Study Start Up Associate II

Job SummaryWe are seeking a highly skilled Study Start Up Associate II to join our team at ICON. As a key member of our team, you will be responsible for collecting, preparing, reviewing, approving, processing, and tracking regulatory and site-level critical documents required for study site activation.Key ResponsibilitiesCollect, prepare, review, approve,...

Job Title: Clinical Research Associate IIAt PSI CRO, we are seeking a highly skilled Clinical Research Associate II to join our team. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials.Key Responsibilities:Conduct and report onsite monitoring visits to ensure the highest quality standards in the industry.Be...

About PSI CROPSI CRO is a leading Contract Research Organization with over 25 years of experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering high-quality and on-time services across a variety of therapeutic indications.Job SummaryWe are seeking a highly skilled Clinical...

Regulatory and Start-Up ExpertJoin IQVIA Argentina as a Regulatory and Start-Up Expert and take on a challenging role in site management. As a key member of our team, you will be responsible for participating in end-to-end site management from feasibility to site closure. Your primary focus will be on serving as a point of contact for investigative sites and...

About the RoleWe are seeking a highly skilled and experienced Study Management Associate Director to join our Clinical Study Leadership team at AbbVie. As a key member of our team, you will be responsible for leading a cohesive regional team of Study Management Associates (SMAs) and providing guidance and support to ensure the successful execution of...

About the RoleWe are seeking a highly skilled Clinical Study Manager II to contribute to the success of our clinical trials team at ICON. As a key member of our team, you will play a pivotal role in designing and executing complex clinical trials, ensuring adherence to regulatory requirements and project timelines.Key ResponsibilitiesStudy Planning and...

Job SummaryAs a Clinical Research Associate at PSI CRO, you will have the opportunity to work on a variety of monitoring tasks and contribute to clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. We are committed to developing our employees in their careers by providing tailored courses and...

Job Title: Quality Assurance Associate IIMarken, a leading provider of clinical drug product storage and distribution services, is seeking a highly skilled Quality Assurance Associate II to join our team.Job Purpose:The Quality Assurance Associate II will be responsible for ensuring the implementation and maintenance of Marken's Quality Management System...

Job Title: Clinical Trial Manager IIAt Syneos Health, we are passionate about developing our people and creating a workplace where everyone feels like they belong. We are seeking a highly skilled Clinical Trial Manager II to join our team in Mexico.Job Summary:The Clinical Trial Manager II will be responsible for site management oversight, clinical...

Job Title: Senior Clinical Research AssociateJob Summary:We are seeking an experienced Senior Clinical Research Associate to join our team at PSI. As a Senior Clinical Research Associate, you will be responsible for conducting and reporting onsite monitoring visits, performing CRF review, source document verification, and query resolution. You will also be...

Job Title: Senior Clinical Research AssociateJob Summary:We are seeking an experienced Senior Clinical Research Associate to join our team at PSI. As a Senior Clinical Research Associate, you will be responsible for conducting and reporting onsite monitoring visits, participating in study startup, and performing CRF review, source document verification, and...

Clinical Research Opportunities at PSI CRO **About the Role** As a Clinical Research Associate at PSI CRO, you will have the opportunity to work on a variety of clinical studies in different therapeutic indications. Our team is committed to delivering high-quality results and providing a supportive environment for our employees to grow and develop in their...

About MedpaceMedpace is a leading full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.Our MissionWe accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach,...

Job Title: Senior Clinical Research AssociateWe are seeking an experienced Senior Clinical Research Associate to join our team at PSI. As a Senior Clinical Research Associate, you will play a key role in the success of our clinical trials by conducting and reporting onsite monitoring visits, performing CRF review, source document verification, and query...

Job Title: Senior Clinical Research AssociateWe are seeking an experienced Senior Clinical Research Associate to join our team at PSI CRO. As a Senior Clinical Research Associate, you will play a key role in the success of our clinical trials by conducting and reporting onsite monitoring visits, performing CRF review, source document verification, and query...

Job Title: FSP Regulatory and Start-Up SpecialistJob Overview:We are seeking a highly skilled Regulatory and Start-Up Specialist to join our FSP team in a Home Based role. As a key member of our team, you will be responsible for performing tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or...

Job DescriptionThe SMAO Line role reports into the Clinical Study Leadership (CSL) SMAO Director and is a people leader responsible for the direct management of a cohesive regional team of Study Management Associates (SMAs), who serve as front-line study execution staff. They are responsible for providing the necessary guidance and support for SMAs to master...

Job OpportunityMedpace, Inc. is seeking a highly organized and detail-oriented Regulatory Submissions Coordinator to support our team in Mexico. As a key member of our Regulatory Submissions department, you will play a vital role in ensuring the timely and accurate submission of regulatory documents.Key ResponsibilitiesProvide administrative support for...

{"Job OverviewAs a Clinical Research Associate at IQVIA, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of clinical trials. Your primary focus will be on monitoring and site management to ensure that sites are conducting the study(ies) and reporting study data as required by the study...

Job OverviewThis position will be responsible for participating in end-to-end site management from feasibility to site closure, serving as a point of contact for investigative sites and the study team members.Key ResponsibilitiesParticipate in the development of in-house model process documents.Act as a primary site contact for end-to-end study activity,...