Top 105 Clinical data coordinator Jobs in San Antonio Tx

Clinical Research Coordinator
U.S. Renal Care —San Antonio, TX
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
- Health insurance
- Dental insurance
6d
Clinical Data Coordinator I (CS6215 - Hamilton Wolfe)
CommuniCare Health Centers (Texas) —San Antonio, TX
- Spanish
- Medical office experience
- HIPAA
Quick Apply
1d
Clinical Research Coordinator I
DM CLINICAL RESEARCH GROUP —San Antonio, TX
- Writing skills
- High school diploma or GED
- Bachelor's degree
Clinical Research Coordinator Assistant
Flourish Research —San Antonio, TX
- Full-time
- Vital signs
- Bachelor's degree
- Data entry
- Disability insurance
- Dental insurance
Quick Apply
5d
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
Clinical Research Coordinator
Pinnacle Clinical Research —San Antonio, TX
- Full-time
- Spanish
- Vital signs
- BLS Certification
- Paid holidays
- Disability insurance
Quick Apply
Pharmacist
Health Outcomes Centers —San Antonio, TX
- $100,000 - $150,000 a year
- Full-time
- Spanish
- Customer service
- Bachelor of Science
- Relocation assistance
- Health insurance
Quick Apply
14d
Advanced Practice Provider (Nurse Practitioner or Physician Assistant)
Health Outcomes Centers —San Antonio, TX
- From $120,000 a year
- Full-time
- Bilingual
- Background check
- Spanish
- Health insurance
- Dental insurance
Quick Apply
Advanced Practice Provider, Oncology
START Center for Cancer Research —San Antonio, TX
- Monday to Friday
- Nursing
- Doctoral degree
- 5 years
Quick Apply
Regional MDS
Tikva Healthcare —Texas
- $80,000 - $100,000 a year
- Full-time
- Anatomy knowledge
- RN License
- HIPAA
- Travel reimbursement
- Health insurance
Quick Apply
8d
Progressive Care Clinical Nurse Coordinator RN
Methodist Hospital —San Antonio, TX
- Full-time
- Mid-level
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply
11d
Charge Nurse CNC FSER Emergency Room
Methodist ER Converse —San Antonio, TX
- Full-time
- Mid-level
- Telemetry
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply
PRN - Direct Support Professional (SUB)
San Antonio —San Antonio, TX
- $10 an hour
- Overtime
- Background check
- CPR Certification
- Pass drug screening
- Health savings account
- Health insurance
Quick Apply
Direct Support Professional - WEEKENDS
San Antonio —San Antonio, TX
- $10 an hour
- Overtime
- Background check
- CPR Certification
- Pass drug screening
- Health savings account
- Health insurance
Quick Apply
Direct Support Professional - WEEKDAYS
San Antonio —San Antonio, TX
- $10 an hour
- Overtime
- Background check
- CPR Certification
- Pass drug screening
- Health savings account
- Health insurance
Quick Apply
MDS Coordinator
Legend Oaks South Healthcare and Rehabilitation —San Antonio, TX
- $61,969.82 - $74,630.33 a year
- Full-time
- Skilled nursing facility
- LVN
- RN License
- Health insurance
- Dental insurance
Quick Apply
6d
Regional MDS Coordinator
Cantex Continuing Care Network —San Antonio, TX
- Full-time
- CPR Certification
- Skilled nursing facility
- RN License
- Continuing education credits
- Health insurance
Quick Apply
2d
FT, Healthcare Data/ Billing Coordinator
Athra Systems —San Antonio, TX
- $17 - $20 an hour
- Full-time
- Medical office experience
- HIPAA
- Mid-level
Quick Apply
15h
Front Desk Coordinator - San Antonio, TX
ProCare Injury Specialists —San Antonio, TX
- $20 - $22 an hour
- Full-time
- Spanish
- High school diploma or GED
- Clinic
- Disability insurance
- Health insurance
Quick Apply
Hospital Billing Coordinator
Deloitte —San Antonio, TX
- $50,000 - $60,000 a year
- Full-time
- Microsoft Excel
- Mid-level
- Bachelor's degree

I want to receive the latest job alert for clinical data coordinator in san antonio tx

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical data coordinator jobs near san antonio tx

Clinical Research Coordinator jobs in San Antonio, TX

Direct Support Professional jobs in San Antonio, TX

Pharmacist jobs in San Antonio, TX

Clinical Data Coordinator jobs in San Antonio, TX

Billing Coordinator jobs in San Antonio, TX

Front Desk Coordinator jobs in San Antonio, TX

Advanced Practice Provider jobs in San Antonio, TX

Mds Coordinator jobs in San Antonio, TX

Nurse Manager jobs in San Antonio, TX

Progressive Care Nurse jobs in San Antonio, TX

Gme Program Coordinator jobs in Texas

Clinical Research Coordinator jobs in Fremont, CA

Clinical Specialist jobs in Orange County, CA

Clinical Research Coordinator jobs in Columbus, GA

Clinical Research Coordinator jobs in Durham, NC

Clinical Research Coordinator jobs in El Paso, TX

Clinical Psychologist jobs in Columbus, OH

Marketing Coordinator jobs in Austin, TX

Direct Support Professional jobs in Cincinnati, OH

Direct Support Professional jobs in Alabama

Clinical Research Coordinator

U.S. Renal Care -
San Antonio, TX

Apply Now

Job Details

Full-time
6 days ago

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

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/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.
One (1) to 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.

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

Apply Now

Refine Your Search

clinical data coordinator jobs in san antonio tx

Clinical Research Coordinator

Clinical Data Coordinator I (CS6215 - Hamilton Wolfe)

Clinical Research Coordinator I

Clinical Research Coordinator Assistant

Clinical Research Coordinator

Clinical Research Coordinator

Pharmacist

Advanced Practice Provider (Nurse Practitioner or Physician Assistant)

Advanced Practice Provider, Oncology

Regional MDS

Progressive Care Clinical Nurse Coordinator RN

Charge Nurse CNC FSER Emergency Room

PRN - Direct Support Professional (SUB)

Direct Support Professional - WEEKENDS

Direct Support Professional - WEEKDAYS

MDS Coordinator

Regional MDS Coordinator

FT, Healthcare Data/ Billing Coordinator

Front Desk Coordinator - San Antonio, TX

Hospital Billing Coordinator

I want to receive the latest job alert for clinical data coordinator in san antonio tx

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected