Start-up Specialist

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...

Job DescriptionJob Title: FSP Regulatory and Start-Up Specialist in ArgentinaLocation: ArgentinaThe Regulatory and Start-Up Specialist will perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and...

Job SummaryWe are seeking a highly skilled Clinical Trials Specialist to join our team. In this role, you will be responsible for coordinating country study start-up activities and performing quality reviews of essential documents.Key Responsibilities:Coordinate country study start-up activities, including interacting with sites and study personnel to...

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...

Are you ready to redefine what’s possible, and discover your extraordinary potential at LabCorp? A career here provides the unique chance to create a lasting impact and difference in our patient’s lives. Joining our team will offer you a rewarding career, an opportunity to work in a high-energy & collaborative workplace, along with access to...

We are looking for a **Regulatory & Start Up Specialist** to join our FSP team in a Home Based role! **What You´ll Do** Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary...

**Job Overview** The **Regulatory & Start Up Specialist 2** will perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance...

Job Summary: Join Medpace in CABA! As a Regulatory Submissions Coordinator you will have the opportunity to work within the Regulatory Submissions team, supporting our many projects and gaining vital experience in the study start up and site activation process of clincial trials. You will be a productive member of the team, and will be mentored and...

The Regulatory and Start-Up Specialist will perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Developing professional...

Site Readiness and Reg Snr Specialist **Labcorp is proud to be an Equal Opportunity Employer**: As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not...

The Sr. Regulatory and Start-Up Specialist will perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Developing professional...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

**What You’ll Do** - Assist/advise project teams on all regulatory requirements for clinical studies - Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings - Review and adapt study specific documents according to each country and site requirements - Perform IRB/EC/CA...

Company OverviewBairesDev is a leading provider of clinical trial solutions, dedicated to delivering high-quality services that meet the evolving needs of our clients.Job DescriptionWe are seeking a highly skilled Clinical Trial Specialist to join our team. In this role, you will be responsible for coordinating country study start-up activities 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 The SSO Finance Specialist is accountable for budget planning, analytics and payment execution in a direct...

**Highlights**: - Base Pay Range: $18K - $24K- Equity compensation- Revenue share compensation **About Us** At Fundraise Up, we are reimagining the fundraising platform to create the most convenient and fastest way to donate to non-profit foundations. Our innovation is aimed at enhancing loading speeds, boosting conversion rates, offering diverse payment...

**Highlights** - OTE (On-Target Earnings): $33,000 - $39,000 - Base Salary: $26,400 - $31,200 - Location: remote in Argentina - Stock options **About Us** At Fundraise Up, we are reimagining the fundraising platform to create the most convenient and fastest way to donate to non-profit foundations. Our innovation is aimed at enhancing loading speeds,...

TALENT ACQUISITON SPECIALIST Modalidad híbrida o 100% remoto para quienes viven en el interior del país. Será responsable de liderar procesos de manera integral, interactuar con clientes internos, desarrollar las estrategias de selección y headhunting para atraer perfiles contables, impositivos, auditores, entre otros, de diversos seniorities. Para...

Job Title: Clinical Trial SpecialistJob SummaryWe are seeking a highly skilled Clinical Trials Specialist to join our team. In this role, you will be responsible for coordinating country study start-up activities and performing quality reviews of essential documents.Key Responsibilities:Oversee country study start-up activities, ensuring timely completion...

At IQVIA LLC, we are seeking a Senior Trade Specialist to join our team. As a key member of the CSA team, you will be responsible for importations and exportation activities in Argentina.Skillset:Import and export processesClinical research experienceInternational trade regulationsAbout the Role:The Senior Trade Specialist will ensure adherence to standard...