Clinical Research Associate II Specialist Role

Clinical Research Associate II SpecialistAt Pharmiweb, we're seeking a highly skilled Clinical Research Associate II Specialist to join our team. As a Clinical Research Associate II Specialist, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative...

Job SummaryWe are seeking a highly skilled Clinical Research Associate II Specialist to join our team at ICON. As a Clinical Research Associate II Specialist, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Key...

Job SummaryWe are seeking a Clinical Research Associate II Specialist to join our team at ICON. As a Clinical Research Associate II Specialist, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Key ResponsibilitiesConduct site...

Job SummaryPharmiweb is seeking a highly skilled Clinical Research Associate II to join our team in Oncology. As a Clinical Research Associate II, you will be responsible for performing site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.Key...

Job SummaryAs a Clinical Research Associate II at Pharmiweb, you will be responsible for assessing the qualifications of potential clinical study sites, implementing clinical studies at participating sites, managing the conduct of clinical studies at sites, ensuring the quality of site performance, and closing clinical studies. This role requires a strong...

Study Start Up Associate II RoleICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence.We are currently seeking a Study Start Up Associate II to join our diverse and dynamic team. As a Study Start Up Associate II at ICON, you will play a pivotal...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.Key ResponsibilitiesLeading...

Job Title: Clinical Research Associate - Oncology TrialsWe are seeking a highly motivated and experienced Clinical Research Associate to join our team in Oncology Trials. As a Clinical Research Associate, you will be responsible for managing clinical trials from start to finish, ensuring compliance with regulatory requirements and Good Clinical Practice...

Job Title: Clinical Research Associate - Oncology TrialsWe are seeking a highly motivated and experienced Clinical Research Associate to join our team in Oncology Trials. As a Clinical Research Associate, you will be responsible for managing clinical trials from start to finish, ensuring compliance with regulatory requirements and Good Clinical Practice...

Job Title: Clinical Research Associate - Oncology TrialsWe are seeking a highly motivated and experienced Clinical Research Associate to join our team in Oncology Trials. As a Clinical Research Associate, you will be responsible for managing clinical trials from start to finish, ensuring compliance with regulatory requirements and Good Clinical Practice...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team in the Oncology Trials department. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials, ensuring compliance with regulatory requirements and Good Clinical Practice guidelines.Key ResponsibilitiesMonitor and manage clinical...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team in Oncology trials. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials, ensuring compliance with regulatory requirements and Good Clinical Practice guidelines.Key ResponsibilitiesMonitor and manage clinical trials,...

Key Responsibilities:As a Study Start Up Associate at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.Prepare and submit regulatory documents, including clinical trial applications, ethics committee...

Job SummaryAs a Clinical Research Associate at Pharmiweb, you will be responsible for managing clinical trials within the pharmaceutical industry. This role involves working on multiple trials, ensuring quality of life for patients, and demonstrating leadership skills. You will be involved in site start-up documents, mentoring junior team members, and...

Job SummaryAs a Clinical Research Associate at Pharmiweb, you will be responsible for monitoring the progress of clinical studies at investigative sites or remotely. Your primary goal will be to ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable...

Quality Assurance Auditor IIICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Quality Assurance Auditor II to join our...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team in supporting phase 1 oncology/haematology trials. As a Senior Clinical Research Associate, you will be responsible for site selection, site initiation, and site management, ensuring compliance with internal SOPs, WIs, policies, and local regulatory requirements.Key...

Job Summary:We are seeking an experienced Clinical Research Associate (CRA) to join our Oncology team. As a CRA, you will be responsible for monitoring clinical trials, ensuring compliance with regulatory requirements, and providing high-quality support to investigators and site staff.Main Responsibilities:Contribute to the selection of potential...

Job SummaryThe Clinical Research Associate will perform site activities for Phase I-IV studies operating as the main point of contact for the site during a study. This role is dedicated to sponsor activities and requires a strong understanding of GCP compliance and regulatory guidelines.Key ResponsibilitiesDrive and execute monitoring plans to ensure site...

Job SummaryAs a Clinical Research Associate at Pharmiweb, you will be responsible for monitoring pharmaceutical industry clinical trials, with a focus on Oncology trials. This role requires a strong understanding of Good Clinical Practice, ICH guidelines, and local regulatory requirements. Key ResponsibilitiesMonitor multiple trials within Oncology, ensuring...