2,265 Advanced Data Analytics Apprentice Remote jobs in Kenya
Senior Data Analyst Apprentice (Remote)
Posted 5 days ago
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Job Description
Our client is seeking ambitious and tech-savvy individuals to join their innovative team as Senior Data Analyst Apprentices in a fully remote capacity. This is a unique opportunity for aspiring data professionals to gain hands-on experience and mentorship within a leading organization. You will work closely with senior data scientists and analysts, contributing to critical projects that involve data collection, cleaning, analysis, and visualization. The apprenticeship is designed to provide a comprehensive understanding of data analytics tools and techniques, enabling you to develop skills in SQL, Python/R, data modeling, and business intelligence platforms. This role requires a strong aptitude for numbers, problem-solving, and a keen eye for detail. As a remote role, you must be highly organized, self-disciplined, and possess excellent communication skills to collaborate effectively with your team members. We are looking for individuals who are eager to learn, passionate about data, and ready to make a significant contribution. This apprenticeship is ideal for recent graduates or individuals looking to transition into a data-focused career. The training will be comprehensive, covering various aspects of data analysis relevant to diverse business needs.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Assist in collecting, cleaning, and organizing large datasets from various sources.
- Perform exploratory data analysis to identify trends, patterns, and insights.
- Support the development and maintenance of data models and databases.
- Create reports and visualizations to communicate findings effectively to stakeholders.
- Collaborate with senior analysts and data scientists on ongoing projects.
- Learn and apply statistical methods and machine learning techniques under guidance.
- Assist in testing and validating data integrity and accuracy.
- Participate in team meetings and contribute to analytical discussions.
- Develop proficiency in relevant data analysis tools and programming languages (SQL, Python, R).
- Contribute to documenting data processes and methodologies.
Qualifications:
- Bachelor's degree in Statistics, Mathematics, Computer Science, Economics, or a related quantitative field.
- Strong analytical and problem-solving skills with a logical mindset.
- Basic understanding of statistical concepts and data analysis principles.
- Familiarity with at least one programming language such as Python or R is a plus.
- Exposure to SQL for data querying is beneficial.
- Excellent attention to detail and ability to work with large datasets.
- Strong written and verbal communication skills.
- Ability to work independently, manage time effectively, and meet deadlines in a remote setting.
- Eagerness to learn and adapt to new technologies and methodologies.
- A genuine interest in data science and analytics.
- Prior experience with data visualization tools (e.g., Tableau, Power BI) is advantageous.
- Previous internship or project experience related to data analysis is a plus.
- Ideal candidate is based in or near Kisumu, Kisumu, KE , but the role is fully remote.
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Advanced Data Analytics Apprentice (Remote)
Posted 22 days ago
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Job Description
Our client is offering an exceptional opportunity for motivated individuals to join their remote apprenticeship program in Advanced Data Analytics. This program is designed for aspiring professionals looking to gain hands-on experience and build a strong foundation in data science and analytics. As a remote apprentice, you will work closely with experienced data scientists and analysts on real-world projects. Your responsibilities will include data cleaning, transformation, and preprocessing; assisting in the development of data visualizations and reports; conducting exploratory data analysis to identify trends and patterns; and supporting the implementation of machine learning models. You will be trained on industry-standard tools and techniques, including Python, R, SQL, and various data visualization platforms. The ideal candidate will possess strong analytical thinking skills, a keen eye for detail, and a genuine passion for data. While prior experience in data analytics is not strictly required, a solid understanding of statistical concepts and a demonstrable ability to learn quickly are essential. You will be expected to participate actively in team meetings, contribute ideas, and take ownership of assigned tasks. This role provides an unparalleled learning experience, allowing you to develop a comprehensive skill set in a supportive and collaborative remote environment. We are looking for individuals who are eager to learn, problem-solve, and contribute to data-driven decision-making. This is a fantastic stepping stone for a career in data science. While the role is fully remote, candidates should be available for virtual collaboration during specified working hours. This traineeship is based out of **Kisumu, Kisumu, KE**, but will be performed remotely.
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Advanced Apprentice - Data Analysis (Remote)
Posted 7 days ago
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Job Description
Our client, a leading data analytics firm, is offering a highly sought-after Advanced Apprenticeship in Data Analysis. This fully remote program is designed for motivated individuals looking to build a career in the exciting field of data science and analytics. You will receive comprehensive training and hands-on experience in collecting, cleaning, analyzing, and visualizing data to derive actionable insights. Working under the guidance of experienced data analysts and scientists, you will contribute to real projects, learning to use industry-standard tools and techniques. This is an exceptional opportunity to develop critical skills and gain practical experience in a supportive, remote-first environment.
Key Learning Opportunities & Responsibilities:
The administrative location for this remote apprenticeship is Eldoret, Uasin Gishu, KE .
Key Learning Opportunities & Responsibilities:
- Learn to collect and clean large datasets from various sources.
- Develop proficiency in data analysis tools such as Python (Pandas, NumPy) and R.
- Master SQL for database querying and data manipulation.
- Create compelling data visualizations using tools like Tableau or Power BI.
- Assist in identifying trends, patterns, and anomalies within data.
- Contribute to the development of reports and dashboards for stakeholders.
- Understand and apply statistical methods to data analysis.
- Learn about data warehousing concepts and ETL processes.
- Collaborate with team members on data-related projects in a virtual setting.
- Receive ongoing mentorship and training from senior data professionals.
- Develop problem-solving skills and learn to interpret complex data effectively.
The administrative location for this remote apprenticeship is Eldoret, Uasin Gishu, KE .
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Senior Clinical Research Associate (Remote)
Posted 20 days ago
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Job Description
Our client, a leading pharmaceutical research organization, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join their globally distributed team in a fully remote capacity. This critical role involves overseeing and managing clinical trial sites, ensuring adherence to study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The ideal candidate will possess a robust understanding of drug development processes, clinical trial methodologies, and regulatory landscapes. You will be responsible for initiating, monitoring, and closing out clinical trial sites, conducting remote source data verification, and ensuring the accuracy, completeness, and quality of clinical data. Key responsibilities include performing remote site visits (feasibility, initiation, interim monitoring, and close-out), training site staff, managing study documentation, and reporting on site performance and progress. You will also collaborate closely with study teams, investigators, and regulatory authorities to resolve study-related issues and ensure patient safety. This position requires exceptional organizational skills, strong attention to detail, and the ability to manage multiple complex trials simultaneously in a virtual environment. The successful candidate must be a proactive problem-solver, adept at communication, and capable of building strong relationships with site personnel remotely. A Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field is required; an advanced degree is a plus. A minimum of 6 years of progressive experience as a Clinical Research Associate, with significant experience in monitoring multiple phases of clinical trials, is mandatory. A strong understanding of ICH-GCP guidelines and relevant regulatory requirements is essential. Excellent written and verbal communication skills, proficiency in clinical trial management systems (CTMS), and electronic data capture (EDC) systems are required. This is an outstanding opportunity to contribute to groundbreaking pharmaceutical research for our client, working remotely and supporting trials impacting regions such as Nairobi, Nairobi, KE .
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Senior Scientific Research Associate - Biotechnology (Remote)
Posted 13 days ago
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Job Description
Our client, a pioneering scientific research and development firm, is searching for a highly skilled and dedicated Senior Scientific Research Associate with a specialization in biotechnology to join their fully remote R&D department. This role is instrumental in driving innovation and advancing scientific understanding in key areas of biotechnology. You will be involved in designing, executing, and analyzing complex research projects, contributing to the development of novel products and technologies. The ideal candidate will possess a strong academic background in biotechnology, molecular biology, biochemistry, or a closely related scientific discipline, coupled with significant hands-on research experience. Your responsibilities will include planning and conducting experiments using advanced laboratory techniques, collecting and interpreting experimental data, and contributing to the preparation of research reports, publications, and patent applications. You will stay current with the latest scientific advancements and methodologies in the field, ensuring our research remains at the forefront of innovation. This position requires exceptional analytical, problem-solving, and critical thinking skills, as well as meticulous attention to detail. You will collaborate effectively with a global team of scientists and researchers through virtual communication platforms, sharing insights and contributing to team-based problem-solving. Excellent written and verbal communication skills are essential for conveying scientific findings clearly and concisely. This is a remote-first position, demanding a high degree of self-motivation, organization, and the ability to work independently and manage multiple research priorities effectively. This is a remarkable opportunity to contribute to cutting-edge scientific research and development that can shape future industries, all while enjoying the flexibility of a remote work setup. The role is fully remote, with extensive remote collaboration expected for scientific teams supporting R&D efforts relevant to advancements in Thika, Kiambu, KE .
