Clinical Coordinator

cu

Colorado

Hybrid

AUD 71,000 - 98,000

Full time

7 days ago
Be an early applicant
Application generator

An application made for this job — a tailored resume and cover letter that speak straight to the posting.

Get past ATS filters

Benefits offered by this job

Medical plans
Dental plans
401(a) Retirement Plan
Paid time off

Job summary

University of Colorado Anschutz Medical Campus is seeking a Clinical Coordinator to manage daily clinical trial operations, obtain consent, gather health data, and coordinate site resources. Hybrid work arrangement with on-campus activities and meetings as needed.

Qualifications include a bachelor’s degree in a health-related field and clinical research experience; familiarity with EMR/EHR systems and regulatory processes is preferred.

Qualifications

  • Bachelor’s degree in public health, public administration, social/behavioral sciences, physical sciences, nursing, healthcare, finance, accounting, business administration, business, or a directly related field.
  • One year of clinical research or related experience for intermediate level.
  • Familiarity with regulatory tasks and IRB submissions is preferred.

Responsibilities

  • Perform day-to-day operations of clinical trials and studies.
  • Obtain medical history and document informed consent processes.
  • Schedule subject participation and coordinate clinical research support.
  • Adhere to regulatory standards and maintain study materials.

Skills

Clinical research
Communication
Regulatory knowledge
IRB submissions
Data management

Education

Bachelor’s degree in public health or related field

Tools

EMR/EHR systems

Job description

University of Colorado Anschutz Medical

Department: Linda Crnic Institute for Down Syndrome

Job Title: Clinical Coordinator

Position #00852084 – Requisition #40822

Job Summary

Clinical Coordinators perform clinical research related functions which includes research conducted with human subjects. This participant-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Clinical Coordinators may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research.

Key Responsibilities
  • Perform day-to-day operations of clinical trials and studies
  • Obtain medical history from consented participants, including follow-up for off-site medical records and completion of a participant health survey. Must be able to reliably transcribe orally reported medical history as written notes.
  • Obtain informed consent and/or assent from study participants and ensure that the process is properly documented, and that informed consent form documents are filed as required.
  • Schedule subject participation in research clinical trials and coordinate the availability of necessary space and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy).
  • Adhere to research regulatory standards.
  • Collect code, and summarize information obtained from research in an accurate and timely manner
  • Master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies
Work Location

Hybrid – this role is eligible for a hybrid schedule of 4 days per week on campus and as needed for in-person meetings.

Why Join Us

The Linda Crnic Institute for Down Syndrome is the largest academic home for Down syndrome research. The Crnic Institute collaborates with prominent scientists and leaders around the globe to enable precision medicine approaches to improve health outcomes in Down syndrome. Learn more at: https://medschool.cuanschutz.edu/linda-crnic-institute.

Why work for the University?

We haveAMAZINGbenefits and offerexceptional amounts of holiday, vacation and sick leave! The University of Colorado offers an excellent benefits package including:

  • 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

There are many additional perks & programs with the CU Advantage.

Qualifications
Minimum Qualifications
Entry Level Professional
  • A bachelor’s degree in public health, public administration, social/behavioral sciences, physical sciences, nursing, healthcare, finance, accounting, business administration, business, or a directly related field from an accredited institution
  • A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year for year basis.
Intermediate Level Professional
  • A bachelor’s degree in public health, public administration, social/behavioral sciences, physical sciences, nursing, healthcare, finance, accounting, business administration, business, or a directly related field from an accredited institution.
  • 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)yearclinicalresearchorrelated experience

Applicants must meet minimum qualifications at the time of hire.

