2406 clinical research associate jobs found

Castle Biosciences Earns a Top Workplaces USA Award for the Third Consecutive Year! You won't find a work culture and benefits package like ours every day. Join our team and a group of colleagues who love working at Castle! Castle Biosciences Inc. is growing, and we are looking to hire full-time Clinical Research Associates with a preferred start date of October 1, 2024 , working remotely from your home-based office, and located near a major airport in the Eastern USA We are in search of someone who strives for excellence in their work with a positive, can-do attitude! If this sounds like the right opportunity for you in the essential biotech field, consider applying today! Learn more at www.CastleBiosciences.com EXCEPTIONAL BENEFIT PACKAGE Excellent Annual Salary + Achievable Annual Bonus Potential of 20% of Annual Salary + 20 accrued PTO Days annually + 10 paid holidays. 401K with a 100% Company match of up to 6% of your allowable Contribution, and No Waiting...

Clinical Research Associate Conducting pre-study, initiation, routine monitoring, and closeout visits Training study investigators and staff Preparing site visit reports Verifying data consistency Ensuring data collection timelines and deliverables Managing query resolution process Reporting protocol deviations Ensuring compliance with ICH/GCP/local regulations Developing and implementing corrective actions Tracking and reporting study progress Collecting, reviewing, and tracking essential documents Uploading documents into eTMF Planning and preparing training materials Managing Investigational Product (IP) inventory Ensuring proper collection and shipment of laboratory specimens Qualifications: Bachelor’s Degree (BA/BS) in life sciences or nursing degree Minimum of five (5) or more years of relevant experience in clinical research or healthcare related industry, including a minimum of 2 years direct field monitoring experience, or...

Description About Ascendion About Ascendion Ascendion is a full-service digital engineering solutions company. We make and manage software platforms and products that power growth and deliver captivating experiences to consumers and employees. Our engineering, cloud, data, experience design, and talent solution capabilities accelerate transformation and impact for enterprise clients. Headquartered in New Jersey, our workforce of 6,000+ Ascenders delivers solutions from around the globe. Ascendion is built differently to engineer the next. Ascendion | Engineering to elevate life We have a culture built on opportunity, inclusion, and a spirit of partnership. Come, change the world with us: Build the coolest tech for the world’s leading brands Solve complex problems – and learn new skills Experience the power of transforming digital engineering for Fortune 500 clients Master your craft with leading training programs and hands-on experience Experience a...

BASIC FUNCTION Apply clinical skills requiring specialized licensing to deliver and evaluate research protocols and clinical trials in the Gastroenterology and Hepatology Division of Internal Medicine. The position requires the academic knowledge of a specific discipline and professional licensure in a clinically-related field related to the study. Key areas of responsibility include research/clinical activities, protocol development and study responsibilities, subject recruitment and enrollment, data collection and monitoring, regulatory guidelines and documents, human resources/leadership and financial responsibility. KEY AREAS OF RESPONSIBILITY Research/Clinical Activities Perform clinical/health care research activities in a skilled/specialized area. Screen patient for study eligibility and consent for clinical trials. Educate patient on scope of study, potential risks and benefits, possible alternatives, and study requirements for patient. Relay...

Position Summary: The Senior CRA has wide-ranging and broad experience and typically handles the most complex and advanced assignments. Responsibilities will be dependent upon the type and timing of the program to which the Senior CRA is assigned and will, at a minimum, include start-up and study implementation activities, on-site monitoring of clinical research studies as well as on-going site management. Incumbents are expected to be able to manage appropriately sized or complex clinical trials, and support Clinical Trial Managers and/or Project Managers with trials as required. An increased focus on training and mentoring junior staff members may be expected. Essential functions of the job include but are not limited to: Independently oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports. Provides...

Position Summary: The Senior CRA has wide-ranging and broad experience and typically handles the most complex and advanced assignments. Responsibilities will be dependent upon the type and timing of the program to which the Senior CRA is assigned and will, at a minimum, include start-up and study implementation activities, on-site monitoring of clinical research studies as well as on-going site management. Incumbents are expected to be able to manage appropriately sized or complex clinical trials, and support Clinical Trial Managers and/or Project Managers with trials as required. An increased focus on training and mentoring junior staff members may be expected. Essential functions of the job include but are not limited to: Independently oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports. Provides...

