2,001 Clinical Trial Managers jobs in Kenya

Clinical Trial Manager

80100 Abothuguchi West KES380000 Annually WhatJobs

Posted 22 days ago

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Job Description

full-time
Our client is seeking a seasoned and highly organized Clinical Trial Manager to oversee the planning, execution, and monitoring of clinical trials. This critical, fully remote role will involve managing all aspects of clinical trials from initiation to close-out, ensuring compliance with regulatory standards and company policies. The ideal candidate will have extensive experience in clinical research, a strong understanding of Good Clinical Practice (GCP) guidelines, and a proven ability to manage complex multi-site studies. You will be responsible for developing study protocols, managing budgets, coordinating with investigators and site staff, and ensuring the timely collection and analysis of trial data. This position requires excellent leadership, communication, and project management skills, enabling effective collaboration with internal teams and external partners in a remote setting. We are looking for a proactive individual who can identify and mitigate risks, ensure data integrity, and drive successful trial outcomes. This is an exceptional opportunity to lead vital research initiatives and contribute to the development of life-saving therapies. Your ability to manage multiple priorities, maintain meticulous documentation, and foster strong relationships with stakeholders will be key to your success. The role demands a dedication to ethical research practices and a passion for advancing medical science through rigorous clinical investigation.
Responsibilities:
  • Plan, manage, and execute clinical trials according to GCP and regulatory requirements.
  • Develop and finalize clinical trial protocols, informed consent forms, and other study documents.
  • Oversee the selection, training, and monitoring of clinical investigators and study sites.
  • Manage trial budgets, timelines, and resources effectively.
  • Ensure accurate and timely collection, review, and reconciliation of clinical data.
  • Monitor trial progress and identify, assess, and mitigate potential risks.
  • Liaise with regulatory authorities, ethics committees, and other stakeholders.
  • Prepare study reports and contribute to regulatory submissions.
  • Manage vendor relationships, including CROs and central laboratories.
  • Ensure compliance with all applicable laws, regulations, and company policies.
  • Communicate study status and key findings to internal teams and management.
Qualifications:
  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; advanced degree preferred.
  • Minimum of 7 years of experience in clinical trial management, with a strong understanding of drug development processes.
  • In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
  • Proven experience managing multiple clinical trials simultaneously.
  • Excellent project management, organizational, and leadership skills.
  • Strong communication, interpersonal, and negotiation abilities.
  • Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
  • Ability to work independently and effectively in a fully remote environment.
  • Experience in data analysis and interpretation is a plus.
  • Commitment to scientific integrity and patient safety.
The job is based in Garissa, Garissa, KE , but is performed remotely.
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Clinical Trial Manager - Remote

20200 Kapsuser KES140000 Annually WhatJobs

Posted 7 days ago

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full-time
Our client, a prominent pharmaceutical company, is seeking a dedicated and experienced Clinical Trial Manager to oversee their global clinical research programs from a fully remote setting. This critical role is responsible for the planning, execution, and successful completion of clinical trials in compliance with all regulatory requirements and ethical standards. You will manage all aspects of clinical trials, including site selection, investigator training, budget management, and data monitoring. The ideal candidate possesses a deep understanding of Good Clinical Practice (GCP) guidelines, regulatory affairs, and clinical trial methodologies. Proven experience in managing multiple clinical trials simultaneously is essential, along with a strong ability to lead and motivate cross-functional teams, including clinical research associates (CRAs), investigators, and site staff. Responsibilities include developing clinical trial protocols, managing vendor relationships, and ensuring timely data collection and analysis. You will be responsible for identifying and mitigating potential risks and ensuring the safety and well-being of trial participants. Excellent organizational, communication, and problem-solving skills are paramount for success in this remote role. You must be proficient in clinical trial management software and possess strong leadership qualities. This is an exceptional opportunity for a seasoned clinical trial professional to contribute to the advancement of innovative therapies and shape the future of healthcare. You will work in a dynamic, collaborative, and fully remote environment, playing a pivotal role in bringing new medicines to patients worldwide. Your expertise in clinical operations will be crucial in ensuring the integrity and efficiency of our client's clinical research endeavors, making a tangible difference in global public health.
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Lead Clinical Trials Coordinator

20137 Dundori KES5800000 Annually WhatJobs

Posted 8 days ago

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full-time
Our client, a pioneering pharmaceutical company, is looking for a Lead Clinical Trials Coordinator to join our globally distributed, remote-first team. This critical role will oversee the planning, execution, and monitoring of clinical trials, ensuring compliance with regulatory standards and company protocols. You will be responsible for managing trial documentation, coordinating with investigators and study sites, and ensuring the integrity and quality of data collected. As a fully remote position, this role demands exceptional organizational skills, proactive communication, and the ability to manage complex projects independently. You will serve as a key point of contact for internal and external stakeholders, providing guidance and support throughout the trial lifecycle. Responsibilities include site selection and initiation, patient recruitment strategies, adverse event reporting, and ensuring adherence to Good Clinical Practice (GCP) guidelines. The ideal candidate will have a strong understanding of drug development processes and clinical trial operations. A Bachelor's degree in a life science, nursing, or a related field is required, coupled with at least 7 years of experience in clinical trial management. Previous experience in a remote or distributed team environment is highly advantageous. We seek a candidate with excellent leadership capabilities, strong interpersonal skills, and the ability to problem-solve effectively under pressure. Proficiency in clinical trial management software and electronic data capture (EDC) systems is essential. This is an excellent opportunity to contribute to groundbreaking research and advance patient care, all while enjoying the flexibility of a fully remote work arrangement. Our client values a collaborative spirit and provides the tools and support necessary for success in a virtual setting. You will be instrumental in ensuring the smooth and efficient conduct of trials, making a tangible difference in bringing new medicines to patients.
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Senior Clinical Trial Manager

01000 Makongeni KES280000 Annually WhatJobs

Posted 20 days ago

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full-time
Our client, a leading pharmaceutical research organization, is seeking an experienced Senior Clinical Trial Manager to oversee complex clinical studies. This critical role is fully remote, empowering you to manage global clinical trials from your home office. You will be responsible for the planning, execution, and completion of clinical trials in accordance with ICH-GCP guidelines, regulatory requirements, and protocol objectives. The ideal candidate will have a strong background in clinical operations, vendor management, and cross-functional team leadership. You will play a pivotal role in bringing life-saving therapies to patients by ensuring the integrity and efficiency of our clinical research programs.

Key Responsibilities:
  • Develop comprehensive clinical trial protocols, study plans, and budgets.
  • Oversee all aspects of clinical trial execution, from site selection to close-out.
  • Manage and mentor clinical research associates (CRAs) and other trial personnel.
  • Ensure adherence to ICH-GCP, FDA regulations, and other applicable guidelines.
  • Select, train, and manage clinical vendors, including CROs, central labs, and IRBs.
  • Monitor trial progress, identify risks, and implement mitigation strategies.
  • Ensure accurate and timely data collection, cleaning, and database lock.
  • Liaise with regulatory authorities, investigators, and study sponsors.
  • Prepare study progress reports, safety reports, and other essential documents.
  • Contribute to the development of standard operating procedures (SOPs) and best practices.
  • Manage study timelines and ensure trials are completed within budget.
  • Conduct site initiation visits, monitoring visits, and close-out visits (virtually or in person as needed).
  • Oversee drug supply management and accountability.
  • Facilitate communication among all study stakeholders.
  • Ensure patient safety and data integrity throughout the trial lifecycle.

Qualifications:
  • Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
  • Minimum of 8 years of experience in clinical trial management within the pharmaceutical or biotech industry.
  • In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
  • Proven experience in managing multiple complex clinical trials simultaneously.
  • Strong leadership and team management skills, with the ability to motivate and guide remote teams.
  • Excellent project management skills, including budget and timeline management.
  • Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
  • Exceptional communication, negotiation, and interpersonal skills.
  • Ability to work independently and make sound decisions in a fast-paced, remote environment.
  • Experience with various therapeutic areas is a plus.
  • Strong understanding of data analysis and statistical concepts.
  • Willingness to travel occasionally for critical meetings or site visits as required.
  • Certification from recognized professional bodies (e.g., ACRP, SoCRA) is highly desirable.

This remote position offers a compelling opportunity for an experienced professional to lead impactful clinical research initiatives from Thika, Kiambu, KE and globally, driving advancements in pharmaceutical therapies.
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Remote Pharmaceutical Clinical Trial Manager

20100 Mwembe KES130000 Annually WhatJobs

Posted 19 days ago

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full-time
Our client, a globally recognized pharmaceutical company, is seeking an experienced and detail-oriented Remote Pharmaceutical Clinical Trial Manager to oversee the execution of clinical trials. This is a fully remote position, allowing you to manage critical aspects of research and development from anywhere, supporting trials that may involve sites in the Nakuru, Nakuru, KE region. You will be responsible for the planning, execution, and monitoring of clinical trials in compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and internal SOPs. Your duties will include developing trial protocols, managing budgets, selecting and overseeing clinical sites and investigators, ensuring data integrity, and managing the safety reporting process. You will collaborate closely with internal teams (e.g., R&D, regulatory affairs, medical affairs) and external partners (e.g., CROs, study sites). The ideal candidate possesses a strong background in pharmaceutical sciences or a related healthcare field, extensive experience in clinical trial management, and a thorough understanding of regulatory landscapes. Exceptional project management, leadership, and communication skills are paramount. This role demands a highly organized, analytical, and proactive individual who can effectively manage complex projects remotely and ensure the successful delivery of high-quality clinical trial data.

Responsibilities:
  • Plan, manage, and execute clinical trials from initiation to close-out.
  • Ensure all clinical trial activities are conducted in compliance with GCP, ICH guidelines, and relevant regulatory requirements.
  • Develop and manage clinical trial budgets and timelines.
  • Oversee the selection and management of clinical investigators and sites.
  • Ensure accurate and timely collection, review, and reporting of clinical trial data.
  • Manage drug supply and investigational product accountability.
  • Oversee the safety reporting process and adverse event monitoring.
  • Collaborate with cross-functional teams to achieve trial objectives.
  • Manage relationships with Contract Research Organizations (CROs) and other vendors.
  • Prepare trial-related documentation, including protocols, informed consent forms, and study reports.
Qualifications:
  • Master's degree or PhD in Pharmacy, Medicine, Life Sciences, or a related field.
  • Minimum of 7 years of experience in clinical trial management within the pharmaceutical or biotechnology industry.
  • In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
  • Proven experience in managing multi-center clinical trials.
  • Excellent project management, organizational, and leadership skills.
  • Strong analytical and problem-solving abilities.
  • Exceptional written and verbal communication skills.
  • Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
  • Ability to work independently, manage complex projects, and make critical decisions in a remote environment.
This is a vital opportunity to contribute to groundbreaking pharmaceutical research from a flexible, remote position.
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Senior Underwriting Specialist - Remote Insurance Operations

60100 Meru , Eastern KES240000 Annually WhatJobs

Posted 22 days ago

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full-time
Our client is seeking a highly analytical and experienced Senior Underwriting Specialist to join their dynamic, remote-first insurance operations team. This pivotal role involves evaluating and accepting insurance risks, ensuring profitability and adherence to company guidelines. You will be responsible for reviewing complex insurance applications, assessing potential risks, and determining appropriate coverage terms and premiums for various policy types. The ideal candidate will possess a comprehensive understanding of insurance principles, risk management, and underwriting best practices across multiple lines of business. You will leverage your expertise to make sound underwriting decisions, balancing risk exposure with market competitiveness. This is a fully remote position, demanding a self-motivated and detail-oriented professional who can manage their workload effectively and collaborate with colleagues and external partners virtually. Responsibilities include analyzing financial statements, medical reports, and other relevant documentation to assess risk comprehensively. You will also play a key role in developing and refining underwriting guidelines, staying abreast of industry trends, and contributing to the training and development of junior underwriters. The ability to communicate complex risk assessments and underwriting decisions clearly and concisely to agents, brokers, and internal stakeholders is essential. Experience with various insurance software systems and data analysis tools is highly desirable. This is an exciting opportunity to contribute to the strategic growth of a leading insurance provider while enjoying the flexibility and autonomy of a remote work environment. We are looking for a seasoned professional who can bring a wealth of knowledge and a proactive approach to our underwriting department, ensuring sound risk selection and profitable growth. You will be instrumental in shaping our risk appetite and driving operational excellence from a remote setting.
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Finance Strategy and Analytics Manager

Nairobi, Nairobi KES2000000 - KES2500000 Y Tala

Posted today

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About Tala
Tala is on a mission to unleash the economic power of the Global Majority – the 4 billion people overlooked by existing financial systems. With nearly half a billion dollars raised from equity and debt, we are serving millions of customers across three continents. Tala has been named by the
Fortune
Impact 20 list,
CNBC
's Disruptor 50 five years in a row,
CNBC
's World's Top Fintech Company,
Forbes'
Fintech 50 list for eight years running, and Chief's The New Era of Leadership Award. We are expanding across product offerings, countries and crypto and are looking for people who have an entrepreneurial spirit and are passionate about our m ission.

By creating a unique platform that enables lending and other financial services around the globe, people in emerging markets are able to start and expand small businesses, manage day-to-day needs, and pursue their financial goals with confidence. Currently, over nine million people across Kenya, the Philippines, Mexico, and India have used Tala products. Due to our global team, we have a remote-first approach, and also have offices in Santa Monica, CA (HQ); Nairobi, Kenya; Mexico City, Mexico; Manila, the Philippines; and Bangalore, India.

Most Talazens join us because they connect with our mission. If you are energized by the impact you can make at Tala, we'd love to hear from you

We are seeking a Market Finance Strategy and Analytics Manager who is passionate about developing a deep understanding of the business and utilizing data to inform strategic analysis and operational decision-making. This role will lead financial planning and business forecasting across the KE market, as well as drive key business initiatives within departments.

What You'll Do

  • Understand the key drivers of the local business (e.g. growth, repayment, conversion, unit economics/lifetime value of customer) and collaborate with both Corporate FP&A and local cross-functional teams to articulate market strategy, monitor critical KPIs and support corporate forecasting
  • Support the head of finance in different analyses and perform detailed financial analysis to model out new investments, business cases, and strategic initiatives, identifying the potential risks & opportunities across different scenarios
  • Report on monthly market financial performance and analyze variances to plan/forecast, articulating the impact to the business from both the vertical (revenue/profit) as well as horizontal (unit economics/LTV) perspective
  • Support annual corporate operational planning and reforecasts, including budgeting for headcount, OPEX, and capital allocation
  • Support local CLT in any analytical need and be an advocate of the market
  • Liaise between in-market teams and country leadership to ensure alignment around business and financial objectives;
  • Other ad-hoc projects and analysis
  • Invest in the team - bring your own personality, quirks, and let's have fun while leveling each other and the business up

What You'll Need

  • Bachelor's Degree in Finance, Business, Economics, or other quantitative degree
  • Experience in Finance or Accounting (minimum of 5 years of experience);
  • Strong communication skills with the ability to influence in an unstructured, cross-functional environment
  • Deeply analytical problem-solver. Bonus points for experience with data analytics languages (e.g. SQL, Python) and/or data visualization tools (e.g. Looker, Amplitude, Tableau)
  • Excellent proficiency in Excel

Our vision is to build a new financial ecosystem where everyone can participate on equal footing and access the tools they need to be financially healthy. We strongly believe that inclusion fosters innovation and we're proud to have a diverse global team that represents a multitude of backgrounds, cultures, and experience. We hire talented people regardless of race, religion, color, national origin, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status.

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Senior Quantitative Analyst (Finance)

60100 Embu, Eastern KES950000 Annually WhatJobs

Posted 4 days ago

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full-time
Our client is a leading financial institution seeking a highly analytical and experienced Senior Quantitative Analyst to join their growing remote team. This role is critical in developing and implementing sophisticated financial models, risk management strategies, and trading algorithms. You will leverage your deep understanding of financial markets, econometrics, and statistical modeling to drive data-driven decision-making across the organization. The ideal candidate will possess exceptional quantitative skills, proficiency in programming languages commonly used in finance, and a strong ability to translate complex analytical findings into actionable insights. Responsibilities include researching and developing new quantitative methodologies, validating existing models, performing backtesting and scenario analysis, and contributing to the design of financial products. You will work closely with portfolio managers, traders, and risk officers to provide analytical support and insights. A key aspect of this role involves staying ahead of market trends, regulatory changes, and technological advancements in quantitative finance. Strong communication skills are essential for presenting complex analysis to both technical and non-technical audiences. This is a fully remote position, requiring self-motivation, excellent time management, and the ability to collaborate effectively within a distributed team environment. While the location **Embu, Embu, KE** is provided for context, qualified candidates worldwide are encouraged to apply. You will be a key player in shaping our quantitative strategies and contributing to the firm's success in a challenging and rewarding remote work setting.
Responsibilities:
  • Develop, implement, and validate complex quantitative models for pricing, risk management, and trading strategies.
  • Conduct in-depth statistical analysis and econometrics on large datasets.
  • Design and execute backtesting and simulation frameworks for model performance evaluation.
  • Collaborate with traders and portfolio managers to understand their needs and provide analytical support.
  • Research and identify new quantitative techniques and market opportunities.
  • Monitor and analyze market data, identifying trends and potential risks.
  • Develop and maintain clear, concise documentation for all models and methodologies.
  • Communicate complex analytical results effectively to stakeholders across different departments.
  • Contribute to the development of new financial products and investment strategies.
  • Stay current with advancements in quantitative finance, machine learning, and data science.
Qualifications:
  • Master's or Ph.D. in a quantitative field such as Finance, Economics, Mathematics, Statistics, Physics, or Computer Science.
  • 5+ years of experience in a quantitative finance role.
  • Strong programming skills in languages like Python (NumPy, Pandas, SciPy), R, or C++.
  • Proficiency in financial modeling techniques and statistical analysis.
  • Solid understanding of financial markets, derivatives, and fixed income instruments.
  • Experience with machine learning algorithms applied to finance is a plus.
  • Excellent problem-solving abilities and attention to detail.
  • Strong written and verbal communication skills, with the ability to explain complex concepts clearly.
  • Proven ability to work independently and collaboratively in a remote team environment.
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Director, Clinical Laboratory Operations

Nairobi, Nairobi KES1500000 - KES3000000 Y IAVI

Posted today

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Job Title: Director, Clinical Laboratory Operations

Location: IAVI - Africa: Nairobi, Kenya, Cape Town, South Africa; OR Remote South Africa, considered

Reports to: Senior Director, Clinical Immunology and Lab Operations

IAVI is seeking a Director, Clinical Lab Operations to lead IAVI's lab operations in Africa. The Director will lead logistical, technical, and regulatory aspects of lab services for clinical trials, while driving lab quality, budget management, vendor oversight, often leveraging technology and data analysis optimizing performance. Director will lead strategy to support the development of vaccines and antibodies for HIV, TB, and emerging infectious diseases. Overseeing the implementation of good clinical lab practices (gCLP) across partner clinical research centers (CRCs) ensuring sustained and robust lab quality systems and operations.

Key Responsibilities

Quality Assurance:

  • Development, implementation and monitoring of quality systems for both the internal IAVI Laboratory Operations unit as well as those of site labs selected, including:
  • Ensuring readiness for technical audits
  • Ensure laboratory operations meet regulatory standards and sponsor requirements
  • Oversee preparation of sites for clinical trials and epidemiology studies.
  • Oversee teams monitoring study progress at site laboratories for the duration of the study/trial.

Budget & Vendor Management:

  • Development and management of operational budgets with budget managers and clinical teams based on study needs.
  • Oversee the development of and implementation of associated integrated work plans and budgets, ensuring that the resources are allocated and deployed effectively.
  • Review budgets and timelines ensuring integration with the overall clinical trials program.
  • Identification and assessment of vendors to support Lab Operations.
  • Development and review of scope of work, task orders and contracts for vendors.
  • Management and oversight of procurement and vendor governance for a cost-effective and sustainable lab ecosystem.

Team Leadership:

  • Building and mentoring a high-performing team, fostering leadership development, and implementing succession planning.
  • Review and approval of all laboratory related documents for studies being implemented.
  • Technology & Data:
  • Leading the adoption of digital systems like LIMS (Laboratory Information Management Systems) and other platforms for enhanced efficiency, data analysis, and performance monitoring.

Regulatory Compliance:

  • Ensuring all laboratory activities comply with Good Clinical Laboratory Practice (GCLP) and other accreditations (e.g. ISO and other relevant regulations and guidelines.
  • Cross-Functional Collaboration:
  • Serve in product development project teams as the laboratory lead.
  • Serving as a key point of contact for CROs, clinical sites, and internal teams, influencing and leading clinical operations outcomes.
  • Representing IAVI and its partners in various areas such as presenting project progress, achievements, and lessons learned to donors, and other key stakeholders in meetings and conferences.

Education and Experience:

  • A Ph.D. in Immunology or related field and a minimum of 7 years of relevant independent research experience, either in a university or corporate setting, with experience working on clinical trials is required OR;
  • A minimum of bachelor's degree in life sciences or related field and 10 years' experience in a safety laboratory will also be considered and clinical trials experience in developing countries is required.
  • Experience working in a certified or accredited lab is required (e.g CLIA, ISO, CAP and GCLP).

Qualifications and Skills:

  • Experience managing clinical laboratory research projects and staff to deliver high quality data to meet project goals and deadlines is required.
  • Broad knowledge of clinical medicine, pathology disciplines, basic medical sciences, clinical laboratory sciences, laboratory operations, and quality management systems required.
  • Experience in safety labs analysis and assay validation and verification, as well as assay development and optimization is required.
  • Experience and understanding of ICH GCP, GCLP and other relevant regulatory requirements for clinical trials.
  • Knowledge of and skills in informatics, data analysis, and business management highly preferred.
  • Experience with vaccine clinical trials and assay development is highly preferred.
  • Understanding of and experience with implementation of Good Clinical laboratory Practices in infectious disease clinical trials conduct is required.
  • Strong organizational skills with proven experience in building strong, coherent and efficient teams.
  • Solid reasoning and analytical skills.
  • Experience in working in a decentralized system, and maintaining close working relationships with various departments, contractors, clinical centers and clinical and basic science laboratories.
  • Excellent verbal and written communication skills.
  • Proven ability to present programs to audiences ranging from high level scientists, clinical investigators and physicians, clinical trials execution teams and non-scientists is highly desirable.
  • Experience working in a multicultural environment is required.
  • Willingness to travel at least 20-25% of the time to IAVI regional and head offices required.
  • Passion for the IAVI Mission.

Organizational Overview:

IAVI is a nonprofit scientific research organization dedicated to addressing urgent, unmet global health challenges including HIV and tuberculosis. We develop vaccines and antibodies in and for the developing world and seek to accelerate their introduction in low-income countries. IAVI programs and partnerships are grounded in the regions of the world where the disease burden is the greatest, and our approach emphasizes sustainability. Our network of clinical research center partners in Africa and India helps strengthen in-country research capacity and supports the training and education of the next generation of scientists. IAVI accelerates scientific discovery and development by fostering unique collaborations among academia, industry, local communities, governments, and funders to explore new and better ways to address public health threats that disproportionately affect people living in poverty. Our global reach, including a clinical research network in five countries in sub-Saharan Africa and in India, has allowed us to make fundamental contributions to understanding the epidemiology, transmission, virology, and immunology of HIV. This work played a key role in facilitating the design of promising HIV vaccine candidates, as well as the discovery of broadly neutralizing antibodies that are now being advanced as promising approaches for HIV prevention. Our integrated capabilities in vaccine and antibody discovery, development, and clinical research take advantage of bio-pharmaceutical industry expertise to accelerate the development and testing of prevention methods for HIV and other diseases.

