Explore 15 Clinical Research Associate Cra jobs in whatjobs
Clinical Research Associate (CRA)
Posted 20 days ago
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Job Description
Our client, a cutting-edge pharmaceutical company, is seeking a diligent and experienced Clinical Research Associate (CRA) to join their team. This role involves significant remote work with occasional travel required to clinical sites. As a CRA, you will play a crucial role in ensuring the smooth execution of clinical trials, upholding the highest standards of data integrity and patient safety. Your primary responsibilities will include monitoring clinical trial sites, verifying data accuracy, ensuring adherence to protocols and regulatory requirements (e.g., GCP, FDA), and managing site staff. You will conduct pre-study, initiation, interim, and close-out visits, providing essential support to investigators and study coordinators. The ideal candidate possesses a Bachelor's degree in a life science, nursing, or a related field; a Master's degree or higher is advantageous. A minimum of 3 years of experience as a CRA in the pharmaceutical or biotech industry is required, with a proven track record of successful trial management. Strong knowledge of clinical trial processes, regulatory guidelines, and medical terminology is essential. Excellent organizational, time management, and communication skills are critical for managing multiple sites and collaborating effectively with cross-functional teams, both in person and remotely. The ability to travel occasionally to designated clinical trial sites is a requirement for this hybrid role. Our client is committed to advancing medical treatments and offers a stimulating work environment with opportunities for professional growth. Join a dedicated team focused on bringing life-changing therapies to patients.
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Clinical Research Associate (CRA)
Posted 20 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their team. This role is essential for ensuring the integrity and quality of clinical trials, from site initiation to study closure. The ideal candidate will have a strong background in clinical research, a thorough understanding of Good Clinical Practice (GCP) guidelines, and regulatory requirements. Responsibilities include selecting, training, and monitoring clinical trial sites, ensuring accurate data collection, and maintaining trial documentation. You will be responsible for conducting site visits, evaluating the quality and accuracy of data, and ensuring compliance with study protocols and regulatory standards. The successful candidate will possess excellent analytical and problem-solving skills, strong organizational abilities, and exceptional attention to detail. Communication and interpersonal skills are crucial for effectively interacting with investigators, site staff, and internal teams. This position requires a proactive approach to identifying and resolving site issues and ensuring patient safety. We are seeking an individual who is committed to upholding the highest ethical standards in clinical research. The role is based in **Kisumu, Kisumu, KE**, and requires regular site visits and potential travel within the region. If you are a qualified CRA with a passion for advancing pharmaceutical research and development, we encourage you to apply for this critical role.
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Clinical Research Associate (CRA)
Posted 22 days ago
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Job Description
Our client, a progressive pharmaceutical company dedicated to improving global health outcomes, is looking for a diligent and motivated Clinical Research Associate (CRA) to join their team in Kitale, Trans-Nzoia, KE . This role offers a hybrid work arrangement, providing a balance between in-office collaboration and remote flexibility. As a CRA, you will play a crucial role in ensuring the smooth and compliant execution of clinical trials, adhering to strict Good Clinical Practice (GCP) guidelines and regulatory requirements. You will be responsible for monitoring clinical trial sites, verifying data accuracy, and ensuring the safety and rights of study participants. This position requires a meticulous approach to detail, strong organizational skills, and the ability to build effective relationships with investigators and site staff. You will travel to various research sites to conduct site visits, including pre-study, initiation, routine monitoring, and close-out visits. Your primary objective will be to ensure that trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and applicable regulatory requirements. This involves reviewing essential documents, checking source data against case report forms (CRFs), and verifying drug accountability. You will also be responsible for identifying and resolving issues at the study sites, training site personnel on study procedures, and ensuring timely submission of all required documentation. The ideal candidate will have a solid understanding of clinical trial processes, therapeutic areas, and regulatory landscapes. Excellent communication and problem-solving skills are paramount, as is the ability to manage multiple priorities effectively. We are seeking individuals who are passionate about advancing medical science and are committed to ethical research practices. The hybrid nature of this role means you'll spend a significant portion of your time working remotely, managing your schedule and tasks, with periodic requirements to be present at our regional office or designated research sites. This is an excellent opportunity for an experienced CRA looking to contribute to impactful pharmaceutical research.
Key Responsibilities:
Key Responsibilities:
- Conduct site visits (remote and on-site) to assess protocol and regulatory compliance.
- Monitor study conduct, data accuracy, and participant safety at assigned clinical trial sites.
- Verify source documentation and ensure its accuracy and completeness against Case Report Forms (CRFs).
- Manage essential trial documents and maintain regulatory files.
- Train and support site staff on study protocols, SOPs, and regulatory requirements.
- Identify, resolve, and escalate site-level issues in a timely manner.
- Ensure compliance with GCP, FDA regulations, and other applicable guidelines.
- Prepare visit reports and follow-up letters promptly.
- Collaborate effectively with internal teams, including project managers, medical monitors, and data management.
- Contribute to the development and review of study-related documents.
- Bachelor's degree in a life science, nursing, or a related field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- Thorough understanding of GCP, ICH guidelines, and clinical trial processes.
- Experience with electronic data capture (EDC) systems.
- Strong knowledge of drug development and regulatory affairs.
- Excellent organizational, time management, and problem-solving skills.
- Proficiency in English, with strong written and verbal communication abilities.
- Ability to travel to clinical sites as required.
- Demonstrated ability to work independently and as part of a hybrid team.
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Clinical Research Associate (CRA)
Posted 8 days ago
Job Viewed
Job Description
A dynamic pharmaceutical company is seeking a diligent and detail-oriented Clinical Research Associate (CRA) to join their expanding clinical operations team in Ruiru, Kiambu, KE . This is a field-based position, requiring regular site visits and a commitment to ensuring the integrity and quality of clinical trial data. The CRA plays a vital role in the successful execution of clinical studies, ensuring compliance with protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements.
Your responsibilities will include initiating, monitoring, and closing clinical study sites. You will be responsible for verifying the accuracy and completeness of study data, ensuring proper investigational product accountability, and maintaining essential regulatory documentation. Building and maintaining strong relationships with investigators, site staff, and study sponsors is crucial. The ideal candidate will have a strong understanding of clinical trial processes, regulatory guidelines, and medical terminology. Excellent organizational, communication, and interpersonal skills are essential for managing multiple sites and effectively interacting with diverse stakeholders.
Key duties involve performing site qualification visits, pre-study visits, initiation visits, routine monitoring visits, and close-out visits. You will also be responsible for resolving data queries, identifying and addressing protocol deviations, and ensuring timely reporting of adverse events. A bachelor's degree in a life science, nursing, or a related healthcare field is typically required, along with significant experience as a CRA or in a similar clinical research role. The ability to travel frequently to assigned clinical sites is a mandatory requirement for this position. If you are passionate about advancing medical research and ensuring patient safety, this Clinical Research Associate role offers a challenging and rewarding career opportunity.
Your responsibilities will include initiating, monitoring, and closing clinical study sites. You will be responsible for verifying the accuracy and completeness of study data, ensuring proper investigational product accountability, and maintaining essential regulatory documentation. Building and maintaining strong relationships with investigators, site staff, and study sponsors is crucial. The ideal candidate will have a strong understanding of clinical trial processes, regulatory guidelines, and medical terminology. Excellent organizational, communication, and interpersonal skills are essential for managing multiple sites and effectively interacting with diverse stakeholders.
Key duties involve performing site qualification visits, pre-study visits, initiation visits, routine monitoring visits, and close-out visits. You will also be responsible for resolving data queries, identifying and addressing protocol deviations, and ensuring timely reporting of adverse events. A bachelor's degree in a life science, nursing, or a related healthcare field is typically required, along with significant experience as a CRA or in a similar clinical research role. The ability to travel frequently to assigned clinical sites is a mandatory requirement for this position. If you are passionate about advancing medical research and ensuring patient safety, this Clinical Research Associate role offers a challenging and rewarding career opportunity.
This advertiser has chosen not to accept applicants from your region.
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Clinical Research Associate (CRA)
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their team in Nyeri, Nyeri, KE . This hybrid role involves a combination of on-site monitoring and remote data management, ensuring the integrity and quality of clinical trials. The CRA will be responsible for site selection, initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements. You will verify the accuracy and completeness of clinical data, manage investigational product, and serve as the primary liaison between the investigative sites and the sponsor. Key responsibilities include developing and executing monitoring plans, identifying and resolving site-level issues, reporting trial progress, and ensuring timely data collection. The ideal candidate will possess a strong understanding of clinical trial processes, regulatory affairs, and pharmaceutical development. Excellent organizational, communication, and interpersonal skills are essential for building and maintaining strong relationships with investigators and site staff. A bachelor's degree in a life science, nursing, or a related field is required, along with proven CRA experience. The ability to travel to clinical sites as needed is also a requirement. This is an exciting opportunity to contribute to the development of life-saving medications and advance your career in a dynamic and challenging field. You will work with a dedicated team committed to ethical research and patient well-being.
This advertiser has chosen not to accept applicants from your region.
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Clinical Research Associate (CRA)
Posted 13 days ago
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Job Description
Our client, a prominent pharmaceutical company, is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their expanding team. This is a fully remote position, allowing you to contribute to groundbreaking research from anywhere in Kenya. The CRA will be responsible for monitoring clinical trials, ensuring compliance with protocols and regulatory standards, and verifying the accuracy and integrity of clinical data. You will play a vital role in bringing life-saving treatments to patients.
Responsibilities:
Qualifications:
This is an excellent opportunity for a skilled CRA to contribute to critical pharmaceutical research remotely, supporting studies relevant to **Naivasha, Nakuru, KE**, and global health initiatives. Our client is committed to scientific advancement and employee development.
Responsibilities:
- Monitor clinical trial sites to ensure compliance with Good Clinical Practice (GCP) guidelines, study protocols, and regulatory requirements.
- Verify the accuracy, completeness, and integrity of clinical trial data through source data verification (SDV).
- Manage and mentor investigative sites, serving as the primary point of contact for study-related matters.
- Conduct site initiation visits (SIVs), interim monitoring visits (IMVs), and close-out visits (COVs).
- Ensure proper drug accountability and storage at trial sites.
- Review and track regulatory documentation from investigational sites.
- Report and resolve any discrepancies or issues identified during monitoring activities.
- Collaborate with study teams, investigators, and site staff to ensure patient safety and data quality.
- Prepare monitoring visit reports and ensure timely submission of all required documentation.
- Participate in investigator meetings and training sessions.
- Stay current with therapeutic area knowledge and clinical research methodologies.
- Contribute to the development and review of study-related documents, such as protocols and informed consent forms.
Qualifications:
- 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 related clinical research role.
- In-depth knowledge of GCP, FDA regulations, and other relevant regulatory guidelines.
- Proven experience in site monitoring, data verification, and regulatory compliance.
- Strong understanding of clinical trial processes and documentation.
- Excellent analytical and problem-solving skills.
- Exceptional organizational skills and attention to detail.
- Strong written and verbal communication skills.
- Ability to work independently, manage time effectively, and travel as required (though this role is remote, site visits may be necessary periodically).
- Proficiency with clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- A valid driver's license and willingness to travel are advantageous.