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Senior Clinical Research Associate, Remote - Mlolongo
Posted 7 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly experienced and meticulous Senior Clinical Research Associate (CRA) to join their globally distributed team. This is a fully remote position, offering the flexibility to manage clinical trials and ensure data integrity from anywhere. The ideal candidate will possess extensive experience in clinical trial monitoring, regulatory compliance, and site management within the pharmaceutical or biotechnology industry. You will be responsible for overseeing the conduct of clinical trials at investigational sites, ensuring adherence to protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. This role demands exceptional attention to detail, strong organizational skills, and the ability to build effective relationships with site personnel and internal study teams. You will conduct site visits (remote or on-site as required), review source documentation, manage data discrepancies, and ensure timely trial progress. The successful candidate will play a critical role in advancing pharmaceutical research and bringing life-saving therapies to market. This is an outstanding opportunity for a seasoned CRA looking to contribute to impactful drug development programs in a challenging and rewarding remote setting. Experience with various therapeutic areas and clinical trial phases is essential.
Responsibilities:
Responsibilities:
- Plan, implement, and manage clinical trial activities at assigned investigational sites.
- Ensure compliance with study protocols, GCP, FDA regulations, and other relevant guidelines.
- Conduct remote and on-site monitoring visits to assess data accuracy, patient safety, and regulatory compliance.
- Train and support site staff on study procedures, protocol requirements, and data management.
- Review and verify source documents, case report forms (CRFs), and investigational product accountability.
- Identify, document, and resolve site-level issues and deviations.
- Manage communication between the sponsor and investigational sites.
- Contribute to the development of clinical trial documents, such as protocols, investigator brochures, and monitoring plans.
- Oversee site readiness and facilitate study start-up activities.
- Ensure timely submission of all required study documentation and reports.
- Bachelor's degree in a life science, nursing, or related field. Advanced degree preferred.
- 5+ years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Proven experience in clinical trial monitoring, site management, and regulatory compliance.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent organizational, time management, and communication skills.
- Ability to work independently and effectively manage responsibilities in a remote environment.
- Experience with various therapeutic areas and phases of clinical trials.
- Relevant professional certifications (e.g., ACRP, SoCRA) are a plus.
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Senior Clinical Research Associate, Remote Monitoring
Posted 6 days ago
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Job Description
Our client, a global leader in pharmaceutical research and development, is actively seeking a highly experienced Senior Clinical Research Associate (CRA) to join their dedicated, fully remote clinical operations team. This critical role involves overseeing and monitoring clinical trials remotely, ensuring data integrity, patient safety, and adherence to regulatory standards (GCP, ICH). You will be responsible for managing site relationships, conducting remote source data verification, reviewing trial documentation, and troubleshooting issues that arise during the trial lifecycle. The ideal candidate will possess a strong background in clinical research, a meticulous attention to detail, and exceptional communication and organizational skills. As this is a 100% remote position, you will leverage advanced technologies and virtual collaboration tools to maintain effective oversight of clinical trial sites and progress. Your expertise will be vital in ensuring the successful execution of critical drug development programs.
Responsibilities:
Responsibilities:
- Conduct remote monitoring of clinical trial sites to ensure adherence to protocols, GCP, and regulatory requirements.
- Perform remote source data verification (SDV) and review case report forms (CRFs) for accuracy and completeness.
