7 Remote Clinical Research Associate Cra jobs in whatjobs
Remote Clinical Research Associate (CRA)
Posted 22 days ago
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Job Description
Our client is actively seeking an experienced and meticulous Clinical Research Associate (CRA) for a fully remote position. This role is integral to ensuring the successful execution and integrity of clinical trials, contributing to the development of life-saving pharmaceuticals. As a remote CRA, you will be responsible for monitoring clinical trial sites, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your primary focus will be on data quality, patient safety, and study integrity, all managed through virtual interactions and site visits as required, though the role is primarily remote. You will conduct site initiation, interim monitoring, and close-out visits (virtually or in person as needed), review source documents, verify data accuracy, and manage investigational product accountability. The ideal candidate possesses a strong understanding of clinical trial processes, excellent communication skills, and the ability to build rapport with investigators and site staff from a distance. Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS) is crucial. This fully remote role demands a high degree of organization, independence, and proactivity. You will be a key liaison between the sponsor and clinical trial sites, ensuring seamless study conduct. We are looking for individuals who are passionate about clinical research, committed to patient well-being, and possess the skills to manage complex projects remotely. Your ability to adapt to evolving trial needs and maintain rigorous standards in a decentralized setting will be paramount. This opportunity, while connected to **Kericho, Kericho, KE**, offers the flexibility of a fully remote work arrangement, making it accessible to qualified professionals across the region. Our client values scientific integrity and efficiency, providing a supportive environment for professionals dedicated to advancing healthcare.
Key Responsibilities:
Key Responsibilities:
- Monitor clinical trial sites remotely and conduct necessary on-site visits as required.
- Ensure compliance with study protocols, SOPs, and regulatory guidelines (e.g., GCP).
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Manage investigational product accountability and site supplies.
- Serve as the primary point of contact for assigned clinical trial sites.
- Facilitate communication between sites, sponsor, and relevant stakeholders.
- Conduct site initiation, interim, and close-out monitoring activities.
- Identify and report potential issues, deviations, and adverse events.
- Prepare monitoring visit reports and track action items.
- Support site staff with study-related queries and training.
- Bachelor's degree in a life science, nursing, or a related healthcare field.
- Minimum of 2-3 years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Proficiency with EDC systems and CTMS software.
- Excellent monitoring and auditing skills.
- Strong written and verbal communication and interpersonal skills.
- Proven ability to work independently, manage time effectively, and meet deadlines.
- High level of organization, attention to detail, and problem-solving abilities.
- Ability to travel as needed for on-site monitoring visits.
- Commitment to patient safety and data integrity.
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Remote Clinical Research Associate (CRA)
Posted 21 days ago
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Job Description
Our client is actively seeking a highly qualified and motivated Remote Clinical Research Associate (CRA) to join their global clinical operations team. This role is fully remote, allowing you to manage clinical trial sites and ensure data integrity from your home office. As a Remote CRA, you will be responsible for monitoring investigational sites to ensure compliance with study protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. You will conduct pre-study visits, site initiation visits, routine monitoring visits (remote or on-site as needed), and close-out visits. Your key focus will be on data accuracy, patient safety, and the ethical conduct of clinical trials. The ideal candidate will possess a strong understanding of pharmaceutical research processes, excellent organizational skills, and the ability to build strong relationships with site staff. You must be adept at utilizing electronic data capture (EDC) systems and other clinical trial management software. This position demands excellent communication, analytical, and problem-solving skills, along with the ability to work independently and travel periodically when necessary.
Key Responsibilities:
Key Responsibilities:
- Monitor investigational clinical trial sites according to protocol and regulatory requirements.
- Conduct site visits, including pre-study, initiation, monitoring, and close-out visits.
- Ensure adherence to GCP, FDA regulations, and study-specific protocols.
- Verify the accuracy, completeness, and integrity of clinical data through source document verification (SDV).
- Oversee patient safety and report adverse events promptly.
- Build and maintain strong working relationships with Principal Investigators and site staff.
- Provide training and ongoing support to study site personnel.
- Manage site supplies and investigational product accountability.
- Review and resolve data queries in the EDC system.
- Prepare and submit monitoring visit reports in a timely manner.
- Identify site issues and implement corrective and preventative actions (CAPAs).
- Ensure regulatory compliance and maintain essential study documents.
- Contribute to protocol development and study design where applicable.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate (CRA).
- Demonstrated experience in monitoring clinical trials across various therapeutic areas.
- Thorough understanding of GCP, ICH guidelines, and regulatory requirements.
- Proficiency with EDC systems and clinical trial management software.
- Excellent verbal and written communication skills.
- Strong organizational, time management, and problem-solving abilities.
- Ability to work independently and manage multiple sites/projects in a remote environment.
- Willingness to travel nationally or internationally as required for site visits.
- Attention to detail and commitment to data accuracy and patient safety.
This advertiser has chosen not to accept applicants from your region.
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Remote Clinical Research Associate (CRA)
Posted 13 days ago
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Job Description
Our client is searching for a highly competent and experienced Remote Clinical Research Associate (CRA) to join their innovative pharmaceutical research division. This is a fully remote role, offering the opportunity to contribute to critical clinical trials from the comfort of your home. You will be responsible for monitoring and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and applicable regulatory requirements.
Your primary duties will include site selection, initiation visits, routine monitoring, and close-out visits for clinical trial sites. You will verify the accuracy and completeness of source documents, case report forms (CRFs), and other study-related documentation. This role requires ensuring the safety and rights of study participants are protected at all times. You will also be responsible for identifying and reporting adverse events, and escalating any study-related issues to the appropriate personnel. Maintaining effective communication with investigators, site staff, and internal project teams is paramount. The successful candidate will play a key role in ensuring data integrity and regulatory compliance throughout the trial lifecycle.
We are looking for candidates with a Bachelor's degree in a life science, nursing, pharmacy, or a related field. A minimum of 3-5 years of experience as a Clinical Research Associate is required, with demonstrated experience in monitoring clinical trials according to ICH-GCP guidelines and relevant local regulations. Strong understanding of medical terminology, clinical trial processes, and drug development is essential. Excellent organizational, time management, and problem-solving skills are crucial. The ability to work independently, manage a remote territory effectively, and travel occasionally as needed is also required. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a must. If you are dedicated to advancing healthcare through meticulous clinical trial oversight, we encourage you to apply.
Your primary duties will include site selection, initiation visits, routine monitoring, and close-out visits for clinical trial sites. You will verify the accuracy and completeness of source documents, case report forms (CRFs), and other study-related documentation. This role requires ensuring the safety and rights of study participants are protected at all times. You will also be responsible for identifying and reporting adverse events, and escalating any study-related issues to the appropriate personnel. Maintaining effective communication with investigators, site staff, and internal project teams is paramount. The successful candidate will play a key role in ensuring data integrity and regulatory compliance throughout the trial lifecycle.
We are looking for candidates with a Bachelor's degree in a life science, nursing, pharmacy, or a related field. A minimum of 3-5 years of experience as a Clinical Research Associate is required, with demonstrated experience in monitoring clinical trials according to ICH-GCP guidelines and relevant local regulations. Strong understanding of medical terminology, clinical trial processes, and drug development is essential. Excellent organizational, time management, and problem-solving skills are crucial. The ability to work independently, manage a remote territory effectively, and travel occasionally as needed is also required. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a must. If you are dedicated to advancing healthcare through meticulous clinical trial oversight, we encourage you to apply.
This advertiser has chosen not to accept applicants from your region.
2
Remote Clinical Research Associate (CRA)
Posted 13 days ago
Job Viewed
Job Description
Our client is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join their expanding pharmaceutical team in a fully remote capacity. This pivotal role involves overseeing clinical trials, ensuring they are conducted, recorded, and reported in accordance with protocol, standard operating procedures (SOPs), and regulatory requirements. As a remote CRA, you will play a critical part in drug development, monitoring patient safety, data integrity, and overall trial compliance. Your responsibilities will include site selection, initiation, monitoring, and close-out visits (requiring travel as per study needs), verifying that investigators and study staff are trained properly, and ensuring the accurate collection and reporting of study data. You will serve as the primary point of contact for clinical sites, fostering strong relationships and providing essential support to investigators and study coordinators. This role demands exceptional organizational skills, a thorough understanding of Good Clinical Practice (GCP) guidelines, and proficiency in clinical trial management systems. The ability to work independently, manage your time effectively, and communicate clearly with diverse stakeholders is paramount. This is an exceptional opportunity for an experienced CRA to advance their career in a flexible, remote-first environment, contributing to the development of life-saving therapies. We are looking for professionals passionate about clinical research and committed to upholding the highest standards of quality and ethics.
Responsibilities:
Responsibilities:
- Perform site selection, initiation, interim monitoring, and close-out visits.
- Ensure study conduct is in compliance with protocol, SOPs, GCP, and regulatory requirements.
- Verify the accuracy, completeness, and quality of clinical data through source document verification.
- Manage study-related supplies and regulatory documentation at clinical sites.
- Serve as the main point of contact for study sites, investigators, and study coordinators.
- Train and mentor site staff on study procedures and data collection.
- Monitor patient safety and report adverse events in a timely manner.
- Prepare and present monitoring visit reports.
- Identify site issues and deviations, and implement corrective and preventive actions (CAPAs).
- Ensure timely resolution of data queries and outstanding issues.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate.
- In-depth knowledge of ICH-GCP guidelines and applicable regulatory requirements.
- Proven experience in monitoring clinical trials across various therapeutic areas.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills.
- Ability to travel to clinical sites as required by study protocols.
- Detail-oriented with a commitment to data quality and patient safety.
- Self-starter with the ability to work independently and manage a remote workload effectively.
This advertiser has chosen not to accept applicants from your region.
3
Remote Clinical Research Associate (CRA)
Posted 5 days ago
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Job Description
Our client is seeking an experienced and highly motivated Clinical Research Associate (CRA) to join their pioneering pharmaceutical team. This is a fully remote position, offering the flexibility to work from anywhere while contributing to critical global health initiatives. As a Remote CRA, you will be instrumental in overseeing clinical trials, ensuring adherence to protocols, regulatory guidelines, and data integrity from a distance. Your responsibilities will include remote site monitoring, data review, issue resolution, and maintaining effective communication with study sites, investigators, and internal project teams. You will leverage cutting-edge technology and digital platforms to conduct your work, requiring a strong aptitude for digital tools and virtual collaboration. The ideal candidate will possess a robust understanding of Good Clinical Practice (GCP), regulatory requirements, and the drug development process. Exceptional organizational skills, meticulous attention to detail, and the ability to work autonomously are paramount for success in this remote role. This is a fantastic opportunity to advance your career in clinical research within a forward-thinking organization that embraces remote work. The role demands a proactive approach to problem-solving, strong analytical skills, and the capacity to manage multiple projects simultaneously. You will be part of a dynamic team dedicated to bringing life-changing therapies to market. We are looking for individuals who are passionate about medical advancements and committed to upholding the highest standards of research ethics and quality. The specific focus of the trials may vary, but will always require a deep commitment to scientific rigor and patient safety. You will conduct remote source data verification, review regulatory documents, and support site initiation and close-out visits virtually. Effective risk assessment and management will be a key component of your daily activities, ensuring that all trials progress smoothly and efficiently. This role requires a high degree of self-discipline and the ability to maintain strong working relationships with clinical sites and internal stakeholders through various communication channels. Our client values innovation, integrity, and a collaborative spirit, fostering an environment where remote professionals can thrive and make a real difference. The assigned geographical region for oversight, while managed remotely, is associated with **Eldoret, Uasin Gishu, KE**.
Responsibilities:
Responsibilities:
- Perform remote monitoring of clinical trial sites to ensure compliance with protocols, SOPs, and regulatory requirements (GCP, FDA, EMA).
- Conduct remote source data verification (SDV) and review clinical trial data for accuracy and completeness.
- Identify, document, and track site issues, proposing and implementing corrective and preventive actions (CAPAs).
- Facilitate remote site initiation, training, and close-out visits.
- Build and maintain strong working relationships with investigators, study coordinators, and site staff.
- Ensure timely submission of essential trial documents and regulatory updates.
- Prepare monitoring reports and contribute to study-level documentation.
- Participate in investigator meetings and team discussions via virtual platforms.
- Stay current with therapeutic area advancements and regulatory changes.
- Contribute to the development and refinement of remote monitoring strategies and tools.
- Bachelor's degree in a life science, nursing, or related field; Advanced degree preferred.
- Minimum of 3 years of direct experience as a Clinical Research Associate.
- Proven experience in remote site monitoring and virtual clinical trial management.
- Strong knowledge of ICH-GCP guidelines and relevant regulatory requirements.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent analytical, problem-solving, and critical-thinking skills.
- Exceptional organizational and time-management abilities.
- Superior written and verbal communication skills for effective remote interaction.
- Ability to work independently with minimal supervision in a remote setting.
- Willingness to travel occasionally as needed (post-pandemic or for essential on-site activities).
This advertiser has chosen not to accept applicants from your region.
4
Remote Clinical Research Associate (CRA)
Posted 6 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical research organization, is seeking a dedicated and meticulous Remote Clinical Research Associate (CRA) to join their global clinical operations team. This is a critical, fully remote position focused on ensuring the quality and integrity of clinical trials. You will be responsible for monitoring clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your role will involve conducting pre-study visits, site initiation visits, interim monitoring visits, and close-out visits, all performed remotely through virtual means and occasional on-site visits when absolutely necessary. You will review and verify patient records, source data, and trial-related documentation to ensure accuracy and completeness. Furthermore, you will manage communication with investigators and site staff, provide training on study procedures, and address any site-related issues or concerns promptly. This role demands exceptional attention to detail, strong organizational skills, and the ability to work autonomously in a remote setting. You will leverage technology for remote monitoring, data review, and reporting. The **Kakamega, Kakamega, KE** location signifies a regional focus, but your work will be conducted remotely, offering significant flexibility. The ideal candidate will possess a strong understanding of pharmaceutical drug development, clinical trial processes, and regulatory landscapes. Excellent communication, interpersonal, and problem-solving skills are essential for success in this role. We are committed to advancing healthcare through rigorous research, and we are looking for individuals who share our passion for making a difference.
Key Responsibilities:
Key Responsibilities:
- Perform remote monitoring of clinical trial sites to ensure protocol adherence and data integrity.
- Verify source data and patient records against case report forms (CRFs).
- Ensure compliance with ICH-GCP guidelines and applicable regulations.
- Conduct remote site initiation, monitoring, and close-out activities.
- Train and support investigators and site staff on study procedures.
- Identify, resolve, and escalate site-related issues in a timely manner.
- Prepare and submit monitoring reports and other required documentation.
- Communicate effectively with internal teams, site personnel, and regulatory authorities.
- Maintain patient confidentiality and data security.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 2 years of experience as a Clinical Research Associate or in a similar role.
- In-depth knowledge of clinical trial processes, ICH-GCP, and regulatory requirements.
- Excellent analytical and problem-solving abilities.
- Strong organizational and time management skills, with the ability to manage multiple sites.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Exceptional written and verbal communication skills.
- Ability to work independently and adapt to a remote work environment.
This advertiser has chosen not to accept applicants from your region.
5
Remote Clinical Research Associate (CRA)
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical research organization, is seeking a dedicated and experienced Remote Clinical Research Associate (CRA) to join their global research team. This fully remote position is crucial for overseeing the conduct of clinical trials, ensuring data integrity, and maintaining compliance with regulatory standards. Your responsibilities will include site initiation visits, regular monitoring visits (virtually or on-site as required by protocols), source data verification, and ensuring adherence to Good Clinical Practice (GCP) guidelines. You will act as the primary liaison between investigative sites and the sponsor, providing support and resolving any issues that arise during the trial. The ideal candidate possesses a strong background in life sciences or a related healthcare field, coupled with significant experience as a CRA or in clinical trial management. Proficiency in CTMS (Clinical Trial Management Systems) and EDC (Electronic Data Capture) systems is essential. Excellent organizational, communication, and problem-solving skills are critical for success in this remote role, as is a meticulous attention to detail and the ability to work independently with minimal supervision. Our client is committed to advancing medical treatments through rigorous and ethical research. This remote-first role offers the flexibility to manage your territory effectively from your home office, contributing to groundbreaking pharmaceutical development worldwide. You will play a vital role in bringing new therapies to patients faster by ensuring the quality and reliability of clinical trial data. The ability to travel occasionally to investigative sites (if necessary) should be considered, though the primary mode of work will be remote. Join a dynamic and mission-driven organization that offers competitive compensation, comprehensive benefits, and opportunities for professional growth within the pharmaceutical industry. This is an excellent opportunity for a skilled CRA to make a significant impact on patient health from a flexible, remote setting. A strong understanding of regulatory requirements in Kenya and international markets is highly valued. You will be empowered to manage your monitoring schedule efficiently and build strong working relationships with site personnel.
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