Start Up Associate

Primary contact and liaison with investigative sites during study maintenance and -when assigned-, site start-up activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB submissions are made within the timelines agreed with project management and Start-up team. - Collect, track and...

Primary contact and liaison with investigative sites during study maintenance and -when assigned-, site start-up activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB submissions are made within the timelines agreed with project management and Start-up team. Essential Job Duties: ...

Trial and site administration: - Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) - Ensure collation and distribution of study tools and documents - Update clinical trial databases (CTMS) and trackers - Clinical supply & non-clinical supply management, in collaboration with other country roles - Manage Labeling requirements and...

**Job Overview**:** 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...

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...

**Study Start Up Associate I - Home-based role** ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all...

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...

**Trial and site administration**: - Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) - Ensure collation and distribution of study tools and documents - Update clinical trial databases (CTMS) and trackers - Clinical supply & non-clinical supply management, in collaboration with other country roles - Manage Labeling requirements and...

Study Start Up Associate I JR093872 Site: Buenos Aires - Argentina At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and...

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...

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...

Techunting is a dynamic company in an ever-changing industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection.As a key member of our clinical development department, you will be responsible for...

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...

100,000. That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations (GCO) touches patients’ lives every day acting as a link between science and medicine. Envision the impact you could have! #GCO Site relationship management role to ensure sustainable trial start-up at Site. The Study Start-Up CRA is...

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...

Provide expertise for local regulations, ICH/GCP and relevant study and Sponsor requirements. - When delegated by Start-up Country Manager (SUCM), oversee and ensure quality data and audit readiness. - Anticipate and prevent issues and service failures from developing in their study, escalating when appropriate, negotiating when required. - Ensure efficient...

Provide expertise for local regulations, ICH/GCP and relevant study and Sponsor requirements.  When delegated by Start-up Country Manager (SUCM), oversee and ensure quality data and audit readiness.  Anticipate and prevent issues and service failures from developing in their study, escalating when appropriate, negotiating when required.  Ensure...

Job DescriptionEnsure successful execution of start-up and maintenance activities for assigned sites and studies.Establish country/site activation plans and priorities, including risk assessment and mitigation plans.Proactively identify and communicate issues impacting delivery and propose solutions.As a US Start-Up Coordinator, you will play a key role in...

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...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives. ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing...