Clinical Research Assistant Jobs

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Job Description : The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required)...

Vocational Tech To assist the Clinical Research Coordinator in conducting clinical trials. The Research Assistant is responsible for collection, process, storage and handling of clinical specimens, scheduling study patients, collection, recording, and filing of clinical data. Performs all job duties in a manner consistent with Corporate Values, FDA, GCP and ICH guidelines. Performs duties and res...

Requisition ID: 16721 Title: Temp Clinical Research Assistant Division: Arthrex, Inc. (US01) Location: INC- Naples, FL (US08) Please note, this is a temporary position and is not eligible for benefits. Main Objective: Support Clinical Research Associate and study site staff in accordance with good clinical practices in FDA regulated trials. Assist in the development and maintenance of El...

Demonstrates through behavior of the company core values of integrity, compassion, balance, excellence, stewardship and teamwork as outlined in the organizations performance excellence Program. Assists the CRN with conducting clinical research trials in accordance with trial protocols, state and federal regulations, and ICH/GCP guidelines by actively screening, assessing eligibility and registerin...

The Clinical Research Assistant position is in Department of Clinical and Regulatory. He/she will be responsible for: Clinical Study Document Management: the storage and archiving of the study related documentation, the creation, updating, maintenance and validation of clinical study databases, both for study and device(s) registry § the computerization of these data § communication with moni...

Description : The Research Assistant provides general office management, subject scheduling and data management. Responsibilities include the creation, updating and maintenance of research charts and case report forms; and the compilation, registration and submission of data. He or She is also responsible for monitor study compliance, ensure effective data flow associated with research protocols...

Seeking a Clinical Trial Assistant for a long-term consulting position at a pharmaceutical client in Fort Worth, TX 76134. Assist Clinical Trial Management to ensure accurate, timely, and coordinated availability of clinical trial materials and documents. Mentor and assist with training of incoming CTAs. Assist with process improvement efforts. Major Accountabilities - 1. Enter and maintain curr...

Braverman IVF & Reproductive Immunology (BRI) is a private medical practice that specializes in the diagnosis and treatment of immunological causes of infertility and recurrent pregnancy loss. Their highly specialized approaches to diagnosis and treatment have helped thousands of women around the world to overcome an inability to initiate or maintain a pregnancy. BRI’s extensive expertise and expe...

Job Description : Essential Function Perform the clinical monitoring aspect of designated projects in accordance with study specific procedures, applicable SOPs, and regulations. Act as PAREXEL’s direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites. Responsibilities include, b...

Overview: The Clinical Research Center Administrative Coordinator provides support to the CRC Nurse Manager and the Section Head of Clinical Research. Working collaboratively with other support staff, s/he maintains office operations and communications and moderates patient flow into the unit. The Coordinator also maintains and organizes database of equipment, maintenance, supplies and billing; r...

Job Description : Essential Function The responsibility of a Senior Clinical Research Associate (SCRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities including performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory...

Job Description : Essential Function The responsibility of a Senior Clinical Research Associate (SCRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities including performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory...

CLINICAL/ RESEARCH LABORATORY TECHNICIAN The Bleeding and Clotting Disorders Institute (BCDI), the only federally recognized bleeding and clotting disorders treatment center of excellence south of Chicago in Illinois, is adding another fulltime Clinical/Research Laboratory Technician to our dynamic expanding medical care team. Duties include performing a wide range of routine and special hemato...

MINIMUM JOB REQUIREMENTS: EXPERIENCE: Three year's cardiac experience required, clinical research exposure required. RN & Regulatory experience a huge plus!! SKILLS : Demonstrate either by experience or education, extensive knowledge of cardiovascular disease processes and appropriate diagnostic, therapeutic, and curative therapies. Self-motivation and direction. Strong prioritization and organi...

This position is located in our MD, Silver Spring facility a. Serve as assistant investigator with scientific and technical skills to develop relevant phenotypic, genotypic and taxonomic assays, models and systems (in vitro and in vivo) related to the cause, effect and clinical management of MDRO surveillance and infections. b. Serve as technical expert in the microbial pathogenesis and relat...

Research Assistant 1/Research Associate 2 - Clinical Pathology About MPI Research: MPI Research, with global headquarters in Mattawan, Michigan, provides discovery, safety evaluation, bioanalytical, and analytical services to the biopharmaceutical, medical device, animal health, and chemical industries. Scientific knowledge and experience, integrity, trust, teamwork, and dedication to strong and...

The Research Specialist Assistant will assist the Research Coordinator with the regulatory and administrative aspects of maintaining adherence to oncology research protocols. Specific functions will include but are not limited to: timely regulatory submissions for continuing review and offsite reports, IRB submissions as mandated by the sponsor or IRB, specimen collection and preparation, document...

Duties include, but are not limited to: Preparing documents, such as protocols, consents, and applications, for IRB and institutional regulatory authorities for study initiation and ongoing review REDCap database development and ongoing support Recruiting and enrolling study participants Study scheduling and tracking subject participation Abstracting data from patient charts Developing data ...

Clinical Research Assistant (Clinical Trials, St. Francis, Full time, Days)-1500005872 Description Job Summary: The Clinical Research Associate (CRA) coordinates the collection, evaluation and processing of clinical trial data. The CRA acts as a liaison among the Cancer Treatment Center team, local physicians, laboratory, pathology, radiology departments, University of Nebraska Medical Center, ...

Job Title : Clinical Research Coordinator,Norton Hospital,Oncology Research,8a-4:30p FT Status : Full-Time Shift : Day Location : Louisville, KY Facility : Norton Hospital About Norton Healthcare For more than 125 years, Norton Healthcares faith heritage has guided its mission to provide quality health care to all those it serves. Today, Norton Healthcare is a leading health care system...