5 Remote Clinical Research Associate jobs in whatjobs
Remote Clinical Research Associate
Posted 22 days ago
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Job Description
Our client, a leading innovator in pharmaceutical research and development, is seeking a dedicated and meticulous Remote Clinical Research Associate to join their global team. This fully remote position allows you to contribute to life-changing medical advancements from the comfort of your home office, with primary responsibilities centered around the **Eldoret, Uasin Gishu, KE** region. You will play a crucial role in the planning, execution, and monitoring of clinical trials, ensuring data integrity and adherence to regulatory standards (GCP, FDA, EMA). Key responsibilities include site selection and initiation visits, ongoing monitoring of study sites, and ensuring all study-related documentation is accurate and up-to-date. You will act as a liaison between the sponsor, investigators, and study personnel, providing essential support and training. This role requires excellent organizational skills, strong attention to detail, and the ability to manage multiple tasks effectively in a virtual environment. Proficiency in clinical trial management systems and electronic data capture (EDC) is essential. You will be responsible for reviewing and resolving data queries, verifying source documents, and ensuring the safety and rights of study participants are protected. The ability to work independently, communicate effectively through digital channels, and adapt to evolving project needs is paramount. We are looking for a proactive individual with a solid understanding of pharmaceutical drug development processes. A Bachelor's degree in a life science, nursing, or related field is required, along with significant experience in clinical research. Excellent written and verbal communication skills, along with strong interpersonal abilities to foster positive working relationships with study sites and internal teams, are essential. The ideal candidate will demonstrate a commitment to ethical research practices and a passion for advancing healthcare. This is an exceptional opportunity to make a significant impact on patient well-being from a flexible, remote setting. Your expertise will directly contribute to bringing innovative therapies to market.
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Remote Clinical Research Associate
Posted 22 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly organized and meticulous Clinical Research Associate (CRA) to join their dynamic team. This is a fully remote position, offering the flexibility to conduct your work from anywhere. You will play a critical role in ensuring the quality and integrity of clinical trials by monitoring study sites, verifying data accuracy, and ensuring compliance with regulatory standards and protocols. The ideal candidate will have a strong understanding of clinical trial processes, good clinical practice (GCP), and excellent communication skills. You will be instrumental in the successful execution of clinical research studies that advance pharmaceutical development.
Responsibilities:
Qualifications:
Responsibilities:
- Conduct remote site monitoring visits and assess study conduct.
- Verify the accuracy, completeness, and consistency of clinical trial data.
- Ensure adherence to study protocols, GCP guidelines, and regulatory requirements.
- Train and support site staff on study procedures and documentation.
- Manage communication between study sites and the sponsor organization.
- Identify and resolve site issues and discrepancies in a timely manner.
- Review regulatory source documents and case report forms (CRFs).
- Prepare monitoring reports and track action items for site follow-up.
- Contribute to the development and review of study-related documents.
- Ensure timely close-out of study sites.
- Stay updated on relevant regulations and industry best practices.
- Maintain effective relationships with investigators and site personnel.
- Participate in study team meetings and contribute to overall study success.
Qualifications:
- Bachelor's degree in a life science, nursing, pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical research role.
- Thorough knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent organizational, time management, and prioritization skills.
- Strong analytical and problem-solving abilities.
- Exceptional written and verbal communication skills.
- Ability to work independently and manage a remote workload effectively.
- Proficiency in Microsoft Office Suite.
- Willingness to travel occasionally for essential on-site meetings or audits if required.
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1
Remote Clinical Research Associate
Posted 14 days ago
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Job Description
Our client, a global pharmaceutical leader, is expanding its remote workforce and is actively seeking a dedicated Remote Clinical Research Associate to join their innovative drug development team. This is a fully remote position, offering the flexibility to work from anywhere within Kenya. You will be responsible for the monitoring and management of clinical trials, ensuring adherence to study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. Your duties will include site selection and initiation visits, interim monitoring visits, and close-out visits. You will collaborate closely with investigators, site staff, and internal study teams to ensure the safety of study participants and the integrity of the data collected. This role requires meticulous attention to detail, excellent organizational skills, and a strong understanding of clinical trial processes. You will review and reconcile source documents, case report forms (CRFs), and query resolution. Effective communication, both written and verbal, is paramount, as you will be interacting with a diverse range of stakeholders, often through virtual platforms. The ideal candidate will have a Bachelor's degree in a life science, nursing, or related field, coupled with significant experience as a Clinical Research Associate. Demonstrated experience in monitoring multi-center clinical trials is essential. You should be adept at using electronic data capture (EDC) systems and other clinical trial management software. This remote role demands a high degree of self-discipline, proactivity, and the ability to manage your workload effectively without direct supervision. We are looking for individuals who are passionate about contributing to life-saving medical advancements and possess the technical acumen to thrive in a virtual research environment. The company offers comprehensive training and support to ensure your success in this remote capacity.
