Research Services Clinical Science Professional (Open Rank: Entry-Intermediate) jobs in United States
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University of Colorado · 3 weeks ago

Research Services Clinical Science Professional (Open Rank: Entry-Intermediate)

The University of Colorado Anschutz Medical Campus is seeking a Research Services Clinical Science Professional to support ongoing grant-funded studies focused on mental health. The role involves assisting with clinical trials, managing research activities, and conducting data analysis in a collaborative environment.

EducationHigher EducationUniversities
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H1B Sponsor Likelynote

Responsibilities

Primarily assist with and oversee the day-to-day operations of clinical trials and studies
Manage and conduct moderately complex research activities that are part of larger project from initiation to close
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)
Identify, screen and consent potential study participants. Interact with clinical staff to confirm eligibility and implement study protocols. Extract relevant data from participant or medical records and enter it into online centralized databases or local data tools
Collect, code, and analyze data obtained from research in an accurate and timely manner
Evaluate data sets for quality and completeness. Set up and or run statistical analyses
Analyze data, including statistical analyses and qualitative assessments of data and data quality. Identify and help solve gaps in data collection
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
Act as a Primary Coordinator on multiple trials/studies
Assist and train junior team members
Create complex data management and tracking tools (REDCap, ACCESS, Excel) to support tracking of project/recruitment activities
Oversee student worker(s) or junior PRAs as it relates to a specific project
Participate in instrument creation and/or analytical structures as appropriate to the project
Collect study data via complex patient visits, surveys, observations or focus groups. Provide leadership in data collection to other PRAs and students
Participate in audits, monitoring visits, and quality control checks of data collection, equipment maintenance, and study procedures
Help develop study findings for presentation to team and external audiences
May lead publication development (abstract/manuscript)
Help with budget management/tracking (under direction of PM/PI)
Lead manuscript preparation for publication or presentation in scientific forums
Work with members of the UCD and UCHealth community as needed to set up labs, participant visits, and access shared University resources
Manage study participant incentive program

Qualification

Clinical research experienceEpidemiological research experienceStatistical analysisClinical Practice (GCP)Data management toolsPsychological health researchGlobal health experienceCustomer service skillsCommunication skillsOrganizational skillsInterpersonal skillsTeam player

Required

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

Preferred

Bachelor's degree in science or health-related field
Master's degree in psychology, public health, or a research-related discipline
Strong interest or previous experience working in psychological health or global health research and/or related efforts
Experience in global health
Experience in military-relevant research

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

Company

University of Colorado

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University of Colorado offers higher education and serving as the catalysts in business, arts, health, and community growth.

H1B Sponsorship

University of Colorado has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (184)
2024 (124)
2023 (163)
2022 (115)
2021 (86)
2020 (95)

Funding

Current Stage
Late Stage
Total Funding
$0.5M
Key Investors
US Department of EnergyUS Department of Commerce, Economic Development Administation
2023-07-27Grant
2023-01-26Grant
2021-04-06Grant· $0.5M

Leadership Team

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Richard Schulick
Professor and Chair of Surgery
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