Top 23 Site director Jobs in Boerne, Tx

Sub l /Nurse Practitioner
Evolution Research Group —San Antonio, TX
- $100,000 - $150,000 a year
- Full-time
- Presentation skills
- Team management
- Neurology
- Health insurance
- Dental insurance
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After School Youth Leader - Boerne/ UTSA area
YMCA San Antonio —Boerne, TX
- $14.50 an hour
- Part-time
- Serving
- Ability to walk for extended periods
- High school diploma or GED
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Risk Management Coordinator
University Health - San Antonio —San Antonio, TX
- $22.10 - $38.25 an hour
- Full-time
- Research
- Mid-level
- Office
Clinical Data Coordinator I (CS3622 - Hamilton Wolfe)
CommuniCare Health Centers (Texas) —San Antonio, TX
- Spanish
- Medical office experience
- HIPAA
Quick Apply
Clinical Research Coordinator
Pinnacle Clinical Research —San Antonio, TX
- Full-time
- Spanish
- Vital signs
- BLS Certification
- Paid holidays
- Disability insurance
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11d
Risk Management Coordinator
University Health —San Antonio, TX
- $22.10 - $38.25 an hour
- Full-time
- Hospital
- Research
- Mid-level
Assistant Manager
CSC Management - San Antonio —San Antonio, TX
- $20 - $22 an hour
- Full-time
- Mid-level
- Office
- Apartments
- Health savings account
- Paid holidays
Quick Apply
10d
STEM and Drone Flying School Year Camp Teacher
DroneTogether —San Antonio, TX
- $25 - $35 an hour
- Part-time
- Background check
- Classroom
- CPR Certification
- Paid training
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11d
After School Program-Site Director- San Antonio Texas
Leaven Kids —San Antonio, TX
- $14.14 an hour
- Part-time
- Background check
- CPR Certification
- Driver's License
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10d
Radiology QA & QC Coordinator
University of Texas Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- Hospital
- Mid-level
- Analysis skills
- AD&D insurance
- Paid holidays
Nurse Navigator
University of Texas Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- CPR Certification
- Nursing
- Microsoft Excel
- AD&D insurance
- Paid holidays
Marketing & Content Assistant
Barshop JCC of San Antonio —San Antonio, TX
- $25,000 a year
- Part-time
- Marketing
- Writing skills
- Office
Laboratory Technician (PRN)
Evolution Research Group —San Antonio, TX
- Weekends as needed
- Vital signs
- Customer service
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
Radiology QA & QC Coordinator
UT Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- Hospital
- Analysis skills
- Organizational skills
- AD&D insurance
- Paid holidays
Nurse Navigator
UT Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- CPR Certification
- Nursing
- Microsoft Excel
- AD&D insurance
- Paid holidays
Medical Director of TDI Diabetes Research Unit (Open Rank)
UT Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- Medicine
- Management
- BC/BE
- AD&D insurance
- Paid holidays
Open Rank Psychiatry Residency Program Director
UT Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- Medicine
- Psychiatry
- Addiction Medicine
- AD&D insurance
- Paid holidays
PRN Physician, Family or Internal Medicine
HEALTH BY DESIGN MEDICAL GROUP —Shavano Park, TX
- No weekends
- Medicine
- BLS Certification
- Internal Medicine
Quick Apply
11d
OB Hospitalist Physician
Methodist Hospital Westover Hills —San Antonio, TX
- Full-time
- Ob/Gyn
- Senior level
- Paid holidays
- Health insurance

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Substitute Teacher - St. Peter the Apostle Catholic School
St Peter the Apostle Catholic School —Boerne, TX
Supervise students in the cafeteria, schoolyard, specials, hallways, on field trips, and/or during before and after school programs.
2026-2027 After School Program Facilitator
South San Antonio Independent School District —San Antonio, TX
Adheres to program standards regarding safety, cleanliness, and adherence to licensing protocol. Follows SSAISD policies and procedures, including those related…
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9d
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Board-certified/eligible in emergency or family medicine with emergency medicine experience. Our flexible scheduling, which focuses on family and the outdoors,…
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Sub l /Nurse Practitioner