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Remote Clinical Research Associate
Posted 12 days ago
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Job Description
Our client is seeking a dedicated and experienced Remote Clinical Research Associate (CRA) to play a vital role in the execution of clinical trials. This position is fully remote, allowing you to contribute to groundbreaking pharmaceutical research from the comfort of your home office. The ideal candidate will be responsible for monitoring clinical trial sites, ensuring compliance with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. You will work closely with investigators and site staff to ensure the accuracy, completeness, and timeliness of trial data.
Responsibilities:
Responsibilities:
- Conduct remote site visits and monitoring activities according to study protocols and SOPs.
- Ensure study participants' rights, safety, and well-being are protected.
- Verify the accuracy, completeness, and integrity of clinical data through source data verification (SDV).
- Train and manage site staff on study-related procedures, regulatory requirements, and data collection.
- Ensure adherence to the investigational plan, protocol amendments, and regulatory guidelines.
- Maintain effective communication with investigators, site staff, and internal study teams.
- Prepare and submit monitoring reports in a timely manner.
- Identify potential risks and issues at study sites and implement corrective actions.
- Ensure all necessary regulatory documentation is maintained at the site and is readily available for review.
- Track subject enrollment and study progress, identifying potential challenges or delays.
- Conduct site initiation visits (remotely where possible) and close-out activities.
- Review essential documents for completeness and accuracy.
- Stay current with ICH-GCP guidelines and other relevant regulatory requirements.
- Participate in investigator meetings and training sessions.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific field.
- Minimum of 3-5 years of experience as a Clinical Research Associate (CRA) or equivalent monitoring role.
- In-depth knowledge of ICH-GCP guidelines, FDA regulations, and other applicable regulatory requirements.
- Proven experience in remote monitoring techniques and technologies.
- Excellent understanding of clinical trial processes and documentation.
- Strong analytical and problem-solving skills.
- Exceptional organizational and time-management abilities.
- Outstanding written and verbal communication skills.
- Ability to work independently with minimal supervision and manage multiple priorities effectively in a remote setting.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Certification from a recognized professional body (e.g., ACRP, SoCRA) is a plus.
This advertiser has chosen not to accept applicants from your region.
3
Remote Clinical Research Associate
Posted 6 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly motivated and experienced Clinical Research Associate (CRA) for a fully remote position. While based conceptually in **Eldoret, Uasin Gishu, KE**, this role allows you to contribute to groundbreaking medical research from the comfort of your home. As a remote CRA, you will play a critical role in ensuring the quality and integrity of clinical trials conducted by our client. Your primary responsibilities will involve monitoring clinical trial sites to ensure adherence to protocols, regulations, and Good Clinical Practice (GCP) guidelines. This includes site selection, initiation, routine monitoring, and close-out activities. You will act as the main point of contact between the study sites and the study team, addressing any issues that arise during the trial.
Key Responsibilities:
Key Responsibilities:
- Conduct remote and on-site (as needed) monitoring visits to assess patient safety, data accuracy, and regulatory compliance.
- Verify that investigational product is dispensed, administered, and accounted for according to the protocol.
- Ensure accurate and timely source data verification against the clinical study report.
- Identify, resolve, and escalate study-related issues and deviations promptly.
- Manage communication and build strong relationships with investigators, site staff, and study sponsors.
- Review and ensure the quality of essential documents maintained at study sites.
- Train site personnel on study procedures, protocols, and regulatory requirements.
- Prepare monitoring visit reports and follow up on action items.
- Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA, ICH-GCP).
- Contribute to the development and review of study protocols and other study-related documents.
- Bachelor's degree in a life science, nursing, or a related field. Advanced degree is a plus.
- Minimum of 3-5 years of experience as a Clinical Research Associate, preferably with pharmaceutical or biotech experience.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven experience in conducting site monitoring visits, data verification, and issue resolution.
- Excellent understanding of medical terminology and clinical trial processes.
- Strong organizational and time management skills, with the ability to manage multiple priorities effectively in a remote setting.
- Exceptional written and verbal communication skills, with the ability to document findings accurately and professionally.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently and as part of a remote, cross-functional team.
- Willingness to travel occasionally for essential site visits or training if required.
This advertiser has chosen not to accept applicants from your region.
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