What Jobs are available for Healthcare in Ongata Rongai?
Showing 2123 Healthcare jobs in Ongata Rongai
Remote Junior Pharmaceutical Quality Control Technician
Posted 1 day ago
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Job Description
Our client is seeking a meticulous and driven Remote Junior Pharmaceutical Quality Control Technician to join their regulatory affairs team. This role offers an exciting entry point into the pharmaceutical industry, with a focus on ensuring product quality and compliance, all within a fully remote work environment. You will support quality control processes by reviewing documentation, analyzing data, and ensuring adherence to regulatory standards and internal protocols. Responsibilities include reviewing batch records and analytical test results for accuracy and completeness, assisting in the preparation of quality control reports, maintaining and organizing quality documentation, and participating in virtual audits and inspections preparation. You will also help track deviations and ensure corrective actions are documented and implemented, and liaise with other departments through virtual communication channels to resolve quality-related issues. The ideal candidate will possess a strong understanding of pharmaceutical quality control principles, good manufacturing practices (GMP), and relevant regulatory guidelines (e.g., FDA, EMA). Familiarity with laboratory data interpretation and documentation is essential. Excellent analytical skills, meticulous attention to detail, and a commitment to data integrity and accuracy are paramount. This remote position requires strong organizational skills, the ability to work independently with minimal supervision, and effective written and verbal communication. Our client is based in **Ongata Rongai, Kajiado, KE**, but this position is fully remote. We are looking for candidates who are dedicated to upholding the highest standards of quality and safety in pharmaceutical manufacturing, eager to learn and contribute to a vital aspect of drug development and production. A Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field is required. Previous experience in a pharmaceutical or quality control setting is a significant advantage.
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Clinical Research Associate - Pharmaceutical
Posted 1 day ago
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Our client, a globally recognized pharmaceutical company dedicated to improving patient lives, is seeking a diligent and organized Clinical Research Associate (CRA) to join their fully remote clinical operations team. This position offers the flexibility to manage clinical trials effectively from anywhere, contributing to the development of life-saving medications.
Responsibilities:
We are looking for individuals with a strong background in life sciences, nursing, or a related field, coupled with hands-on experience in clinical trial monitoring. Excellent understanding of Good Clinical Practice (GCP) and regulatory guidelines is paramount. Exceptional organizational, communication, and problem-solving skills are required. The ability to work independently and manage multiple tasks in a remote setting is crucial. This role is based in Mlolongo, Machakos, KE but offers a fully remote working environment.
Responsibilities:
- Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements.
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Screen, recruit, and inform potential study participants.
- Conduct site initiation visits, interim monitoring visits, and close-out visits.
- Manage communication between the sponsor, research sites, and investigators.
- Train site personnel on study-specific procedures and protocols.
- Oversee the safe and ethical conduct of clinical trials.
- Identify and resolve site issues and discrepancies in a timely manner.
- Ensure the proper handling and storage of investigational products and biological samples.
- Prepare monitoring reports and provide feedback to the clinical study team.
We are looking for individuals with a strong background in life sciences, nursing, or a related field, coupled with hands-on experience in clinical trial monitoring. Excellent understanding of Good Clinical Practice (GCP) and regulatory guidelines is paramount. Exceptional organizational, communication, and problem-solving skills are required. The ability to work independently and manage multiple tasks in a remote setting is crucial. This role is based in Mlolongo, Machakos, KE but offers a fully remote working environment.
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1
Remote Pharmaceutical Quality Control Specialist
Posted 1 day ago
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Job Description
Our client, a reputable pharmaceutical company committed to producing high-quality medicines, is actively seeking an experienced Remote Pharmaceutical Quality Control Specialist to join their virtual team. In this fully remote role, you will play a crucial part in ensuring that all pharmaceutical products meet stringent quality and safety standards. Your responsibilities will include reviewing batch records, analyzing analytical data, monitoring manufacturing processes remotely, and ensuring compliance with regulatory guidelines such as Good Manufacturing Practices (GMP). You will also be involved in the investigation of quality deviations, the implementation of corrective and preventive actions (CAPA), and the maintenance of quality documentation. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field, along with significant experience in pharmaceutical quality control or quality assurance. Strong knowledge of regulatory requirements and analytical techniques is essential. You must possess excellent analytical, problem-solving, and documentation skills, with the ability to work independently and manage your workload effectively in a remote setting. This is a vital opportunity to contribute to the integrity and safety of pharmaceutical products, supporting our client’s mission to improve global health outcomes from a remote capacity. We are looking for a detail-oriented professional dedicated to upholding the highest standards of quality in the pharmaceutical industry.
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2
Clinical Research Associate (CRA) - Pharmaceutical
Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly motivated and experienced Clinical Research Associate (CRA) for a fully remote position. This critical role will involve overseeing and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and applicable regulations. You will be responsible for site selection, initiation, monitoring, and close-out visits, ensuring data integrity and patient safety. This remote position offers significant flexibility while maintaining vital oversight of research sites.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct site selection and feasibility assessments for potential clinical trial sites.
- Initiate clinical trial sites, ensuring all necessary documentation is in place and staff are adequately trained.