This is an excellent opportunity for a skilled CRA to contribute to critical pharmaceutical research remotely, supporting studies relevant to **Naivasha, Nakuru, KE**, and global health initiatives. Our client is committed to scientific advancement and employee development.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate (CRA)
Posted 8 days ago
Job Viewed
Job Description
Our client is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join our fully remote clinical operations team. As a CRA, you will play a pivotal role in ensuring the quality, integrity, and compliance of clinical trials conducted according to Good Clinical Practice (GCP) guidelines and regulatory requirements. You will be responsible for site monitoring, data verification, and ensuring patient safety throughout the trial lifecycle. This position requires a strong understanding of clinical trial processes, excellent organizational skills, and the ability to build effective relationships with investigative sites.
Responsibilities:
Responsibilities:
- Conduct site initiation, monitoring, and close-out visits to ensure protocol compliance and data accuracy.
- Verify the accuracy, completeness, and integrity of clinical trial data through source document verification.
- Ensure adherence to regulatory requirements, Standard Operating Procedures (SOPs), and protocol guidelines.
- Monitor patient safety and report adverse events promptly.
- Build and maintain positive working relationships with investigators, site staff, and study sponsors.
- Provide training and support to site personnel on trial procedures and requirements.
- Manage study supplies and drug accountability at clinical sites.
- Resolve site-level issues and discrepancies in a timely and efficient manner.
- Prepare detailed monitoring visit reports and follow up on action items.
- Contribute to the development of study-related documents, such as protocols and case report forms (CRFs).
- Ensure all trial-related documentation is maintained in compliance with regulatory standards.
- Actively participate in investigator meetings and teleconferences.
- Identify potential risks and implement mitigation strategies at the site level.
- Bachelor's degree in a life science, nursing, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate (CRA) or in a similar clinical trial monitoring role.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with various therapeutic areas is advantageous.
- Proficiency in EDC (Electronic Data Capture) systems and CTMS (Clinical Trial Management Systems).
- Excellent attention to detail and organizational skills.
- Strong written and verbal communication abilities.
- Ability to work independently, manage time effectively, and travel occasionally if required by specific project needs (though the role is predominantly remote).
- Problem-solving skills and the ability to handle challenging situations professionally.
- Proactive approach to identifying and addressing potential issues.
- Commitment to patient safety and data integrity.
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Clinical Research Associate (CRA)
Posted 11 days ago
Job Viewed
Job Description
Our client is seeking a diligent and experienced Clinical Research Associate (CRA) to join their growing pharmaceutical team. This role offers a hybrid work arrangement, combining remote flexibility with occasional site visits. As a CRA, you will be instrumental in ensuring the quality and integrity of clinical trials by monitoring study sites, verifying data accuracy, and ensuring compliance with protocols, FDA regulations, and Good Clinical Practice (GCP) guidelines. You will be responsible for site selection, initiation, monitoring, and close-out visits. Your role involves meticulous record-keeping, communication with investigators and study staff, and problem-solving to ensure the smooth progression of clinical studies. The ideal candidate possesses a strong understanding of clinical trial processes, excellent attention to detail, and robust communication skills.
Key Responsibilities:
Key Responsibilities:
- Conduct pre-study, initiation, routine monitoring, and close-out visits for clinical trial sites.
- Verify the accuracy and completeness of study data by reviewing source documents and case report forms (CRFs).
- Ensure adherence to study protocols, Standard Operating Procedures (SOPs), and regulatory requirements (e.g., FDA, ICH-GCP).
- Train site personnel on study procedures, protocol requirements, and regulatory compliance.
- Monitor study drug accountability and investigate discrepancies.
- Identify and report potential risks and issues to the study team and implement corrective actions.
- Serve as the primary liaison between the sponsor and the clinical sites.
- Prepare comprehensive monitoring visit reports and follow up on action items.
- Ensure timely submission of essential study documents.
- Maintain confidentiality and security of all study-related information.
- Participate in Investigator Meetings and other study-related training sessions.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or equivalent role in the pharmaceutical industry.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with various therapeutic areas is a plus.
- Strong understanding of clinical trial processes and documentation.
- Excellent organizational, time management, and problem-solving skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong written and verbal communication skills.
- Ability to travel to study sites as required for monitoring visits.
- Detail-oriented and able to work independently within a hybrid work structure.
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Associate (CRA)
Posted 8 days ago
Job Viewed
Job Description
Our client, a global pharmaceutical company at the forefront of medical innovation, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their expanding, fully remote clinical operations team. This role is crucial in ensuring the successful execution of clinical trials, maintaining data integrity, and adhering to regulatory standards. As a CRA, you will play a key part in bringing life-changing therapies to patients worldwide.
Responsibilities:
This position is based within the **Ruiru, Kiambu, KE** region but offers the flexibility of being a fully remote role, allowing for a global talent pool. The ideal candidate will possess a strong understanding of clinical trial processes, excellent organizational skills, and the ability to work independently and manage multiple priorities. A Bachelor's degree in a life science, nursing, or a related field is required, along with significant experience as a CRA. Our client is committed to advancing healthcare and seeks individuals passionate about making a difference. Proficiency in clinical trial management systems and data management software is essential.
Responsibilities:
- Conduct site initiation, monitoring, and close-out visits for clinical trials in accordance with protocol, GCP, and regulatory requirements.
- Ensure accurate, complete, and timely collection of clinical data.
- Verify the safety and rights of study subjects.
- Train and support study site personnel.
- Resolve data queries and ensure adherence to study protocols.
- Prepare monitoring reports and maintain study documentation.
- Communicate effectively with investigators, site staff, and internal project teams.
- Identify and report adverse events and safety concerns.
- Stay updated on ICH-GCP guidelines and relevant regulations.
This position is based within the **Ruiru, Kiambu, KE** region but offers the flexibility of being a fully remote role, allowing for a global talent pool. The ideal candidate will possess a strong understanding of clinical trial processes, excellent organizational skills, and the ability to work independently and manage multiple priorities. A Bachelor's degree in a life science, nursing, or a related field is required, along with significant experience as a CRA. Our client is committed to advancing healthcare and seeks individuals passionate about making a difference. Proficiency in clinical trial management systems and data management software is essential.
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Associate (CRA)
Posted 21 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical research organization, is seeking a highly qualified and experienced Clinical Research Associate (CRA) to join their dedicated, fully remote team. This critical role involves overseeing clinical trials, ensuring compliance with study protocols, and maintaining the integrity of data collected. You will be responsible for site selection, initiation, monitoring, and close-out visits to clinical trial sites, as well as ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements. The ideal candidate will possess a strong scientific background, meticulous attention to detail, and excellent communication and interpersonal skills. You will build and maintain effective relationships with investigators, study coordinators, and other site personnel. Your responsibilities will include reviewing and verifying source documents, monitoring patient safety, and ensuring timely reporting of adverse events. The ability to interpret complex clinical trial protocols and regulatory documents is essential. This position requires a proactive approach to problem-solving and a commitment to maintaining the highest ethical standards in clinical research. Proficiency in clinical trial management software and electronic data capture systems is highly desirable. This is an excellent opportunity for a seasoned CRA to contribute to life-saving research in a flexible, remote work environment. You will play a pivotal role in the successful execution of clinical studies and the advancement of new therapeutic options. Thorough understanding of drug development processes and regulatory affairs is a must.
Key Responsibilities:
Key Responsibilities:
- Conduct site visits for initiation, monitoring, and close-out of clinical trials.
- Ensure compliance with study protocols, SOPs, and regulatory requirements (e.g., GCP).
- Monitor patient safety and data accuracy at clinical trial sites.
- Review and verify source documentation and case report forms (CRFs).
- Manage communication and relationships with investigators and site staff.
- Identify and resolve site-level issues and deviations.
- Ensure timely reporting of study progress and any significant findings.
- Assist in the preparation of study-related documents.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum 3-5 years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with various clinical trial management and EDC systems.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills.
- Ability to work independently and manage multiple sites remotely.
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