JR140855 Clinical Site Associate ICON plc is a world-leading healthcare intelligence and clinical research..., and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Site Associate to join our diverse...
), is currently seeking a dedicated and experienced Clinical Research Associate (CRA) to join their growing team in Malaysia.... Responsibilities: Oversee all aspects of clinical research activities, ensuring strict adherence to study protocols, ICH-GCP guidelines...
. collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start Up Associate (RSA), prepare site essential...The Clinical Research Associate (CRAII - SCRA), is primarily responsible for ensuring the rights and wellbeing of trial...
Description Clinical Research Associate II, Malaysia (remote) Syneos Health is a leading fully integrated... to create a place where everyone feels like they belong. Job Responsibilities Conduct on-site and remote monitoring of clinical...
of clinical development We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team.... As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting...
discipline or healthcare At least 1 year of on-site monitoring experience Good knowledge of GCP and clinical research.... You will be building a flexible, meaningful and fulfilling career with no limits. Your responsibilities will include: Performing site...
Summary Of Responsibilities Site management responsibility for clinical studies according to Fortrea's Standard... training records. Conducts site monitoring responsibilities for clinical trials according to Fortrea's Standard Operating...
Job Description & Requirements 1. Responsible for performing all monitoring aspects of clinical trials and assist... in strict adherence to good clinical practices, regulatory obligations, investigator integrity and compliance with project...
start-up, clinical monitoring and site management activities on the country/regional level. You will become one of our first... is about conducting clinical research of novel medications. We work at the interface of R&D, pharmaceutical industry and healthcare...
future of clinical development We are currently seeking a Lead Clinical Research Associate (CRA) to join our diverse...Lead CRA ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud...
future of clinical development We are currently seeking a Clinical Research Associate II to join our diverse and dynamic... team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials...
to create a place where everyone feels like they belong. Job Responsibilities Conduct on-site and remote monitoring of clinical... clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study...
to create a place where everyone feels like they belong. Job Responsibilities Conduct on-site and remote monitoring of clinical... clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study...
. Assesses factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site... such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP):Assesses...
factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site... such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP):Assesses...
. Assesses factors that might affect subject/patientâs safety and clinical data integrity at an investigator/physician site... such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP...
like they belong. Job Responsibilities Conduct on-site and remote monitoring of clinical research studies to ensure compliance... and other relevant software Certifications: Certified Clinical Research Associate (CCRA) or equivalent certification preferred Necessary...
at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site.... May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures...