Clinical Study Manager

Join us at IQVIA LLC as a Global Study Manager! In this role, you will be responsible for overseeing global study activities, ensuring compliance with GCP/ICH and regulatory requirements. You will work closely with SSO Study Start-Up Managers, SSO Clinical Project Managers, and SSO Contracting Specialists to develop and implement effective study plans,...

Job SummaryWe are seeking a skilled and dedicated Clinical Trial Assistant to support our clinical research activities. As a key member of our team, you will play a critical role in ensuring the accuracy and completeness of clinical documentation, managing study files, and coordinating with the clinical team.Key Responsibilities:Support clinical research...

Job Description:Clinical Payments SpecialistAt IQVIA LLC, we are seeking a Clinical Payments Specialist to join our team. The successful candidate will be responsible for budget planning, analytics, and payment execution in a direct country or extended study group (OPC and satellite countries) in close collaboration with the SSO Study Start-Up Managers, SSO...

Company DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services...

About the JobAs a Senior Clinical Project Manager at IQVIA Argentina, you will play a critical role in leading clinical trials from start to finish. Your expertise and leadership skills will be essential in driving project delivery, productivity, and quality. You will work closely with cross-functional teams to ensure seamless project execution and...

Job OverviewClinical Project Leads are essential members of the core project team responsible for delivering clinical studies to meet contractual requirements in accordance with SOPs, policies and practices.The focus is on leveraging therapeutic expertise and IQVIA's suite of solutions to drive operational excellence and strategic leadership with customers.

Project Management Professional - Clinical TrialsWe are seeking an experienced Project Management Professional to lead clinical trials from initiation to closure. As a key member of our clinical project management team, you will be responsible for developing and implementing project plans, managing resources, and ensuring timely delivery of projects. Your...

Parexel International is a global leader in clinical research outsourcing, revolutionizing healthcare by harnessing the power of science to benefit people, society, and the planet.The company is a vital part of their global network, hosting colleagues from every life sciences value chain segment. Their science-driven approach aims to transform healthcare and...

Job OverviewWe are seeking a highly motivated and organized Clinical Trial Assistant to join our team at IQVIA. The successful candidate will be responsible for supporting the clinical research process, ensuring accurate and complete documentation, and providing exceptional customer service.Essential Functions:Assist with updating and maintaining clinical...

Job SummaryThe Investigator Payments Analyst role is responsible for budget planning, financial analysis, and payment execution in direct countries or extended country groups (OPC and satellite countries) in collaboration with Study Start-Up Managers, Clinical Project Managers, and Contracting Specialists.This position ensures compliance with GCP/ICH and...

Job OverviewWe are seeking a seasoned Clinical Trial Manager to join our team at Syneos Health, Inc.This role will involve overseeing site management, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol compliance, and data integrity.The successful candidate will have prior experience in leading teams and...

Job OverviewIQVIA Argentina is seeking an experienced Clinical Research Project Lead to join our team. As a key member of our clinical project management team, you will be responsible for leading clinical trials from initiation to closure. Your expertise and leadership skills will be essential in driving project delivery, productivity, and...

ResponsibilitiesThe Clinical Trial Site Coordinator role requires the ability to work independently and as part of a team to achieve project goals.Key SkillsFlexibility in working hours may be required depending on the schedule of study procedures and/or patient visits.Ability to effectively communicate with sponsors, investigators, and other stakeholders.

What You'll DoServe as a key liaison between Trial Grants Experts and sites to ensure accurate feedback and Grant Plan leveling.Implement innovative and efficient processes to enhance study delivery and site satisfaction.Manage internal controls and maintain adherence to financial standards, prevailing legislation, ICH/GCP, IRB/IEC, Health Authority, and SOP...

QualificationsBachelor's Degree in Life Sciences or related field required. 5 years of prior relevant experience including > 1 year project management experience.Advanced knowledge of clinical trials and broad knowledge of other related job areas.Strong written and verbal communication skills, problem solving skills, leadership skills and organizational...

**Syneos Health, Inc.**We are a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of everything that we...

About the RoleThe Clinical Research Contracts Specialist is responsible for ensuring that all contracting activities are completed efficiently and effectively to meet our clients' needs.Main Responsibilities:Develop and coordinate the development of investigator grants and estimates, contracting strategies, and proposal text to support the proposal...

About the RoleThis is an exciting opportunity to join our team as a Study Site Activation Specialist. In this role, you will be responsible for managing the site activation process for clinical trials, working closely with sites, sponsors, and other stakeholders to ensure successful trial execution.You will be part of a dynamic team that values innovation,...

About the RoleThis position plays a critical role in ensuring the successful execution of clinical studies at investigative sites.Key ResponsibilitiesServe as Single Point of Contact (SPOC) for assigned studies, providing timely and accurate support to site staff.Evaluate and Maintain Compliance with Standard Operation Procedures (SOPs), work instructions...

**Company Overview**Syneos Health is a leading provider of biopharmaceutical solutions, combining late-stage clinical development services, data analytics, intelligence, and full-phase management. Our goal is to transform the way healthcare companies develop and deliver innovative medicines and devices that improve patients' lives.As a Country Operations...