What Jobs are available for Healthcare in Eldoret?
Showing 1285 Healthcare jobs in Eldoret
Remote Pharmaceutical Clinical Research Associate (CRA)
Posted 2 days ago
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing healthcare through innovative drug development, is seeking a highly motivated and experienced Remote Pharmaceutical Clinical Research Associate (CRA). This fully remote position offers the opportunity to contribute to groundbreaking clinical trials from the comfort of your home. You will be responsible for monitoring clinical trial sites to ensure adherence to protocols, regulations, and ethical standards, as well as collecting and verifying trial data. This role requires a deep understanding of Good Clinical Practice (GCP) guidelines, regulatory requirements, and the drug development process. The ability to manage multiple sites, build strong relationships with investigators and site staff, and maintain meticulous documentation is essential.
Key Responsibilities:
Key Responsibilities:
- Perform remote site monitoring activities, including pre-study visits, initiation visits, routine monitoring visits, and close-out visits.
- Ensure all clinical trial activities are conducted in accordance with the study protocol, GCP guidelines, and applicable regulations.
- Verify the accuracy, completeness, and integrity of clinical trial data through source data verification (SDV).
- Train and support site personnel on study-related procedures and data collection requirements.
- Manage and oversee the conduct of clinical trials at assigned investigator sites.
- Identify, document, and report deviations and adverse events in a timely manner.
- Collaborate with internal study teams (e.g., project managers, medical monitors) to address site-specific issues.
- Ensure proper drug accountability and maintenance of essential study documents at the sites.
- Prepare monitoring visit reports and follow up on action items with site staff.
- Contribute to the continuous improvement of clinical trial processes and quality standards.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 3 years of experience as a Clinical Research Associate (CRA) or similar role in the pharmaceutical industry.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience in therapeutic areas relevant to the company's pipeline is a plus.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent monitoring, auditing, and problem-solving skills.
- Strong organizational skills and the ability to manage multiple sites and tasks effectively.
- Exceptional communication, interpersonal, and negotiation skills.
- Ability to work independently and proactively in a remote setting.
- Willingness to travel occasionally for essential site visits as required.
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Clinical Research Associate - Pharmaceutical
Posted 2 days ago
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing global health, is seeking a meticulous and driven Clinical Research Associate (CRA) to join their esteemed team. This hybrid role offers a dynamic blend of on-site engagement and remote flexibility, based in **Kitale, Trans-Nzoia, KE**. The CRA will play a critical role in ensuring the successful execution of clinical trials, adhering to stringent regulatory guidelines and ethical standards. You will be responsible for monitoring clinical trial sites, verifying data integrity, and ensuring patient safety throughout the trial process. The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) and regulatory requirements, excellent organizational skills, and a commitment to quality and precision in all aspects of their work. This position requires frequent travel to clinical trial sites within the region.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct pre-study, initiation, monitoring, and close-out visits at clinical trial sites according to study protocols and standard operating procedures (SOPs).
- Verify the accuracy, completeness, and integrity of clinical trial data by reviewing source documents and case report forms (CRFs).
- Ensure compliance with study protocols, GCP, and all applicable regulatory requirements.
- Monitor patient safety and report adverse events and serious adverse events promptly.
- Train site staff on study procedures, protocols, and regulatory requirements.
- Manage site-specific documentation and maintain essential trial files.
- Build and maintain positive working relationships with investigators and site staff.
- Identify and resolve site-specific issues and escalate critical issues to the clinical operations manager as needed.
- Participate in the preparation of study-related documents and reports.
Qualifications:
- Bachelor's degree in a life science, nursing, pharmacy, or a related scientific field.
- Minimum of 3 years of experience as a Clinical Research Associate or equivalent role in the pharmaceutical industry.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Proven experience in monitoring clinical trial sites and ensuring data quality.
- Excellent understanding of medical terminology and clinical trial processes.
- Strong organizational, time management, and problem-solving skills.
- Exceptional written and verbal communication skills, with the ability to effectively interact with healthcare professionals.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness and ability to travel frequently to assigned clinical trial sites.
- Ability to work effectively both independently and as part of a hybrid team.
