Admissions Coordinator Salary at University Of Kansas BETA

Put your talents to work at PCM! Whether you work in our Home Care, Clinical Research, Impairments, or Catastrophic Care division, you will support our mission to deliver care and other services that enhance the quality of life of our clients. Be a part of our dynamic client-focused team and make a difference in your career! As an on-site Clinical Research Coordinator (CRC), you will provide technical and administrative support to your assigned clinical operations team in the field as well as direct patient care of research study participants. You work with a high attention to detail, reviewing documentation, coordinating clinical study project details, and maintaining data systems - all with a sense of urgency aligned with that of our customers. The position will involve the conduct of trial coordinator activities for EmVenio Research' decentralized network. This will include assessing and following trial participants along with other trial protocol-related activities. In this role th

Job Description Job Description We are seeking a highly organized and detail-oriented Admissions Coordinator to join our Automotive Management Training Department. The ideal candidate will be responsible for managing various NCM Institute administrative tasks, including processing registrations and cancellations for training classes, answering inbound NCMi phone calls, responding to NCMi emails, and providing support to the Institute coordinators. This role requires excellent communication skills, the ability to multitask, and a strong commitment to customer service. This role requires an in-office presence 4-5 days a week in our office located on the Country Club Plaza. Responsibilities: Registration and Cancellation Processing: Handles all aspects of NCMi student registrations and cancellations for Institute classes, ensuring accuracy and efficiency in maintaining records and managing logistics. Student Follow-ups: Proactively follow up with students to reschedule cancelled classes a

**Seeking a Clinical Research Coordinator in Lenexa, Kansas** Position: Clinical Research Coordinator Location: Lenexa, Kansas Hours: Monday-Friday; Onsite Pay: $55,000-60,000 Duties: • Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study • Administer sponsor required questionnaires (i.e. VFQ) • Works with team member responsible for ordering study supplies (lab kits, shippers, etc.) to ensure adequate inventory is on hand • Ensures study staff is properly trained on study-related information (i.e. protocol, ICF, manuals, etc.) and that the training is documented • Creates, manages, and maintains source documents for each trial • Attends teleconferences and Investigator Meetings as requested by research director • Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections • Works with other members of the study team and clin

PLEASE NOTE: Must be authorized to work lawfully in the United States for any employer without sponsorship. Kelly® Science & Clinical is seeking a Clinical Research Analyst for a temporary position (with potential to extend/covert) at a leading client in Kansas City, MO. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. Pay Rate: $30-38.00/Hour (commensurate with experience) Overview: A Clinical Research Analyst plays a critical role in the identification of qualified clinical study participants and in the collection of data required to support the development of new diagnostic and screening solutions and other medical treatments and therapies. This position requires attention to detail, a commitment to ethical research practices, and a strong ability to work in a collaborative, interdisciplinary environment. Schedule: Friday – Monday, 1st/Day: Standard Hours Responsibil

Key Responsibilities: Manage the receipt, storage, preparation, and dispensing of investigational products. Maintain accurate drug accountability records and ensure compliance with study protocols. Coordinate randomization and unblinded study documentation. Communicate with the pharmacy and unblinded study personnel regarding drug preparation and administration. Ensure proper documentation of dose modifications, side effects, and treatment adherence. Maintain strict separation from blinded study staff to prevent accidental unblinding. Assist with regulatory compliance, audits, and inspections related to investigational products. Train and educate relevant staff on unblinded procedures and compliance requirements. Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study Conducts recruitment, screening, enrollment, and consenting of participants Execute data management tasks

Overview: The Aquatics Program Coordinator II is responsible and accountable for assisting with the administration and supervision of the aquatics program area under the supervision of the Aquatics Director. YMCA Benefits Paid professional development training FREE Y family membership Opportunities for career advancement Medical/Vision/Dental Y Retirement Fund OUR CULTURE: The YMCA of Greater Kansas Citys mission and core values are brought to life by our culture. Its who we are, who we aspire to be and how we show up every day. We are cause-driven. We dont just show up, we show up with purpose. We are welcoming: we are open to all. We are a place where you can belong and become. We are genuine: we value you and embrace your individuality. We are hopeful: we believe in you and your potential to become a catalyst in the world. We are nurturing: we support you in your journey to develop your full potential. We are determined: above all else, we are on a relentless quest to make our commu

Key and scan data from toxicology requisition forms into CRL computer system. ESSENTIAL FUNCTIONS: Enter/double demographic information from requisition forms received from laboratory into computer system. Enter sample setup information from requisit Data Entry, Clerk, Technology, Healthcare, Data, Information

Job Description Job Description We are seeking a Data Entry Specialist/ Administrative Support role for our business office M-F 8:00 a.m – 5:00 p.m, in Kansas City MO. This is an important support role within our business office. A large portion of this position will consist of working with our buyers and entering purchase orders into our data base. A smaller portion of this position will include administrative support duties. This is a very detail oriented position requiring fluent Microsoft Excel skills. Some knowledge of NetSuite would be helpful, but not necessary. The starting pay for this position is $18 /hr. Requirements: High School Diploma or equivalent Ability to complete and pass pre-employment screening Previous experience in data entry or administrative support is preferred but not mandatory. Strong attention to detail, precision, and a commitment to maintaining data accuracy. Fluent in Microsoft Excel Ability to multitask effectively and accurately Excellent organizationa