Research Services Clinical Sciences Professional OPEN RANK (Intermediate - Senior)

University of Colorado Anschutz Medical Campus Department: SOM - Orthopedics Job Title: Research Services Clinical Sciences Professional OPENRANK (Intermediate – Senior) Position #: 00837810 – Requisition #:40318 Job Summary This position will act as a clinical research coordinator for the Emily Lindley Research Lab, assisting with studies related to non‑opioid alternatives for treatment of chronic musculoskeletal pain. The role is posted as “open rank,” meaning the selected candidate may be hired at either the intermediate or senior level, depending on experience and business needs. Intermediate Clinical Science Professionals perform clinical research related functions which may include patient‑oriented research or research conducted with human subjects. Patient‑oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Senior Clinical Science Professionals perform clinical research related functions which may include patient‑oriented research or research conducted with human subjects. Patient‑oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Senior Clinical Science Professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research. Some Assignments will not move beyond this level. Key Responsibilities All Levels: Assist with and oversee the day‑to‑day operations of clinical trials and studies Obtain study subject's medical history and current medication information, review research protocol inclusion/exclusion criteria, and confirm eligibility of subject to participate in clinical trial Perform informed consent process or ensure 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 contacts and personal interviews Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy) Collect, code, and analyze data obtained from research in an accurate and timely manner Senior Level Only: All duties stated above, plus: Assist with developing or develop protocol‑specific systems and documents including process flows, training manuals, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs). Maintain subject‑level documentation and prepare documents, equipment and/or supplies Assist with identifying issues related to operational efficiency and share results with leadership Collect information to determine feasibility, recruitment and retention strategies. Employ, evaluate and assist with the implementation of innovative solutions to maximize recruitment and retention Serve as a resource and participate in study initiation and close‑out duties Additional Duties & Responsibilities Drive cargo van (e.g., Sprinter Van) that is converted into a Mobile Pharmacology Lab to research subjects' homes. A second study team member will always accompany the driver. Draw blood samples from research subjects Work Location Onsite – this role is expected to work onsite and is located in Aurora, CO. Qualifications Minimum Qualifications Intermediate Level: Bachelor's degree in any field. One (1) year clinical research or related experience. Senior Level: Bachelor's degree in any field. Two (2) years clinical research or related experience. Preferred Qualifications Bachelor's degree in science or health related field. Three (3) years of clinical research or related experience. Experience with electronic data capture systems (e.g., EMR or EHR and data management systems). Competencies, Knowledge, Skills, & Abilities Knowledge and understanding of federal regulations and Good Clinical Practice (GCP). Ability to communicate effectively, both in writing and orally. Ability to establish and maintain effective working relationships with employees at all levels throughout the institution. Outstanding customer service skills. Knowledge of basic human anatomy, physiology, medical terminology. Ability to interpret and master complex research protocol information. How to Apply For full consideration, please submit the following document(s): Curriculum vitae / Resume Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address Questions should be directed to: Emily Lindley, View email address on click.appcast.io. Equal Employment Opportunity Statement CU is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing nondiscrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity, and we encourage individuals from all backgrounds to apply, including protected veterans and individuals with disabilities. ADA Statement The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at View email address on click.appcast.io. Background Check Statement The University of Colorado Anschutz Medical Campus is dedicated to ensuring a safe and secure environment for our faculty, staff, students and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees. Vaccination Statement CU Anschutz strongly encourages vaccination against the COVID‑19 virus and other vaccine‑preventable diseases. If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. In addition, if you work in certain research areas or perform certain safety‑sensitive job duties, you must enroll in the occupational health medical surveillance program. #J-18808-Ljbffr US Anesthesia Partners