- Manage and build strong relationships with principal investigators and site staff.
- Oversee patient safety and ensure timely reporting of adverse events (AEs) and serious adverse events (SAEs).
- Review essential trial documents, including investigational plans, consent forms, and regulatory binders.
- Identify, document, and track site issues and implement corrective and preventative actions (CAPAs).
- Provide training and guidance to clinical trial site personnel on study protocols and procedures.
- Ensure timely site initiation, monitoring visits (remote or on-site as needed), and site closure.
- Prepare monitoring reports and communicate findings to the clinical study team and management.
- Contribute to the development of study-related documents, including monitoring plans and risk assessment tools.
- Maintain up-to-date knowledge of regulatory guidelines and industry best practices.
- Effectively utilize clinical trial management systems (CTMS) and electronic data capture (EDC) systems for remote monitoring activities.
- Bachelor's degree in a life science, nursing, or a related field.
- Minimum of 5 years of experience as a Clinical Research Associate (CRA) or in a similar clinical trial management role.
- Extensive knowledge of GCP, ICH guidelines, and other relevant regulatory requirements.
- Proven experience in remote clinical trial monitoring and data verification.
- Strong understanding of clinical trial processes from study start-up to close-out.
- Excellent organizational, time management, and prioritization skills.
- Exceptional written and verbal communication skills, with the ability to clearly articulate findings and recommendations.
- Proficiency with clinical trial software, including CTMS and EDC systems.
- Ability to work independently and as part of a remote, cross-functional team.
- Detail-oriented with a strong commitment to quality and patient safety.
- Willingness to travel on-site occasionally as required by specific study needs (though the role is primarily remote).
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Senior Clinical Research Associate - Remote (Pharmaceutical)
Posted 3 days ago
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Job Description
Our client, a rapidly expanding pharmaceutical company focused on innovative drug development, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join our fully remote global clinical operations team. This critical role will oversee and manage clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. The ideal candidate will have a comprehensive understanding of the drug development lifecycle, extensive experience in clinical monitoring, and a proven ability to manage multiple complex clinical trials. Your responsibilities will include conducting site qualification, initiation, interim monitoring, and close-out visits (remotely or in-person as required, but the role itself is remote-based). You will be responsible for verifying the accuracy and completeness of clinical data, ensuring patient safety, and managing site personnel to achieve trial objectives. Strong communication and interpersonal skills are essential for building and maintaining effective relationships with investigators, site staff, and internal project teams. This position requires a meticulous attention to detail, exceptional organizational skills, and the ability to proactively identify and resolve issues. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is mandatory. As this is a fully remote role, you must possess strong self-management capabilities, excellent virtual collaboration skills, and the ability to work independently with minimal supervision. Travel may be required for essential site visits, but the base role is remote. Contributions to study documentation, including protocols, informed consent forms, and study reports, will also be part of your remit. A background in life sciences, nursing, or a related healthcare field, coupled with significant CRA experience, is essential. This is an exceptional opportunity to contribute to life-changing pharmaceutical research from anywhere, supporting global clinical operations that impact patient care worldwide, including potentially near **Nairobi, Nairobi, KE**. Our client offers a competitive salary, comprehensive benefits, and opportunities for professional growth within a cutting-edge pharmaceutical environment.
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Senior Clinical Research Associate (CRA) - Remote
Posted 12 days ago
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Job Description
Our client, a leading pharmaceutical company committed to advancing global health, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join their entirely remote clinical operations team. This role offers the flexibility to manage clinical trials from anywhere, contributing to the development of life-changing medicines. You will be responsible for monitoring clinical trial sites to ensure adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The ideal candidate possesses extensive experience in clinical trial monitoring, strong knowledge of regulatory affairs, and exceptional organizational skills. You will build and maintain strong relationships with investigators and site staff, providing training and support to ensure data integrity and patient safety. We are looking for an individual with exceptional attention to detail, excellent problem-solving abilities, and superior communication and interpersonal skills, capable of thriving in an independent remote work environment. Responsibilities include conducting pre-study, initiation, interim monitoring, and close-out visits, as well as verifying data accuracy and completeness. You will also be involved in resolving site issues, ensuring timely subject recruitment, and preparing monitoring reports. The ability to manage your own schedule, travel as needed (within reasonable parameters for remote roles), and effectively advocate for patient safety and data quality is crucial. This is an exceptional opportunity to contribute to groundbreaking pharmaceutical research while enjoying the autonomy of a remote position. You will be an integral part of a dedicated team focused on bringing innovative therapies to patients worldwide. Our client is committed to professional development and offers a supportive environment for career growth within the pharmaceutical industry.
