We have other current jobs related to this field that you can find below
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Clinical Research Coordinator
2 weeks ago
Charleston, United States Wake Research Full timeJob DescriptionJob DescriptionCompany DescriptionM3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the...
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Clinical Research Coordinator
3 months ago
Charleston, United States Alcanza Clinical Research Full timeJob DescriptionJob DescriptionDescriptionAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general...
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Clinical Research Nurse
3 months ago
Charleston, United States Alcanza Clinical Research Full timeJob DescriptionJob DescriptionDescriptionAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general...
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Clinical Research Coordinator- 232512
1 week ago
Charleston, United States Medix™ Full timePosition Overview:In this role you will ensure IRB approved protocols are implemented and followed; execute theinformed consent process and monitor patient status and safety; collect and organize researchdata; schedule and conduct study-specific training and site in-services to study related staff onnew or amended protocols, and educate patients and their...
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Clinical Research Coordinator
1 month ago
Charleston, West Virginia, United States Massachusetts General Hospital Full timeGENERAL SUMMARY/ OVERVIEW STATEMENT:The Harvard Aging Brain study and affiliated studies at Massachusetts General Hospital and Brigham and Women's Hospital is looking to hire a highly motivated Clinical Research Coordinator. The team works across MGH and BWH to better understand the changes in the brain that may lead to Alzheimer's disease and to investigate...
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Clinical Research Coordinator I
1 month ago
Charleston, West Virginia, United States The MGH Institute of Health Professions Full timeJob Summary:The Clinical Research Coordinator I (full-time) will join the BEAM (Brain Education, and Mind) Lab at MGH IHP to manage staff, lead projects, and take on oversight responsibilities for current projects.Job Duties:The position will include oversight of general lab management tasks (IRBs, administrative tasks, organization) executed by this...
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Clinical Research Manager
2 months ago
Charleston, United States Charleston ENT & Allergy Full timeJob DescriptionJob DescriptionWe are an eclectic team inspired by intellectual curiosity and a passion for exceptional patient care. Here we lead with compassion, direction, and focus. As a Clinical Research Manager, we define success by five main components.Outstanding patient careWe strive to provide our patients with excellent customer service and...
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Clinical Research Manager
3 weeks ago
Charleston, United States Charleston ENT & Allergy Full timeJob DescriptionJob DescriptionWe are an eclectic team inspired by intellectual curiosity and a passion for exceptional patient care. Here we lead with compassion, direction, and focus. As a Clinical Research Manager, we define success by five main components.Outstanding patient careWe strive to provide our patients with excellent customer service and...
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Laboratory Services Manager
5 days ago
Charleston, West Virginia, United States Alcanza Clinical Research Full timeJob OverviewAlcanza Clinical Research is a dynamic and expanding organization engaged in multi-site, multi-phase clinical trials across various therapeutic areas, including vaccine research, neurology, dermatology, psychiatry, and general medicine. We are committed to maintaining high standards in clinical research and laboratory operations.Position...
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Clinical Research Specialist
2 hours ago
Charleston, West Virginia, United States Medix™ Full timePosition Overview:The Clinical Research Specialist plays a crucial role in ensuring that Institutional Review Board (IRB) approved protocols are executed effectively. This position involves managing the informed consent process, monitoring patient well-being and safety, and meticulously collecting and organizing research data.Key Responsibilities:● Prepare...
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Clinical Research Operations Manager
6 days ago
Charleston, South Carolina, United States Charleston ENT & Allergy Full timeClinical Research Manager at Charleston ENT & AllergyAt Charleston ENT & Allergy, we are a forward-thinking organization committed to advancing healthcare through research and innovation. Our mission is rooted in compassion, clarity, and a dedication to enhancing patient outcomes. As a Clinical Research Manager, your contributions will be measured against...
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Clinical Research Manager
4 days ago
Charleston, United States Charleston ENT & Allergy Full timeJob DescriptionJob DescriptionSingle location Clinical Research ManagerWe are an eclectic team inspired by intellectual curiosity and a passion for exceptional patient care. Here we lead with compassion, direction, and focus. As a Clinical Research Manager, we define success by five main components.Outstanding patient careWe strive to provide our patients...
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Clinical Research Operations Manager
5 days ago
Charleston, South Carolina, United States Charleston ENT & Allergy Full timeClinical Research Manager at Charleston ENT & AllergyAt Charleston ENT & Allergy, we are a progressive organization committed to advancing healthcare through innovative research and exceptional patient care. Our mission is built on the principles of empathy, transparency, and meaningful impact. As a Clinical Research Manager, your contributions will be...
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Clinical Research Operations Leader
5 days ago
Charleston, South Carolina, United States Charleston ENT & Allergy Full timeClinical Research Manager at Charleston ENT & AllergyAt Charleston ENT & Allergy, we are committed to advancing healthcare through innovative research and patient-centered care. Our mission is rooted in compassion, clarity, and purpose. As a Clinical Research Manager, your contributions will be evaluated through five essential pillars:Exceptional Patient...
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Clinical Trials Coordinator
5 hours ago
Charleston, West Virginia, United States Medix™ Full timePosition Overview:The Clinical Trials Coordinator plays a crucial role in ensuring that Institutional Review Board (IRB) approved protocols are effectively executed and adhered to. This position involves overseeing the informed consent process, monitoring patient safety and status, and systematically collecting and organizing research data.Key...
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Emergency Medicine Research Program Coordinator
6 hours ago
Charleston, West Virginia, United States Medical University of South Carolina Full timePosition OverviewThe Medical University of South Carolina is seeking a dedicated individual to fill the role of Research Program Coordinator I in the Emergency Medicine department. This position involves critical responsibilities in the recruitment and management of study participants according to established criteria.Key Responsibilities:Recruit study...
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Emergency Medicine Research Program Coordinator
6 hours ago
Charleston, West Virginia, United States Medical University of South Carolina Full timePosition Overview The Medical University of South Carolina is seeking a dedicated individual to fulfill the role of Research Program Coordinator I in the Emergency Medicine department. This position involves a variety of responsibilities aimed at supporting clinical research initiatives. Key Responsibilities Recruit study participants according...
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Manager, Laboratory Services
3 weeks ago
Charleston, United States Alcanza Clinical Research Full timeJob DescriptionJob DescriptionDescriptionAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general...
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Senior Clinical Research Specialist
6 days ago
Charleston, West Virginia, United States Thermo Fisher Scientific Full timeAbout the Company: Thermo Fisher Scientific stands at the forefront of scientific exploration and innovation, dedicated to empowering clients to enhance health outcomes and drive advancements in research. Become a part of our dynamic team and engage in meaningful work that has a global impact. Job Title: Senior Clinical Research Specialist - Bilingual...
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Registered Nurse 1 Clinical Research
1 month ago
Charleston, United States CAMC Health System Full timeJob Summary Administers research protocols for CAMC. Responsibilities • Manage research elements essential to study. • Supervise sub-center activities. • Develop and coordinate ancillary sub-studies; coordinate multiple studies simultaneously. • Manage clinical care of participants. • Serve as resource for participants and study physicians. •...
Clinical Research Coordinator
2 months ago
Clinical Research Coordinator (Must be Bi-lingual - English/Spanish)Department: Operations Employment Type: Full TimeLocation: Coastal Carolina Research Center | Charleston, SCReporting To: Nikki ShebelskieDescriptionAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs. Key ResponsibilitiesIn collaboration with other members of the clinical research site team works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: Screening of patients for study enrollment;Patient consents;Patient follow-up visits;Documenting in source clinic charts;Entering data in EDC and answers queries;Obtaining vital signs and ECGs;Performing blood draws as needed;May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests;Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;Scheduling subjects for study visits and conducts appointment reminders;Building/updating source as needed;Conducting monitoring visits and resolves issues as needed in a timely manner;Ensuring study related reports and patient results are reviewed by investigator in a timely manner;o Filing SAE/Deviation reports to Sponsor and IRB as needed;o Documenting and reporting adverse events;o Reporting non-compliance to appropriate staff in timely manner;o Maintaining positive and effective communication with clients and team members;o Always practicing ALCOAC principles with all documentation;Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed;Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed;Assist with training of new research assistants and coordinators;Assist with scheduling and planning for visit capacity for assigned studies;May set up, train and maintain all technology needed for studies;May assist with study recruitment, patient enrollment, and tracking as needed;May handle more complex study assignments and volumes;May participate in community outreach / education events;Maintaining confidentiality of patients, customers and company information, and;Performing all other duties as requested or assigned.Skills, Knowledge and ExpertiseMinimum Qualifications: A Medical Assistant diploma, LPN/LVN, EMT credential AND 2+ years of clinical research coordination experience, OR an equivalent combination of education and experience, is required. Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred. CCRC or CCRP credential and BLS certification preferred. Bi-lingual (English / Spanish) proficiency is required. Required Skills: Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etcStrong organizational skills and attention to detail.Well-developed written and verbal communication skills. Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.Must be professional, respectful of others, self-motivated, and have a strong work ethic.Must possess a high degree of integrity and dependability.Ability to work under minimal supervision, identify problems and implement solutions.Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines. BenefitsFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
