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

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

$54K/yr - $73K/yr

Education

Higher Education

Universities

Responsibilities

• Assist with and oversee the day-to-day operations of clinical trials and studies
• Obtain study subject’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial
• Perform informed consent process or ensures 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
• Assist with developing or develops protocol-specific systems and documents including process flows, training manuals, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs). Maintains subject level documentation and prepares documents, equipment and/or supplies
• Assist with identifying issues related to operational efficiency and shares 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
• 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

Preferred

• 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)

Benefits

• Medical: Multiple plan options
• Dental: Multiple plan options
• Additional Insurance: Disability, Life, Vision
• Retirement 401(a) Plan: Employer contributes 10% of your gross pay
• Paid Time Off: Accruals over the year
• Vacation Days: 22/year (maximum accrual 352 hours)
• Sick Days: 15/year (unlimited maximum accrual)
• Holiday Days: 10/year
• Tuition Benefit: Employees have access to this benefit on all CU campuses
• ECO Pass: Reduced rate RTD Bus and light rail service
• Glassdoor
• 3.7
• University of Colorado offers higher education and serving as the catalysts in business, arts, health, and community growth.
• Denver, Colorado, USA
• https://www.cu.edu
• Distribution of Different Job Fields Receiving Sponsorship
• Represents job field similar to this job
• Education and Training
• Engineering and Development
• Customer Service and Support
• Management and Executive
• Marketing
• Accounting and Finance
• Arts and Entertainment
• Human Resources
• Public Sector and Government
• Creatives and Design
• Legal and Compliance
• Trends of Total Sponsorships

Qualifications

• Bachelor's degree in any field
• A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor's degree on a year for year basis
• One (1) year clinical research or related experience
• Two (2) years clinical research or related experience
• 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
• 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)
• A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year for year basis.
• One (1) year clinical research or related experience.
• Two (2) years clinical research or related experience.

Required skills

• Clinical Practice (GCP), Clinical Research, Clinical Research Protocols, Electronic Health Records (EHR), Electronic Medical Records (EMR), Federal Regulations, Human Anatomy, Medical Terminology, Physiology, Relationship Management

Preferred skills

• Bachelor's degree in science or health related field, Three (3) years of clinical research or related experience

Experience

• 1-2 years