Clinical Pharmacist Salary at Axion Healthcare Llc BETA

Job Summary: All shifts as needed (6:45-15:15, 14:45-23:15, 22:45-07:15) possibly 12 hour shifts too (primarily weekend 06:45-19:15, 18:45-07"15) or doubles on the weekend 06:45-23:15. For orientation must have the ability to dedicate approximately 6 weeks on all 3 shifts for training Required Skills: ICU is preferred, telemetry, or emergency room experience At least 1year experience Active Illinois license Responsibilities: • Participate in the execution of protocol activities of a Phase I clinical research study conducted at the Phase 1 Unit. • Maintain safety and confidentiality of study subjects throughout the study • Evaluate adverse events and manage safety reporting activities in a timely manner. • Review protocols and informed consent forms for scheduled studies, identify, and communicate potential issues to the appropriate personnel. • Participate in nursing study related activities as required by protocol in compliance with corporate, divisional, and depart-mental SOP’s and e

Responsibilities: Review and adhere to study protocols and perform study-specific activities as assigned. Communicate professionally and appropriately with study subjects and unit personnel to ensure effective study operations. Maintain accurate and complete source data documentation. Perform study protocol-related procedures. Phlebotomy and sample processing. Electrocardiogram (ECG) collection. Vital signs measurement (e.g., blood pressure, heart rate). Height and weight collection. Ensure the safety, confidentiality, and well-being of study subjects throughout the study. Adhere to Standard Operating Procedures (SOPs), FDA regulations, and Good Clinical Practice (GCP) guidelines. Requirements: High School Diploma or equivalent required. 1-2 years of work experience in a clinical, research, or patient care setting. 1-2 years of experience with phlebotomy responsibilities. Proficiency in clinical tasks such as lab work, ECG collection, and vital signs assessment. Strong understanding of

Open 24/7, will work 8 hour shifts. There is no guarantee of hours. Some weeks may have no shifts whereas others may have 4 or 5. Shift options: day shift for training, then PM and AM, PM, night weekend shifts for contract. Schedule comes out every 2 weeks, Name of Functional Area/Department: Clinical Pharmacology & Pharmacometrics Research Unit (Located in Grayslake) Minimum Education Required: High School Diploma or equivalent Preferred Education: Clinical Medical Assistant, EMT, Paramedic, military medic with recent clinical experience, or higher Minimum Experience Required: •1-2 years of work experience in a clinical or research environment, or in a patient care setting; and •1-2 years of work experience in a role with phlebotomy responsibilities Major Job Responsibilities: •Review protocols and comply with study-specific activities •Communicates in an appropriate and professional manner with study subjects and unit personnel. •Maintain accurate and complete source data. •Perform s

Clinical Research Coordinator Must Haves: Must have phlebotomy experienced and have 1+ years of experience as a Clinical Research Coordinator Hours: 40 hours per week, normal business hours, hybrid schedule (4 days onsite, 1 day remote). Contract Duration: Direct Hire - permanent employee from day one. Benefits: Medical, Dental, Vision, PTO, 401k (employer pays into, no match required), bonus structures and raises based on performance, etc. Job Summary responsible for day-today-management and coordination of 2-3 clinical trials at once, 10-20 patient visits per week, ensuring the safety of participants and adherence to protocols and regulations Minimum Qualifications Must have phlebotomy experience Coordinator who has experience with everything- consent, phlebotomy, audits, IRB, prefer previous CNS experience Candidate must be flexible, will mainly work day shift but could need to come in occasional evenings or early mornings to see patients, no overnights Apply Today!

Job Description: Be a part of a world-class academic healthcare system at UChicago Medicine as an Ambulatory Medication Access Coordinator in the DCAM Outpatient/UCMC Pharmacy Services- Mail Order Pharmacy Call Center- Burr Ridge. In this role you will be responsible for assistance with conducting and completing necessary third party (insurance) prior authorization requests and associated services related to high-cost medications, maximizing efficiency for patients and clinic staff. UChicago Medicine Duchossois Center for Advanced Medicine - Hyde Park, also known as DCAM, is our flagship outpatient facility and is home to dozens of primary and specialty clinics as well as a pharmacy. Job Summary In this role, the Ambulatory Medication Access Coordinator, or AMAC, performs necessary functions to ensure optimal reimbursement for high cost, take home medications for patients receiving care in UCMC ambulatory clinics. Other areas of responsibility include pre-screening patients for viable

Job Summary JOB SUMMARY Conduct and manage human clinical trials and other research related activities with direction from other Clinical Operations management or designee and in accordance with ICH International Committee for Harmonization and Good Clinical Practices (ICH/GCP) guidelines, and Medline Industries, LP. Standard Operating Procedures (SOPs). Job Description MAJOR RESPONSIBILITIES Collaborate with the Medical Affairs (MA) teams to develop or update study protocol(s) and any related forms, templates, or tools such as the Informed Consent Forms (ICFs, the CRFs (Case Report Forms), Clinical Monitoring Plan, recruitment materials, and any other study related documents for both Internal and External clinical trials. Collaborates with other Medical Affairs team members on study strategy and budget development (ex: Fair Market Value software). With support and supervision, plans, conducts, and executes all types of monitoring visits in compliance with ICH/GCP, FDA Code of Federal

Monopar is a growing biotech company seeking a bright, motivated, and collaborative Clinical Research Data Scientist to support the company’s late-stage rare disease and Phase 1 radiopharmaceutical pipeline. You will join a growing, talented team and will be a member of the core cross-functional team that is leading an FDA New Drug Application for Monopar’s Wilson disease candidate with significant opportunities for impact and growth. What you'll do... The Clinical Research Data Scientist applies advanced data analysis and statistical methodologies to clinical trial data, synthesizes findings into clear and concise summaries for internal and external communication, and supports future commercial operations. This role will work cross-functionally with scientists, clinicians, statisticians, and management to generate actionable insights that support the company’s regulatory filings and scientific publications. The main activities include analysis and reporting of clinical trial data, cre

Amergis Healthcare is hiring a Pharmacist for a Corrections Facility in Chicago, IL! JOB SUMMARY: The Clinical Pharmacist provides comprehensive pharmaceutical care to patients by delivering clinically oriented pharmacy services in the inpatient, outpatient areas and/or correctional facility. These responsibilities include patient education and counseling of medications, performing medication histories and ensuring optimum patient outcomes or therapy. In addition, provide training and teaching to pharmacy students and residents, medical students and residents, and ancillary professional staff, i.e., pharmacists, pharmacy technicians, dieticians, nurses, respiratory therapists and others. + Shift: 9AM-5PM + Schedule: Monday-Friday Only Typical Duties + Monitors drug therapy by routinely analyzing patients' drug therapy with respect to potential problems, laboratory data and special procedures + Provides consultation on the selection of drug therapy and appropriate dosing regimens, deter