517 Clinical Research Associate 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
Posted 22 days ago
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Job Description
Our client, a leading pharmaceutical research organization, is seeking a dedicated and experienced Clinical Research Associate to join their team in Nyeri, Nyeri, KE . This role involves overseeing and managing clinical trials to ensure adherence to protocols, regulatory requirements, and ethical standards. You will be responsible for site selection, initiation, monitoring, and close-out activities. This hybrid position requires a balance of on-site visits to research facilities and remote work for data analysis and reporting. The ideal candidate will possess a strong understanding of clinical trial phases, Good Clinical Practice (GCP) guidelines, and regulatory affairs. Excellent organizational skills, attention to detail, and the ability to communicate effectively with investigators, site staff, and internal stakeholders are crucial. You will play a vital role in the successful execution of clinical studies, contributing to the development of new and innovative pharmaceutical products. Responsibilities include monitoring patient recruitment, ensuring data integrity, managing study documentation, and addressing any issues that arise during the trial.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct site visits to assess trial progress, compliance, and patient safety.
- Ensure adherence to study protocols, SOPs, and GCP guidelines.
- Monitor data accuracy and completeness, and resolve data queries.
- Manage study-related documentation and regulatory binders.
- Facilitate communication between the study sponsor, investigators, and site personnel.
- Oversee patient recruitment and retention efforts.
- Identify and report adverse events and deviations from the protocol.
- Prepare site monitoring reports and track action items.
- Participate in study initiation and close-out visits.
- Contribute to the overall success of clinical research projects.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, 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 various therapeutic areas is a plus.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent communication, interpersonal, and problem-solving skills.
- Ability to travel to research sites as required for monitoring activities.
- Strong organizational skills and ability to manage multiple tasks effectively.
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Clinical Research Associate II
Posted 13 days ago
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Job Description
Our client is seeking a dedicated and detail-oriented Clinical Research Associate II (CRA II) to join their growing pharmaceutical research team. This hybrid role offers a blend of remote work flexibility and essential on-site engagement. As a CRA II, you will play a vital role in ensuring the quality and integrity of clinical trials by monitoring study sites, verifying data accuracy, and ensuring compliance with protocols, regulations, and Good Clinical Practice (GCP) guidelines. You will be responsible for site selection, initiation, monitoring, and close-out visits, as well as resolving data discrepancies and addressing protocol deviations. The ideal candidate will possess strong organizational skills, excellent communication abilities, and a thorough understanding of clinical trial processes. This position requires the ability to travel to study sites as needed while also effectively managing tasks remotely. You will contribute to the development of life-saving medicines by maintaining high standards throughout the clinical research process.
Responsibilities:
Responsibilities:
- Conduct pre-study, initiation, routine monitoring, and close-out visits to clinical trial sites.
- Verify that study conduct is in compliance with the approved protocol, GCP, and applicable regulations.
- Ensure accurate, complete, and timely collection and review of clinical data.
- Train and support site staff on study procedures and requirements.
- Resolve data queries and address protocol deviations.
- Manage site-level regulatory documentation.
- Build and maintain strong working relationships with investigators and site staff.
- Prepare visit reports and communicate findings to the study team.
- Ensure adherence to project timelines and budgets.
- Contribute to the development of study-related documents.
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate (CRA).
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Experience with various therapeutic areas is a plus.
- Proficiency in using electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent written and verbal communication skills.
- Strong organizational, time management, and problem-solving abilities.
- Ability to travel up to 50% of the time to study sites.
- Detail-oriented with a commitment to data quality and integrity.
- Experience in pharmaceutical or biotechnology settings is preferred.
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Lead Clinical Research Associate
Posted 19 days ago
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Job Description
Our client, a progressive pharmaceutical company, is seeking a highly experienced Lead Clinical Research Associate (CRA) for a fully remote position. This critical role involves overseeing and managing clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. The ideal candidate will possess extensive experience in clinical trial management, including site monitoring, data collection oversight, and regulatory submissions within the pharmaceutical or biotech industry. Strong leadership skills and the ability to mentor and guide junior CRAs are essential. As a remote CRA, you will conduct remote monitoring of study sites, engage with investigators and study staff via virtual platforms, and ensure the integrity and accuracy of trial data. Your responsibilities will include developing study protocols, managing investigational product logistics, ensuring subject safety, and facilitating timely completion of trials. You will also be responsible for performing risk-based monitoring, preparing monitoring reports, and resolving site-specific issues. The ability to work autonomously, manage multiple priorities effectively, and maintain meticulous documentation in a remote setting is crucial. This is an outstanding opportunity for a seasoned CRA to take on a leadership role, contributing to life-saving research and development efforts that impact public health, remotely supporting trials relevant to **Naivasha, Nakuru, KE**, and global health outcomes.
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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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Clinical Research Associate (CRA)
Posted 19 days ago
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Job Description
Our client, a cutting-edge pharmaceutical company, is seeking a diligent and experienced Clinical Research Associate (CRA) to join their team. This role involves significant remote work with occasional travel required to clinical sites. As a CRA, you will play a crucial role in ensuring the smooth execution of clinical trials, upholding the highest standards of data integrity and patient safety. Your primary responsibilities will include monitoring clinical trial sites, verifying data accuracy, ensuring adherence to protocols and regulatory requirements (e.g., GCP, FDA), and managing site staff. You will conduct pre-study, initiation, interim, and close-out visits, providing essential support to investigators and study coordinators. The ideal candidate possesses a Bachelor's degree in a life science, nursing, or a related field; a Master's degree or higher is advantageous. A minimum of 3 years of experience as a CRA in the pharmaceutical or biotech industry is required, with a proven track record of successful trial management. Strong knowledge of clinical trial processes, regulatory guidelines, and medical terminology is essential. Excellent organizational, time management, and communication skills are critical for managing multiple sites and collaborating effectively with cross-functional teams, both in person and remotely. The ability to travel occasionally to designated clinical trial sites is a requirement for this hybrid role. Our client is committed to advancing medical treatments and offers a stimulating work environment with opportunities for professional growth. Join a dedicated team focused on bringing life-changing therapies to patients.
