Clinical Trials Research Associate - Data Capture & Study Coordination
ViziRecruiter,LLC.
ViziRecruiter,LLC. is seeking a Clinical Research Coordinator I to assist in the conduct of clinical trials. This role involves collecting and managing patient clinical data, obtaining informed consent, and ensuring compliance with Good Clinical Practice. The ideal candidate should have a Bachelor's degree, with a Master's degree preferred, along with relevant certifications. Responsibilities include data collection, subject screening, and coordination of study activities. #J-18808-Ljbffr ViziRecruiter,LLC.
- ...A healthcare organization is seeking a Research Associate to work with Principal Investigators in clinical research studies. Responsibilities include overseeing data integrity, managing study information, and preparation of research presentations. Candidates should have...Data
$19.47 - $19.81 per hour
...Perelman School of Medicine in Philadelphia, PA is seeking a Clinical Research Assistant B to assist with ongoing clinical research studies under supervision. Responsibilities include general trial support, coordination with CRCs/CRNs, and preparing regulatory documents. The...DataHourly pay- ...Worldwide Clinical Trials seeks a Senior Clinical Research Associate (CNS) to support Midwest and Southeast regions with remote options... ...lead site management across CNS studies, coordinating regulatory docs, budgets, and data capture while ensuring patient safety and regulatory...DataRemote workWorldwide
$38 - $40 per hour
...Baim Institute for Clinical Research Director, Human... ...Clinical Research Associate/Field Monitor... ...Interim Monitoring and Study Close-out Visits,... ...manner, in coordination with SM Lead and/... ...CRA Comply with Trial Master File (TMF)... ...Knowledgeable of Electronic Data Capture System (e.g...DataPart timeFor contractorsInterim roleRemote workWork from home10 hours per week- ...Montefiore New Rochelle seeks a Research Associate I to oversee multiple clinical trials, acting as a primary contact for patients and study teams. The role involves coordinating with multiple departments to... ...trial workflows, manage data entry and patient consent, and...Data
- ...Clinical Research AssistantJoin Us in Shaping the Future... ...leading clinical trial site network... ...deliver uncompromising data quality, safety,... ...and outpatient studies.We are seeking... ...confirm appointments, coordinate transportation,... ....Ensure accurate capture and upload of...DataWork at office
$4,000 - $9,000 per month
...Clinical Research AssociateDotLab is transforming the diagnosis... ...a Clinical Research Associate to join our team and... ...DotLab clinical trials. This role will initially... ...including monitoring of study data in accordance with... ...with an electronic data capture (EDC) system and eTMF...DataWork at officeRemote workWorldwideFlexible hours$58.66k - $81.68k
...Job Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities... ...# Estimates, orders and coordinates shipments of clinical study... ...Identifies and documents data errors or items requiring...DataTraineeshipLocal area$103k - $130k
...Sr. Clinical Research Associate (Sr. CRA) The Sr. Clinical Research Associate... ...device clinical trials at external clinical... ...Oversee clinical study protocol execution at... ...out, ensuring timely data collection and compliance... ..., including site coordination, investigational product...DataContract workRemote workNight shift- ...We translate unique clinical, medical affairs and... ...safety and clinical data integrity at an investigator... ...of the clinical study data review and capture. Verifies site... ...Verifies issues or risks associated with blinded or... ...of the ISF with the Trial Master File (TMF). Ensures...DataContract workInterim roleLocal areaImmediate startRemote workWork from homeFlexible hours
$96.2k - $151.4k
...ensures compliance of study conduct with ICH/... ...all phases of a clinical research study, taking... ...all phases of the trial. Performs... ...Monitoring Plan and associated documents. Gains... ...procedures. Coordinates & manages various... ...tools to ensure: Data generated at site...DataFor contractorsLocal areaRemote work2 days per week3 days per week$100k
...Works on assigned studies to ensure that... ..., Good Clinical Practice (GCP),... ...followed. • Coordinates and manages clinical... ...adverse events, trial master file maintenance... .... • Supports data management in... ...of clinical research processes and... ...Clinical Research Associates (SoCRA) or...DataContract workInterim roleLocal areaRemote work$70k - $100k
...Title: Senior Associate, Clinical Operations Location... ...or more clinical trials. The Senior Associate... ...of a clinical study (feasibility, start... ...‑based clinical research associates... ...Support internal data review, as needed... ...preparation and coordination of Investigator Meetings...DataFlexible hours- ...in New York is seeking a Clinical Research Associate to support field-based trials across diverse therapeutic areas. You will coordinate site activities, ensure... ...documents in collaboration with study teams. IQVIA emphasizes... ...empowering teams with data, smarter technology and...Data
