Senior Clinical Science Professional - Pediatrics, Section of Endocrinology

• Senior Clinical Science Professional
• Pediatrics, Section of Endocrinology
• Description
• University of Colorado Anschutz

• Department:

  Pediatrics | Section of Endocrinology

• Job Title:

  Senior Clinical Science Professional
• Pediatrics, Section of Endocrinology
• Position #: 00848586
• Requisition #:40013

• Job Summary:

• Key Responsibilities:

• Clinical Research Coordination (30%) + Serve as senior study coordinator for multiple investigator-led clinical research studies, including tracking milestone progress. + Lead subject recruitment efforts, including preparing recruitment materials, identifying eligible patients, and conducting informed consent.

• Work Location:

• Onsite

• Why Join Us:

• Why work for the University?
• +

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

• Qualifications:

• Minimum Requirements
• + Bachelor's degree in science or a health-related field.
• _How to

Apply:

_

• _For full consideration, please submit the following document(s):_ _1.

A letter of interest describing relevant job experiences as they relate to the listed job qualifications and interest in the position_ _2. Curriculum vitae / Resume_ _3. Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address_ _Questions should be directed to: Shanlee.davis@cuanschutz.edu (https://apptrkr.com/get\_redirect.php?id=7177065⌖URL=Shanlee.davis@cuanschutz.edu)_

• _

Screening of Applications Begins:

_

• _Immediately and closes five (5) days after the posting date._
• _

Anticipated Pay Range:

_

• _The starting salary range (or hiring range) for this position has been established as $35,223 to $47,199 (calculated for 0.

6 FTE)._ _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 (https://apptrkr.com/get\_redirect.php?id=7177065⌖URL=http://www.cu.edu/node/153125)_

• _

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 (https://apptrkr.com/get\_redirect.php?id=7177065⌖URL=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 (https://apptrkr.com/get\_redirect.php?id=7177065⌖URL=https://www.cdc.gov/vaccines/schedules/downloads/adult/adult-combined-schedule.pdf) . 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 (https://apptrkr.com/get\_redirect.php?id=7177065⌖URL=https://research.cuanschutz.edu/ehs/home/divisions/occupational-health/oh-enrollment) ._ _

Application Materials Required:

Cover Letter, Resume/CV, List of References_

• _Job Category_
• _: Research Services_
• _Primary Location_
• _:

Aurora Department:

U0001

• Anschutz Med Campus or Denver
• 20971
• SOM-PEDS Endocrinology-GenOps_
• _Schedule_
• _: Part-time_
• _Posting Date_
• _: May 20, 2026_
• _Unposting Date_
• _: May 26, 2026, 5:59:00

AM Posting Contact Name:

Shanlee.davis

Posting Contact Email:

Shanlee.davis@cuanschutz.edu (https://apptrkr.com/get\_redirect.php?id=7177065⌖URL=Shanlee.davis@cuanschutz.edu)

Position Number:

00848586_

• _To apply, visit https://cu.taleo.net/careersection/2/jobdetail.ftl?job=40013⟨=en (https://apptrkr.com/7177065)_
• _Copyright 2025 Jobelephant.com Inc. All rights reserved._ _Posted by the FREE value-added recruitment advertising agency (https://www.jobelephant.com/)_ _jeid-ee65fc4f0040114898c66a7c5519d504_ Senior Clinical Science Professional
• Pediatrics, Section of Endocrinology
• 40013 University Staff The eXtraOrdinarY Kids Team is seeking a highly motivated Senior Clinical Research Services Professional to lead and support a diverse portfolio of investigator-initiated clinical research studies focused on children and adolescents with sex chromosome aneuploidies and related conditions.

This senior role integrates clinical research coordination, regulatory oversight, data management, and scientific writing within a dynamic, multidisciplinary environment. The ideal candidate will bring advanced experience in human subjects research, a strong commitment to participant-centered care, and the ability to independently manage complex studies while mentoring junior staff and contributing to the team's broader mission of improving outcomes through innovative, translational research. + Schedule and conduct virtual and in-person study visits according to study protocol, including anthropometrics, standardized assessments, ancillary service coordination, and biospecimen collection. + Coordinate and manage wearable devices, including distribution, data downloads, and diary monitoring. + Maintain compliance with HIPAA, GCP, and institutional policies.

Regulatory (15%) + Draft and revise study documents, including protocols, consent forms, case report forms, and IRB applications, amendments, and continuing reviews. + Maintain electronic regulatory binders. + Support study start-up and close out, including all institutional requirements for conducting human subjects research. + Register and/or maintain studies on clinicaltrials.gov.

Data Management (15%) + Collect, code, and analyze data obtained from research in an accurate and timely manner. + Develop, manage, and maintain REDCap databases, including instrument creation, data entry, validation, cleaning, and report generation. + Collaborate with statisticians and research teams on data cleaning and analysis.

Scientific Writing (15%) + Draft and review abstracts, posters, and manuscripts. + Copyediting and ensuring compliance with submission guidelines. + Support grant proposals, including drafting human subjects sections, recruitment plans, budget justifications, Just-in-Time documentation, and annual reports.

Mentorship & Supervision (15%) + Oversee student research assistants, including onboarding, training, task management, and feedback. + Assist with the orientation and training of new team members. + Oversee and provide informal leadership to the team members, including managing day-to-day priorities, evaluating and redistributing workloads on a temporary basis, and mentoring junior staff. + Organize and lead study team meetings.

Community Engagement (10%) + Maintain and update the team website with publications, team updates, and announcements. + Engage with patient advocacy organizations to support participant-centered research. + Translate scientific work into materials digestible for lay audiences. + Attend applicable community events, as needed.

This description is a summary only and describes the general level of work being performed; it is not intended to be all-inclusive. The duties of this position may change from time to time and/or based on business need. We reserve the right to add or delete duties and responsibilities at the discretion of the supervisor and/or hiring authority.

• this role is expected to work onsite and is located in Aurora, CO.

The interdisciplinary eXtraOrdinarY Kids team leads the nation in care and research for children with sex chromosome aneuploidies, including Turner syndrome, Klinefelter syndrome, Trisomy X syndrome, XYY, and XXYY syndrome. The eXtraOrdinarY Kids team includes developmental-behavioral pediatrics, endocrinology, gynecology, genetic counseling, child psychology, cardiology, otolaryngology, audiology, neuropsychology, speech therapy, occupational therapy, nursing, social work, research associates, graduate students, and other medical subspecialists. Our multifaceted clinical-translational research program has the overarching goal to improve the lives of children with X&Y chromosome variations, and our work is funded by the NIH, foundations, and family advocacy organizations. Our vibrant team is committed to impactful clinical care and research, advocacy, and education.

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

There are many additional perks & programs with the CU Advantage (https://apptrkr.com/get\_redirect.php?id=7177065⌖URL=https://advantage.cu.edu/) . : + Two (2) years of clinical research experience.

Applicants must meet minimum qualifications at the time of hire.

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.

• Conditions of Employment:

• + Must be willing and able to pass national criminal and sex offender background checks + Must successfully pass a 10-panel drug screen through Children's Hospital Colorado _
• For questions regarding Children's Hospital drug testing requirements, please contact Children's Human Resources at 720-777-8598. Some positions may require testing if access to Children's Hospital or their systems is needed at any time during employment with the University. If drug testing is required, it will be listed in the job posting._
• _

Preferred Qualifications:

_

• + _Master's degree in a health sciences-related field.

_ + _Five (5) years of clinical research or related experience._ + _Experience with scientific writing (e.g., grant and manuscript preparation)._ + _Experience with data analysis and visualization._ + _One (1) year project or program development, management, and/or evaluation in a clinical and/or research domain._ + _Experience with electronic data capture systems (e.g., EHR and data management systems)._ + _Experience with managing institutional review board submissions._

• _

Knowledge, Skills, and Abilities:

_

• + _Strong written, oral, and interpersonal communication skills; ability to engage effectively with participants, families, and interdisciplinary teams.

_ + _Commitment to diversity, equity, inclusion, professionalism, and ethical conduct in research._ + _Knowledge of ethical research practices, including Good Clinical Practice (GCP) and federal guidelines._ + _Ability to coordinate study visits, biospecimen handling, and logistics efficiently while working collaboratively in interdisciplinary teams._ + _Ability to work compassionately with individuals with neurodevelopmental differences or behavioral challenges._ + _Ability to interpret and implement complex research protocols accurately._ + _Ability to achieve proficiency with electronic data capture systems (e.g., REDCap, OnCore) and EHR systems (e.g., EPIC)._ + _Strong organizational skills, attention to detail, and ability to manage multiple studies, tasks, and deadlines._ + _Proactive, solution-oriented, and able to anticipate issues to keep studies on track._ + _Adaptable and flexible in a dynamic, multi-site research environment, with a strong desire to learn, grow, and excel._The University of Colorado does not discriminate on the basis of race, color, national origin, sex, age, pregnancy, disability, creed, religion, sexual orientation, gender identity, gender expression, veteran status, political affiliation, or political philosophy. All qualified individuals are encouraged to apply.