3,129 Research Associate jobs in Kenya
Clinical Research Associate
10100 Nyeri Town
KES80000 Annually
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Job Description
Our client, a leading pharmaceutical research organization, is seeking a dedicated and experienced Clinical Research Associate to join their team in Nyeri, Nyeri, KE . This role involves overseeing and managing clinical trials to ensure adherence to protocols, regulatory requirements, and ethical standards. You will be responsible for site selection, initiation, monitoring, and close-out activities. This hybrid position requires a balance of on-site visits to research facilities and remote work for data analysis and reporting. The ideal candidate will possess a strong understanding of clinical trial phases, Good Clinical Practice (GCP) guidelines, and regulatory affairs. Excellent organizational skills, attention to detail, and the ability to communicate effectively with investigators, site staff, and internal stakeholders are crucial. You will play a vital role in the successful execution of clinical studies, contributing to the development of new and innovative pharmaceutical products. Responsibilities include monitoring patient recruitment, ensuring data integrity, managing study documentation, and addressing any issues that arise during the trial.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct site visits to assess trial progress, compliance, and patient safety.
- Ensure adherence to study protocols, SOPs, and GCP guidelines.
- Monitor data accuracy and completeness, and resolve data queries.
- Manage study-related documentation and regulatory binders.
- Facilitate communication between the study sponsor, investigators, and site personnel.
- Oversee patient recruitment and retention efforts.
- Identify and report adverse events and deviations from the protocol.
- Prepare site monitoring reports and track action items.
- Participate in study initiation and close-out visits.
- Contribute to the overall success of clinical research projects.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with various therapeutic areas is a plus.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent communication, interpersonal, and problem-solving skills.
- Ability to travel to research sites as required for monitoring activities.
- Strong organizational skills and ability to manage multiple tasks effectively.
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0
Clinical Research Associate
20200 Kapsuser
KES250000 Annually
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Our client, a leading pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their team. This hybrid role offers a blend of remote flexibility and in-office collaboration, based in **Kericho, Kericho, KE**. The CRA plays a crucial role in ensuring the successful execution of clinical trials, upholding the highest standards of data integrity, patient safety, and regulatory compliance. Your primary responsibilities will include site selection, initiation, monitoring, and close-out of clinical trial sites. You will build and maintain strong relationships with investigators and site staff, providing them with the necessary guidance and support to conduct trials according to protocol and Good Clinical Practice (GCP) guidelines. This involves regular site visits (both in-person and remotely) to review study documentation, verify data accuracy, ensure protocol adherence, and address any issues that may arise. The ideal candidate will possess excellent organizational skills, a strong understanding of clinical trial processes, and the ability to effectively communicate with diverse stakeholders. You must be adept at problem-solving, proactive in identifying potential risks, and committed to ensuring the ethical and scientific integrity of the research conducted.
Responsibilities:
Responsibilities:
- Perform site qualification, initiation, interim, and close-out visits.
- Monitor clinical trial activities at assigned sites to ensure compliance with protocol, SOPs, and GCP.
- Verify accuracy and completeness of clinical data through source data verification (SDV).
- Ensure patient safety and rights are protected throughout the trial.
- Train and guide site staff on study procedures and regulatory requirements.
- Manage investigational product accountability and reconciliation.
- Communicate effectively with study teams, investigators, and regulatory authorities.
- Prepare monitoring reports and follow up on action items.
- Contribute to the development of study-related documents as needed.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical research role.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven experience in monitoring clinical trials across various therapeutic areas.
- Excellent written and verbal communication skills.
- Strong organizational, time management, and problem-solving abilities.
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Ability to travel to sites as required and work effectively in a hybrid model.
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1
Clinical Research Associate
01000 Mangu
KES380000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is looking for a dedicated Clinical Research Associate (CRA) to join their growing team in **Machakos, Machakos, KE**. This hybrid role offers a unique opportunity to contribute to groundbreaking drug development while maintaining a flexible work-life balance. The CRA will be responsible for monitoring clinical trials to ensure compliance with protocols, government regulations, and Good Clinical Practice (GCP) guidelines. You will play a crucial role in safeguarding the integrity of trial data and ensuring the safety and well-being of study participants.
