Open Rank Intermediate and Senior Research Services Clinical Sciences Professional (Nights/Weekends)

Open Rank Intermediate and Senior Research Services Clinical Sciences Professional (Nights/Weekends)

$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
• Adhere to research regulatory standards
• Maintain detailed records of studies to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures and other regulatory guidelines
• Participate in subject recruitment efforts, including communicating with patients expressing an interest and all pre-screening/screening activities
• Ensure that the necessary supplies and equipment for studies are in stock and in working order
• Independently master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies
• Independently perform study related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies
• Assist Team Leads, Supervisors and/or management with creation and implementation of processes and procedures and quality improvement initiatives
• Develops or assists with developing 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

Preferred

• Bachelor's degree in science or health related field
• Two (2) years of clinical trials experience
• Experience with electronic data capture systems (e.g. EMR or EHR and data management systems)
• Three (3) years of clinical trials or related experience

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: 15/year
• Tuition Benefit: Employees have access to this benefit on all CU campuses
• ECO Pass: Reduced rate RTD Bus and light rail service
• Glassdoor
• 3.6
• 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
• Late Stage
• Total Funding
• $0.5M
• Key Investors
• US Department of Energy
• "US Department of Commerce, Economic Development Administation"
• 2023-07-27
• Grant
• 2023-01-26
• 2021-04-06
• Grant· $0.5M
• Leadership Team
• Richard Schulick
• Professor and Chair of Surgery
• Recent News

Qualifications

• Bachelor's degree in any field
• One (1) year clinical trials or related experience
• A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor's degree on a year for year basis
• Two (2) years clinical trials or related experience
• Applicants must be legally authorized to work in the United States without requiring sponsorship. We are unable to provide work visa sponsorship or employment authorization for this position now or in the future
• 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
• Demonstrated commitment and leadership ability to advance diversity and inclusion
• 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
• Two (2) years of clinical trials experience
• Experience with electronic data capture systems (e.g. EMR or EHR and data management systems)
• Three (3) years of clinical trials or related experience
• A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year for year basis.

Required skills

• Clinical Practice (GCP), Clinical Trials, Data Management Systems, Electronic Data Capture Systems, Electronic Medical Records (EMR/EHR), Federal Research Regulations, Human Anatomy, Medical Terminology, Physiology, Research Protocol Interpretation

Preferred skills

• Bachelor's degree in science or health related field, Three (3) years of clinical trials or related experience, Two (2) years of clinical trials experience

Experience

• 1-2 years