Manage and resolve data queries in collaboration with investigators and study staff.
- Train and provide ongoing support to site staff.
- Oversee regulatory compliance at study sites.
- Prepare and present monitoring visit reports.
- Liaise effectively between the sponsor, investigators, and other stakeholders.
- Ensure timely submission of study-related documents.
- Proven experience as a Clinical Research Associate (CRA) or similar role in clinical research.
- In-depth knowledge of GCP guidelines, ICH regulations, and local regulatory requirements.
- Experience in site monitoring, data verification, and query resolution.
- Strong understanding of clinical trial processes and documentation.
- Excellent organizational and time management skills.
- Exceptional attention to detail and accuracy.
- Strong written and verbal communication skills.
- Ability to work independently and travel as needed (though the role is primarily remote).
- Bachelor's degree in a life science, nursing, or related field.
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Clinical Research Associate - Pharmaceuticals
Posted 7 days ago
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Job Description
Our client is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their fully remote pharmaceutical team. This role is critical in managing and monitoring clinical trials to ensure the safety, efficacy, and integrity of new pharmaceutical products. You will be responsible for overseeing all aspects of clinical study conduct at investigator sites, including site initiation, monitoring, and close-out. The ideal candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines, regulatory requirements, and clinical trial processes. This is a remote-first position, requiring excellent organizational, analytical, and communication skills to effectively manage relationships with investigators, site staff, and internal stakeholders. You will conduct site visits (as needed, often virtually) to verify data accuracy, ensure protocol compliance, and address any study-related issues. Responsibilities include reviewing source documents, Case Report Forms (CRFs), and study logs; resolving data queries; and ensuring that all trial activities are conducted in accordance with the approved protocol and applicable regulations. A Bachelor's degree in a life science, nursing, or a related field is required; a Master's degree is a plus. A minimum of 3-5 years of experience as a CRA or in a similar clinical research role within the pharmaceutical industry is essential. Strong knowledge of drug development processes and therapeutic areas is highly desirable. You must be proficient in using electronic data capture (EDC) systems and other clinical trial management software. Excellent written and verbal communication skills, strong problem-solving abilities, and the capacity to work independently and manage multiple projects simultaneously are paramount. This is an excellent opportunity to contribute to the development of life-saving medications from the comfort of your home, with a competitive salary and comprehensive benefits.
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Senior Clinical Research Associate - Pharmaceutical Development
Posted 21 days ago
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Job Description
Our client is seeking a highly experienced and meticulous Senior Clinical Research Associate (CRA) to join their fully remote pharmaceutical development team. This role is integral to the successful execution of clinical trials, ensuring adherence to protocols, regulatory standards, and data integrity. You will be responsible for monitoring clinical trial sites, verifying data accuracy, managing investigational product, and ensuring patient safety. The ideal candidate possesses a deep understanding of Good Clinical Practice (GCP) guidelines, pharmaceutical development processes, and a strong ability to manage multiple sites and complex trial requirements remotely. This position offers a unique opportunity to contribute to life-saving drug development from the convenience of a remote work environment, collaborating with a global network of researchers and clinicians.
Key Responsibilities:
Key Responsibilities:
- Conduct remote site initiation, monitoring, and close-out visits according to protocol and GCP.
- Verify the accuracy, completeness, and consistency of clinical data through source data verification (SDV).
- Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA) and study protocols.
- Manage investigational product accountability and ensure proper storage and handling at trial sites.
- Serve as the primary point of contact for assigned clinical trial sites, addressing site staff queries and issues.
- Identify, track, and resolve data discrepancies and protocol deviations.
- Ensure timely reporting of adverse events (AEs) and serious adverse events (SAEs).
- Provide training and ongoing support to site personnel.
- Prepare and present site monitoring reports.
- Collaborate with internal teams, including clinical operations, data management, and regulatory affairs.
- Bachelor's degree in a life science, nursing, pharmacy, or a related discipline. Advanced degree preferred.
- Minimum of 5 years of progressive experience as a Clinical Research Associate.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven experience in monitoring clinical trials across various therapeutic areas.
- Strong understanding of clinical trial processes, from study start-up to close-out.
- Excellent analytical, problem-solving, and organizational skills.
- Exceptional communication, interpersonal, and negotiation skills, particularly in managing remote relationships.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently, manage time effectively, and travel as needed (though the role is primarily remote).
- Relevant certifications (e.g., ACRP, SoCRA) are a plus.
This advertiser has chosen not to accept applicants from your region.
3
Remote Clinical Research Associate - Pharmaceutical Development
Posted 8 days ago
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing global health, is seeking a meticulous and dedicated Remote Clinical Research Associate (CRA) to join their clinical development team. This fully remote position plays a vital role in ensuring the successful execution of clinical trials according to Good Clinical Practice (GCP) guidelines and regulatory requirements. You will be responsible for monitoring clinical trial sites, ensuring data accuracy and integrity, and verifying compliance with study protocols. The ideal candidate will possess a strong understanding of clinical trial processes, regulatory affairs, and medical terminology. Key responsibilities include performing site initiation, monitoring, and close-out visits remotely where feasible and in-person as required, reviewing source documents and case report forms (CRFs), and managing study-related documentation. You will also serve as a key liaison between the investigative sites and the sponsor, addressing study-related queries and ensuring timely resolution of issues. This role demands excellent organizational, analytical, and communication skills, along with a high degree of accuracy and attention to detail. The ability to work independently, manage time effectively, and maintain strong professional relationships with site staff in a remote capacity is crucial. A Bachelor's degree in a life science, nursing, or related field, coupled with previous experience as a CRA or in a related clinical research role, is required. Relevant certifications are a plus. This is a fully remote opportunity offering the flexibility to contribute to life-saving research from anywhere, while adhering to the highest standards of scientific integrity. Join our client in their mission to discover and develop innovative medicines that improve patient lives.
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Senior Clinical Research Associate - Pharmaceuticals
Posted 7 days ago
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Job Description
Our client is actively seeking an experienced Senior Clinical Research Associate (CRA) to join their fully remote clinical operations team. This position plays a critical role in ensuring the successful execution of clinical trials for innovative pharmaceutical products. As a Senior CRA, you will be responsible for monitoring clinical trial sites, ensuring compliance with protocols, regulations, and Good Clinical Practice (GCP) guidelines. Your expertise in site management, data integrity, and regulatory adherence will be crucial for the success of our client's drug development programs. This is a remote-first opportunity, allowing you to contribute significantly to medical advancements from the comfort of your home.
Key Responsibilities:
Key Responsibilities:
- Conduct remote and on-site (as needed) trial-related monitoring visits to assess protocol adherence, patient safety, and data accuracy.
- Verify the collection, documentation, and reporting of clinical trial data; ensure data integrity and quality.
- Manage assigned clinical trial sites, serving as the primary point of contact for investigators and site staff.
- Ensure compliance with all applicable regulatory requirements, including ICH-GCP, FDA regulations, and local regulatory guidelines.
- Facilitate investigator meetings and training sessions on study protocols and procedures.
- Oversee site readiness, initiate sites, monitor site progress, and close out sites upon completion of the trial.
- Review and approve essential documents, including site regulatory binders and source documents.
- Identify and escalate potential issues and risks to clinical operations management and implement corrective action plans.
- Participate in the development and review of clinical trial protocols, case report forms (CRFs), and other study-related documents.
- Contribute to the development and implementation of risk-based monitoring strategies.
- Maintain effective communication with study teams, investigators, and internal stakeholders.
- Bachelor's degree in a life science, nursing, or related discipline. Advanced degree (Master's, PharmD, PhD) is a plus.
- Minimum of 5 years of experience as a Clinical Research Associate, with a strong understanding of pharmaceutical development.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Proven experience in site monitoring, patient safety assessment, and data review.
- Excellent understanding of clinical trial processes from site selection to close-out.
- Strong organizational, time management, and problem-solving skills.
- Exceptional written and verbal communication skills, with the ability to effectively communicate with diverse stakeholders.
