Country Start Up Specialist

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 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 submission of regulatory documents and providing exceptional support to our projects.Key...

Job OverviewWe are seeking a highly skilled Regulatory and Start-Up Specialist to join our team at IQVIA. As a key member of our FSP 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 international regulations, standard operating procedures (SOPs),...

Job SummaryMedpace, Inc. is seeking a highly skilled Regulatory Submissions Coordinator to join our team in Mexico. As a key member of our Regulatory Submissions department, you will have the opportunity to work on various projects, gaining valuable experience and developing your skills.Key ResponsibilitiesProvide daily support to the department and...

Job OverviewWe are seeking a highly skilled Regulatory and Start-Up Specialist to join our team at IQVIA in a Home-Based role.Key ResponsibilitiesAct as the Single Point of Contact (SPOC) for investigative sites, ensuring seamless communication and coordination with the Site Activation Manager (SAM), Project Management team, and other departments.Ensure...

Job SummaryWe are seeking a highly skilled Regulatory Submissions Manager to join our Study Start Up team in Mexico City. This role plays a critical part in the clinical trial management process at Medpace.Key ResponsibilitiesManage and execute all aspects of global start-up efficiently;Perform quality checks on submission documents and site essential...

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 AbbVieAbbVie is a leading biopharmaceutical company dedicated to discovering and delivering innovative medicines and solutions that address serious health issues. Our mission is to make a remarkable impact on people's lives across various therapeutic areas, including immunology, oncology, neuroscience, and eye care.Job DescriptionThe Area Study Start...

Job SummaryThe Area Study Start Up Lead is responsible for the on-time, budget, and quality delivery and execution of start-up and maintenance activities for assigned pipeline and Global Medical Affairs clinical studies within the area. This role reports to the Area SSU Head and serves as a single point of accountability for site start-up and maintenance...

Job SummaryThe Area Study Start Up Lead is a critical role responsible for the on-time, budget, and quality delivery and execution of start-up and maintenance activities for assigned pipeline and Global Medical Affairs clinical studies within the area. This position reports to the Area SSU Head and serves as a single point of accountability for site start-up...

Regulatory and Start Up SpecialistWe are seeking a highly skilled Regulatory and Start Up Specialist to join our team in Mexico. As a key member of our FSP 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 international regulations, standard...

Regulatory & Start Up SpecialistWe are seeking a highly skilled Regulatory & Start Up Specialist to join our cFSP team in a Home Based role.Key Responsibilities:Perform country-level tasks associated with Site Activation (SA) activities in accordance with local and international regulations, SOPs, project requirements, and contractual guidelines.Act as the...

Job Overview:As a leading global contract research organization (CRO), Fortrea is seeking a highly skilled Regulatory Specialist to join our team. 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,...

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,...

Site Activation LeadWe are seeking a highly skilled Site Activation Lead to advance clinical trial start-up activities at ICON. As a key member of our team, you will play a crucial role in understanding client objectives and developing plans for country and site distribution.Key Responsibilities:Lead clinical trial start-up activities, ensuring timely and...

Job Overview As a Pharmacovigilance Specialist at IQVIA, you will play a critical role in ensuring the safety and efficacy of pharmaceutical products in clinical trials. Under moderate supervision, you will execute feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project...

Job OverviewUnder moderate supervision, executes the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level.Key ResponsibilitiesExecute pharmacovigilance processes applicable to RSU.Submit safety reports (periodic and expedited) in a...

Job OverviewUnder moderate supervision, executes the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level for IQVIA.Key ResponsibilitiesExecute pharmacovigilance processes applicable to research sites.Submit safety reports (periodic...

Job SummaryAs a Site Activation Lead at ICON, you will play a critical role in advancing clinical trial start-up activities by understanding client objectives and assisting in the development of plans for country and site distribution.Key ResponsibilitiesLead Clinical Trial Start-Up Activities: Oversee the day-to-day delivery of all aspects of site...

{"Job Title": "Quality Assurance Specialist", "Job Summary": "We are seeking a highly skilled Quality Assurance Specialist to join our team at Dr. Reddy's Laboratories Ltd. As a Quality Assurance Specialist, you will be responsible for ensuring the quality of our pharmaceutical products by performing line clearance, material verification, and in-process...