Average salary: $49,296 /yearly
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- A leading healthcare provider in Florissant, MO is looking for a manager to oversee daily operations, manage staff, and ensure quality service delivery. This role requires a Bachelor's degree in a relevant field, along with 2-5 years of supervisory experience and relevant...Suggested
$79.8k - $139.6k
...techniques. Find solutions to problems related to the application of bioanalytical methods. Supervise and/or drive improvements in laboratory activity processes (method development and validation). Write and review bioanalytical method SOPs. Review scientific...SuggestedRemote workFlexible hours- Parexel FSP has an exciting opportunity for a Sr. CTM. This candidate is responsible for : Manages all operational aspects for implementation of one or more clinical trials and all activities from study start-up through database lock, ensuring Good Clinical Practices...SuggestedContract workRemote work
PAREXEL
Jefferson City, MO1 day ago - ...Directs and manages all technical and administrative aspects of the laboratory. Administer Boone Health policy as well as setting local... ...Physical/Life Science or related field Experience: 5-10 Years Supervisor Experience: 2-5 Years Licenses & Certification: MT/MLS-ASCP...SuggestedLocal areaMonday to FridayShift workDay shift
- Description :Job Profile Summary The responsibility of the Clinical Research Coordinator I is to assist in providing the overall administration and operation of clinical research trials at CoxHealth. This position requires basic knowledge of clinical protocols and good...SuggestedWork at office
$3,000 per month
About the Data Entry Research Participant position We are looking for dependable, trustworthy individuals from various work experience backgrounds such as customer service, administrative assistant, nurse, construction and others to participate in various research studies...SuggestedFor contractorsWork experience placementRemote workFocusGroupPanel
Jefferson City, MO2 days ago$50 - $60 per hour
Join to apply for the Research Director role at DataAnnotation . We are looking for a Research Director to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model...SuggestedHourly payFull timeContract workPart timeRemote workDataAnnotation
California, MO2 days ago- A biotech company is seeking a Clinical Trial Manager to oversee clinical trial execution from start to finish, ensuring compliance, and managing vendors. The ideal candidate will have a Bachelor's degree and 5+ years of clinical trial experience, particularly in oncology...SuggestedFull timeFlexible hours
- ...documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging and laboratory handling manuals, etc.). Adhere to an IRB approved protocol Assist in the informed consent process of research subjects. Support...SuggestedFull timeCasual workLocal areaAfternoon shift
- Senior Clinical Research Coordinator - Internal Medicine (Nephrology) page is loaded## Senior Clinical Research Coordinator - Internal Medicine (Nephrology)locations: Kansas City Metro Areatime type: Full timeposted on: Posted Todayjob requisition id: JR009664## **Department...SuggestedFull timeContract workWork experience placement
- · Manages clinical trials, including those conducted through Contract Research Organizations (CROs)· May participate in developing and recommending operational strategies for clinical trials in collaboration with cross-functional teams· May serve as a mentor and provide...SuggestedContract workLocal area
- A prominent educational institution in St. Louis is seeking a motivated full-time Clinical Research Coordinator to manage the ADAPT initiative, focusing on psychedelic medicine. The role requires coordination of study operations, participant recruitment, and compliance ...SuggestedFull time
- ...assistants and other study staff.* Ensure proper maintenance of laboratory equipment.This job description is not designed to cover or... ...responsibilities, though occasional remote work may be permitted with supervisor approval.**Required Qualifications****Work Experience:*** Four...SuggestedFull timeWork experience placementCasual workRemote work
- Washington University in St. Louis is seeking a Clinical Research Coordinator to assist investigators with managing multiple research studies. Responsibilities include implementing study protocols, recruiting participants, and ensuring compliance with regulatory agencies...Suggested
- * Independently coordinate and manage day-to-day operations of multiple funded clinical research studies, including domestic and international projects.* Implement and oversee all phases of assigned study protocols in accordance with institutional policies, study timelines...SuggestedTraineeship
- ...professionalism including scheduling and conducting appointments, procedures, assessing eligibility, communicating with the Nursing staff, Laboratory and/or Investigators, educating study volunteers, recording adverse events, ensuring oversight Maintain contact with sponsors/...Work experience placement
- * Assists in developing plans for research projects and discusses the interpretation of results; collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies; assists in the preparation of amendments to protocols...Traineeship
- The University of Kansas Medical Center is seeking a Clinical Research Coordinator to oversee day-to-day clinical research activities, especially studies involving patients with cancer. Candidates should have at least four years of relevant experience, preferably with a...Casual workRemote work
- ...(CCRP) or certification eligible**Work Experience:*** Experience with procedures related to clinical research.* Experience with laboratory safety and regulatory requirements.**Skills*** Interpersonal skills* Communication* Computer skills* Attention to detail**Required...Full timeWork experience placementAfternoon shift
- A leading research university is seeking a Clinical Research Coordinator II to assist in managing complex clinical studies. The ideal candidate will have a Bachelor's degree and at least 2 years of clinical research experience. Responsibilities include overseeing study ...
- Clinical Research Coordinator (CRC) We are seeking a highly organized and motivated CRC to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance...Work at office
- Overview Founded in 1965, UC Irvine is a member of the prestigious Association of American Universities and is ranked among the nation’s top 10 public universities by U.S. News & World Report. The campus has produced five Nobel laureates and is known for its academic achievement...Work experience placementWork at officeLocal areaFlexible hoursWeekend workAfternoon shift
- The Senior Clinical Trial Manager plays a critical role in the strategic planning and execution of clinical trials from study start-up through close-out. This individual will oversee CROs, vendors, and clinical trial sites, while partnering cross-functionally to ensure ...
- Overview Job Title: Clinical Research Coordinator Employment Type: Full-Time (40 hours per week) Schedule: Monday to Friday, No evenings, weekends, or holidays Company Overview: Join Missouri Cancer Associates, a prestigious healthcare practice renowned for its specialization...Full timeTemporary workWork at officeMonday to FridayWeekend workAfternoon shift
- A local healthcare institution in Kansas City is seeking a Clinical Research Coordinator to join its innovative research team. In this role, you will assist with coordinating patient care in various research studies, manage scheduling, and maintain study data. Ideal candidates...Local area
- Your Role Under the direction of the Assistant Director of Clinical Research Operations, the Clinical Research Coordinator (CRC) will support the clinical research efforts of the UCI Alpha Cell Clinic by coordinating and managing data for sponsored clinical trials in compliance...Work at officeFlexible hoursWeekend workAfternoon shift
$52.6k - $78.9k
Position Summary Assists investigators as coordinator of a complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; manages and records...Work experience placementWork at office- ...and sponsor organizations.* Assist in audits, monitoring visits, and responses to queries from regulatory agencies.**Clinical & Laboratory Responsibilities:*** Coordinate sample collection, processing, and shipping according to study requirements.* Assist with study-related...Full timeWork experience placementAfternoon shift
- A major research institution located in St. Louis is seeking a research assistant who will assist in developing research plans, manage study protocols, and ensure compliance with regulatory guidelines. Ideal candidates will have a relevant degree and strong skills in data...
- A reputable healthcare practice in Columbia, MO seeks a Clinical Research Coordinator to manage and coordinate clinical research studies. The ideal candidate will screen patients, ensure protocol compliance, and collaborate with healthcare providers. Required qualifications...Full time