- Proficiency in using electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Ability to work independently and manage multiple projects simultaneously in a remote setting.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate - Pharmaceutical
Posted 23 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their dynamic team. This role plays a crucial part in the development of new life-saving medicines. The CRA will be responsible for monitoring clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and regulatory guidelines. You will act as the primary point of contact for clinical investigators and study sites, ensuring data accuracy and subject safety. The position requires extensive travel to study sites, but offers flexibility through a hybrid work model, allowing for remote work on non-site visit days. A strong understanding of Good Clinical Practice (GCP) and regulatory affairs is essential.
Responsibilities:
Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits in accordance with GCP and protocol requirements.
- Monitor study conduct to ensure compliance with protocol, SOPs, regulatory requirements, and ethical principles.
- Verify the accuracy, completeness, and integrity of clinical data collected at study sites through source data verification.
- Ensure subject safety and well-being, reporting any adverse events or protocol deviations promptly.
- Train and support site staff, providing guidance on study procedures and regulatory requirements.
- Manage relationships with investigators and site personnel, fostering effective collaboration.
- Review and ensure accurate and timely submission of study-related documents.
- Oversee drug accountability and ensure proper storage and dispensing of investigational products.
- Prepare and present monitoring visit reports, addressing any identified issues and action items.
- Ensure the timely retrieval of essential study documents from study sites.
- Participate in study team meetings and contribute to study planning and execution.
- Maintain up-to-date knowledge of therapeutic areas, drug development processes, and relevant regulations.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. Advanced degree preferred.
- Minimum of 3-5 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical industry.
- In-depth knowledge of ICH-GCP guidelines and relevant regulatory requirements (e.g., FDA, EMA).
- Proven experience in monitoring clinical trials across various phases.
- Excellent understanding of medical terminology and clinical trial processes.
- Strong attention to detail and accuracy in data management and reporting.
- Excellent organizational, communication, and interpersonal skills.
- Ability to travel frequently to study sites (up to 60%).
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work effectively both independently and as part of a hybrid team.
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Remote Clinical Research Associate - Pharmaceutical
Posted 21 days ago
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Job Description
Our client, a leading pharmaceutical company focused on developing innovative treatments, is actively seeking a dedicated and meticulous Remote Clinical Research Associate (CRA). In this fully remote role, you will play a crucial part in overseeing and managing clinical trials conducted at various sites, ensuring compliance with protocols, regulations, and good clinical practice (GCP). Your responsibilities will include monitoring trial progress, ensuring data accuracy and integrity, and facilitating effective communication between the sponsor, investigators, and study sites. The ideal candidate possesses extensive knowledge of clinical trial processes, strong regulatory understanding, and excellent organizational and interpersonal skills. You will contribute to bringing life-changing therapies to patients globally, all while working remotely.
Responsibilities:
Qualifications:
Responsibilities:
- Perform remote site monitoring visits and assess protocol compliance.
- Ensure accurate and timely collection, review, and verification of clinical trial data.
- Verify that study participants are enrolled and monitored according to the clinical trial protocol.
- Ensure the rights, safety, and well-being of study participants are protected.
- Train and support investigators and site staff on study procedures and requirements.
- Manage communication between study sites, the sponsor, and other stakeholders.
- Prepare and submit monitoring visit reports and action items.
- Oversee site adherence to GCP, FDA regulations, and other applicable guidelines.
- Track study milestones and timelines, identifying and resolving any potential delays.
- Maintain comprehensive study documentation and regulatory binders.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline.
- Minimum of 3-5 years of experience as a Clinical Research Associate or in a similar clinical research role.
- In-depth knowledge of clinical trial phases, GCP, ICH guidelines, and regulatory requirements.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills.
- Ability to work independently and travel occasionally if required for specific site visits (though the role is primarily remote).
- Proficiency in Microsoft Office Suite.
- A secure home office environment with a reliable high-speed internet connection.
- Demonstrated ability to manage multiple tasks and prioritize effectively.
