Senior Clinical Trial Coordinator Lead

About the CompanyAt TN Poland, we are committed to delivering high-quality clinical trials that meet the needs of our clients. Our team of professionals works closely together to ensure that our trials are conducted efficiently and effectively.Job DescriptionThe Clinical Trial Coordinator will be responsible for coordinating the day-to-day activities of...

At Rho, Inc., we are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our team. As a member of our organization, you will play a vital role in the success of our clinical trials.About UsRho, Inc. is a leading Contract Research Organization (CRO) dedicated to providing exceptional service and expertise to pharmaceutical companies...

Transforming lives through clinical research is at the core of our mission at Thermo Fisher Scientific. As a leading global contract research organization, we are dedicated to improving health outcomes that people and communities depend on. Our purpose is to help customers deliver life-changing therapies, and our strategy is to bend the cost and time curve...

Job OverviewWe are seeking a highly skilled Clinical Country and Site Lead to join our team at Biogen. This role will be responsible for providing strategic direction and oversight for clinical trials in Poland.The ideal candidate will have extensive experience in managing clinical trial activities, including sponsor oversight activities in an outsourced...

OverviewJoin us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges.At Rho, we're committed to you just as you're committed to us. You'll have the opportunity to...

Medpace, a full-service clinical contract research organization (CRO), is seeking a Clinical Trial Leader to accelerate the global development of safe and effective medical therapeutics. The successful candidate will be responsible for providing medical management and expertise for clinical trials, contributing medical expertise to study reports, regulatory...

Rho, Inc. is a leading Contract Research Organization (CRO) dedicated to providing exceptional service and expertise to pharmaceutical companies worldwide. Our mission is to improve human health by advancing medical research and development.About the JobWe are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our team. As a...

Company Overview:IQVIA Argentina is a leading provider of healthcare insights, technology, and services.We are seeking an experienced Clinical Trial Operations Specialist to join our team.Job Description:The successful candidate will be responsible for coordinating the operational and strategic aspects for clinical trial submissions.Essential Functions:Lead...

We are seeking a highly skilled Clinical Operations Assistant to join our team at Parexel International. As a key member of the site management team, you will be responsible for supporting the efficient management of clinical trials.This may include tasks related to site payments, management of site supplies, trial master file, site activation, Clinical...

We are currently hiring a Freelance Regional Clinical Trial Coordinator to join our team This can be home-based in Poland, Estonia, Lithuania, or LatviaResponsibilitiesThe Freelance Regional Clinical Trial Coordinator will be responsible for supporting the preparation of Investigator Site Files, maintaining the Trial Master File, and ensuring timely...

This role offers an exciting opportunity to join a dynamic team and contribute to the success of our clinical trials. The Freelance Regional Clinical Trial Coordinator will support the preparation of Investigator Site Files, maintain the Trial Master File, and ensure timely documentation submissions to regulatory authorities.About the RoleThis is a freelance...

Clinical Trial Manager II, Dermatology & RheumatologyJob Summary:The Clinical Trial Manager II (CTM II) is responsible for the operational management and oversight of clinical investigative sites as well as clinical monitoring deliverables of clinical trials.Responsibilities:Ensures timely quality deliverables and in accordance with applicable standard...

We are seeking a skilled Freelance Regional Clinical Trials Coordinator to join our team at Rho, Inc. as a freelance professional.Job DescriptionThe Freelance Regional Clinical Trials Coordinator will be responsible for supporting the preparation of Investigator Site Files (ISFs), maintaining the Trial Master File (TMF), and uploading country and site level...

Rho, Inc. is seeking a skilled Clinical Research Project Coordinator Freelancer to join our team as a freelance professional.Job SummaryThe Clinical Research Project Coordinator Freelancer will be responsible for supporting the preparation of Investigator Site Files (ISFs), maintaining the Trial Master File (TMF), and uploading country and site level...

Worldwide Clinical Trials is a global leader in the CRO industry, and we are seeking a talented Clinical Trial Agreement Manager to join our team. In this role, you will work closely with our seasoned team of contract specialists to analyze and draft clinical research site contracts.Your excellent negotiation and communication skills will enable you to...

**Job Description** At IQVIA Argentina, we are seeking an experienced Senior Statistical Programmer to join our team. **Key Responsibilities:**Collaborate with study teams to design data structure and specifications for ad hoc and study deliverables.Ensure the quality and accuracy of clinical data as required by authorities (SDTM, ADaM, tables, figures,...

We are seeking a skilled Freelance Clinical Trial Operations Specialist to join our team at Rho, Inc. as a freelance professional.Job OverviewThe Freelance Clinical Trial Operations Specialist will be responsible for supporting the preparation of Investigator Site Files (ISFs), maintaining the Trial Master File (TMF), and uploading country and site level...

About You:To be successful as a Therapeutic Strategy Lead, you'll need:A deep and current knowledge of the scientific, clinical operations, real-world, regulatory, operational, commercial, and competitive landscape in applicable therapeutic areas.Strong global knowledge and awareness/understanding of the biopharma industry, drug development lifecycle, and...

GSK is expanding its Oncology Clinical Development organization and seeks experienced professionals to join our exciting journey.About the Position:We are looking for a highly motivated Clinical Trial Medical Review expert to join our team. The successful candidate will be responsible for ensuring the medical consistency and robustness of clinical data...

Clinical Programming ExpertiseWe are seeking a seasoned Clinical Programmer to join our team at Advanced Clinical. As a Clinical Programmer, you will be responsible for delivering high-quality data review and trial management solutions. Your primary responsibility will be to design, develop, and implement data review listings, exception reports, QTL/KRIs,...