2 Senior Clinical Research Associate Pharmaceuticals Remote jobs in whatjobs
Senior Clinical Research Associate - Pharmaceuticals (Remote)
Posted 21 days ago
Job Viewed
Job Description
Our client is a leading pharmaceutical company dedicated to advancing global health, seeking a highly experienced Senior Clinical Research Associate (CRA) to join their remote clinical operations team. This position is 100% remote, offering flexibility and the opportunity to contribute to critical drug development programs from your home. You will be responsible for monitoring clinical trials, ensuring data integrity, adherence to protocols, and compliance with regulatory requirements. Your role is crucial in bringing life-changing therapies to market.
Responsibilities:
Qualifications:
Responsibilities:
- Conduct remote site monitoring visits and assessments to ensure protocol adherence and data accuracy.
- Manage and mentor clinical trial sites, providing guidance and support to investigators and site staff.
- Verify the accuracy, completeness, and consistency of clinical trial data.
- Ensure compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols.
- Identify, evaluate, and select potential clinical trial sites.
- Prepare monitoring reports and escalate any site issues or concerns promptly.
- Train site personnel on study procedures, data collection, and regulatory requirements.
- Manage drug accountability and investigational product supply at sites.
- Contribute to the development and review of clinical trial documents.
- Collaborate effectively with internal project teams, including project managers, data managers, and biostatisticians.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 5 years of experience as a Clinical Research Associate, with significant experience in remote monitoring.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven ability to conduct thorough site monitoring and data review.
- Strong understanding of pharmaceutical drug development process.
- Excellent communication, interpersonal, and organizational skills.
- Ability to work independently and manage time effectively in a remote environment.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel occasionally as required (though the role is primarily remote).
This advertiser has chosen not to accept applicants from your region.
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Senior Clinical Research Associate - Pharmaceuticals (Remote)
Posted 18 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly qualified and meticulous Senior Clinical Research Associate (CRA) to join their expanding global team. This position is 100% remote, enabling you to contribute to critical drug development from your home office. As a Senior CRA, you will play a pivotal role in ensuring the quality and integrity of clinical trials, adhering strictly to Good Clinical Practice (GCP) guidelines, FDA regulations, and ICH guidelines. You will be responsible for monitoring clinical trial sites, verifying data accuracy, and ensuring patient safety throughout the trial lifecycle. Your expertise will be crucial in managing relationships with investigators and site staff, resolving issues promptly, and ensuring timely study completion. Key responsibilities include:
Qualifications:
This is a fantastic opportunity to contribute to life-saving research from a remote location, working with cutting-edge therapies and a collaborative international team.
- Conducting remote and on-site (when required) monitoring visits to assess trial conduct and data integrity.
- Ensuring compliance with protocols, regulatory requirements, and company SOPs at assigned investigational sites.
- Verifying source data against case report forms (CRFs) and electronic data capture (EDC) systems.
- Managing and resolving site-level issues, providing training and support to site personnel.
- Maintaining accurate and up-to-date trial documentation and records.
- Communicating effectively with investigators, study coordinators, and internal study teams.
- Participating in protocol development and review, contributing clinical trial expertise.
- Identifying and escalating potential risks and challenges to study management.
- Contributing to the development and implementation of risk-based monitoring strategies.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. Advanced degree preferred.
- Minimum of 5 years of experience as a Clinical Research Associate, with a significant portion in a senior capacity.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Proven experience with EDC systems and clinical trial monitoring techniques.
- Excellent organizational, communication, and interpersonal skills.
- Ability to work independently and manage time effectively in a remote setting.
- Strong critical thinking and problem-solving abilities.
- Experience in specific therapeutic areas is a plus.
This is a fantastic opportunity to contribute to life-saving research from a remote location, working with cutting-edge therapies and a collaborative international team.
This advertiser has chosen not to accept applicants from your region.
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