Responsibilities:
Responsibilities:
- Monitor clinical trial sites to ensure compliance with study protocols, SOPs, GCP, and regulatory requirements.
- Conduct pre-study, initiation, routine monitoring, and close-out visits according to monitoring plan.
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Identify, resolve, and escalate site-related issues in a timely manner.
- Build and maintain positive relationships with investigators, site staff, and study teams.
- Provide training and ongoing support to clinical trial site personnel.
- Ensure subject safety and data privacy are maintained throughout the study.
- Prepare and submit comprehensive monitoring reports and follow-up on action items.
- Participate in study team meetings and contribute to study planning and execution.
- Manage a portfolio of clinical trial sites and ensure timely completion of monitoring activities.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. Advanced degree preferred.
- Minimum of 5 years of progressive experience as a Clinical Research Associate (CRA) or equivalent role.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven experience in monitoring Phase I-IV clinical trials across various therapeutic areas.
- Exceptional understanding of clinical trial processes and documentation.
- Strong analytical and problem-solving skills, with meticulous attention to detail.
- Excellent written and verbal communication skills, with the ability to effectively communicate with diverse stakeholders.
- Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Ability to travel as required for site visits (typically up to 40-60%, depending on study needs).
- Demonstrated ability to work independently, manage time effectively, and prioritize tasks in a remote setting.
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Senior Clinical Research Associate - Pharmaceuticals (Remote)
Posted 19 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly qualified and meticulous Senior Clinical Research Associate (CRA) to join their expanding global team. This position is 100% remote, enabling you to contribute to critical drug development from your home office. As a Senior CRA, you will play a pivotal role in ensuring the quality and integrity of clinical trials, adhering strictly to Good Clinical Practice (GCP) guidelines, FDA regulations, and ICH guidelines. You will be responsible for monitoring clinical trial sites, verifying data accuracy, and ensuring patient safety throughout the trial lifecycle. Your expertise will be crucial in managing relationships with investigators and site staff, resolving issues promptly, and ensuring timely study completion. Key responsibilities include:
Qualifications:
This is a fantastic opportunity to contribute to life-saving research from a remote location, working with cutting-edge therapies and a collaborative international team.
- Conducting remote and on-site (when required) monitoring visits to assess trial conduct and data integrity.
- Ensuring compliance with protocols, regulatory requirements, and company SOPs at assigned investigational sites.
- Verifying source data against case report forms (CRFs) and electronic data capture (EDC) systems.
- Managing and resolving site-level issues, providing training and support to site personnel.
- Maintaining accurate and up-to-date trial documentation and records.
- Communicating effectively with investigators, study coordinators, and internal study teams.
- Participating in protocol development and review, contributing clinical trial expertise.
- Identifying and escalating potential risks and challenges to study management.
- Contributing to the development and implementation of risk-based monitoring strategies.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. Advanced degree preferred.
- Minimum of 5 years of experience as a Clinical Research Associate, with a significant portion in a senior capacity.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Proven experience with EDC systems and clinical trial monitoring techniques.
- Excellent organizational, communication, and interpersonal skills.
- Ability to work independently and manage time effectively in a remote setting.
- Strong critical thinking and problem-solving abilities.
- Experience in specific therapeutic areas is a plus.
This is a fantastic opportunity to contribute to life-saving research from a remote location, working with cutting-edge therapies and a collaborative international team.
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