Clinical Research Contracts Specialist

Job Title: Clinical Research SpecialistJob Summary:We are seeking a highly skilled Clinical Research Specialist to join our team at Innovaderm Research. As a key member of our Site Selection and Contracting team, you will work closely with project teams and the legal/contract department to prepare, negotiate, and execute budgets and contracts with...

Key Responsibilities:As a Contracts Specialist 2, you will play a crucial role in preparing and negotiating site agreements, confidentiality agreements, and other contracts for Sponsors who contract Fortrea to perform clinical studies. Your primary responsibilities will include:Preparing and negotiating site agreements, confidentiality agreements, and other...

Job SummaryThe Site Budget and Contract Specialist is a key member of the Site Selection and Contracting team at Innovaderm Research. This role involves working closely with project teams and the legal/contract department to prepare, negotiate, and execute budgets and contracts with investigator sites across Canada and internationally.Key Responsibilities:...

Job Summary:The Site Budget and Contract Specialist will be a key member of the Site Selection and Contracting team at Innovaderm Research. This role will involve working closely with project teams and the legal/contract department to prepare, negotiate, and execute budgets and contracts with investigator sites across Canada and internationally.Key...

Key Responsibilities:As a Clinical Research Specialist at ICON plc, you will be responsible for leading strategic calls and meetings with clients to discuss how to best apply digital measures and DHTs to all therapeutic areas covered in the client's portfolio. You will provide expert guidance on best practices, potential challenges, and solutions for...

Company OverviewWorldwide Clinical Trials is a leading global contract research organization (CRO) that partners with biotechnology and pharmaceutical companies to create customized solutions for advancing new medications.Job SummaryWe are seeking a Senior Specialist, Site Contracts to join our team in Spain. As a key member of our contracts team, you will...

Job Overview:The Clinical Contracts Manager will oversee the execution of Clinical Contracts to ensure consistency and quality while identifying and solving any issues that potentially would delay the negotiation and execution of site contracts. The Lead directly supports the study Project Manager by collaboration with Clinical Trial Regulatory Manager...

Key Responsibilities:• Gather information from technical contacts (medical writers, physicians, statisticians, regulatory affairs, and pharmacovigilance team members).• Create and update abbreviated protocols, amended protocols, and lay protocol synopsis.• Co-write and write clinical study reports for phase 1 to 4 studies.• Draft various clinical...

About UsWe're a global, mid-sized Contract Research Organization (CRO) that fosters innovation and excellence in clinical trials. Our mission is to improve lives by working with passion and purpose every day. At Worldwide Clinical Trials, we're committed to a diverse and inclusive environment that promotes collaboration and creativity.Our TeamWe're a global...

Job SummaryThe Site Contracts Template Specialist plays a crucial role in identifying and prioritizing opportunities to maintain an appropriate inventory of site contract templates. This position requires revising global, country, and site-specific templates to align with changing external and internal requirements.Key ResponsibilitiesAs a divisional subject...

Job SummaryThe Clinical Research Vendor Manager is responsible for managing vendors during study start-up and maintaining oversight and issue resolution management during study conduct. This role requires close collaboration with the project management team for all project-specific vendors' needs. The ideal candidate will have experience working with vendors...

The Clinical Research Associate Specialist at Parexel plays a crucial role in the start-up phase of clinical trials. This position involves performing all study start-up activities, from site identification to pre-initiation. The specialist will be responsible for managing and driving the strategy for the Pre SIV/start-up tasks of the study, ensuring quality...

Deliver Quality and Accuracy in Clinical ResearchAt Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Our Clinical Operations colleagues provide end-to-end support for clinical trials from study start-up to monitoring through to study close-out, across commercial and government contracts.As a Clinical...

About the RoleWe are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team at Innovaderm Research. As a key member of our site activation team, you will play a critical role in ensuring the successful execution of clinical trials.Key ResponsibilitiesPrepare Investigator Sites for clinical trials by reviewing and...

About the Role:Innovaderm Research is seeking a highly skilled Clinical Research Vendor Manager to join our team. As a key member of our project management team, you will be responsible for establishing and managing project supplier and vendor scope, timelines, and costs for awarded opportunities throughout the project life cycle.Key Responsibilities:•...

About the Role:The Contract Specialist plays a pivotal part in overseeing the negotiation and preparation of contracts and related documents for participation in industry-sponsored clinical trials. This role involves producing site-specific contracts from country clinical trial agreement (CTA) templates, negotiating budget and contract terms with sites and...

About the RoleWe are seeking a skilled Clinical Research Specialist to join our team in Spain. As a Regulatory Start-up/Site Activation Specialist, you will play a vital role in ensuring the successful activation and management of clinical sites.About IQVIAIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research...

Job Overview:The Clinical Contracts Strategist will oversee the cross-functional execution of Clinical Contracts to ensure consistency and quality while identifying and solving any issues that potentially would delay the negotiation and execution of site contracts. The role directly supports the study Project Manager by collaboration with Clinical Trial...

Job SummaryAs a Clinical Research Associate at Premier Research, you will play a crucial role in transforming life-changing ideas into reality. You will be working in a friendly environment with colleagues who are genuinely supportive.Responsibilities:Deliver high-quality, timely monitoring reports for sponsor approval per Clinical Monitoring Plan...

**About ICON Plc**ICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment driving innovation and excellence, and we welcome you to be a part of our mission to shape the future of clinical development.**Job Overview**We are seeking a Clinical Research Outcomes Specialist to join our team at...