Primary responsibilities include site initiation visits, routine monitoring visits, and close-out visits; verifying the accuracy, completeness, and source documentation of clinical data; ensuring compliance with study protocols and regulatory requirements; identifying and resolving site issues; providing training and support to clinical site staff; and preparing monitoring reports. The ideal candidate will possess a strong understanding of clinical trial processes, regulatory affairs, and medical terminology. Excellent communication, organizational, and interpersonal skills are essential. You must be able to travel to clinical sites as needed, with flexibility for remote work when appropriate. A Bachelor's degree in a life science, nursing, or related field is required. Previous experience as a CRA or in a similar clinical research role is highly preferred. We are committed to fostering an environment where scientific advancement and employee well-being go hand in hand. If you are passionate about making a difference in patient lives and possess the meticulous attention to detail required for clinical research, we encourage you to apply.
Primary responsibilities include site initiation visits, routine monitoring visits, and close-out visits; verifying the accuracy, completeness, and source documentation of clinical data; ensuring compliance with study protocols and regulatory requirements; identifying and resolving site issues; providing training and support to clinical site staff; and preparing monitoring reports. The ideal candidate will possess a strong understanding of clinical trial processes, regulatory affairs, and medical terminology. Excellent communication, organizational, and interpersonal skills are essential. You must be able to travel to clinical sites as needed, with flexibility for remote work when appropriate. A Bachelor's degree in a life science, nursing, or related field is required. Previous experience as a CRA or in a similar clinical research role is highly preferred. We are committed to fostering an environment where scientific advancement and employee well-being go hand in hand. If you are passionate about making a difference in patient lives and possess the meticulous attention to detail required for clinical research, we encourage you to apply.
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2
Clinical Research Associate
01100 Ngong
KES190000 Monthly
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Posted 3 days ago
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Job Description
Our client is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join their pharmaceutical team. This role plays a crucial part in ensuring the integrity and quality of clinical trials, contributing to the development of life-saving medications. As a CRA, you will be responsible for monitoring clinical trial sites to ensure compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your duties will include site initiation visits, interim monitoring visits, and close-out visits. You will review patient records, assess data accuracy, and ensure proper documentation is maintained. Building and maintaining strong relationships with investigators and site staff is paramount to facilitate the smooth running of trials. You will identify and report adverse events, troubleshoot site issues, and provide training and support to clinical site personnel. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with significant experience as a CRA or in a similar clinical research role. Strong knowledge of GCP, ICH guidelines, and regulatory requirements is essential. Excellent organizational, communication, and problem-solving skills are required. The ability to travel to sites as needed is also a key requirement for this role. This position offers a **hybrid** work model, allowing for a combination of remote work and on-site visits to trial locations. Our client is committed to professional development and offers opportunities for career growth within the pharmaceutical industry. This is an excellent opportunity to contribute to groundbreaking medical research and patient care.
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3
Clinical Research Associate
60200 Meru , Eastern
KES150000 Annually
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Posted 5 days ago
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Job Description
Our client, a leading pharmaceutical company, is looking for a dedicated and meticulous Clinical Research Associate to oversee clinical trials. This hybrid role offers a balance between remote work and on-site responsibilities in Meru, Meru, KE . The ideal candidate will possess a strong background in scientific research, regulatory compliance, and project management within the pharmaceutical sector. Key responsibilities include site selection and initiation, monitoring trial progress, ensuring data accuracy and integrity, and verifying that trials are conducted in accordance with Good Clinical Practice (GCP) guidelines and relevant protocols. You will be responsible for managing relationships with investigators, site staff, and other stakeholders, providing training on study procedures, and resolving any issues that may arise during the trial. This role involves extensive data review, source document verification, and the preparation of monitoring visit reports. You will also play a crucial role in the submission of regulatory documents and ensuring the safety of study participants. Qualifications require a Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, or a related discipline. A minimum of 3 years of experience as a Clinical Research Associate or in a similar role within the pharmaceutical industry is essential. In-depth knowledge of clinical trial phases, drug development processes, and regulatory requirements (e.g., ICH-GCP) is mandatory. Strong analytical and problem-solving skills, attention to detail, excellent organizational and communication abilities are highly valued. The ability to travel to clinical sites as needed for monitoring visits and audits is also a requirement. This is an excellent opportunity for a motivated professional to contribute to groundbreaking medical advancements.
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4
Clinical Research Associate
60100 Embu, Eastern
KES115000 Annually
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Posted 7 days ago
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Job Description
Our client is seeking a detail-oriented and motivated Clinical Research Associate to join their growing pharmaceutical team. This role offers a hybrid work arrangement, balancing remote responsibilities with necessary on-site activities. You will be instrumental in supporting the planning, execution, and monitoring of clinical trials, ensuring compliance with regulatory standards and protocols. Your responsibilities include site initiation visits, regular monitoring of study sites to ensure data accuracy and integrity, and managing investigational product. You will also be involved in data collection, source document verification, and reporting adverse events. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with prior experience in clinical research. Strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements is essential. Excellent organizational, analytical, and problem-solving skills are crucial for managing multiple study sites and complex data. You must possess strong interpersonal and communication skills to effectively interact with investigators, site staff, and internal teams. Proficiency with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is required. This hybrid role demands flexibility, adaptability, and the ability to work independently while also collaborating effectively within a team. You will play a vital role in bringing new therapies to patients, contributing to meaningful advancements in healthcare. This position requires travel to study sites, balanced with significant remote work capabilities.
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5
Graduate Research Associate
80101 Nairobi, Nairobi
KES30000 Monthly
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Posted 7 days ago
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Our client, a renowned research institution at the forefront of scientific discovery, is offering an exciting Graduate Research Associate opportunity to bright and ambitious individuals. This is a fully remote internship, providing invaluable hands-on experience in a dynamic research environment without the need for physical relocation. The Graduate Research Associate will support senior researchers in ongoing projects across various disciplines, contributing to data collection, analysis, and literature reviews. Key responsibilities include assisting with experimental design and execution, preparing research materials, documenting findings, and contributing to research reports and presentations. The ideal candidate is currently pursuing or has recently completed a Bachelor's or Master's degree in a relevant scientific or technical field (e.g., Biology, Chemistry, Computer Science, Physics, Engineering, Mathematics). Strong analytical and critical thinking skills are essential, along with a keen interest in conducting research. Proficiency in basic statistical analysis and common research methodologies is expected. As this is a remote role, excellent organizational skills, self-motivation, and the ability to work independently are crucial. Effective communication skills, both written and verbal, are necessary for collaborating with the research team and documenting progress. Familiarity with research software and data management tools is a plus. This internship offers a unique chance to gain practical research experience, develop new skills, and contribute meaningfully to scientific advancement. We are looking for enthusiastic individuals eager to learn and contribute. This program is based conceptually in **Mombasa, Mombasa, KE**, but the role is entirely remote, allowing interns from across the country to participate.
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6
Clinical Research Associate
00200 Ngong
KES400000 Annually
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Posted 7 days ago
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Our client, a leading pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) for a fully remote position. This role is pivotal in ensuring the successful execution of clinical trials, adhering strictly to protocol and regulatory guidelines. As a remote CRA, you will be responsible for site monitoring, data verification, and ensuring the safety and rights of study participants. Your responsibilities will include conducting pre-study, initiation, routine, and close-out monitoring visits (often remotely, with occasional on-site requirements), verifying source data against case report forms, and ensuring compliance with Good Clinical Practice (GCP) and applicable regulations. You will serve as the primary point of contact for study sites, providing essential support and guidance to investigators and study staff. Strong communication and interpersonal skills are crucial for building and maintaining positive relationships with research sites. You will also manage trial-related documentation, track study progress, and report findings to the clinical trial manager. The ideal candidate will possess a strong understanding of clinical trial processes, drug development, and regulatory requirements within the pharmaceutical industry. A Bachelor's degree in a life science or healthcare-related field is required, along with demonstrable experience as a CRA. This exciting remote opportunity is ideal for professionals looking to contribute to groundbreaking research in the pharmaceutical sector, impacting healthcare advancements relevant to **Ruiru, Kiambu, KE**.