- Monitor clinical trial sites regularly (remotely and on-site as needed) to verify compliance with protocol, SOPs, and Good Clinical Practice (GCP) guidelines.
- Ensure the accuracy, completeness, and integrity of clinical data collected at trial sites.
- Manage communication with investigators, study coordinators, and site staff.
- Resolve data queries and ensure timely resolution of issues identified during monitoring visits.
- Oversee patient recruitment and retention efforts at assigned sites.
- Manage investigational product accountability and drug supplies at sites.
- Prepare monitoring reports and document all site activities thoroughly.
- Ensure all regulatory requirements and ethical guidelines are followed.
- Participate in study team meetings and contribute to the overall success of the clinical trial.
- Maintain a strong understanding of therapeutic areas and study protocols.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific field. Advanced degree is a plus.
- Minimum of 5 years of experience as a Clinical Research Associate, with a strong understanding of GCP, ICH guidelines, and regulatory requirements.
- Proven experience in monitoring clinical trials across various phases and therapeutic areas.
- Excellent understanding of clinical trial processes, from initiation to close-out.
- Strong analytical and problem-solving skills, with meticulous attention to detail.
- Exceptional organizational and time management skills, with the ability to manage multiple priorities effectively in a remote setting.
- Outstanding written and verbal communication and interpersonal skills.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as required (though the role is predominantly remote).
- Self-motivated, proactive, and able to work independently with minimal supervision.
- Commitment to patient safety and data integrity.
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3
Senior Clinical Research Associate - Pharmaceutical
Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical company dedicated to improving global health, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join their fully remote team. This role is essential for overseeing the successful execution of clinical trials, ensuring data integrity and adherence to regulatory standards. You will play a critical role in bringing life-saving treatments to market.
Responsibilities:
Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits for clinical trial sites.
- Ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), ICH-GCP guidelines, and all applicable regulations.
- Verify the accuracy and completeness of clinical trial data through source document verification and source data review.
- Manage communication between clinical investigators, study coordinators, and the sponsor.
- Identify, document, and escalate trial-related issues and risks to the Clinical Trial Manager.
- Train and mentor junior CRAs and site personnel on study protocols and procedures.
- Ensure all study-related documentation is maintained in the Trial Master File (TMF).
- Monitor study progress and ensure timely patient recruitment and data collection.
- Prepare monitoring reports and follow up on action items.
- Contribute to the development of study protocols, case report forms (CRFs), and other study documents.
- Participate in investigator meetings and provide training to site staff.
- Ensure compliance with site-specific policies and procedures.
- Communicate effectively with internal teams, including project management, data management, and regulatory affairs.
- Stay updated on therapeutic area advancements and regulatory changes.
- This position is fully remote, supporting global clinical operations, with an administrative presence linked to **Ongata Rongai, Kajiado, KE**.
- Bachelor's degree in a life science, nursing, pharmacy, or a related discipline.
- Minimum of 5 years of experience as a Clinical Research Associate, with a strong understanding of clinical trial phases and methodologies.
- In-depth knowledge of ICH-GCP guidelines and other relevant regulatory requirements.
- Proven experience in conducting all types of clinical monitoring visits.
- Excellent understanding of medical terminology and disease processes.
- Strong critical thinking, problem-solving, and organizational skills.
- Exceptional written and verbal communication skills, with the ability to build strong relationships with site personnel.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel as needed (though this role is remote, occasional site visits may be required).
- Ability to work independently and manage time effectively in a remote environment.
- Certification from a recognized professional body (e.g., SoCRA, ACRP) is a plus.
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4
Remote Automotive Technician - Diagnostics Specialist
Posted 1 day ago
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Job Description
Join a leading automotive innovation company as a Remote Automotive Technician specializing in diagnostics. This is a fully remote position, allowing you to leverage your expertise from anywhere. You will be responsible for remotely diagnosing complex vehicle issues, providing technical support to field technicians, and contributing to the development of diagnostic software and tools. Your deep understanding of automotive systems, electrical components, and engine performance will be crucial.
Responsibilities:
Qualifications:
Responsibilities:
- Perform remote diagnostic analysis on a wide range of vehicle makes and models using advanced diagnostic tools and software.
- Interpret diagnostic data, fault codes, and sensor readings to pinpoint root causes of issues.
- Provide clear, concise, and actionable technical guidance to field service technicians.
- Document diagnostic findings, troubleshooting steps, and resolutions in a comprehensive manner.
- Collaborate with engineering teams to report recurring issues and suggest product improvements.
- Stay updated with the latest automotive technologies, diagnostic techniques, and manufacturer repair procedures.
- Contribute to the creation and refinement of diagnostic knowledge bases and troubleshooting guides.
- Participate in virtual team meetings and knowledge-sharing sessions.
Qualifications:
- Proven experience as an Automotive Technician with a strong focus on diagnostics.
- Expertise in using automotive diagnostic equipment, scan tools, and software (e.g., OEM-specific tools, aftermarket scanners).
- In-depth knowledge of vehicle electrical systems, engine management, emissions control, and powertrains.
- Strong analytical and problem-solving skills with the ability to troubleshoot complex technical issues.
