Clinical Associate

Clinical Research Associate I Job DescriptionWe are seeking a highly skilled Clinical Research Associate I to join our team at Pharmiweb. As a Clinical Research Associate I, you will be responsible for conducting site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and...

Clinical Research Associate II Job SummaryWe are seeking a highly motivated and detail-oriented Clinical Research Associate II to join our team at Pharmiweb. As a Clinical Research Associate II, you will be responsible for conducting site monitoring responsibilities for clinical trials according to our Standard Operating Procedures (SOPs), ICH guidelines,...

Job SummaryAs a leading global contract research organization (CRO), Fortrea is seeking a highly skilled Clinical Research Associate II to join our team. With a passion for scientific rigor and decades of clinical development experience, we provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient...

Job Title: Clinical AssociateWe are seeking a highly skilled Clinical Associate to join our team in Barcelona, Spain. As a Clinical Associate, you will play a crucial role in the planning, execution, and monitoring of clinical trials.Key Responsibilities:Assist in the planning and execution of clinical trials, ensuring adherence to protocol requirements,...

Job SummaryWe are seeking a highly skilled Clinical Research Associate I to join our team. As a Clinical Research Associate I, 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 ResponsibilitiesPerform site...

Job SummaryPharmiweb is seeking a highly motivated and detail-oriented Clinical Research Associate II to join our team. As a Clinical Research Associate II, you will be responsible for conducting site monitoring responsibilities for clinical trials, ensuring the protection of subjects, and safeguarding data integrity.Key Responsibilities:Conduct site...

Job SummaryAs a Clinical Research Associate II at Pharmiweb, you will play a critical role in the success of our pharmaceutical trials. We are seeking a highly skilled and experienced professional to join our team as a Site Management Expert.Key ResponsibilitiesConduct site monitoring responsibilities for clinical trials according to our Standard Operating...

Job SummaryAs a Principal Biostatistician at Syneos Health, you will play a key role in leading clinical research projects, collaborating with cross-functional teams, and developing statistical plans to ensure high-quality data analysis.Key ResponsibilitiesLead the development of statistical analysis plans, including the creation of mock-up displays for...

Job SummaryAs a Senior Biostatistics Team Lead at Pharmiweb, you will serve as a statistical department resource, mentoring biostatisticians on job skills and overseeing training plans or materials for Biostatistics associates. You will direct the activities of other biostatistics personnel on assigned projects to ensure timely completion of high-quality...

Job SummaryAs a Senior Biostatistics Lead at Syneos Health, you will serve as a statistical department resource, mentoring biostatisticians on job skills and overseeing training plans for Biostatistics associates. Your expertise will be invaluable in conducting training sessions, enhancing the skills of existing personnel, and directing the activities of...

Job SummaryThe Procurement Specialist will provide a confidential, proactive, and highly professional personal service to contribute to operational procurement activities, carrying out sourcing and supplier management activities. A key element of this role is the coordination of Purchase To Pay (P2P) activities between the Procurement Teams and the Accounts...

Senior Manager, Clinical Trial Management ICON 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. At ICON, it’s our people that set us apart. Our...

As a Clinical Research Associate (CRA) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently or as part of the client and ICON team. You will be managing...