Clinical Research Associate

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Thermo Fisher Scientific. As a Clinical Research Associate, you will be responsible for coordinating all aspects of the clinical monitoring and site management process.Key ResponsibilitiesMonitor investigator sites to ensure the accuracy and validity of CRF entries in...

Position Overview:The Senior Clinical Research Associate plays a pivotal role in overseeing and coordinating all facets of clinical monitoring and site management in compliance with ICH GCP, FDA regulations, local laws, and Thermo Fisher Scientific's standard operating procedures.Key Responsibilities:Conduct site visits to evaluate adherence to protocols and...

Job DescriptionThis role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally.The CRM could be responsible for a particular...

Job DescriptionThis role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards and adverse event reporting requirements internally and externally.The Clinical Research Manager (CRM) could be...

Job SummaryWe are seeking a highly skilled Clinical Research Manager to join our team at MSD. As a Clinical Research Manager, you will be responsible for the end-to-end performance and project management of assigned protocols in a country, ensuring compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards, and...

Position Overview:The Senior Clinical Research Associate (Sr CRA) plays a pivotal role in overseeing and coordinating all facets of clinical monitoring and site management in compliance with industry standards and regulations.Key Responsibilities:Conduct site evaluations to ensure adherence to protocols and regulatory requirements.Maintain ongoing...

About the RoleWe are seeking a highly skilled Clinical Operations Lead to join our team at Amgen. As a key member of our clinical operations team, you will be responsible for overseeing clinical trials processes and operations, ensuring compliance with regulatory requirements, and driving strategic alignment with local and regional teams.Key...

Position Overview:The Senior Clinical Research Associate (Sr CRA) plays a pivotal role in overseeing and coordinating the clinical monitoring and site management processes. This position is essential in ensuring compliance with ICH GCP, FDA regulations, local laws, and internal standard operating procedures.Key Responsibilities:Conducts thorough site visits...

**About Us**BOG Fortrea Colombia Ltda. is a leading global contract research organization (CRO) with a strong commitment to scientific rigor and a rich history of clinical development expertise. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across...

About CDS Fortrea Inc.CDS Fortrea Inc. is a leading global contract research organization (CRO) 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 access, and technology solutions across more than 20...

About the RoleWe are seeking an experienced Clinical Lead to join our team at IQVIA. As a Clinical Lead, you will be responsible for providing leadership of the clinical team, in support of the project leader, and in collaboration with other functional teams, to achieve the delivery of the project's overall objectives to the Sponsor's satisfaction per...

**Career Opportunities that Transform Lives****A Day in the Life of a Clinical Specialist Associate****Key Responsibilities:**Support field personnel to deliver exceptional results and services to Medtronic clients.Collaborate with sales colleagues to develop and execute sales plans within one or more business units.Participate in conferences, forums, and...

Job DescriptionJob Title: Clinical Lead - Project ManagementJob Summary:We are seeking an experienced Clinical Lead to join our team at IQVIA. The successful candidate will provide leadership of the clinical team, in support of the project leader, and in collaboration with other functional teams, to achieve the delivery of the project's overall objectives to...

As a prominent global contract research organization (CRO) dedicated to scientific excellence and extensive clinical development expertise, CDS Fortrea Inc. offers pharmaceutical, biotechnology, and medical device clients a comprehensive array of clinical development, patient access, and technological solutions across over 20 therapeutic areas. With a...

As a prominent global contract research organization (CRO) dedicated to scientific excellence and equipped with extensive clinical development expertise, CDS Fortrea Inc. offers pharmaceutical, biotechnology, and medical device clients a comprehensive array of clinical development, patient access, and technological solutions across more than 20 therapeutic...

Overview: The Clinical Trial Coordinator plays a pivotal role in providing both administrative and technical assistance to the Project Team. This position is crucial for maintaining audit readiness by ensuring that documentation is reviewed in accordance with the organization's Standard Operating Procedures (SOP) and departmental guidelines. The...

As a prominent global contract research organization (CRO) dedicated to scientific excellence and with extensive experience in clinical development, CDS Fortrea Inc. offers pharmaceutical, biotechnology, and medical device clients a comprehensive array of clinical development, patient access, and technological solutions across over 20 therapeutic areas....

About the RoleWe are seeking a highly skilled Clinical Data Science Lead to join our team at ICON Plc. As a key member of our Full Service IOD Clinical Data Science team, you will be responsible for leading and managing clinical data review activities, ensuring timely and high-quality delivery of data fit for analysis.Key ResponsibilitiesLead Clinical Data...

Overview:As a Clinical Trial Coordinator II, you will provide essential administrative and technical assistance to the Project Team. Your role will be pivotal in maintaining audit readiness by ensuring that files are reviewed in accordance with the established schedule outlined in the organization's Standard Operating Procedures (SOP) and departmental...

Job OverviewAs a key member of the IQVIA team, the Centralized Monitoring Lead will provide leadership and guidance to the centralized monitoring team to ensure the successful delivery of clinical trials. This role will work closely with project and clinical leads to achieve project objectives, optimize speed, quality, and cost of delivery, and ensure...