Clinical Research Coordinator _hospital Ana Nery _salvador De Bahia

Clinical Research Coordinator _Hospital Ana Nery _ Salvador de Bahia - Part time & fixed termJoin to apply for the Clinical Research Coordinator _Hospital Ana Nery _ Salvador de Bahia - Part time & fixed term role at IQVIAClinical Research Coordinator _Hospital Ana Nery _ Salvador de Bahia - Part time & fixed term6 days ago Be among the first 25 applicantsJoin to apply for the Clinical Research Coordinator _Hospital Ana Nery _ Salvador de Bahia - Part time & fixed term role at IQVIAAre you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking Clinical Research Coordinator.This role has an immediate start working 24 hours a week for a period of months to support the site. The study coordinator should have experience clinically or nursing background as tasks includes perform EKG, collect vital signs.As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.Day to day responsibilities will include:
Verifying and/or correcting research study information on source documents;
researching queries andvariances;
providing feedback to the site data collectorAccurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS)Preparing and maintaining study files, and timely submission of informationCollecting, submitting and assisting in maintaining relevant regulatory and ethics documentsScheduling visits with research subjects, generating appropriate reports and documentationOther administrative support functions such as reception, office organization and supply management.We are looking for candidates with the following skills and experience:
BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.G. clinical research coordinator, nurse, medical assistant, other medical professionBasic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedulesBasic knowledge of medical terminologyStrong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and WordExcellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clientGood organizational skills with the ability to pay close attention to detail.As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.Day to day responsibilities will include:
Verifying and/or correcting research study information on source documents;
researching queries andvariances;
providing feedback to the site data collectorAccurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS)Preparing and maintaining study files, and timely submission of informationCollecting, submitting and assisting in maintaining relevant regulatory and ethics documentsScheduling visits with research subjects, generating appropriate reports and documentationOther administrative support functions such as reception, office organization and supply management.We are looking for candidates with the following skills and experience:
BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.G. clinical research coordinator, nurse, medical assistant, other medical professionBasic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedulesBasic knowledge of medical terminologyStrong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and WordExcellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clientGood organizational skills with the ability to pay close attention to detail.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at />//jobs.Iqvia.ComSeniority levelSeniority levelNot ApplicableEmployment typeEmployment typePart-timeJob functionJob functionResearch, Analyst, and Information TechnologyIndustriesPharmaceutical ManufacturingReferrals increase your chances of interviewing at IQVIA by 2xClinical Research Coordinator NUPEC -Belo Horizonte_ Part timelSite Navigator - Start Up Specialist - For PortugalFSP - Regulatory and Start-Up Specialist in BrazilClinical Research Associate II / SR. CRA (Level depends on experience)CRA I - Sponsor dedicated - Brazil Home BasedWe're unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.#J-18808-Ljbffr

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