Stanford University is seeking a Clinical Research Coordinator Associate at 90% FTE to perform duties related to the coordination of clinical studies, assessing the efficacy of telehealth video therapy platforms on engagement in youth with anxiety and mood conditions. The research associate would be responsible for managing aspects related to clinical trials, including recruitment, data acquisition and coordination with study participants. The research associate will work under close direction of the principal investigators and/or study coordinator/supervisor. Duties include: Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. Coordinate collection of study specimens and processing. Collect and manage patient and laboratory data for clinical...

BASIC FUNCTION Apply clinical skills requiring specialized licensing to deliver and evaluate research protocols and clinical trials in the Gastroenterology and Hepatology Division of Internal Medicine. The position requires the academic knowledge of a specific discipline and professional licensure in a clinically-related field related to the study. Key areas of responsibility include research/clinical activities, protocol development and study responsibilities, subject recruitment and enrollment, data collection and monitoring, regulatory guidelines and documents, human resources/leadership and financial responsibility. KEY AREAS OF RESPONSIBILITY Research/Clinical Activities: Perform clinical/health care research activities in a skilled/specialized area. Screen patient for study eligibility and consent for clinical trials. Educate patient on scope of study, potential risks and benefits, possible alternatives, and study requirements for patient. Relay...

BASIC FUNCTION Apply clinical skills requiring specialized licensing to deliver and evaluate research protocols and clinical trials in the Gastroenterology and Hepatology Division of Internal Medicine. The position requires the academic knowledge of a specific discipline and professional licensure in a clinically-related field related to the study. Key areas of responsibility include research/clinical activities, protocol development and study responsibilities, subject recruitment and enrollment, data collection and monitoring, regulatory guidelines and documents, human resources/leadership and financial responsibility. KEY AREAS OF RESPONSIBILITY Research/Clinical Activities: Perform clinical/health care research activities in a skilled/specialized area. Screen patient for study eligibility and consent for clinical trials. Educate patient on scope of study, potential risks and benefits, possible alternatives, and study requirements for patient. Relay...

Full job description BASIC FUNCTION Apply clinical skills requiring specialized licensing to deliver and evaluate research protocols and clinical trials in the Gastroenterology and Hepatology Division of Internal Medicine. The position requires the academic knowledge of a specific discipline and professional licensure in a clinically-related field related to the study. Key areas of responsibility include research/clinical activities, protocol development and study responsibilities, subject recruitment and enrollment, data collection and monitoring, regulatory guidelines and documents, human resources/leadership and financial responsibility. KEY AREAS OF RESPONSIBILITY Research/Clinical Activities: Perform clinical/health care research activities in a skilled/specialized area. Screen patient for study eligibility and consent for clinical trials. Educate patient on scope of study, potential risks and benefits, possible alternatives, and study...

Job Profile Summary This role focuses on performing work related to research and development of new products, innovation, and improvement of products and processes. In addition, this role focuses on performing the following Research Programs and Projects duties: Supports the development of new products and innovation. Includes Clinical roles focused on research projects. Positions in this family perform basic, translational, and/or clinical research towards solving a specific problem for an entity or community. A professional individual contributor role that may direct the work of other lower level professionals or manage processes and programs. The majority of time is spent overseeing the design, implementation or delivery of processes, programs and policies using specialized knowledge and skills typically acquired through advanced education. An experienced level role that applies practical knowledge of job area typically obtained through advanced education and work...

Job Profile Summary This role focuses on performing work related to research and development of new products, innovation, and improvement of products and processes. In addition, this role focuses on performing the following Research Programs and Projects duties: Supports the development of new products and innovation. Includes Clinical roles focused on research projects. Positions in this family perform basic, translational, and/or clinical research towards solving a specific problem for an entity or community. A professional individual contributor role that may direct the work of other lower level professionals or manage processes and programs. The majority of time is spent overseeing the design, implementation or delivery of processes, programs and policies using specialized knowledge and skills typically acquired through advanced education. An experienced level role that applies practical knowledge of job area typically obtained through advanced education and work...

Position Summary: The Stephens Family Clinical Research Institute of the Carle Foundation Hospital in Urbana, IL is building the Carle Clinical Imaging Research Program (CCIRP) with a position to be filled at the Assistant or Associate Professor level. The Carle Foundation is a vertically integrated healthcare system with almost 17,000 employees, a multi-specialty physician group, eight hospitals, and health plans. Carle also collaborates extensively with the University of Illinois at Urbana-Champaign (Illinois) in a number of initiatives. These include the Carle Illinois College of Medicine, the world's first engineering-based medical school, and the Carle Illinois Advanced Imaging Center (CIAIC). In addition to the primary appointment at Carle, additional academic appointments are possible in the relevant Illinois departments and at the Beckman Institute for Advanced Science and Technology. Carle is making a multi-million dollar investment in its research infrastructure,...

The Department of Otolaryngology - Head and Neck Surgery at The University of Iowa Hospitals and Clinics is seeking a Clinical Trials Research Associate to design, plan, promote and control clinical trials and coordinate the processing and analysis of trials data. Key areas of responsibility include protocol development/management and study responsibilities; research/clinical activities, subject recruitment and enrollment, data collection and monitoring; regulatory guidelines, documents and submission; and human resources/leadership. Duties to include: Protocol Development/Management and Study Responsibilities: Assist in the design, development, execution, administration and maintenance of protocols and clinical studies. Oversee CRF development Review query reports. Meet with study monitor. Resolve all monitoring issues. Develop complex research study materials. Initiate IRB submissions, renewals and communication with constituents. Liaise with multi-center health...

Position Summary The Stephens Family Clinical Research Institute of the Carle Foundation Hospital in Urbana, IL is building the Carle Clinical Imaging Research Program (CCIRP) with a position to be filled at the Assistant or Associate Professor level. The Carle Foundation is a vertically integrated healthcare system with almost 17,000 employees, a multi-specialty physician group, eight hospitals, and health plans. Carle also collaborates extensively with the University of Illinois at Urbana-Champaign (Illinois) in a number of initiatives. These include the Carle Illinois College of Medicine, the world's first engineering-based medical school, and the Carle Illinois Advanced Imaging Center (CIAIC). In addition to the primary appointment at Carle, additional academic appointments are possible in the relevant Illinois departments and at the Beckman Institute for Advanced Science and Technology. Carle is making a multi-million dollar investment in its research infrastructure,...

The Department of Otolaryngology - Head and Neck Surgery at The University of Iowa Hospitals and Clinics is seeking a Clinical Trials Research Associate to design, plan, promote and control clinical trials and coordinate the processing and analysis of trials data. Key areas of responsibility include protocol development/management and study responsibilities; research/clinical activities, subject recruitment and enrollment, data collection and monitoring; regulatory guidelines, documents and submission; and human resources/leadership. Duties To Include Protocol Development/Management and Study Responsibilities: Assist in the design, development, execution, administration and maintenance of protocols and clinical studies. Oversee CRF development Review query reports. Meet with study monitor. Resolve all monitoring issues. Develop complex research study materials. Initiate IRB submissions, renewals and communication with constituents. Liaise with...

Full job description The Department of Otolaryngology - Head and Neck Surgery at The University of Iowa Hospitals and Clinics is seeking a Clinical Trials Research Associate to design, plan, promote and control clinical trials and coordinate the processing and analysis of trials data. Key areas of responsibility include protocol development/management and study responsibilities; research/clinical activities, subject recruitment and enrollment, data collection and monitoring; regulatory guidelines, documents and submission; and human resources/leadership. Duties to include: Protocol Development/Management and Study Responsibilities: Assist in the design, development, execution, administration and maintenance of protocols and clinical studies. Oversee CRF development Review query reports. Meet with study monitor. Resolve all monitoring issues. Develop complex research study materials. Initiate IRB submissions, renewals and communication...

Clinical Research Coordinator – Brain (Neuro) Team - 34852 University Staff Description University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: Clinical Research Coordinator – Brain (Neuro) Team Position #: 00783932 – Requisition #: 34852 Job Summary: The Cancer Center is looking to hire a full-time Clinical Research Coordinator (CRC) to work at our Aurora, CO location on the Brain (Neuro) team. Key Responsibilities: Entry Level or CRC I: Assist with and oversee the day-to-day operations of clinical trials and studies Obtain study subject's medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required...

University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: Clinical Research Coordinator – Brain (Neuro) Team Position #: 00783932 – Requisition #: 34852 Job Summary: The Cancer Center is looking to hire a full-time Clinical Research Coordinator (CRC) to work at our Aurora, CO location on the Brain (Neuro) team. Key Responsibilities: Entry Level or CRC I: Assist with and oversee the day-to-day operations of clinical trials and studies Obtain study subject’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required Interview prospective subjects for a variety of research clinical trials. Educate potential subjects on the details of the studies...

POEMS Clinical Research Supervisor - 34850 University Staff Description University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: POEMS Clinical Research Supervisor Position #: 00693007 – Requisition #: 34850 Job Summary: As an important member of the POEMS research team, the Clinical Research Supervisor will report to the team manager This position works with Phase I-IV industry-sponsored, co-operative group and or investigator-initiated clinical trials in accordance with the trial protocols, FDA Regulations, and ICH/GCP Guidelines. It is accountable for meeting study-specific goals and timelines, while also performing and assisting with clinical tasks related to study-specific tests, procedures, and treatments as assigned based on appropriate licensure and/or completion of competency documentation and team needs. This position is responsible for coordinating study subject appointments throughout the study as well as...

University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: POEMS Clinical Research Supervisor Position #: 00693007 – Requisition #: 34850 Job Summary: As an important member of the POEMS research team, the Clinical Research Supervisor will report to the team manager This position works with Phase I-IV industry-sponsored, co-operative group and or investigator-initiated clinical trials in accordance with the trial protocols, FDA Regulations, and ICH/GCP Guidelines. It is accountable for meeting study-specific goals and timelines, while also performing and assisting with clinical tasks related to study-specific tests, procedures, and treatments as assigned based on appropriate licensure and/or completion of competency documentation and team needs. This position is responsible for coordinating study subject appointments throughout the study as well as scheduling, coordinating, and preparing for monitoring visits and audits. The incumbent is...

Clinical Research Coordinator – Melanoma Team - 34818 University Staff Description University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: Clinical Research Coordinator – Melanoma Team Position #: 740773 – Requisition #: 34818 Job Summary: The Cancer Center is looking to hire a full-time Clinical Research Coordinator (CRC) to work at our Aurora, CO location on the Melanoma team. Key Responsibilities: Assist with and oversee the day-to-day operations of clinical trials and studies Obtain study subject's medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required Interview prospective subjects for a variety of...

University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: Clinical Research Coordinator – Brain (Neuro) Team Position #: 00783932 – Requisition #: 34852 Job Summary: The Cancer Center is looking to hire a full-time Clinical Research Coordinator (CRC) to work at our Aurora, CO location on the Brain (Neuro) team. Key Responsibilities: Entry Level or CRC I: Assist with and oversee the day-to-day operations of clinical trials and studies Obtain study subject’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required Interview prospective subjects for a variety of research clinical trials. Educate potential subjects on the...

University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: Clinical Research Coordinator – Melanoma Team Position #: 740773 – Requisition #: 34818 Job Summary: The Cancer Center is looking to hire a full-time Clinical Research Coordinator (CRC) to work at our Aurora, CO location on the Melanoma team. Key Responsibilities: Assist with and oversee the day-to-day operations of clinical trials and studies Obtain study subject’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required Interview prospective subjects for a variety of research clinical trials. Educate potential subjects on the details of the studies through phone...