Evolution Research Group -
San Antonio, TX

Quick Apply

Job Details

Full-time
$100,000 - $150,000 a year

Benefits

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

Qualifications

Computer operation
Presentations for conferences or internal meetings
ICH guidelines
Nurse Practitioner (NP)
Advanced practice provider
Computer skills
Clinical quality assurance standards
Medical terminology
FDA regulations

Full Job Description

About Company:

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.

Why join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.

Job Description:

The Sub-Investigator acts as the secondary physician in charge of medical and clinical issues at the clinical research site, acting in place of the Principal Investigator, as requested, or required. Works with the Principal Investigator and the site to evaluate clinical trials and ensure that all study-related procedures are completed properly from a clinical and a regulatory perspective.

Ensures adherence to protocol requirements, protecting the rights and welfare of study subjects, assuring the integrity of data generated at the site. In executing these position responsibilities, the Sub-Investigator is guided by and promotes the adherence to Good Clinical Practices (GCP), International Committee on Harmonization (IHP) guidelines, and company standard operating procedures and policies.

Responsibilities:

Planning and Management

Assist in recruitment of additional research studies, especially through professional/clinical, and industry relationships.
Provide input to the Principal Investigator and/or Site Director about study protocols (e.g., with respect to enrollment/retention potential, office capacity and capabilities, profit potential, and other determinants of success).
Provide input to the Principal Investigator and/or Site Director as to which studies to pursue.
Conduct medical office visits with subjects in active studies and ensure compliance with requirements of protocols for said studies.
Act as liaison with study monitors for active studies.
Represents ERG at conferences sponsored by potential clients (i.e., pharmaceutical firms) as requested.
Aid Patient Recruitment personnel in recruiting patients for studies, with a particular emphasis upon working with other physicians and hospitals.
Ensure proper compliance and execution of the Informed Consent processes.

Investigator Qualifications and Agreements

Maintain a current, up to date curriculum vitae.
Maintain current licensure to practice.
Provide the sponsor and IRB with documentation of credentials as requested.
Demonstrate the proper education, training, and experience to conduct the clinical investigation.
Assume responsibility for the conduct of the clinical investigation.
Sign the Form FDA 1572 as appropriate.
Sign the protocol as required.
Sign sponsor contract(s) as appropriate
Disclosing conflicts of interest as described in the regulations.

Ensure Protocol Compliance

Possess a thorough understanding of the requirements of each protocol.
Participate in sponsor investigator meetings whenever possible.
Determine that inclusion/exclusion criteria are applicable to the study population.
Ensure recruitment goals are reasonable and attainable.
Follow the trial's randomization procedures.
Will not implement any protocol deviation or changes without agreement by the sponsor and prior review and approval by the IRB (except to eliminate immediate hazards to the subject)
Review the inclusion /exclusion criteria, schedule of visits, end point criteria and investigational article use with the research team.

Ensure Adequate Review by A Duly Constituted Institutional Review Board (IRB)

Provide the IRB with adequate information to initially review the study (i.e., protocol, investigator's brochure, informed consent form, recruitment advertisements and any written information to be given to subject(s)
Provide the IRB with documents for ongoing review (i.e., amendments to the protocol, adverse events, deviations, or new information)
Secure written IRB approval prior to initiating the study or instituting any changes to the protocol as approved.
Provide written summaries of the trial status to the IRB annually, or as requested.
Provide the IRB with all documents subject to their review.

Manage the Care of Subjects

Assess subject compliance with the test article and follow-up visits.
Assess subject's response to therapy.
Evaluate adverse experiences per protocol guidelines.
Ensure that medical care is provided to a subject for any adverse event(s)
Inform a subject when medical care is needed to treat an intercurrent illness(es)
Inform the subject's primary physician about their participation in the trial.