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1
Clinical Research Associate - Pharmaceutical Development
Posted 2 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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2
Principal Pharmaceutical Scientist - Drug Discovery
Posted 2 days ago
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Job Description
Our client is seeking a highly experienced and visionary Principal Pharmaceutical Scientist to lead cutting-edge drug discovery initiatives. This is a fully remote position, offering a unique opportunity for a distinguished scientist to drive innovation from anywhere. You will be responsible for spearheading the research and development of novel therapeutic agents, from target identification through to preclinical candidate selection. This role demands a deep understanding of medicinal chemistry, pharmacology, and drug development processes, along with strong leadership and strategic planning capabilities.
Key responsibilities include:
Qualifications:
Key responsibilities include:
- Leading the design, synthesis, and optimization of small molecule drug candidates.
- Developing and implementing innovative drug discovery strategies and methodologies.
- Identifying and validating novel drug targets in various therapeutic areas.
- Overseeing in vitro and in vivo preclinical studies to assess drug efficacy and safety.
- Collaborating with cross-functional teams, including biologists, toxicologists, and clinical researchers.
- Interpreting complex experimental data and making critical decisions on project direction.
- Authoring scientific publications, patents, and regulatory submissions.
- Mentoring and guiding junior scientists and research associates.
- Managing research budgets and resources effectively.
- Staying abreast of the latest scientific advancements and technological trends in pharmaceutical R&D.
- Contributing to the strategic pipeline planning and business development activities.
Qualifications:
- Ph.D. in Medicinal Chemistry, Organic Chemistry, Pharmacology, or related field.
- 8-10 years of experience in pharmaceutical drug discovery.
- Proven track record in advancing drug candidates.
- Expertise in medicinal chemistry and preclinical development.
- Strong leadership and strategic planning skills.
- Excellent scientific communication and publication record.
- Demonstrated ability to work effectively in a remote environment.
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3
Remote Sanitation and Hygiene Specialist
Posted 2 days ago
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Job Description
Our client is actively seeking a dedicated and knowledgeable Remote Sanitation and Hygiene Specialist to join their innovative team. In this fully remote role, you will be instrumental in developing, implementing, and monitoring comprehensive sanitation and hygiene protocols across various client sites without the need for on-site presence. Your expertise will ensure compliance with all relevant health and safety regulations, contributing to a safe and healthy environment for all stakeholders. You will leverage digital tools and remote communication to assess needs, provide guidance, train staff virtually, and conduct audits. This position requires a keen eye for detail, a deep understanding of best practices in cleaning and disinfection, and the ability to effectively communicate complex information to diverse audiences. You will work independently and collaboratively with on-site managers to uphold the highest standards of cleanliness and public health.
Key Responsibilities:
Key Responsibilities:
- Develop and update sanitation and hygiene policies and procedures tailored to specific operational needs.
- Provide remote guidance and support to on-site teams on best practices for cleaning, disinfection, and waste management.
- Conduct virtual assessments and audits of sanitation protocols, identifying areas for improvement.
- Develop and deliver online training modules for staff on proper hygiene practices.
- Research and recommend appropriate cleaning chemicals, equipment, and technologies.
- Monitor compliance with regulatory requirements and industry standards.
- Analyze incident reports related to hygiene and implement corrective actions.
- Maintain detailed records of sanitation activities, inspections, and training.
- Advise on pandemic preparedness and response strategies related to sanitation.
- Collaborate with cross-functional teams to integrate hygiene measures into all operational aspects.
- Stay informed about emerging trends and scientific advancements in sanitation and public health.
- Bachelor's degree in Public Health, Environmental Science, Microbiology, or a related field.
- Proven experience in sanitation, hygiene management, or a related role, with a strong understanding of cleaning science.
- Demonstrated ability to develop and implement effective sanitation programs.
- Excellent virtual communication and presentation skills.
- Proficiency in using remote collaboration tools and digital documentation platforms.
- Knowledge of relevant health and safety regulations (e.g., WHO, CDC guidelines).
- Strong analytical and problem-solving capabilities.
- Ability to work independently and manage multiple projects simultaneously.
- Detail-oriented with a commitment to accuracy.
- Experience in training development and delivery is a plus.
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