SAS Programmer Position in Clinical Research

About the RoleWe are seeking a highly skilled and motivated Clinical Research Coordinator to join our team at Icon Research. As a key member of our research team, you will be responsible for coordinating and conducting clinical trials, ensuring that all research activities are conducted in accordance with Good Clinical Practice and Icon policies.Key...

About the RoleWe are seeking a highly skilled and motivated Clinical Research Coordinator to join our team at Research at Icon Group. As a key member of our research team, you will be responsible for coordinating and conducting clinical trials, ensuring compliance with Good Clinical Practice and Icon policies.Key Responsibilities:Provide high-level support...

Clinical Research Coordinator Role SummaryWe are seeking a highly skilled and motivated Clinical Research Coordinator to join our research team at Icon Group. As a key member of our team, you will play a crucial role in the conduct and day-to-day management of clinical trials. Your primary responsibility will be to provide high-level support to our Principal...

Company OverviewAt Research at Icon Group, we are committed to providing exceptional cancer care services. With a growing reach into New Zealand and Asia, our company has over 3,500 employees company-wide.We have more than half of our locations participating in clinical trials, making us Australia's largest private cancer clinical trials program.About the...

Clinical Research Associate RoleAs a Clinical Research Associate at Pharmiweb, you will be part of the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence.The Clinical Research Associate is responsible for the initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with...

Clinical Research Associate RoleWe are seeking a highly skilled Clinical Research Associate to join our team at Pharmiweb. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials.Key Responsibilities:Site Qualification and Monitoring: Conduct site qualification, initiation, monitoring, and close-out visits for...

About the Role:The Patient Recruitment Associate is an integral part of our team, responsible for encouraging patients to participate in clinical research studies. This role involves conducting phone screens, reviewing patient medical information, discussing research opportunities, maintaining patient databases, and reporting recruitment outcomes.Key...

The University of Tasmania invites applications for a Project Manager to coordinate and oversee medical student professional practice projects (MD projects) at the Hobart Clinical School.This role will facilitate development of research projects and ensure a positive experience for students and supervisors participating in MD projects. The successful...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team in a key role within our Oncology Trials department. As a Clinical Research Associate, you will be responsible for managing clinical trials, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to deliver high-quality results.Key...

Job DescriptionWe are seeking a highly skilled Clinical Research Associate II to join our team at Pharmiweb. As a Clinical Research Associate II, 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...

Job SummaryAs a Senior Clinical Research Associate at Pharmiweb, you will play a critical role in the success of our clinical trials. Your primary responsibility will be to ensure the smooth execution of clinical studies, from site qualification to close-out. You will work closely with cross-functional teams to identify and mitigate risks, and develop...

Job Summary:We 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 Responsibilities:Conduct...

Job Title: Clinical Research Associate I - HistologistAt ICON, we are committed to providing a comprehensive and competitive total reward package that comprises an excellent level of base pay, as well as a wide range of variable pay and recognition programs. Our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to...

**Clinical Site Manager Job Description**About the Role: We are currently seeking a highly motivated and experienced Clinical Site Manager to join our team in Switzerland. As a Clinical Site Manager, you will be responsible for maximizing site performance and site engagement in our client-conducted clinical studies.About the Job: As a Clinical Site Manager,...

Job SummaryThe Clinical Haematology Registrar will be responsible for the day-to-day management of public inpatients and outpatients within the hospital, providing on-call cover for the Clinical Haematology unit and occasional after-hours emergency cover. This is a fixed-term, full-time position with a salary range of $134,930 - $189,005 per annum.Key...

We are seeking a Clinical Research Associate to strengthen our clinical operations team in Spain (Madrid or Barcelona). This role will be responsible for all activities required to set up and oversee a study, complete study status reports, and maintain study documentation. You will participate in the submission of protocols, consent documents for ethics/IRB...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team in a key role within our global clinical trials organization. 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...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team in the pharmaceutical industry. As a Clinical Research Associate, you will be responsible for monitoring pharmaceutical industry clinical trials, ensuring compliance with regulatory requirements, and providing high-quality support to our clients.Key...

**Job Opportunity:** Clinical Haematology RegistrarThe successful candidate will be responsible for the day-to-day management of public inpatients and outpatients within the hospital, providing on-call cover for the Clinical Haematology unit, and infrequent after-hours emergency cover.**Key Responsibilities:**Manage public inpatients and outpatients within...

We're seeking a highly skilled Clinical Research Associate II to join our team at Syneos Health. As a Clinical Research Associate II, you will be responsible for performing site qualification, initiation, monitoring, and close-out visits, ensuring regulatory compliance and site performance.Key Responsibilities:Verify informed consent processes and protect...