2,092 Senior Clinical Research Associate Pharmaceutical jobs in Kenya
Senior Data Analyst - Healthcare Analytics
Posted 23 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 19 days ago
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Job Description
Our client, a leading innovator in pharmaceutical research, is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join their esteemed, fully remote clinical development team. This crucial role involves overseeing and managing clinical trial activities, ensuring compliance with regulatory standards, and safeguarding the integrity of data collected. The CRA will be responsible for site selection, initiation, monitoring, and close-out activities, acting as a vital liaison between the sponsor and investigational sites. This position requires a strong understanding of Good Clinical Practice (GCP) guidelines, clinical trial protocols, and pharmaceutical research methodologies.
Responsibilities:
Qualifications:
Responsibilities:
- Conduct site visits (remote and/or on-site as required, with travel as needed) to assess protocol and regulatory compliance, data accuracy, and overall site performance.
- Ensure that investigational sites adhere strictly to the study protocol, GCP, and all applicable regulatory requirements.
- Manage communication with clinical investigators and site staff, providing necessary training and ongoing support.
- Review and verify source documents, case report forms (CRFs), and other study-related records for accuracy and completeness.
- Identify, document, and resolve deviations and adverse events promptly and appropriately.
- Assist in the preparation and distribution of study-related documents and essential regulatory documents.
- Track study progress, identify potential risks, and implement mitigation strategies to ensure timely completion of study milestones.
- Participate in investigator meetings and training sessions as required.
- Contribute to the development and refinement of study protocols and clinical research processes.
Qualifications:
- A Bachelor's degree in a life science, nursing, pharmacy, or a related healthcare field. Advanced degree preferred.
- Minimum of 3-5 years of direct experience as a CRA in the pharmaceutical or biotechnology industry.
- Thorough knowledge of GCP, ICH guidelines, FDA regulations, and other relevant regulatory standards.
- Experience in monitoring various phases of clinical trials.
- Excellent organizational skills, with the ability to manage multiple priorities and deadlines effectively.
- Strong written and verbal communication skills, with the ability to document findings clearly and concisely.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently and collaboratively in a remote team environment.
- This role supports global initiatives but is specifically aligned with operational oversight relevant to the Eldoret, Uasin Gishu, KE geographical area, requiring adherence to local regulatory nuances.
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Clinical Research Associate - Pharmaceuticals
Posted 7 days ago
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Job Description
Our client, a leading pharmaceutical research organization, is seeking a diligent and experienced Clinical Research Associate (CRA) to join their fully remote team. In this critical role, you will be responsible for monitoring clinical trials, ensuring data integrity, and verifying compliance with protocols and regulatory guidelines. Your expertise will be crucial in advancing the development of life-saving medications. This position demands a thorough understanding of Good Clinical Practice (GCP), clinical trial conduct, and excellent interpersonal skills.
Key Responsibilities:
Key Responsibilities:
- Conduct site initiation visits, interim monitoring visits, and close-out visits for clinical trials, ensuring adherence to study protocols and regulatory requirements.
- Verify the accuracy, completeness, and integrity of clinical trial data by reviewing source documents and case report forms (CRFs).
- Ensure all trial-related activities and documents are in compliance with Good Clinical Practice (GCP), FDA regulations, and other applicable guidelines.
- Monitor patient safety and report any adverse events or protocol deviations according to established procedures.
- Build and maintain strong working relationships with investigators, site staff, and other study stakeholders.
- Provide training and ongoing support to clinical trial sites on study procedures and data collection.
- Manage study supplies and equipment at clinical sites, ensuring proper storage and handling.
- Prepare and submit monitoring visit reports in a timely manner, documenting findings and action items.
- Track and resolve data queries and discrepancies identified during monitoring.
- Ensure timely retrieval and archiving of all essential study documents.
- Participate in investigator meetings and clinical trial team discussions.
- Stay updated on current regulatory requirements and industry best practices in clinical research.
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- In-depth knowledge of GCP guidelines, ICH regulations, and clinical trial conduct.
- Experience with various therapeutic areas is a plus.
- Strong understanding of clinical trial protocols and study documentation.
- Excellent organizational, time management, and prioritization skills.
- Exceptional attention to detail and accuracy in data review.
- Outstanding communication, interpersonal, and problem-solving skills.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently, travel as required (if applicable, though this role is remote), and manage responsibilities effectively in a remote setting.
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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.
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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 12 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly motivated and experienced Senior Clinical Research Associate (CRA) to join their dynamic, fully remote team. This role is integral to the successful execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. The Senior CRA will be responsible for site selection, initiation, monitoring, and closing out clinical trial sites, meticulously documenting all trial-related activities. You will play a crucial role in data integrity, patient safety, and the overall progress of critical drug development programs. This is an exceptional opportunity to contribute to life-saving medical advancements from the convenience of your home office.
Key Responsibilities:
Key Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits for clinical trials in accordance with protocol and GCP guidelines.
- Ensure timely and accurate data collection, verification, and source document review.
- Monitor patient safety and adverse event reporting.
- Verify compliance with study protocols, SOPs, and regulatory requirements.
- Build and maintain strong relationships with investigators, site staff, and study sponsors.
- Identify, evaluate, and resolve site-level issues and risks.
- Prepare and present site performance reports to study management.
- Ensure all trial-related documentation is maintained in the trial master file.
- Participate in study team meetings and contribute to protocol development as needed.
- Maintain up-to-date knowledge of regulatory guidelines and industry best practices.
This advertiser has chosen not to accept applicants from your region.
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Clinical Research Associate - Pharmaceutical
Posted 23 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly motivated and experienced Clinical Research Associate (CRA) to join their global clinical development team. This fully remote position allows you to play a crucial role in advancing groundbreaking medical treatments by overseeing clinical trials from initiation to closeout. You will be responsible for ensuring that trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and regulatory requirements. This remote-first role demands exceptional organizational skills, a keen eye for detail, and the ability to manage multiple sites and complex data sets. You will leverage advanced communication and monitoring technologies to collaborate with investigators, site staff, and internal teams, ensuring data integrity and patient safety. The ideal candidate possesses a strong understanding of Good Clinical Practice (GCP) guidelines and a passion for contributing to pharmaceutical research. Responsibilities include:
Qualifications:
- Monitoring clinical trial progress at assigned sites to ensure compliance with protocols, SOPs, and GCP.
- Conducting pre-study, initiation, interim, and close-out visits at clinical trial sites.
- Verifying the accuracy, completeness, and integrity of clinical trial data.
- Ensuring timely submission of regulatory documents and ethical committee approvals.
- Communicating effectively with investigators, site staff, and study sponsors.
- Identifying and resolving site-level issues and escalating problems as needed.
- Maintaining accurate and up-to-date trial documentation and records.
- Assisting with the recruitment and selection of study sites and investigators.
- Monitoring subject safety and reporting adverse events promptly.
- Preparing monitoring visit reports and following up on action items.
Qualifications:
- Bachelor's degree in a life science, nursing, or related healthcare field.
- Minimum of 5 years of experience as a Clinical Research Associate or in a similar clinical trial management role.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Experience with various therapeutic areas and trial phases.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to build rapport with site personnel.
- Ability to work independently, manage a remote workload effectively, and travel as required for site visits.
- Detail-oriented with a strong commitment to data accuracy and patient safety.
- Fluency in English is essential; additional language skills are a plus.
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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 23 days ago
Job Viewed
Job Description
Our client, a pioneering pharmaceutical company at the forefront of medical innovation, is actively seeking a highly competent and dedicated Clinical Research Associate (CRA) to join their globally distributed, fully remote clinical operations team. This role is paramount in ensuring the successful execution of clinical trials in accordance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and protocol objectives. As a CRA, you will be responsible for monitoring clinical trial sites to ensure data integrity, patient safety, and adherence to study protocols. Your duties will include conducting pre-study visits, initiation visits, interim monitoring visits, and close-out visits for assigned clinical sites. You will verify the accuracy, completeness, and source data verification of clinical trial documentation, including patient records, lab results, and adverse event reporting. Building and maintaining strong relationships with investigators and site staff is crucial for fostering effective collaboration and ensuring compliance. This role requires a thorough understanding of clinical trial processes, regulatory frameworks, and ethical considerations in research. You will identify and report any deviations from protocol or GCP, escalate issues as needed, and implement corrective and preventive actions (CAPAs). Contributing to the development of study-related documents, such as protocols and case report forms, may also be part of your responsibilities. This fully remote position demands exceptional organizational skills, meticulous attention to detail, and the ability to work autonomously while collaborating effectively with internal study teams and external site personnel.
Key Responsibilities:
Key Responsibilities:
- Monitor assigned clinical trial sites to ensure compliance with protocol and GCP.
- Conduct pre-study, initiation, monitoring, and close-out visits.
- Verify accuracy and completeness of source data and CRFs.
- Ensure patient safety and rights are protected throughout the trial.
- Build and maintain strong relationships with investigators and site staff.
- Identify, document, and resolve protocol deviations and GCP non-compliance issues.
- Implement CAPAs and track their effectiveness.
- Ensure timely reporting of adverse events and safety information.
- Review and manage essential trial documents.
- Communicate effectively with study teams, sponsors, and regulatory authorities.
- Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
- Minimum of 3-5 years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Experience in site monitoring and clinical trial conduct.
- Strong understanding of medical terminology and disease states.
- Excellent critical thinking, problem-solving, and decision-making skills.
- Exceptional organizational, time management, and documentation skills.
- Proficiency with clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Excellent written and verbal communication skills.
- Ability to work independently and travel as needed (if applicable for site visits).
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8
Senior Clinical Research Associate - Pharmaceutical
Posted 20 days ago
Job Viewed
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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