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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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Principal Clinical Research Associate
Posted 22 days ago
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Job Description
Our client, a globally recognized pharmaceutical company, is actively seeking a Principal Clinical Research Associate to oversee critical aspects of clinical trials. This is a fully remote position requiring extensive experience in clinical trial management, regulatory compliance, and data integrity. You will be responsible for ensuring that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. The ideal candidate will possess a deep understanding of the drug development process, strong project management skills, and the ability to lead and mentor junior CRAs. Your role will involve site selection, initiation, monitoring, and close-out activities. You will conduct site visits to assess protocol compliance, review case report forms (CRFs), and ensure the accurate and timely collection of data. Exceptional communication and interpersonal skills are crucial for building strong relationships with investigators, site staff, and internal project teams. This position demands a proactive and meticulous approach to quality assurance, a commitment to patient safety, and the ability to thrive in a highly regulated and demanding remote environment. We are looking for a seasoned professional who can drive the successful execution of clinical studies and contribute to bringing vital new therapies to patients. This is an outstanding opportunity to play a pivotal role in pharmaceutical innovation from a remote location, offering significant career growth potential.
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Lead Clinical Research Associate (CRA)
Posted 22 days ago
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Job Description
Our client, a pioneering pharmaceutical firm, is actively searching for an experienced and dedicated Lead Clinical Research Associate (CRA) to join their expanding research team. This is a fully remote position, enabling you to contribute to groundbreaking drug development from the comfort of your home. As a Lead CRA, you will play a pivotal role in overseeing and managing clinical trial activities, ensuring compliance with regulatory standards, and driving the successful execution of studies. Your responsibilities will include coordinating and monitoring clinical trial sites, performing site visits (pre-study, initiation, routine monitoring, and close-out), ensuring data integrity and accuracy, and verifying adherence to protocols and Good Clinical Practice (GCP) guidelines. You will also be responsible for mentoring and training junior CRAs, serving as a key point of contact for investigators and site staff, and resolving site-level issues promptly. This role demands a deep understanding of pharmaceutical research, regulatory affairs, and clinical trial management. The ideal candidate will possess exceptional organizational, communication, and interpersonal skills, with a proven ability to manage multiple tasks and priorities effectively. Experience in therapeutic areas such as oncology, cardiology, or infectious diseases is highly valued. A strong track record of successful site management and a commitment to quality and patient safety are essential. You will work collaboratively with internal teams, including data management, biostatistics, and regulatory affairs, to ensure seamless trial progression. This remote role requires self-discipline, proactivity, and a results-driven approach. A Bachelor's degree in life sciences, nursing, or a related field is mandatory. Advanced degrees or relevant certifications (e.g., ACRP, SoCRA) are a plus. This is an exceptional opportunity to advance your career in clinical research within a supportive and innovative environment. Be part of a team that is committed to improving global health through cutting-edge pharmaceutical development. Your expertise will directly contribute to bringing life-changing therapies to patients worldwide. Embrace a flexible work model that prioritizes outcomes and professional growth.
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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 experienced Clinical Research Associate (CRA) to join their expanding global team. This is a fully remote position, offering unparalleled flexibility and the chance to make a significant impact on drug development from your home base. As a remote CRA, you will be responsible for monitoring clinical trials to ensure adherence to protocols, regulatory requirements, and good clinical practice (GCP) guidelines. You will conduct site visits (virtually or in-person as needed, though the role is predominantly remote), verify data accuracy, manage investigational product, and ensure the safety and rights of study participants. This role requires exceptional organizational skills, meticulous attention to detail, and a deep understanding of clinical trial processes. You will serve as a key liaison between the study sponsor, investigative sites, and regulatory authorities. We are looking for a self-starter who can manage their workload independently, maintain strong relationships with site staff, and contribute to the successful execution of clinical studies. The ideal candidate will possess strong therapeutic area knowledge and a commitment to ethical research practices. This is an exciting opportunity to advance your career in clinical research within a forward-thinking and supportive remote environment. You will have the opportunity to work on groundbreaking therapies and contribute to bringing life-changing medicines to patients. Your ability to adapt to a remote work environment, coupled with your professional expertise, will be critical to your success in this role.
Responsibilities:
Responsibilities:
- Monitor clinical trial sites to ensure compliance with study protocols, SOPs, and GCP.
- Verify the accuracy, completeness, and integrity of clinical data.
- Conduct pre-study, initiation, monitoring, and close-out visits (remote or in-person as required).
- Manage investigational product accountability and drug accountability at sites.
- Ensure the rights, safety, and well-being of study participants.
- Act as a primary point of contact for investigative sites and study sponsors.
- Prepare and submit monitoring visit reports in a timely manner.
- Facilitate communication between sites, sponsors, and regulatory bodies.
- Ensure all required regulatory documentation is complete and maintained.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with various therapeutic areas is advantageous.
- Proficiency in Electronic Data Capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication and interpersonal skills.
- Ability to work independently and effectively in a remote setting, travel may be required occasionally.
- Registered Nurse (RN) or equivalent clinical background is a plus.
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