Preferred Qualifications
Entry Level Professional
  • Bachelor’sdegreeinscienceorhealthrelated field
  • Experiencewithelectronicdatacapturesystems(e.g.EMRorEHRanddatamanagement systems)
  • Experience working with individuals with Down syndrome or other intellectual disability
  • Demonstrate ability to think conceptually about project design and implementation; anticipate potential problems and study needs
  • One year of experience working directly with IRB submissions and familiarity with basic regulatory tasks required in a clinical trial.
Intermediate Level Professional
  • Two(2)yearsofclinicalresearchorrelated experience
Conditions of Employment
  • 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, Skills and Abilities
  • KnowledgeandunderstandingoffederalregulationsandGoodClinicalPractice(GCP)
  • Abilitytocommunicateeffectively,bothinwritingandorally
  • English/Spanish bilingual is beneficial
  • Abilitytoestablishandmaintaineffectiveworkingrelationshipswithemployeesatalllevels throughout the institution
  • Outstandingcustomerservice skills
  • Knowledgeofbasichumananatomy,physiologymedical terminology
  • Abilitytointerpretandmastercomplexresearchprotocol information
  • Organized and able to complete multi-step tasks independently
  • Knowledge of electronic data capture systems (e.g., EMR or HER and data management systems)
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 hr.adacoordinator@cuanschutz.edu.

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.

Anticipated Pay Range

The starting salary range (or hiring range) for this position has been established as:

  • Entry Level: $49,899 – $63,472
  • Intermediate Level: $54,302 - $69,072

The above salary range (or hiring range) represents the University’s good faith and reasonable estimate of the range of possible compensation at the time of posting. This position may be eligible for overtime compensation, depending on the level.

Your total compensation goes beyond the number on your paycheck. The University of Colorado provides generous leave, health plans and retirement contributions that add to your bottom line.

Total Compensation Calculator

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Clinical Research Coordinator (open rank) - LCPC / CPS Team
Clinical Research Coordinator (open rank) - LCPC / CPS Team

cu • Denver (CO)

Hybrid
AUD 71,000 - 84,000
Tuition Benefit
Paid Time Off
Medical/Dental options
Open Rank Clinical Trial Coordinator (Entry – Senior) – Cardiology
Open Rank Clinical Trial Coordinator (Entry – Senior) – Cardiology

University of Colorado System • Aurora (CO)

On-site
USD 50,000 - 72,000
Health insurance
Tuition benefit
Paid time off
+1
Open Rank Clinical Trial Coordinator (Entry - Senior) - Cardiology
Open Rank Clinical Trial Coordinator (Entry - Senior) - Cardiology

University of Colorado Anschutz • Aurora (CO)

On-site
USD 50,000 - 72,000
Research Services Professional
Research Services Professional

CU Denver • Aurora (CO)

On-site
USD 49,899 - 66,865
Research Services Clinical Sciences Professional OPEN RANK (Intermediate - Senior)
Research Services Clinical Sciences Professional OPEN RANK (Intermediate - Senior)

University of Colorado Anschutz • Aurora (CO)

On-site
USD 54,302 - 78,665
Research Services Professional (Pre/Post Award) (Open Rank: Entry – Senior)
Research Services Professional (Pre/Post Award) (Open Rank: Entry – Senior)

University of Colorado • Aurora (CO)

Hybrid
USD 50,000 - 75,000
Health insurance options
Retirement 401(a) plan
Paid time off
+3
Research Services Clinical Sciences Professional OPEN RANK (Intermediate - Senior)
Research Services Clinical Sciences Professional OPEN RANK (Intermediate - Senior)

CU Denver • Aurora (CO)

On-site
USD 55,000 - 78,000
Open Rank Clinical Research Coordinator (Entry – Senior)
Open Rank Clinical Research Coordinator (Entry – Senior)

University of Colorado • Aurora (CO)

On-site
USD 49,899 - 78,665
Open Rank Clinical Data Coordinator (Entry - Senior)
Open Rank Clinical Data Coordinator (Entry - Senior)

University of Colorado Anschutz • Aurora (CO)

On-site
USD 60,000 - 78,000
Research Services Clinical Services Professional (Open Rank – Entry and Intermediate Level)
Research Services Clinical Services Professional (Open Rank – Entry and Intermediate Level)

cu • Colorado

Hybrid
AUD 74,000 - 100,000
Medical plans
Dental plans
Retirement 401(a) plan
+1