Clinical Research Associate

Job SummaryWe are seeking a highly organized and detail-oriented individual to join our team as a Trial Master File Associate. In this role, you will be responsible for contributing to the development and management of both paper and electronic Trial Master File (TMF) systems for clinical trials.Key ResponsibilitiesDevelop and manage TMF systems to ensure...

Job SummaryWe are seeking a highly skilled Clinical Research Associate II to join our team at CPC Clinical Research. As a key member of our clinical trials team, you will be responsible for ensuring the smooth execution of clinical trials, from site initiation to close-out.Key ResponsibilitiesSite Monitoring: Conduct regular site visits to ensure compliance...

Job Opportunity: Clinical Research InternCPC Clinical Research is seeking a highly motivated and detail-oriented Clinical Research Intern to join our team. As a Clinical Research Intern, you will have the opportunity to gain hands-on experience in clinical research management, working closely with our experienced team of researchers and clinicians.Key...

Job DescriptionJob Summary:CPC Clinical Research is seeking an experienced Senior Clinical Trial Manager to lead and manage clinical trials site operations. The ideal candidate will have a strong background in clinical research, excellent communication and organizational skills, and the ability to work independently with minimal supervision.Key...

Job DescriptionJob Summary:CPC Clinical Research is seeking an experienced Senior Clinical Trial Manager to lead and manage clinical trials site operations. The ideal candidate will have a strong background in clinical research, excellent communication and organizational skills, and the ability to work independently with minimal supervision.Key...

Job DescriptionJob Summary:CPC Clinical Research is seeking an experienced Clinical Operations Manager II to oversee clinical operations management activities, define and monitor project scope, timelines, and deliverables, and provide expert advice in the design, writing, and/or review of all project-related essential documents.Key Responsibilities:Project...

Job SummaryCPC Clinical Research is seeking a highly experienced Clinical Trial Manager to lead and manage clinical trials from start to finish. As a key member of our team, you will be responsible for ensuring the successful execution of clinical trials, from site initiation to close-out.Key ResponsibilitiesDevelop and implement clinical trial strategies to...

Job SummaryWe are seeking a highly organized and detail-oriented Research Assistant I to support our clinical research team.Key ResponsibilitiesProvide administrative support for clinical trials, including data management, document preparation, and communication with investigational sites.Assist in the preparation of study materials, including protocols,...

Job SummaryWe are seeking a highly organized and detail-oriented Research Assistant I to support our clinical research team.Key ResponsibilitiesProvide administrative support for clinical trials, including data management, document preparation, and communication with investigational sites.Assist in the preparation of study materials, including protocols,...

Job SummaryWe are seeking a highly organized and detail-oriented Research Assistant II to support our clinical research team. The successful candidate will have a strong understanding of Good Clinical Practice guidelines and applicable regulations, as well as excellent communication and organizational skills.Key ResponsibilitiesProvide administrative support...

Job SummaryWe are seeking an experienced Clinical Operations Manager to join our team at CPC Clinical Research. The successful candidate will be responsible for managing clinical trials from initiation to close-out, ensuring compliance with regulatory requirements and company policies.Key ResponsibilitiesManage site identification, evaluation, initiation,...

Position Overview We are looking for a dedicated Trial Master File Associate to become a vital part of our organization.Key Responsibilities:Assist in the creation and oversight of Trial Master File systems for clinical studiesManage the uploading of study documentation into electronic TMF platformsGuarantee the prompt and precise organization of essential...

Job Overview We are looking for a dedicated Trial Master File Associate to become a vital part of our organization.Key Responsibilities:Assist in the creation and oversight of Trial Master File systems for clinical studiesUpload essential study documentation into electronic TMF platformsGuarantee the prompt and precise organization of critical documentsWork...

Job SummaryCPC Clinical Research is seeking an experienced Clinical Operations Manager II to oversee clinical operations management activities, define and monitor project scope, timelines, and deliverables, and provide expert advice in the design, writing, and review of project-related essential documents.Key ResponsibilitiesOversee clinical operations...

Job Title: Senior Clinical Operations ManagerWe are seeking a highly experienced Senior Clinical Operations Manager to join our team at CPC Clinical Research. As a key member of our clinical operations team, you will be responsible for managing clinical trials from initiation to close-out, ensuring compliance with regulatory requirements and company...

Job OverviewCPC Clinical Research is looking for a dedicated professional to fill the role of Clinical Trial Drug Supply Specialist.The Clinical Trial Drug Supply Specialist will oversee regulatory and investigational product management to facilitate our clinical studies. This role involves supervising both internal protocols and external partners, including...

Job OverviewCPC Clinical Research is looking for a dedicated professional to fill the role of Clinical Trial Drug Supply Specialist.The Clinical Trial Drug Supply Specialist will oversee the management of regulatory and investigational product activities essential for our clinical studies. This role involves supervising both internal processes and external...

Job OverviewCPC Clinical Research is looking for a dedicated professional to fill the role of Clinical Trial Drug Supply Specialist.The Clinical Trial Drug Supply Specialist will play a crucial role in overseeing regulatory and investigational product functions essential for our clinical studies. This position entails managing both internal workflows and...

Job DescriptionJob Summary:CPC Clinical Research is seeking a highly skilled Clinical Trial Manager I to serve as the primary point of contact for clinical trials site operations. As a key member of our team, you will be responsible for ensuring the smooth execution of clinical trials at our partner sites.Key Responsibilities:Site Operations Management:...

Job Title: Clinical Operations Manager IWe are seeking a highly skilled Clinical Operations Manager I to join our team at CPC Clinical Research. This role is ideal for an individual who can motivate teams to do great work collaboratively in order to produce the best quality outcomes possible.Key Responsibilities:Manage site identification and evaluation to...