Clinical Study Start-Up Expert

About FeverupWe are a leading company in the Pharmaceutical /CRO industry, dedicated to delivering high-quality services to our clients. Our team is passionate about innovation and excellence, and we are seeking a talented Senior Study Start-Up Expert to join us.As a Senior Study Start-Up Expert, you will be responsible for ensuring the smooth execution of...

Job Description: As a Global Study Coordinator - Start-Up, you will play a critical role in the successful launch of clinical trials in countries worldwide. Your primary responsibility will be to oversee and lead country study start-up activities, working closely with cross-functional teams to ensure timely and efficient site activation.Key Tasks:Collect and...

Job SummaryWe are seeking an experienced Study Start-Up Specialist to join our team at Novo Nordisk Argentina.About the RoleDeveloping functional short and long-term strategic plans for Study Start-Up (SSU) in accordance with global/regional KPIs.Building and managing high-performing start-up teams to ensure timely trial deliverables.Establishing and...

Job Summary: We are seeking a highly motivated Clinical Trial Start-Up Specialist to join our team. As a key member of our start-up group, you will be responsible for ensuring the timely and successful activation of clinical trials in countries around the world.Key Responsibilities:Oversee and lead country study start up (SSU) activities, collaborating with...

Study Start up Lead Category: Clinical DevelopmentLocation: Vicente Lopez, Buenos Aires, ARAre you ready for a life-changing career at Novo Nordisk Argentina?Join us.Working at Novo Nordisk is never just a job, it is an opportunity to have a life-changing career - you grow professionally.The PositionActivities and Responsibilities Developing Study Start-Up...

Study Start up LeadCategory: Clinical DevelopmentLocation: Vicente Lopez, Buenos Aires, ARAre you ready for a life-changing career at Novo Nordisk Argentina? Join us. Working at Novo Nordisk is never just a job, it is an opportunity to have a life-changing career - you grow professionally.The PositionActivities and ResponsibilitiesDeveloping Study Start-Up...

Role Description Study-Start-Up/QC Specialist: Purpose: Study Start Up/QC Specialist is responsible for country study start up (SSU) activities and performing quality review of essential documents.The SSU/QC Specialist is responsible for overseeing and leading SSU activities in collaboration with country team members (CLM and CRA) with the objective to...

Role Description Study-Start-Up/QC Specialist:Purpose: Study Start Up/QC Specialist is responsible for country study start up (SSU) activities and performing quality review of essential documents. The SSU/QC Specialist is responsible for overseeing and leading SSU activities in collaboration with country team members (CLM and CRA) with the objective to...

The Ideal CandidateBachelor's Degree required, preferably in a health care or scientific field.A minimum of 1-2 years of clinical research experience and +1 year of study start-up management experience supporting US.Advanced English level.You should have good analytical and critical thinking skills, as well as excellent communication and interpersonal...

Job Description: Clinical Research Associate (CRA)The Clinical Research Associate (CRA) will work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate, and close-out investigational sites for clinical studies in phases II-IV. The role involves independent, proactive work to set up and...

About the RoleOur clinical trial activities in Latin America are growing rapidly, and we seek a Regulatory Submissions Manager to join our Study Start Up team. This position plays a key role in the clinical trial management process at Medpace, where you can develop and grow your career.

Study Activation and Quality Assurance Specialist: We are seeking an experienced professional to join our start-up group as a Study Activation and Quality Assurance Specialist. In this role, you will be responsible for ensuring the timely and successful activation of clinical trials in countries around the world.Key Responsibilities:Oversee and lead country...

Key QualificationsAt least 4 years of regulatory submissions/start-up management experience (leading regulatory/start-up project teams);Knowledge and experience of Clinical Trial Applications within LATAM;Strong oral and written communication skills;Team-oriented approach and strong leadership skills;Willing to work in an office-based model;Fluency in...

Primary ResponsibilitiesThe Clinical Site Identification and Feasibility specialist is responsible for supporting the administration of clinical systems and tools utilized by Development Operations, working closely with Development Operations teams, study start-up, and/or CROs to provide key inputs, metrics, and outputs to support the selection of the most...

About the PositionThe Global Study Activation Coordinator will play a pivotal role in ensuring the timely and successful execution of start-up and maintenance activities for assigned studies and sites in the US. Key responsibilities include establishing country/site activation plans, identifying and mitigating risks, and coordinating with regulatory...

We are looking for a highly skilled Project Start Up Expert to join our team at Beiersdorf S.A. (Argentina). In this role, you will be responsible for performing start up and site activation activities, working closely with sponsors and project teams to ensure successful project delivery.The ideal candidate will have experience with external commerce in...

IQVIA Regulatory & Start Up Specialist, cFSP - US Support Location: Argentina - Full Home Based rolePurpose: The RSU Specialist 1 proactively drives and executes all start up and maintenance related activities and deliverables for assigned studies and sites in their assigned country: US.Responsibilities: Ensuring successful and on time and quality execution...

Job SummaryWe are seeking a highly skilled SITE ID AND FEASIBILITY SPECIALIST to join our team at IQVIA. As a key member of our clinical operations team, you will play a critical role in supporting the administration of clinical systems and tools.Key Responsibilities:Data Management: Work closely with clinical study teams to ensure the accuracy of data in...

IQVIARegulatory & Start Up Specialist, cFSP - US SupportLocation: Argentina - Full Home Based rolePurpose: The RSU Specialist 1 proactively drives and executes all start up and maintenance related activities and deliverables for assigned studies and sites in their assigned country: US.Responsibilities:Ensuring successful and on time and quality execution of...

**Clinical Research Associate Role Overview**We are seeking highly motivated and experienced Clinical Research Associates to join our team in executing high-quality clinical research programs. Your primary responsibility will be to manage research activities at study sites, including identifying potential sites, performing study start-up activities, and...