$60k - $80k
...Behavioral Medicine is seeking a Clinical Research Associate I. In this role the Clinical... ...Research Associate I will manage and coordinate a large-scale research study on temporomandibular disorders... ...examinations to obtain clinical data and to collect oral and biological...Data- Overview As a clinical research associate (CRA), you are responsible for... ..., evaluate clinical data, and create reports... ...Responsibilities Develop and write trial protocols (outlining... ...report forms (CRFs) Coordinate with the ethics... ...reports Archive study documentation and correspondence...DataRelocationVisa sponsorship
- Clinical Research Associate - Full-Service Syneos Health is a fully integrated... ...affect subject safety and data integrity. Assess site... ...effective conduct of clinical study data review and capture, and verify site... ...completeness, reconcile it with the Trial Master File (TMF), and...DataInterim roleLocal areaImmediate startRemote workFlexible hours
- Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study data, and assist with grant applications. The role involves collaborating with investigators and research...Data
- NYU Grossman School of Medicine invites applications for a Research Coordinator in Obstetrics and Gynecology. The role supports studies in maternal‑fetal medicine, manages regulatory documents, and coordinates data collection and analysis across multiple studies. The...Data
- ...Medical Center in New York seeks a Clinical Research Coordinator to manage and assist in clinical trials. The role involves conducting... ...research and organizing study information under supervision.... ...position is crucial for ensuring data accuracy and patient consent. The...DataHourly pay
- Mount Sinai Health System seeks a Clinical Research Coordinator to support daily study activities, obtain informed consent, and manage study data with meticulous attention to regulatory requirements. The role also assists in preparing grant documentation and coordinating...Data
- The Mount Sinai Health System in New York seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and manage study data. Responsibilities include data collection, maintaining source documents, assisting with grant...Data
$71.9k - $169.3k
...OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and... ...execution of clinical trials. In this position, you will... ...sites to ensure compliance with study protocols, regulatory... ...quality of clinical research data.Key ResponsibilitiesConduct...DataFull timePart timeImmediate startWorldwide$71.9k - $189k
...sites are conducting the study(ies) and reporting study data as required by the study protocol... ...scope of work and Good Clinical Practice.• Work with sites... ...for filing in the Trial Master File (TMF) and verify... ...applying, applicable clinical research regulatory requirements.•...DataFull timePart timeLocal areaImmediate startWorldwide- ...in Germany is seeking a CRA I to join our clinical solutions team. This role supports site... ...protect patient confidentiality, and assess safety and data integrity at investigator sites, collaborating with cross-functional teams to drive study success. #J-18808-Ljbffr...DataRemote work
- ...oncology/neurology work (home-based in GA/SC). The role involves site qualification, monitoring, data review, and regulatory compliance across real-world late-phase studies. Travel up to 30% is required, with on-site or remote activities and collaboration with sponsor teams...DataRemote workWork from home
- ...Worldwide is seeking a Clinical Operations Site Management professional to join our global team in the United States. You will ensure data from study sites is accurately collected and promptly reported, supporting sponsor expectations and patient safety. The role emphasizes...DataWorldwide
- ...Piper Companies seeks a Senior Clinical Research Associate (Oncology) to support... ...sponsored Phase II-III oncology trials. This remote role requires... ...Phase II-III oncology studies, conduct site initiation, monitoring... ...-out visits, and review data to ensure high quality,...DataRemote work
- ...Worldwide Clinical Trials is seeking a Clinical Research Associate (CRA) to oversee research activities at sites involved in our clinical trials... ...ensure regulatory compliance, training, and data integrity throughout the study lifecycle. The ideal candidate has 5+ years...DataWorldwide
$53.29k - $55k
...Clinical Research Assistant Research -- Administration... ...research team and performs study coordination tasks under the... ...support of clinical trials as applicable. Job... ...eligibility packets to Data Coordination Unit (DCU... ...Preferred Qualifications: Associate degree, preferably in...DataFull time
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