- Excellent communication and interpersonal skills, with the ability to explain technical information clearly.
- Ability to work autonomously and manage time effectively in a remote setting.
- Relevant certifications (e.g., ASE) are highly desirable.
- Familiarity with data logging and remote access tools.
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5
Remote Pharmaceutical Clinical Trials Specialist
Posted 1 day ago
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Job Description
Our client is a leading pharmaceutical research organization seeking a highly skilled and dedicated Remote Pharmaceutical Clinical Trials Specialist. This is a fully remote position, offering a fantastic opportunity to contribute to groundbreaking medical advancements from your home office. You will be responsible for managing and coordinating various aspects of clinical trials, ensuring compliance with regulatory standards and ethical guidelines. This role requires a deep understanding of pharmaceutical development, clinical trial processes, and excellent organizational and communication skills.
Key Responsibilities:
Key Responsibilities:
- Coordinate and manage all phases of clinical trials, from study initiation to closure, ensuring adherence to protocols and timelines.
- Develop and maintain comprehensive trial documentation, including protocols, case report forms (CRFs), and investigator brochures.
- Liaise with investigators, site staff, ethics committees, regulatory authorities, and other stakeholders to ensure smooth trial execution.
- Monitor trial progress, identify potential risks and issues, and implement corrective actions as needed.
- Oversee patient recruitment and retention efforts, ensuring compliance with inclusion/exclusion criteria.
- Manage study budgets, track expenses, and ensure timely submission of financial reports.
- Ensure data integrity and accuracy by reviewing CRFs, source documents, and performing data cleaning activities.
- Implement and oversee Good Clinical Practice (GCP) guidelines and other relevant regulatory requirements.
- Manage the procurement and distribution of study materials, including investigational products and lab kits.
- Conduct remote site monitoring visits and provide support and training to site personnel.
- Prepare and submit regulatory documents and reports to relevant authorities.
- Contribute to the design and development of new clinical trial protocols.
- Stay current with advancements in pharmaceutical research, clinical trial methodologies, and regulatory landscape.
- Communicate trial status and key findings to internal teams and external partners.
- Maintain patient confidentiality and data privacy in accordance with HIPAA and other regulations.
- Bachelor's degree in Pharmacy, Medicine, Life Sciences, Nursing, or a related healthcare field. Advanced degree preferred.
- Minimum of 5 years of direct experience in clinical trial management within the pharmaceutical or biotech industry.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Proven experience in managing multiple clinical trials simultaneously.
- Strong understanding of drug development processes and therapeutic areas.
- Excellent project management, organizational, and time management skills.
- Exceptional communication, interpersonal, and negotiation skills.
- Proficiency in clinical trial management systems (CTMS), Electronic Data Capture (EDC) systems, and common office software.
- Ability to work independently, make informed decisions, and thrive in a remote, fast-paced environment.
- Attention to detail and commitment to data quality and patient safety.
- Must be legally authorized to work in Kenya.
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6
Remote Clinical Research Associate (Pharmaceutical)
Posted 1 day ago
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Job Description
Our client, a dynamic pharmaceutical company committed to advancing healthcare, is seeking a dedicated and meticulous Remote Clinical Research Associate (CRA) to join their globally distributed clinical operations team. This position operates entirely remotely, focusing on the planning, execution, and monitoring of clinical trials. You will play a critical role in ensuring trials are conducted according to protocol, regulatory requirements, and Good Clinical Practice (GCP) standards, all while working from your home office.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Perform remote site selection, initiation, monitoring, and close-out visits in accordance with study protocols and regulatory requirements.
- Ensure adherence to Good Clinical Practice (GCP), protocol amendments, and applicable regulatory guidelines.
- Monitor study conduct, data quality, and patient safety through remote review of source documents and data.
- Verify accuracy and completeness of clinical data through source data verification (SDV).
- Oversee site personnel training on study procedures, protocols, and regulatory requirements.
- Manage communication between study sites, investigators, and the clinical trial team.
- Prepare and submit monitoring visit reports and follow-up letters in a timely manner.
- Identify and address site-level issues and deviations, implementing corrective and preventative actions (CAPA).
- Maintain accurate and up-to-date trial documentation in electronic trial master files (eTMF).
- Ensure timely reporting of adverse events and protocol deviations.
- Support investigational product accountability and drug supply management at sites.
- Contribute to the development and review of clinical study protocols, informed consent forms, and other trial-related documents.
Qualifications:
- Bachelor's degree in a life science, nursing, pharmacy, or a related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate, preferably with site monitoring experience.
- Thorough understanding of GCP, ICH guidelines, and local regulatory requirements.
- Proven ability to conduct remote monitoring and data review effectively.
- Excellent organizational, time management, and prioritization skills.
- Strong written and verbal communication skills, with the ability to interact professionally with healthcare professionals.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently with minimal supervision and manage a remote caseload.
- Detail-oriented with strong analytical and problem-solving skills.
- Willingness to travel occasionally for essential site visits or training as required (though the role is primarily remote).
- Relevant certifications (e.g., ACRP, SoCRA) are a plus.
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