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Clinical Research Associate - Pharmaceutical Trials
Posted 11 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their cutting-edge research team. This is a fully remote position, empowering you to manage clinical trials from anywhere while making a significant impact on healthcare advancements. As a CRA, you will play a pivotal role in ensuring the quality, integrity, and compliance of clinical studies by monitoring investigational sites and verifying that data collected is accurate and complete. You will be responsible for site selection, initiation, monitoring, and close-out activities, ensuring adherence to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements. This role demands exceptional organizational skills, meticulous attention to detail, and strong interpersonal abilities to build and maintain effective relationships with investigators, site staff, and internal stakeholders. You will conduct source data verification, review case report forms (CRFs), and ensure timely reporting of adverse events. The ideal candidate possesses a strong background in clinical research, a deep understanding of pharmaceutical development, and a proven track record of successfully managing multiple study sites. A Bachelor's degree in a life science, nursing, or a related field is required, with advanced degrees being a distinct advantage. Previous experience as a CRA, preferably within a pharmaceutical or contract research organization (CRO) setting, is essential. Familiarity with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is highly desirable. This role requires a proactive approach to problem-solving and a commitment to upholding the highest ethical standards in clinical research. As a remote employee, you will have the flexibility to manage your workload effectively while ensuring all monitoring activities are completed to the highest standards. Our client is dedicated to fostering a collaborative and innovative research environment.
Responsibilities:
Responsibilities:
- Perform site selection, initiation, interim monitoring, and close-out visits.
- Ensure study conduct is in compliance with protocol, GCP, and regulatory requirements.
- Verify source data and CRFs for accuracy, completeness, and consistency.
- Manage study supplies and investigational product accountability.
- Identify and report deviations and implement corrective actions.
- Serve as the primary liaison between study sites and the sponsor.
- Train site staff on study procedures and documentation.
- Participate in study team meetings and contribute to study progress reports.
- Bachelor's degree in Life Sciences, Nursing, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with EDC and CTMS systems.
- Strong monitoring and auditing skills.
- Excellent communication, negotiation, and interpersonal skills.
- Ability to travel to sites occasionally if required, although the role is primarily remote.
- Proficiency in English, both written and verbal.
This advertiser has chosen not to accept applicants from your region.
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Senior Clinical Research Associate - Pharmaceutical
Posted 20 days ago
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Job Description
Our client, a fast-growing pharmaceutical company committed to developing life-changing medications, is seeking a highly motivated and experienced Senior Clinical Research Associate (CRA) to join their fully remote team. This position offers the flexibility to work from home while playing a critical role in the successful execution of clinical trials. The Senior CRA will be responsible for monitoring clinical trial sites to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
Key Responsibilities:
Qualifications:
This role, based conceptually in **Nyeri, Nyeri, KE**, is designed for a dedicated professional who thrives in a remote work environment and is passionate about advancing pharmaceutical research.
Key Responsibilities:
- Conduct pre-study, initiation, interim, and close-out monitoring visits to clinical trial sites.
- Ensure accurate, complete, and timely collection of clinical data.
- Verify the rights and well-being of trial subjects.
- Ensure that the trial is conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), and regulatory requirements.
- Oversee site personnel to ensure they are properly trained and conduct the trial in accordance with the protocol.
- Resolve data queries and ensure timely data entry.
- Manage communication with investigators and site staff.
- Prepare and present monitoring visit reports.
- Identify site issues and develop corrective action plans.
- Maintain Trial Master File (TMF) documentation.
- Participate in the selection and qualification of new clinical trial sites.
- Contribute to the development and review of clinical trial protocols and other study documents.
- Ensure compliance with all applicable local and international regulations.
Qualifications:
- Bachelor's degree in a life science, nursing, or a related field. Advanced degree preferred.
- Minimum of 5 years of experience as a Clinical Research Associate.
- Thorough understanding of ICH-GCP guidelines and other relevant regulatory requirements.
- Proven experience in monitoring multiple clinical trials across various therapeutic areas.
- Excellent organizational skills and attention to detail.
- Strong communication, interpersonal, and negotiation skills.
- Ability to work independently and manage time effectively in a remote setting.
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Willingness to travel occasionally for essential meetings or site visits, if required, though the role is predominantly remote.
This role, based conceptually in **Nyeri, Nyeri, KE**, is designed for a dedicated professional who thrives in a remote work environment and is passionate about advancing pharmaceutical research.
This advertiser has chosen not to accept applicants from your region.
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