Top 353 Enrollment Jobs in Boerne Tx

Clinical Research Coordinator
U.S. Renal Care —San Antonio, TX
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
- Health insurance
- Dental insurance
Director of Admissions
Fusion Academy —San Antonio, TX
- $65,000 - $75,000 a year
- Full-time
- Background check
- Marketing
- Business development
- Commuter assistance
- Paid holidays
Enrollment Advisor
Hallmark University —San Antonio, TX
- $52,000 - $70,000 a year
- Full-time
- Microsoft Outlook
- High school diploma or GED
- University
Quick Apply
Registrar
Innovative Network of Knowledge —San Antonio, TX
- Full-time
- Remote
- School experience
- 5 years
- Mid-level
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11d
Enrollment Manager
Galen College of Nursing —San Antonio, TX
- Weekends as needed
- Mid-level
- Travel
- Ability to sit for extended periods
- Employee stock purchase plan
- Disability insurance
Quick Apply
Director, Enrollment CRM Systems
University of Texas at San Antonio —San Antonio, TX
- Up to $115,000 a year
- Extended hours
- Background check
- Office
- Master's degree
Student Enrollment Coordinator - IDEA Ingram Hills (Immediate Opening)
IDEA Public Schools —San Antonio, TX
- $20.74 - $25.93 an hour
- Weekends as needed
- School experience
- Spanish
- Ability to walk for extended periods
- Disability insurance
- Dental insurance
Clinical Data Coordinator I (CS3622 - Hamilton Wolfe)
CommuniCare Health Centers (Texas) —San Antonio, TX
- Spanish
- Medical office experience
- HIPAA
Quick Apply
Admissions Representative
ECPI University LLC —San Antonio, TX
- University
- Bachelor's degree
- Computer skills
Quick Apply
Clinical Research Coordinator
Pinnacle Clinical Research —San Antonio, TX
- Full-time
- Spanish
- Vital signs
- BLS Certification
- Paid holidays
- Disability insurance
Quick Apply
Admissions Advisor
CHCP Healthcare and Educational Services LLC —San Antonio, TX
- Full-time
- In-person
- Communication skills
- Entry level
Quick Apply
Human Resources Analyst - Generalist
University Health - San Antonio —San Antonio, TX
- $22.10 - $38.25 an hour
- Full-time
- Mid-level
- Bachelor's degree
- Recruiting
Higher Education Sales Consultant - Texas
Kendall Hunt Publishing —San Antonio, TX
- From $70,000 a year
- Full-time
- Hybrid work
- Clean driving record
- Mid-level
- Office
- Profit sharing
- Paid holidays
Quick Apply
SPG Call Center Team Member, (Clearance Required, TS/SCI with Poly) Onsite, San Antonio, TX
Hewlett Packard Enterprise —San Antonio, TX
- $71,500 - $164,400 a year
- 12 hour shift
- Mid-level
- Analysis skills
- Team management
Assistant or Associate Dean, Initiatives & Operations - College of AI, Cyber and Computing (CAICC)
University of Texas at San Antonio —San Antonio, TX
- Full-time
- Background check
- 7 years
- Office
Senior Community Outreach Specialist
University Health —San Antonio, TX
- $19.05 - $26.75 an hour
- Full-time
- School experience
- Mid-level
- Bachelor's degree
13d
Underwriting Assistant
Brown & Brown —San Antonio, TX
- Full-time
- Bilingual
- Mid-level
- Office
- Employee stock purchase plan
- Paid holidays
Financial Aid Coordinator
Universal Technical Institute —San Antonio, TX
- $20 - $22 an hour
- Monday to Friday
- Microsoft Outlook
- Computer literacy
- Writing skills
- Paid training
- Paid parental leave
Research Regulatory Associate I
Urology San Antonio —San Antonio, TX
- From $20.50 an hour
- Full-time
- Entry level
Quick Apply
Campus Registrar
Galen College of Nursing —San Antonio, TX
- Full-time
- Ability to walk for extended periods
- Mid-level
- Travel
- Employee stock purchase plan
- Disability insurance
Quick Apply

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Clinical Research Coordinator

U.S. Renal Care -
San Antonio, TX

Apply Now

Job Details

Full-time

Benefits

Health insurance
Dental insurance
Paid time off
Vision insurance
401(k) matching
Life insurance

Qualifications

Microsoft Excel
Microsoft Outlook
Documentation tools
Clinical quality assurance standards
Technical Proficiency
FDA regulations

Full Job Description

Responsibilities:

SUMMARY

The Clinical Research Coordinator (CRC) is responsible for the coordination of daily clinical trial activities. USRC has a research Partnership with the principal investigator (PI) and their physician practice. The local oversight and direction for activities related to the conduct of the clinical research is directed by the PI. The CRC will work collaboratively with the principal investigator (PI), the Sr. Clinical Research Coordinator (SCRC), the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure Execution of the clinical trial in accordance with the Study Protocol, the Food and Drug Administration (FDA), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) and applicable state and local regulations. The CRC will assist the PI in protecting the rights, safety and welfare of all study participants.

Essential Duties and Responsibilities include the following. Other duties and tasks may be assigned.

Coordinate all aspects of participant care from screening through study completion as defined by the protocol and PI delegation.
Ensure and document that the informed consent process has occurred properly according to the Code of Federal Regulations (45 CFR part 46).
Assist in the process of maintaining and updating each study participant's source records, including collection of medical history, assessment of eligibility and documentation of all study related procedures and relevant information.
Promptly report adverse events, protocol deviations and unanticipated problems involving risk to human subjects or others to the PI, the Sponsor, the IRB and in accordance with the Federal Code of Regulations (21 CFR 312), with assistance as applicable.
Ensure thorough, individualized, protocol-based study subject education on all study processes including but not limited to informed consent, study participation obligations, appropriate use of investigational product (IP), IP side effects and safety, communication with study staff and research rights.
Provide timely and accurate exchange of participant information with the PI and research team as it pertains to study conduct and patient safety.
Adhere to the Health Insurance Portability and Accountability Act (HIPAA Privacy Rule) and protect participant confidentiality at all times.
Dispense, administer and instruct participants on proper use of the investigational product (IP) in accordance with the protocol, coordinator's scope of practice and at the direction of the PI, with assistance as needed.
Collaborate with the USRC clinical team. Participate in trial implementation, and ensure compliance with the study protocol by our clinical partners, with assistance as needed.
Perform accurate and timely data collection, source documentation, and entry into the USRC databases and sponsor Case Report Forms (CRFs)/ interactive web response systems (IWRS). Address queries and sponsor requests in a timely manner.
Aid in the coordination of long-term storage of research records in accordance with contractual requirements, with direction from the Director of Clinical Research.
Assist in the preparation of and attendance during site initiation meetings, monitoring visits, audit visits or regulatory authority inspections.
Responsible for the preparation and ongoing maintenance of Essential Documents (The Trial Master File). This includes those documents that will allow for the evaluation of the clinical trial and demonstrate compliance of the sponsor and PI with the study protocol and GCP. (Including but not limited to: Form FDA 1572, financial disclosures, laboratory certifications, protocol, investigator brochure, institutional review board (IRB) related documents, IND reports delegation of authority (DOA), study specific enrollment logs, monitoring reports, with assistance as needed.
Assists in the coordination of efforts of internal and external resources (industry partners, clinical research organizations) to ensure efficient trial selection, proper patient recruitment, achieving target enrollment goals and trial plan execution.
Fosters a patient-care culture that emphasizes patient safety and quality in all aspects.
Responsible for the patient stipend automated payment process including registration into the system and processing payments per the USRC policy and ongoing maintenance of payments during the trial.
Adheres to the USRC Research quality assurance program guidelines.
Travel to Investigator Meetings or similar research related meetings is required.
Travel may be required between dialysis facilities or nephrology practices within the community.
Develops a working knowledge of current clinical research practice standards and regulatory requirements. For example, but not limited to; (FDA Federal Code of Regulations Good Clinical Practice (GCP), Health Insurance Portability and Accountability Act (HIPPA), International Air and Transportation Association (IATA) - Shipping of Dangerous Goods. Maintains their industry standard licensures and certifications.
May provide training and oversight of Clinical Research Coordinators and/or Research Assistants.
Actively promotes GUEST customer service standards; develop effective relationships at all levels of the organization.
Participate in team concepts and promote a team effort; perform duties in accordance with company policies and procedures.
Participate in staff meetings as required.
Regular and reliable attendance is required for the job.
Actively promotes GUEST customer service standards; develops effective relationships at all levels of the organization.
Participates in team concepts and promote a team effort; performs duties in accordance with company policies and procedures.
Regular and reliable attendance is required for the job.

Qualifications:

Qualifications/Requirements:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

Requirements include:

Bachelor's degree in related field preferred.
Three (3) years of experience in clinical research required; nephrology experience preferred.
Basic knowledge of FDA regulations, IRB requirements and Good Clinical Practice.
Basic knowledge of kidney care and/or End-Stage Kidney Disease (ESKD) or similar field is a plus.
Strong verbal and written communication skills required.
Must have intermediate computer skills, including Microsoft Office (Word, Excel, Outlook and web based tools); proficiency in USRC applications required within 90 days of hire.

Benefit Details

All Full-Time employees are eligible for the following benefits:

Medical / Pharmacy
Dental
Vision
Voluntary benefits
401k with employer match
Virtual Care
Life Insurance
Voluntary Benefits
PTO

All Part Time employees are eligible for the following benefits:

401k with employer match
PTO

Company (Career Site Brand): U.S. Renal Care

Apply Now

Refine Your Search

enrollment jobs in boerne tx

Clinical Research Coordinator

Director of Admissions

Enrollment Advisor

Registrar

Enrollment Manager

Director, Enrollment CRM Systems

Student Enrollment Coordinator - IDEA Ingram Hills (Immediate Opening)

Clinical Data Coordinator I (CS3622 - Hamilton Wolfe)

Admissions Representative

Clinical Research Coordinator

Admissions Advisor

Human Resources Analyst - Generalist

Higher Education Sales Consultant - Texas

SPG Call Center Team Member, (Clearance Required, TS/SCI with Poly) Onsite, San Antonio, TX

Assistant or Associate Dean, Initiatives & Operations - College of AI, Cyber and Computing (CAICC)

Senior Community Outreach Specialist

Underwriting Assistant

Financial Aid Coordinator

Research Regulatory Associate I

Campus Registrar

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