Trial Protocol Expert

Job Overview:The RFT Group, a leading recruitment agency in the life sciences industry, is seeking an experienced Clinical Trials Expert to join our team. As a Pharmacovigilance Manager, you will play a crucial role in ensuring the safety of patients participating in clinical trials.About the Job:This is a full-time permanent hybrid role, requiring presence...

Job Description Job Description Our client is a young innovative clinical stage Biotech company with a strong development pipeline, now have approval for a new position for a Trial Master File (TMF) Expert within the Clinical Development and Operations group. There is flexibility for this hire to work remotely / from home office, with occasional...

Key Responsibilities:Provide clinical leadership and medical strategic input for deliverables in the assigned project/program, including sections of individual protocols, data review, program specific standards, clinical components of regulatory documents, and publications.Drive execution of the section of the program in partnership with global line...

Our client, a pharmaceutical company based in Dublin, is currently recruiting for a Clinical Monitor to join their growing team on a permanent basis. As Clinical Monitor, you will collaborate with the Clinical Project Manager to oversee and ensure the compliance and quality of clinical trials. This role requires extensive travel (at least 50% of the time) to...

Your new company Here, in Hays Life Sciences, our Multinational Clinical Trials client in Dublin is hiring a Clinical Trails Manager.The Clinical Program Manager will be a valued member of the Clinical Operations team. They will work with the Clinical Program Manager and study teams to manage global clinical trials or regional components of global clinical...

Job Overview:Clinical Trial Vendor Associate Director is a key leadership position responsible for managing all clinical vendor-related aspects of global clinical trials. As a core member of the Clinical Trial Team, you will independently oversee study outcomes within schedule, budget, quality/compliance and performance standards.Main Responsibilities:Serve...

About UsWe're proud to foster an inclusive environment driving innovation and excellence. At ICON, diversity, inclusion & belonging are fundamental to our culture and values.We are currently seeking a Sample Management Coordinator I to join our diverse and dynamic team. This role involves coordinating the receipt, tracking, and storage of clinical trial...

About the JobThis Clinical Trials Manager position is available at Syneos Health, Inc. The selected candidate will be responsible for managing scheduling and time constraints across multiple projects, setting goals based on priorities from management, and discussing time estimates for completion of study-related activities with biostatistics management.Key...

What are we looking for in our Clinical Scientific Expert I? Exciting Career Opportunity - Clinical Scientific Expert I in Dublin 4 - 06 months contract - Hybrid role with 3 days onsite Join one of the world's premier pharmaceutical companies making a significant impact on patients lives and the Irish economy.  We are...

About the Role: As a key member of our clinical trial team, you will independently manage all vendor-related aspects of global clinical trials to deliver study outcomes within schedule, quality, and performance standards.Your Responsibilities:Serve as the leader of the CTT vendor sub-team, working closely with the study lead and other team members throughout...

At WEP Clinical, we are seeking a highly experienced Clinical Research Lead to join our team. This key role plays a crucial part in ensuring the success of clinical trials and Expanded Access Programs (EAPs) by providing expert medical guidance and scientific oversight.About the Role:The Medical Director will serve as the primary medical and scientific...

About the PositionWe are seeking a highly motivated Global Trial Manager to join our clinical operations team. As a key member of the team, you will be responsible for planning, managing, and executing clinical trials from start to finish.About the RoleLead cross-functional teams in collaboration with the Clinical Operations Program Head (COPH) to deliver...

About the JobWe are seeking a skilled professional to lead and oversee the alignment with Novartis-wide financial cycles and Governance boards. This individual will execute enhanced "fast track" Early Trial pricing support to support Business Development and Licensing (BD&L) deal assessments.Responsibilities:Develop strategic forecasts for pre-IMB...

Job Description Summary Are you ready to become a Clinical Trial Vendor Associate Director?As a Clinical Trial Vendor Associate Director, you will be a core member of the Clinical Trial Team, independently managing all clinical vendor-related aspects of global clinical trials to deliver study outcomes within schedule, budget, quality/compliance and...

Job SummaryAs a Senior Clinical Trials Professional at TN Ireland, you will play a key role in managing the strategic planning and execution of clinical supply chain projects, ensuring seamless delivery and compliance with regulatory requirements.Key ResponsibilitiesInterpret clinical trial protocols to create effective clinical trial supply chain...

Are you ready to become a Clinical Trial Vendor Senior Manager?As a Clinical Trial Senior Manager, you will be a core member of the Clinical Trial Team, independently managing all vendor-related aspects of global clinical trials to deliver study outcomes within schedule, budget, quality/compliance and performance standards and be accountable for vendor...

About the Job OpportunityJoin our Clinical Trials team as an experienced Associate Director. As a key member of the team, you will be responsible for managing all clinical vendor-related aspects of global clinical trials.ResponsibilitiesLead the CTT vendor sub-team, overseeing the translation of vendor-related protocol sections into external service...

About the JobWe are seeking an experienced Associate Director to join our Clinical Trials team. As a key member of the team, you will be responsible for managing all clinical vendor-related aspects of global clinical trials.ResponsibilitiesLead the CTT vendor sub-team, overseeing the translation of vendor-related protocol sections into external service...

IRC recruitment is hiring on behalf of a client for the role of a Clinical Scientific Expert within the pharmaceutical sector. Location: Dublin 4 Pay rate: €20/hr Contract type: 6-month contract Working model: hybrid ( must be available to come to the Dublin 4 office each week- number of days in the office will vary depending on demand) Working...

Clinical Sample Processor I Job Description:As a Clinical Sample Processor I, you will be responsible for collecting, processing, and tracking clinical trial samples. You will work closely with our team to ensure the highest level of quality and accuracy in all aspects of sample processing.Key Responsibilities:Collecting, receiving, and logging clinical...