Protect the Rights and Welfare of Subjects

Report all serious adverse events immediately to the sponsor and IRB.
Ensure that the informed consent form contains all the elements required by regulatory agencies.
Obtain a signed and dated informed consent from the subject or subject's legal representative prior to initiating any study-related procedures.
Inform the subject or legal representative about all aspects of the clinical trial.
Provide new information about the study or test article(s)

Ensure Validity of The Data Reported to The Sponsor

Ensure the accuracy, completeness, legibility, and timeliness of case report forms.
Ensure that case report forms accurately reflect source documents.
Explain any discrepancies between source documents and case report forms.
Endorse changes or corrections to a case report form.

Ensure Documentation of Study-Related Procedures, Processes and Events

Document deviations from the approved protocol
Document and explaining premature unblinding of the investigational product(s)
Document that informed consent has been obtained from the subject or legal representative.
Ascertain the reason for a patient's premature study withdrawal.
Document adverse experiences
Comply with written procedures to document changes to data and/or case report forms.
Maintain trial documents as required by the regulations and sponsor for the appropriate timeframe and under secure conditions.
Provide study reports as requested by the sponsor, IRB, and regulatory authority(is)

Ensure the Proper Use and Storage of Investigational Agents

Being thoroughly familiar with the use of the investigational products(s)
Read the current investigator's brochure, product insert, or other source information.
Assume responsibility for the investigational product at the trial site (when necessary)
Ensure the proper use and storage of the investigational product(s) at the trial site.
Assign responsibility to the appropriate research pharmacy personnel.
Review the proper use of the study article(s) by the subject(s)

Direct Site Operations

Communicate effectively with subjects, research team, IRB, and sponsor.
Ensure that all research staff are informed about the protocol and investigational agents.
Be knowledgeable about regulatory requirements and GCP standards.
Prepare for and attending investigator and start-up meetings whenever necessary.
Participate in monitoring visits and audits as appropriate.
Permit monitoring and auditing by the sponsor and appropriate regulatory authorities.
Make available to monitors, auditors, IRB and regulatory authorities all requested trial-related records.
Delegate authority at the site appropriately
Ensure that all research staff are informed about their trail-related duties and functions.

Maintains Professional and Technical Knowledge

Attend educational workshops.
Review professional publications.
Participate in professional societies.

Skills and Qualifications:

Education and experience
- NP required
- Experience as a Sub-Investigator in industry-sponsored clinical trials preferred.
Requirements
- Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
- Knowledgeable in medical terminology
- Skilled in persuading potential sponsors to place research with the site.
- Demonstrate the initiative to act independently, initiate activity as required and make appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy.
- Able to initiate or modify behavior to achieve desired outcomes despite environmental factors, priorities, or problems that might not be well defined or that are subject to change.
- Experienced negotiation skills
- Formal presentation skills
- Ability to perform overnight business travel.
- Excellent persuasive/selling skills.
- Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.
- Excellent communication skills (interpersonal, written, verbal)
- Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)

#ERGHP

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Refine Your Search

site director jobs in boerne, tx

Sub l /Nurse Practitioner

After School Youth Leader - Boerne/ UTSA area

Risk Management Coordinator

Clinical Data Coordinator I (CS3622 - Hamilton Wolfe)

Clinical Research Coordinator

Risk Management Coordinator

Assistant Manager

STEM and Drone Flying School Year Camp Teacher

After School Program-Site Director- San Antonio Texas

Radiology QA & QC Coordinator

Nurse Navigator

Marketing & Content Assistant

Laboratory Technician (PRN)

Radiology QA & QC Coordinator

Nurse Navigator

Medical Director of TDI Diabetes Research Unit (Open Rank)

Open Rank Psychiatry Residency Program Director

PRN Physician, Family or Internal Medicine

OB Hospitalist Physician

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