931 Remote Clinical Research Associate Pharmaceutical jobs in Kenya
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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Remote Clinical Research Associate (Pharma)
Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a dedicated and experienced Remote Clinical Research Associate (CRA) to support groundbreaking drug development. This position is fully remote, offering flexibility and the opportunity to contribute to critical clinical trials from the comfort of your home office. As a Remote CRA, you will play a vital role in monitoring study conduct, ensuring data integrity, and upholding regulatory compliance across multiple research sites. The ideal candidate will possess a strong understanding of clinical trial processes, GCP guidelines, and excellent analytical and interpersonal skills. You will be responsible for conducting remote site visits, reviewing study documentation, and communicating effectively with investigators, site staff, and internal teams.
Key Responsibilities:
This role is based in Nakuru, Nakuru, KE , but operates as a fully remote position. We are looking for a self-motivated individual with a keen eye for detail and a commitment to advancing pharmaceutical research. Strong organizational skills and the ability to manage multiple tasks effectively in a remote setting are essential. If you are passionate about clinical research and seeking a challenging yet rewarding remote opportunity, we encourage you to apply.
Key Responsibilities:
- Conduct remote monitoring activities for clinical trials, including source data verification, regulatory document review, and protocol adherence assessment.
- Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and other applicable guidelines.
- Initiate, monitor, and close-out clinical trial sites remotely, performing necessary virtual visits and evaluations.
- Build and maintain strong relationships with investigators and site staff, providing guidance and support.
- Review and reconcile essential documents, ensuring accuracy and completeness.
- Identify and report adverse events and protocol deviations promptly.
- Prepare and present monitoring visit reports, documenting findings and action plans.
- Collaborate with internal study teams, including data management, regulatory affairs, and project management.
- Participate in site qualification, initiation, and close-out visits (potentially some on-site travel may be required as per project needs, though the role is primarily remote).
- Contribute to the development and review of study protocols and other clinical trial documents.
This role is based in Nakuru, Nakuru, KE , but operates as a fully remote position. We are looking for a self-motivated individual with a keen eye for detail and a commitment to advancing pharmaceutical research. Strong organizational skills and the ability to manage multiple tasks effectively in a remote setting are essential. If you are passionate about clinical research and seeking a challenging yet rewarding remote opportunity, we encourage you to apply.
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Remote Clinical Research Associate - Pharmaceutical Studies
Posted today
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Job Description
Our client, a leading pharmaceutical research organization, is seeking a dedicated and meticulous Remote Clinical Research Associate (CRA) to join their global clinical operations team. This fully remote position will involve overseeing and managing all aspects of clinical trial conduct from a distance, ensuring adherence to protocols, regulations, and ethical standards. You will be responsible for site selection, initiation, monitoring, and close-out activities, as well as ensuring data integrity and patient safety. The ideal candidate will possess a strong understanding of Good Clinical Practices (GCP), clinical trial processes, and regulatory requirements. You should have excellent communication, organizational, and analytical skills, with the ability to work independently and collaboratively in a remote setting. This is an excellent opportunity to contribute to the development of life-saving medicines and advance your career in clinical research.
Responsibilities:
Responsibilities:
- Perform remote site monitoring activities to ensure compliance with study protocols, SOPs, and regulatory requirements (e.g., GCP, FDA, ICH).
- Conduct pre-study visits (PSVs), site initiation visits (SIVs), interim monitoring visits (IMVs), and close-out visits (COVs) remotely or on-site as needed.
- Verify the accuracy, completeness, and consistency of clinical trial data through source data verification (SDV).
- Ensure timely query resolution and data clarification with study sites.
- Train and support site staff on study procedures, protocol requirements, and regulatory compliance.
- Monitor patient safety and report adverse events (AEs) and serious adverse events (SAEs) according to protocol and regulatory guidelines.
- Manage relationships with investigators and site staff, fostering a collaborative research environment.
- Ensure the proper documentation and archiving of all essential study documents.
- Prepare monitoring visit reports and communicate findings and action items to study teams and management.
- Participate in investigator meetings and clinical trial team meetings.
- Bachelor's degree in a life science, nursing, pharmacy, or a related scientific discipline.
- Minimum of 3-5 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 is advantageous.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong understanding of medical terminology and clinical trial processes.
- Excellent organizational, time management, and problem-solving skills.
- Exceptional written and verbal communication skills, with the ability to build rapport with site personnel.
- Ability to work independently, manage travel (if required for occasional on-site visits), and meet strict deadlines in a remote setting.