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7
Clinical Research Associate
50200 Tuwan
KES140000 Annually
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Posted 7 days ago
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Job Description
Our client, a global leader in pharmaceutical research and development, is looking for a dedicated and meticulous Clinical Research Associate (CRA) to join their fully remote clinical operations team. This is an exceptional opportunity for an experienced CRA to contribute to vital clinical trials from anywhere in Kenya, enhancing patient care and advancing medical science. You will be responsible for monitoring clinical trial sites, ensuring adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Key responsibilities include site initiation, monitoring, and close-out visits, data collection and review, adverse event reporting, and maintaining accurate trial documentation. You will serve as the primary point of contact between study sites and the sponsor, ensuring effective communication and issue resolution. This is a fully remote role, requiring extensive travel to clinical sites as needed, with the ability to manage your schedule and administrative tasks remotely. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with a minimum of 3 years of experience as a Clinical Research Associate. A thorough understanding of clinical trial processes, ICH-GCP guidelines, and regulatory requirements is essential. Proven experience in site monitoring, data management, and regulatory compliance is required. Excellent communication, interpersonal, and organizational skills are paramount for building strong relationships with investigators, site staff, and internal teams. You must be adept at problem-solving, critical thinking, and maintaining meticulous records. The ability to work independently, manage multiple study sites, and travel frequently (as required by specific trials) is crucial. Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems is highly desirable. Join our client's mission-driven team and play a vital role in bringing life-changing therapies to patients, operating remotely while supporting trials that may involve sites near **Bungoma, Bungoma, KE**.
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8
Clinical Research Associate
30100 Tuwan
KES250000 Annually
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Posted 11 days ago
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Job Description
Our client is seeking a highly skilled and meticulous Clinical Research Associate to join their fully remote global research team. This role is vital for the successful execution of clinical trials, ensuring compliance with protocols, regulatory requirements, and ethical standards. You will be responsible for monitoring clinical trial sites, verifying data accuracy, and managing study documentation. This is a remote-first position, requiring exceptional organizational skills and the ability to conduct site visits as needed, while primarily managing responsibilities from a distance. You will collaborate closely with investigators, study coordinators, and internal stakeholders to ensure the integrity and quality of research data. Key responsibilities include:
The ideal candidate will hold a Bachelor's degree in a life science, nursing, or a related discipline. A Master's degree is a plus. A minimum of 3-5 years of experience as a Clinical Research Associate (CRA) or in a similar clinical trial monitoring role is required. Thorough knowledge of ICH-GCP guidelines and regulatory requirements (e.g., FDA, EMA) is essential. Experience with various clinical trial phases and therapeutic areas is highly desirable. Strong analytical and problem-solving skills, excellent organizational abilities, and exceptional attention to detail are critical for this role. Outstanding written and verbal communication skills, along with the ability to work independently and manage a remote workload effectively, are paramount. This is an exceptional opportunity to contribute to groundbreaking pharmaceutical research on a global scale.
- Monitoring assigned clinical trial sites to ensure compliance with protocols, SOPs, and Good Clinical Practice (GCP) guidelines.
- Verifying the accuracy, completeness, and integrity of clinical trial data through source data verification.
- Ensuring timely collection of all necessary study documents from study sites.
- Building and maintaining strong working relationships with investigators and site staff.
- Managing communication between clinical trial sites and the sponsor/CRO.
- Identifying, documenting, and resolving any site-level issues or deviations.
- Conducting pre-study visits, initiation visits, interim monitoring visits, and close-out visits.
- Ensuring all regulatory requirements are met and documented at the study sites.
- Providing training and ongoing support to clinical trial site personnel.
- Coordinating with the clinical operations team on study progress and site performance.
- Maintaining accurate and up-to-date study site files and databases.
- Contributing to the development and review of clinical trial protocols and other study documents.
The ideal candidate will hold a Bachelor's degree in a life science, nursing, or a related discipline. A Master's degree is a plus. A minimum of 3-5 years of experience as a Clinical Research Associate (CRA) or in a similar clinical trial monitoring role is required. Thorough knowledge of ICH-GCP guidelines and regulatory requirements (e.g., FDA, EMA) is essential. Experience with various clinical trial phases and therapeutic areas is highly desirable. Strong analytical and problem-solving skills, excellent organizational abilities, and exceptional attention to detail are critical for this role. Outstanding written and verbal communication skills, along with the ability to work independently and manage a remote workload effectively, are paramount. This is an exceptional opportunity to contribute to groundbreaking pharmaceutical research on a global scale.
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