Study Site Facilitator

Main ResponsibilitiesParticipate in feasibility studies with delegated tasks from FS responsible;Site selection and qualification evaluation under supervision of senior personnel;Assist during study set-up regarding submission and approval process and preparation of documentation as per local requirements;Collect all ECs requirements per allocated...

Job DescriptionMSD is seeking an experienced Clinical Research Manager to oversee the execution of clinical trials.This role will involve managing project timelines, ensuring quality standards are consistently met, and facilitating successful outcomes.The ideal candidate will have a strong background in clinical research, project management, and site...

Responsibilities and ExpectationsServe as the single point of contact (SPOC) for assigned studies, collaborating with investigative sites to ensure adherence to Standard Operation Procedures (SOPs), work instructions (WIs), and project timelines.Perform Regulatory Start-up and Maintenance activities, distribute completed documents, and prepare site...

Directly reporting to the Director (Turkey)About Us:Study Now is a leading education consultancy firm, dedicated to assisting students in finding the best study opportunities worldwide. We work closely with universities, colleges, and other educational institutions to facilitate the recruitment and admission process. We are committed to providing...

Parexel FSP is hiring an Associate Clinical Study Director to join us on a permanent full-time, 3 days office based.If you're driven by the potential of science to create meaningful change and eager to explore your capabilities, join us.Dedicated to a single sponsor in BioPharma, who is revolutionizing healthcare by harnessing the power of science to benefit...

Job SummaryMerck Gruppe - MSD Sharp & Dohme is seeking a highly skilled Clinical Research Manager to lead our team in delivering exceptional results in clinical trials. The ideal candidate will possess strong project management skills, excellent communication abilities, and a passion for maintaining the integrity of clinical research.Responsibilities:Manage...

Tech Research Studies is a division of Voxelmaps, dedicated to gathering valuable user insights that drive technological innovation. This department specializes in in-person paid focus groups, connecting individuals with some of the world's leading brands to provide feedback on existing products and upcoming innovations.With a focus on user experience and...

Milestone One's mission is to empower clinical study sites to achieve their full potential. Our Site Coordinators play a vital role in helping us deliver on this promise.Job DescriptionThis position involves coordinating all aspects of clinical trials at our partner sites, including communication with sponsors and CRAs, data management, and site training.You...

Job ResponsibilitiesUnder general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites.Ensure adherence to Standard Operation Procedures (SOPs), work instructions (WIs), quality of designated deliverables and project timelines.Perform Regulatory Start-up and Maintenance activities according to applicable...

Role and ResponsibilitiesRegulatory Expertise: Utilize your expertise to perform Regulatory Start-up and Maintenance activities, preparing site regulatory documents and ensuring compliance with applicable regulations, SOPs, and WIs.Communication: Serve as the primary point of contact for assigned studies, maintaining open communication with investigative...

About the RoleThe Commercial Contract Manager will be responsible for developing and implementing commercial contracting strategies to support the growth of IQVIA Argentina. This role requires strong legal, financial and technical writing skills, as well as the ability to communicate effectively with sponsors, stakeholders and colleagues.Key...

Job DescriptionAs a Clinical Research Manager, you will be responsible for managing and overseeing all aspects of clinical trials. This includes everything from the initial study design to the execution phase. Your role will involve ensuring that all project timelines are adhered to and quality standards are consistently met throughout the trial process. By...

Site Contracts Specialist II or Senior - Turkey home based - Sponsor dedicatedUpdated: January 27, 2025Location: Europe-TurkeyJob ID:25001260Syneos Health is 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...

About UsIQVIA Argentina is a leading provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are seeking a skilled Regulatory Affairs Contract Lead to join our team and contribute to the development and implementation of regulatory contracting strategies to support the growth of our company.Key...

Role OverviewThe Regulatory Affairs Contract Lead is responsible for leading the development and implementation of regulatory contracting strategies to support the growth of IQVIA Argentina. This role requires strong knowledge of regulated clinical trial environment and drug development process, as well as the ability to communicate effectively with...

Job DescriptionAs a Clinical Research Manager, you will be responsible for managing and overseeing all aspects of clinical trials. This includes everything from the initial study design to the execution phase. Your role will involve ensuring that all project timelines are adhered to and quality standards are consistently met throughout the trial process. By...

Job OverviewDevelop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor's requirements.Essential FunctionsDevelop and coordinate the development of investigator grants and estimates, contracting strategies and proposal...

Milestone One is a global Site Enabling Services organization, dedicated to supporting clinical study sites in delivering strong study outcomes.Job OverviewWe are seeking an experienced Clinical Trial Site Coordinator to join our team. As a key member of our site enablement team, you will be responsible for providing support to trial sites throughout the...

Essential Functions and Other Job InformationParticipation in feasibility studies with delegated task from FS responsible; approaching investigators and collects the requested information within the shortest possible timelines in compliance with all terms of confidentiality and current applicable SOPs.Site selection and qualification evaluation under...

Job DescriptionThe Clinical Payment Specialist role involves supporting the budget planning, analytics and payment execution in a direct country or extended study group. This requires close collaboration with SSO Study Start-Up Managers, SSO Clinical Project Managers and SSO Contracting Specialists to ensure compliance with regulatory requirements.Main...