IAVI CORE VALUES:

  • Dedication to the Mission: We are committed to the translation of scientific discoveries into affordable, globally accessible public health solutions.
  • Innovative Evolution: We are committed to solving complex problems in creative and innovative ways, learning from our mistakes and successes and never giving up
  • Integrity: We are committed to meeting the highest ethical and professional standards in everything we do and to taking responsibility for our actions to earn respect
  • Collaboration: We are committed to embracing diversity, the power of global teamwork and the belief that by working as one we can make a difference

Disclaimer: Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be an exhaustive list of all duties, responsibilities and skills required of personnel so classified. This document does not create an employment contract, implied or otherwise, other than an "at-will" relationship. IAVI is an equal opportunity employer and applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

IAVI IS AN EQUAL OPPORTUNITY EMPLOYER actively committed to fostering a diverse and inclusive global organization. IAVI believes that diversity and inclusion among our teammates is critical, and we seek to recruit, develop and retain the most talented people from a representative candidate pool. At IAVI, we celebrate the spectrum of colleagues' experiences and believe that dedication to our mission above all is essential to our success as a scientific global non-profit. IAVI upholds these principles through IAVI's Global Diversity and Inclusion Committee.

Compensation And Benefits Information:

Salary is paid in local currency, and is commensurate and competitive with the local labor market. Please note, there may be some variation based on experience level. In addition, this position offers competitive benefits including: generous retirement savings plan employer contributions; competitive health, dental and vision insurance plans; competitive paid time off policy; potential for annual bonuses based on performance; and other benefits. More information can be found on IAVI's career page.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the
Know Your Rights
notice from the Department of Labor.

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Remote Actuarial Analyst (General Insurance)

00100 Tuwan KES160000 Annually WhatJobs

Posted 22 days ago

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full-time
Our client, a dynamic insurance provider, is actively seeking an accomplished Remote Actuarial Analyst to join their growing team. This position is fully remote, offering the flexibility to work from any location while contributing to critical actuarial functions within the general insurance sector. You will be responsible for developing and validating pricing models, assessing risk, and forecasting financial outcomes. This role requires a strong foundation in actuarial science, excellent analytical and quantitative skills, and proficiency in relevant software. The ideal candidate will possess a keen eye for detail, a commitment to accuracy, and the ability to communicate complex actuarial concepts effectively.

Responsibilities:
  • Develop, implement, and maintain pricing models for various general insurance products.
  • Analyze historical claims data to assess trends, identify patterns, and forecast future loss costs.
  • Perform reserving analyses to ensure adequate financial provisions for outstanding claims.
  • Conduct profitability studies and provide insights into product performance.
  • Support the development and implementation of risk management strategies.
  • Collaborate with underwriting, claims, and product development teams to provide actuarial support and guidance.
  • Assist in the preparation of regulatory filings and reporting requirements.
  • Utilize actuarial software and programming languages (e.g., R, Python, SQL, SAS) for data analysis and modeling.
  • Stay updated on industry best practices, regulatory changes, and emerging actuarial techniques.
  • Mentor junior actuarial staff and contribute to the overall development of the actuarial function.
Qualifications:
  • Bachelor's degree in Actuarial Science, Mathematics, Statistics, or a related quantitative field.
  • Minimum of 3 years of actuarial experience, with a focus on general insurance.
  • Progress towards actuarial certifications (e.g., ACAS, FCAS, FIA) is highly desirable.
  • Proficiency in actuarial modeling software and programming languages such as R, Python, SQL, or SAS.
  • Strong understanding of insurance principles, product lines, and regulatory requirements.
  • Excellent analytical, problem-solving, and quantitative skills.
  • Ability to interpret complex data and translate it into actionable insights.
  • Strong written and verbal communication skills, with the ability to explain technical concepts to non-technical audiences.
  • Proven ability to work independently and manage projects effectively in a remote environment.
  • High level of accuracy and attention to detail.
This is a remote position, offering the opportunity to work from anywhere while supporting our client's operations in Eldoret, Uasin Gishu, KE . If you are a dedicated actuary looking for a challenging and rewarding remote role, we encourage you to apply.
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  50. local_hospital Military & Public Safety
  51. local_hospital Mining
  52. medical_services Nursing
  53. local_gas_station Oil & Gas
  54. biotech Pharmaceutical
  55. checklist_rtl Project Management
  56. shopping_bag Purchasing
  57. home_work Real Estate
  58. person_search Recruitment Consultancy
  59. store Retail
  60. point_of_sale Sales
  61. science Scientific Research & Development
  62. wifi Telecoms
  63. psychology Therapy
  64. pets Veterinary
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