955 Remote Senior Clinical Research Associate Cra jobs in Kenya

• Conduct remote monitoring of clinical trial sites to ensure protocol adherence and GCP compliance.
• Verify the accuracy, completeness, and integrity of clinical trial data.
• Review essential regulatory documents and site files.
• Manage site selection, initiation, monitoring, and closure activities remotely.
• Ensure compliance with all applicable regulatory requirements (FDA, EMA, ICH).
• Identify, document, and resolve site-level issues and deviations.
• Communicate effectively with investigators, site staff, and internal project teams.
• Prepare monitoring reports and track action items.
• Oversee drug accountability and investigational product management at sites.
• Contribute to the development of clinical trial protocols and case report forms (CRFs).
• Support audits and regulatory inspections as required.
• Maintain up-to-date knowledge of oncology clinical trials and relevant regulations.

• Bachelor's degree in a life science, nursing, pharmacy, or a related healthcare field.
• Minimum of 3-5 years of experience as a Clinical Research Associate (CRA) or similar role.
• Specific experience in monitoring Oncology clinical trials is essential.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Strong understanding of medical terminology and clinical trial processes.
• Excellent analytical, problem-solving, and decision-making skills.
• Exceptional organizational and time management abilities.
• Outstanding written and verbal communication skills.
• Ability to work independently, manage travel (if required for occasional in-person visits), and maintain productivity in a remote setting.
• RN or advanced degree is a plus.

• 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.

• Collect, clean, and validate clinical trial data from various sources.
• Perform statistical analysis on trial data to identify trends, patterns, and significant findings.
• Develop and maintain databases and data management systems.
• Generate comprehensive reports and visualizations of data analysis results.
• Collaborate with clinical research associates, statisticians, and medical writers.
• Ensure data integrity and compliance with regulatory guidelines (e.g., ICH GCP).
• Assist in the design of clinical trial databases and data collection instruments.
• Identify data discrepancies and implement corrective actions.
• Stay updated on pharmaceutical research methodologies and data analysis tools.
• Contribute to the interpretation of study results and the preparation of regulatory documentation.

• Proven experience as a Data Analyst, preferably within the pharmaceutical or healthcare industry.
• Strong understanding of clinical trial processes and data management.
• Proficiency in statistical software packages such as SAS, R, or SPSS.
• Experience with database management systems (e.g., SQL).
• Excellent analytical, critical thinking, and problem-solving skills.
• Detail-oriented with a high degree of accuracy.
• Effective communication and collaboration skills for remote teamwork.
• Bachelor's degree in Statistics, Mathematics, Computer Science, Pharmacy, or a related scientific field.
• Experience with data visualization tools (e.g., Tableau, Power BI) is a plus.
• Minimum of 3 years of relevant experience in data analysis.

Duty Station: Uganda (with travel across the region)

Contract Type: Consultancy / Full-time Assignment

About the Role

Teriya Management Inc. is seeking an International Agriculture Insurance Specialist to contribute to a high-impact data and analytics initiative in agriculture, climate, and rural livelihoods.

The Agriculture Insurance Specialist will support premium calculation and accurate loss modeling for agricultural insurance products.

Qualifications and Experience

Education

• Master's or its equivalent in actuarial science, Agriculture insurance, mathematics and statistics, Agriculture/Agronomy

General Experience

• 5–6 years demonstrated experience in agricultural insurance, including environmental risk assessment, premium calculations, loss modeling, and agricultural risk evaluation.
• Track record of delivering solutions that reflect a deep understanding of farming systems, crop cycles, and economic drivers of agriculture.
• Proficiency in both spoken and written English

Technical Expertise

• Agricultural Insurance Capability
• Expertise in agricultural insurance, including environmental risk assessment, premium calculations, loss modeling, and agricultural risk evaluation
• Good interpretation of digital data from metrology, hydrology and economic data

Additional InformationThe position will require regional travel, including within Uganda.

Candidates must be able to lead a diverse, cross-functional team and collaborate with multiple stakeholders.

Why Join Us ?

This role offers the opportunity to shape innovative data solutions for agriculture, climate, and rural development in Africa. You will work at the intersection of technology, policy, and impact, contributing to scalable solutions that improve decision-making and resource allocation across the agricultural sector.

How to Apply:

Submit your CV (3 pages maximum) and a brief motivation note to:

Please note: Applications sent through other channels will not be accepted; only email submissions will be reviewed.

• Review and analyze life insurance applications, medical reports, and financial information.
• Assess applicant risk based on established underwriting guidelines and policies.
• Determine policy eligibility, premiums, and coverage limits.
• Communicate effectively with agents, brokers, and applicants to gather necessary information.
• Ensure compliance with regulatory requirements and industry standards.
• Identify potential fraudulent applications and escalate concerns as needed.
• Maintain accurate and organized underwriting files and records.
• Contribute to the development and refinement of underwriting policies and procedures.
• Stay current with industry trends, medical advancements, and underwriting best practices.
• Utilize underwriting software and other technology tools effectively.

• Bachelor's degree in Finance, Business, Actuarial Science, or a related field.
• Proven experience as a Life Insurance Underwriter.
• Strong understanding of risk assessment, medical terminology, and financial analysis.
• Excellent analytical, problem-solving, and decision-making skills.
• Proficiency in underwriting software and Microsoft Office Suite.
• Strong attention to detail and ability to manage multiple applications simultaneously.
• Excellent written and verbal communication skills for effective remote interaction.
• Ability to work independently and manage workload efficiently.
• Relevant professional certifications (e.g., LOMA) are a significant advantage.

• Analyze insurance applications, assessing risks associated with applicants and proposing appropriate coverage terms, conditions, and premiums.
• Evaluate complex risks across various insurance lines, making sound underwriting decisions that align with company guidelines and profitability targets.
• Interpret and apply insurance policies, regulations, and underwriting manuals to ensure compliance and mitigate risk.
• Develop and maintain strong relationships with brokers and agents, providing expert advice and support on underwriting matters.
• Conduct in-depth risk assessments for large or complex accounts, potentially involving site visits (remotely coordinated) or detailed documentation review.
• Review and approve or decline insurance proposals based on risk appetite and underwriting standards.
• Collaborate with claims, actuarial, and product development teams to provide insights on risk trends and market conditions.
• Monitor portfolio performance, identifying adverse trends and recommending corrective actions.
• Stay current with industry developments, regulatory changes, and emerging risks that may impact underwriting.
• Mentor and train junior underwriters, sharing expertise and best practices.
• Contribute to the development and refinement of underwriting guidelines and procedures.
• Prepare reports on underwriting performance, risk exposures, and market analysis for management.
• Ensure the efficient and accurate processing of all underwriting documentation.

• Bachelor's degree in Business Administration, Finance, Economics, or a related field. Relevant professional designations (e.g., ACII, CPCU) are highly desirable.
• Minimum of 7 years of progressive experience in insurance underwriting, with a specialization in a specific line of business (e.g., property, casualty, life).
• Proven ability to analyze and underwrite complex risks effectively.
• In-depth knowledge of insurance products, legal requirements, and industry best practices.
• Strong analytical, decision-making, and problem-solving skills.
• Excellent communication, negotiation, and interpersonal skills.
• Ability to work independently and manage a demanding workload in a remote setting.
• Proficiency in underwriting software and standard office productivity tools.
• Commitment to ethical conduct and regulatory compliance.
• Experience in managing broker relationships is a plus.

• 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.