- Self-motivated, detail-oriented, and committed to maintaining high standards of quality and ethical conduct.
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2
Remote Pharmaceutical Quality Control Analyst (Trainee)
Posted 16 days ago
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Job Description
Our client, a leading pharmaceutical entity, is seeking a driven and detail-oriented individual for a fully remote Pharmaceutical Quality Control Analyst Trainee position. This is a groundbreaking opportunity to enter the pharmaceutical industry and develop critical skills in quality assurance and control from a remote setting. You will be trained on rigorous testing procedures, data analysis, and regulatory compliance standards that govern pharmaceutical product development and manufacturing. Responsibilities will include reviewing batch records, analyzing laboratory data (virtually), preparing reports on quality testing outcomes, and assisting in the implementation of quality improvement initiatives. The ideal candidate will possess a strong scientific aptitude, meticulous attention to detail, and a solid understanding of basic chemistry and biology principles. Familiarity with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is advantageous, though not required as comprehensive training will be provided. You must be able to work independently, manage your time effectively in a remote environment, and communicate clearly and concisely with team members and supervisors. This role requires a proactive approach to learning and a commitment to maintaining the highest standards of quality and safety. The successful candidate will gain invaluable experience in a highly regulated industry, contributing to the development of life-saving medications. While the position is fully remote, we are looking for individuals based in or with a strong connection to **Naivasha, Nakuru, KE**, and surrounding regions who are ready to embark on a challenging yet rewarding career path. This is an excellent opportunity for aspiring professionals to gain specialized knowledge and contribute to pharmaceutical excellence from a distance.
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Remote Clinical Research Associate - 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 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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5
Job Description
Our client is seeking a bright and enthusiastic Biotechnology Research Associate Intern to join their dynamic, fully remote research team. This internship is designed for recent graduates or current Master's students eager to gain hands-on experience in a fast-paced research environment. You will support ongoing projects in molecular biology, cell culture, and genetic engineering. Responsibilities include preparing reagents, performing experiments under supervision, meticulously documenting results, and assisting with data analysis and presentation. You will work collaboratively with senior researchers using advanced virtual communication tools, fostering a strong team spirit despite the remote setting. The ideal candidate will have a solid foundation in general biology, molecular biology, or a related life science discipline. Prior laboratory experience, even from academic coursework, is highly valued. Familiarity with standard laboratory techniques such as PCR, Western blotting, ELISA, and sterile cell culture techniques is beneficial. Proficiency in data recording and analysis, along with strong organizational skills, is essential. You should possess excellent written and verbal communication skills, with the ability to clearly convey experimental findings. This remote position requires a high degree of self-discipline, proactivity, and a genuine passion for scientific discovery. You will have the opportunity to learn state-of-the-art techniques and contribute meaningfully to research initiatives aimed at developing innovative biotechnological solutions. This is an excellent stepping stone for a career in scientific research. The position is based in **Kitale, Trans-Nzoia, KE**.
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Senior Quality Control Analyst (Pharmaceuticals) - Remote
Posted 20 days ago
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Job Description
Our client is seeking a meticulous and experienced Senior Quality Control Analyst specializing in pharmaceuticals to join their dedicated remote team. This critical role involves ensuring the highest standards of quality and compliance for all manufactured pharmaceutical products. You will be responsible for developing, validating, and implementing analytical methods, conducting rigorous testing, and interpreting results to guarantee product integrity. This is an excellent opportunity to leverage your expertise in quality assurance within a flexible, home-based work setting. Your contributions will directly impact patient safety and product efficacy.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Develop, validate, and optimize analytical methods for raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, spectroscopy, and titrimetry.
- Perform routine quality control testing according to established protocols and specifications.
- Analyze and interpret test results, identifying any deviations or out-of-specification (OOS) findings.
- Investigate OOS results, implement corrective and preventive actions (CAPAs), and document all findings thoroughly.
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory guidelines (e.g., FDA, EMA).
- Maintain and calibrate laboratory equipment, ensuring its proper functioning and adherence to calibration schedules.
- Prepare Certificates of Analysis (CoA) and other quality-related documentation.
- Participate in internal and external audits, providing necessary information and demonstrating compliance.
- Train and mentor junior QC analysts on analytical techniques, procedures, and compliance requirements.
- Contribute to continuous improvement initiatives within the Quality Control department.
Qualifications:
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field.
- A minimum of 5 years of experience in pharmaceutical quality control, with a strong understanding of analytical techniques.
- Extensive hands-on experience with analytical instrumentation (HPLC, GC, UV-Vis, FTIR, etc.).
- In-depth knowledge of GMP, GLP, and regulatory requirements for pharmaceutical manufacturing.
- Proven experience in method validation and OOS investigations.
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent attention to detail and organizational abilities.
- Proficiency in documentation and report writing.
- Ability to work independently and manage workload effectively in a remote environment.
- Familiarity with pharmaceutical manufacturing processes relevant to **Kakamega, Kakamega, KE** or similar regions is a plus.
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7
Remote Pharmaceutical Research Associate
Posted 23 days ago
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Job Description
Our client, a leading innovator in the pharmaceutical sector, is seeking a skilled and dedicated Remote Pharmaceutical Research Associate. This is a unique opportunity to contribute to groundbreaking research and development from a fully remote setting. While the role is aligned with **Mombasa, Mombasa, KE**, it is a remote-first position, offering unparalleled flexibility. You will play a key role in various stages of pharmaceutical research, from study design to data analysis and reporting, working with cutting-edge technologies and collaborating with a global team of experts.
Your Responsibilities Will Include:
Your Responsibilities Will Include:
- Designing and conducting laboratory experiments or in-silico studies related to drug discovery and development.
- Collecting, analyzing, and interpreting complex research data using statistical software and bioinformatics tools.
- Preparing detailed research reports, manuscripts for publication, and presentations.
- Collaborating with cross-functional teams, including chemists, biologists, and clinicians, in a virtual environment.
- Maintaining accurate and organized records of experimental procedures, results, and observations.
- Ensuring compliance with all relevant regulatory guidelines and company SOPs.
- Troubleshooting experimental issues and developing innovative solutions.
- Contributing to the development of new research methodologies and protocols.
- Staying abreast of the latest scientific literature and advancements in pharmaceutical sciences.
- Presenting research findings at virtual scientific conferences or internal meetings.
- Master's degree or Ph.D. in Pharmacology, Biochemistry, Molecular Biology, Chemistry, or a related life science field.
- Proven experience in pharmaceutical research, with a strong understanding of drug development processes.
- Proficiency in relevant research techniques and methodologies (e.g., cell culture, PCR, Western blotting, chromatography, molecular modeling).
- Strong analytical skills and experience with statistical analysis and data interpretation.
- Excellent written and verbal communication skills, essential for remote collaboration.
- Ability to work independently with minimal supervision and manage multiple projects simultaneously.
- Proficiency in relevant software (e.g., GraphPad Prism, R, Python, Schrödinger Suite).
- A meticulous approach to record-keeping and experimental execution.
- Demonstrated ability to critically evaluate scientific data and draw sound conclusions.
- Experience with regulatory affairs and Good Laboratory Practice (GLP) is a plus.
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8
Quality Control Analyst (Pharmaceutical)
Posted 22 days ago
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Job Description
Our client is seeking a meticulous and detail-oriented Quality Control Analyst to join their pharmaceutical division. This role plays a crucial part in ensuring the safety, efficacy, and quality of our pharmaceutical products. The position offers a hybrid work model, combining remote flexibility with essential on-site laboratory work. The successful candidate will be responsible for performing a range of analytical tests and procedures according to established protocols and regulatory standards.
Responsibilities:
Responsibilities:
- Conduct routine and non-routine analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
- Prepare reagents, solutions, and standards required for testing.
- Maintain accurate and detailed laboratory records, documenting all procedures, results, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Calibrate and maintain laboratory equipment, ensuring proper functioning and adherence to calibration schedules.
- Investigate out-of-specification (OOS) results, identify root causes, and participate in deviation investigations.
- Assist in the validation and transfer of analytical methods.
- Review and approve testing data and reports.
- Stay informed about current pharmacopeial methods (e.g., USP, BP, EP) and relevant regulatory guidelines.
- Participate in internal and external audits as required.
- Contribute to the continuous improvement of quality control processes and procedures.
- Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific field.
- Minimum of 3 years of experience in a pharmaceutical quality control or analytical laboratory setting.
- Proficiency in operating and maintaining analytical instrumentation, particularly HPLC and GC.
- Solid understanding of GMP, GLP, and relevant regulatory requirements.
- Experience with pharmacopeial testing and monographs.
- Strong problem-solving skills and ability to troubleshoot analytical issues.
- Excellent attention to detail and accuracy in data recording and analysis.
- Good organizational and time management skills.
- Effective written and verbal communication abilities.
- Ability to work independently and collaboratively in a hybrid environment, balancing remote tasks with essential on-site laboratory duties.
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