Clinical Research Associate

Job SummaryWe are seeking an experienced Clinical Research Associate to join our team at Pharmiweb. As a Clinical Research Associate, you will be responsible for clinical monitoring activities, site relationships, and study site management in accordance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, and Protocol.Key Responsibilities:Develop strong...

Clinical Research Associate Role SummaryThe successful candidate will join Pharmiweb, the world's largest clinical research organisation, to work on Oncology trials. They will collaborate with country operations teams and site personnel to ensure site activation and study timelines are met.Main Responsibilities:Perform Site Qualification VisitsBuild...

Job Summary ICON is seeking a highly motivated and detail-oriented Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.Key...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team in a key role within our pharmaceutical 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 ResponsibilitiesMonitor...

Clinical Research Associate II Job SummaryWe are seeking a highly skilled Clinical Research Associate II to join our team in Miami, FL. As a Clinical Research Associate II, you will be responsible for conducting clinical trial site visits, overseeing and reporting on the conduct of clinical trials, and proactively managing sites.Key Responsibilities:Conduct...

Job Title: Senior Clinical Research Associate - Cambridge, MAWe are seeking a highly skilled Senior Clinical Research Associate to join our team in Cambridge, MA. As a Senior CRA, you will be responsible for monitoring the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in...

Key Responsibilities:As a Clinical Research Associate in our Vascular Devices team, you will be responsible for monitoring study progress, ensuring compliance with regulations, and developing policies and procedures. Additional Duties:Support clinical trial management systems, maintain trial master files, and manage study Investigators. Leverage your...

Job DescriptionAt ICON, we are seeking an experienced Senior Clinical Research Associate to join our team in Italy and Hungary. As a Senior Clinical Research Associate, you will be responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with sponsor's procedural documents, international...

About the Role: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 be a part of our mission to shape the future of clinical development.We are currently seeking an Associate Outcomes Researcher to join our diverse and...

The Clinical Research Associate II will perform site activities for Phase I-IV studies as the primary point of contact for the site during a study. This role involves driving and executing monitoring plans, ensuring site GCP compliance, writing trip reports, resolving issues, and facilitating open issue resolution. Additionally, the CRA will conduct site...

Job SummaryClinical Research Associate II in Oncology - Sponsor dedicated - Paris Area Home BasedSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical...

Job Title: Clinical Research Associate - Oncology Trials SpecialistAs a Clinical Research Associate - Oncology Trials Specialist, you will be responsible for working on multiple trials within Oncology, with a focus on start-up activities. Your primary goal will be to collaborate with country operations teams to identify, select, and activate clinical trial...

Job DescriptionWe are seeking a highly skilled Senior Clinical Research Associate to join our team in Cambridge, MA. As a Senior CRA, you will play a key role in the execution of clinical studies, ensuring high-quality data is delivered to sponsors on time, within budget, and in compliance with all applicable regulations and procedures.Key...

Job Role OverviewWe are seeking a highly skilled Clinical Research Associate to join our team in a Sponsor Dedicated role for Immunology and Rare Disease Experience. As a Site Management Associate, you will be responsible for performing site qualification, site initiation, interim monitoring, site management, and close-out visits, ensuring regulatory,...

Unlock a Rewarding Career as a Senior Academic LeaderBond University, a leading private not-for-profit institution based on Australia's stunning Gold Coast, invites applications for a highly competitive position as Research Director and Clinical Research Professor. This full-time, fixed-term appointment for 3 years offers a unique opportunity to contribute...

Job DescriptionAs a Clinical Research Associate, you will be responsible for managing clinical trials in the oncology field. Your primary goal will be to ensure the smooth execution of trials, from site qualification to activation and maintenance.Key ResponsibilitiesConduct site qualification visits to assess the eligibility of sites for participation in...

About the OpportunityBond University, a leading private not-for-profit university in Australia, is seeking an exceptional individual to fill the role of Lead Clinical Research Director. This senior academic leadership position will be based at Bond University's Robina campus and the Evidence-Based Practice Unit at Gold Coast Hospital, Southport.The...

Hire a Senior Clinical Scientist to lead clinical/scientific execution of clinical protocol(s). Collaborate with medical monitoring, Clinical Research and Pharmacovigilance teams. Key responsibilities include designing CRFs, monitoring clinical data, and providing scientific mentorship. You will also assist with data analysis, presentation, and manuscript...

Job SummaryWe are seeking a highly skilled Clinical Research Oversight Specialist to join our team at Pharmiweb. As an Oversight Monitor, you will be responsible for developing and implementing comprehensive oversight monitoring plans tailored to our organization's specific clinical trials and research activities.Key ResponsibilitiesDevelop and implement...

Job DescriptionAs a Clinical Research Feasibility Specialist at Pharmiweb, you will play a crucial role in the start-up phase of clinical trials. Your primary responsibility will be to coordinate and manage the feasibility assessments of potential study sites, ensuring that they meet the necessary criteria for conducting clinical trials.Key...