Top 85 Research compliance coordinator Jobs in San Antonio, Tx

Clinical Research Coordinator
U.S. Renal Care —San Antonio, TX
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
Research Compliance Coordinator
University of the Incarnate Word —San Antonio, TX
- $63,000 - $65,000 a year
- Extended hours
- Microsoft Outlook
- Mid-level
- Master's degree
- 403(b) matching
- AD&D insurance
Clinical Research Coordinator
Bering-Alaka`ina Holdings, LLC —San Antonio, TX
- Current TB test
- Mid-level
- Bachelor's degree
- Paid holidays
- Disability insurance
3d
PG Project Manager I
CPS Energy —San Antonio, TX
- Research
- Mid-level
- Bachelor's degree
7d
PG Project Manager I
CPS Energy —San Antonio, TX
- Research
- Mid-level
- Bachelor's degree
7d
PLE Construction Coordinator
Calance US —San Antonio, TX
- $50 an hour
- Weekends as needed
- Microsoft Excel
- Construction site
- Engineering
- AD&D insurance
- Disability insurance
3d
Research Coordinator
UT Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- Microsoft Excel
- Customer service
- Mid-level
- AD&D insurance
- Paid holidays
13d
Quality Assurance Coordinator-Associate
UT Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- Up to 50% travel
- Mid-level
- High school diploma or GED
- AD&D insurance
- Paid holidays
Animal Research Coordinator
Bering-Alaka`ina Holdings, LLC —San Antonio, TX
- Vital signs
- Current TB test
- Mid-level
- Paid holidays
- Disability insurance
3d
Research Coordinator
UT Health San Antonio —San Antonio, TX
- 8 hour shift
- Microsoft Excel
- Customer service
- Mid-level
- AD&D insurance
- Paid holidays
Quick Apply
3d
Clinical Research Coordinator
START Center for Cancer Research —San Antonio, TX
- Monday to Friday
- Mid-level
- High school diploma or GED
- 2 years
- Health savings account
- Paid holidays
Quick Apply
Career Navigator
Texas A&M University - San Antonio —San Antonio, TX
- Weekends as needed
- Microsoft Excel
- Microsoft Outlook
- Experience working with individuals with disabilities
23h
Clinical Research Coordinator
Pinnacle Clinical Research —San Antonio, TX
- Full-time
- Spanish
- Vital signs
- BLS Certification
- Paid holidays
- Disability insurance
Quick Apply
Clinical Research Coordinator
Tekton Research Inc —San Antonio, TX
- Full-time
- Nursing
- Mid-level
- High school diploma or GED
Quick Apply
Emergency Preparedness Coordinator
Dept of State Health Services —San Antonio, TX
- $4,263.16 - $6,779.25 a month
- Online Application
- Microsoft Excel
- Research
- Mid-level
- Health insurance
Quick Apply
22h
Contract Coordinator (Grant Funded)
City of San Antonio —San Antonio, TX
- $64,097.02 - $96,145.66 a year
- Full-time
- Computer literacy
- Mid-level
- Office
- Disability insurance
- Health insurance
13d
Head Start Facilitator
South San Antonio Independent School District —San Antonio, TX
- $59,953 - $88,079 a year
- Weekends as needed
- Background check
- Experience working with individuals with disabilities
- Computer literacy
5d
Coordinator Referrals -
Christus Health —San Antonio, TX
- Full-time
- Medical office experience
- Research
- Mid-level
7d
CAMPUS COORDINATOR-GIFTED & TALENTED
Harmony Public Schools —San Antonio, TX
- Nights as needed
- School experience
- Classroom
- Word processing
6d
DISTRICT CHARACTER EDUCATION COORDINATOR
School of Science & Technology —San Antonio, TX
- $68,040 - $96,040 a year
- Weekends as needed
- School experience
- Writing skills
- Mid-level
Quick Apply

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Clinical Research Coordinator

U.S. Renal Care -
San Antonio, TX

Apply Now

Job Details

Full-time

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.

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

Apply Now

Refine Your Search

research compliance coordinator jobs in san antonio, tx

Clinical Research Coordinator

Research Compliance Coordinator

Clinical Research Coordinator

PG Project Manager I

PG Project Manager I

PLE Construction Coordinator

Research Coordinator

Quality Assurance Coordinator-Associate

Animal Research Coordinator

Research Coordinator

Clinical Research Coordinator

Career Navigator

Clinical Research Coordinator

Clinical Research Coordinator

Emergency Preparedness Coordinator

Contract Coordinator (Grant Funded)

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Coordinator Referrals -

CAMPUS COORDINATOR-GIFTED & TALENTED

DISTRICT CHARACTER EDUCATION COORDINATOR

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