Intermediate Clinical Sciences Coordinator

at  University of Colorado

Aurora, Colorado, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate10 Nov, 2024USD 66088 Annual11 Aug, 2024N/APhysiology,Outlook,Human Anatomy,Teams,Excel,Redcap,Writing,Federal Regulations,Medical Terminology,Clinical Research,Customer Service SkillsNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

JOB SUMMARY:

We are seeking an Intermediate Clinical Sciences Coordinator to join our clinical colorectal cancer screening and prevention research program. The successful candidate will be part of a team that includes supportive research personnel (regulatory, budget, coordinators) and medical personnel (nurses, genetic counselors, physicians)—all led by the principal investigator and the GI division research leadership. The candidate will participate in clinical research projects including studies examining different colorectal cancer prevention strategies in prospective clinical trials, studies examining the prevalence of genetic syndromes that increase risk of cancer among patients with colorectal polyps, cancer prevention vaccine trials, development of mobile/digital applications to help patients improve cancer prevention care and many more. The position requires an ability to work independently, but collaboratively, have attention to detail, and be able to maintain organized protocol documentation and data. Furthermore, the Intermediate Clinical Science Professional will have the opportunity to manage and lead teams. The studies we conduct require in-person and telephone interactions with participants/patients/staff, thus we are seeking a candidate who is a “people person” and can interact well with others.

MINIMUM QUALIFICATIONS:

  • 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.
    Applicants must meet minimum qualifications at the time of hire.

PREFERRED QUALIFICATIONS:

  • Bachelor’s degree in science or health related field.
  • Two (2) years of clinical research or related experience.
  • Experience with electronic data capture systems (e.g. Electronic Medical Record (EMR) or Electronic Health Record (EHR), REDCap, and data management systems).

KNOWLEDGE, SKILLS, AND 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.
  • Demonstrated commitment and leadership ability to advance diversity and inclusion.
  • Knowledge of basic human anatomy, physiology, and medical terminology.
  • Ability to interpret and master complex research protocol information.Proficiency in Microsoft office tools (Outlook, Excel, Teams, etc.).
-

QUALIFICATIONS

Application Materials Required: Cover Letter, Resume/CV, List of References
Job Category: Research Services
Primary Location: Hybrid
Department: U0001 - Anschutz Med Campus or Denver - 20189 - SOM-MED-Gastroenterology
Schedule: Full-time
Posting Date: Aug 9, 2024
Unposting Date: Ongoing
Posting Contact Name: Demi Sclafani
Posting Contact Email: demi.sclafani@cuanschutz.edu
Position Number: 0082594

Responsibilities:

  • 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.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Hospital/Health Care

Pharma / Biotech / Healthcare / Medical / R&D

Health Care

Graduate

Any field

Proficient

1

Aurora, CO, USA