Urology San Antonio
Clinical Research Data Coordinator
Urology San Antonio - San Antonio, Texas, United States, 78208
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Overview
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Clinical Research Data Coordinator
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Clinical Research Data Coordinator
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The Clinical Research Data Coordinator is responsible for the collection, coordination, processing, and quality control of all clinical trial data. They may assist with screening patients for research guidelines along with maintaining research protocol information, regulatory documents, and other research files as applicable. Works in compliance with Urology San Antonio Research Department (USARD), Standard Operating Procedure (SOP), principles of Good Clinical Practice, and all applicable federal, state, and local regulations. Job Summary
The Clinical Research Data Coordinator is responsible for the collection, coordination, processing, and quality control of all clinical trial data. They may assist with screening patients for research guidelines along with maintaining research protocol information, regulatory documents, and other research files as applicable. Works in compliance with Urology San Antonio Research Department (USARD), Standard Operating Procedure (SOP), principles of Good Clinical Practice, and all applicable federal, state, and local regulations.
Duties And Essential Job Functions
Extrapolates data, completes case report forms, and ensures timely data submission in accordance with USARD SOP. Actively prepares/participate in monitoring and auditing activities. Assists in ensuring that all queries are resolved in a timely manner in accordance with USARD SOP and sponsor requirements. Responsible for processing, filing, and maintaining protocol regulatory documents. May assist with screening patients for potential study enrollment. Responsible for assisting with patient scheduling for procedures required to maintain protocol compliance. Responsible for assisting with coordinating patient follow-up visits and timely data submission. Responsible for assisting with the collection and processing of specimens, imaging documents, or other items required for research purposes. Responsible for ordering and maintaining research supplies. Responsible for assisting in the investigational drug accountability process. Maintains research records in a confidential manner according to practice policies, sponsor confidentiality agreements, HIPAA guidelines, and any other applicable regulations. May lead and mentor other data coordinators at the site/location May be responsible for coordinating patient billing and research payout/payment tracking.
Other Functions And Responsibilities
This job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
COMPETENCIES
Patient & Customer Focus Ethical Conduct Flexibility Initiative Personal Effectiveness/Credibility Stress Management/Composure EDC Platforms: RAVE, imedidata, Inform, Medrio
Qualifications
Required
Associates of Science Degree (or related field) Bachelor's Degree preferred
Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
Job function Research, Analyst, and Information Technology Industries Medical Practices Referrals increase your chances of interviewing at Urology San Antonio by 2x Sign in to set job alerts for “Clinical Data Coordinator” roles.
Clinical Research Coordinator 2 (Recent Grads)- San Antonio, TX - Office Based
Clinical Research Coordinator 2 - San Antonio, TX - Office Based
San Antonio, Texas Metropolitan Area $80,000.00-$120,000.00 2 weeks ago Research Coordinator (Emergency Medicine- Regulatory)
PRN Research Technician - San Antonio, TX - Office Based **New Grads Welcome**
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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Clinical Research Data Coordinator
role at
Urology San Antonio 1 day ago Be among the first 25 applicants Join to apply for the
Clinical Research Data Coordinator
role at
Urology San Antonio Get AI-powered advice on this job and more exclusive features. Job Summary
The Clinical Research Data Coordinator is responsible for the collection, coordination, processing, and quality control of all clinical trial data. They may assist with screening patients for research guidelines along with maintaining research protocol information, regulatory documents, and other research files as applicable. Works in compliance with Urology San Antonio Research Department (USARD), Standard Operating Procedure (SOP), principles of Good Clinical Practice, and all applicable federal, state, and local regulations. Job Summary
The Clinical Research Data Coordinator is responsible for the collection, coordination, processing, and quality control of all clinical trial data. They may assist with screening patients for research guidelines along with maintaining research protocol information, regulatory documents, and other research files as applicable. Works in compliance with Urology San Antonio Research Department (USARD), Standard Operating Procedure (SOP), principles of Good Clinical Practice, and all applicable federal, state, and local regulations.
Duties And Essential Job Functions
Extrapolates data, completes case report forms, and ensures timely data submission in accordance with USARD SOP. Actively prepares/participate in monitoring and auditing activities. Assists in ensuring that all queries are resolved in a timely manner in accordance with USARD SOP and sponsor requirements. Responsible for processing, filing, and maintaining protocol regulatory documents. May assist with screening patients for potential study enrollment. Responsible for assisting with patient scheduling for procedures required to maintain protocol compliance. Responsible for assisting with coordinating patient follow-up visits and timely data submission. Responsible for assisting with the collection and processing of specimens, imaging documents, or other items required for research purposes. Responsible for ordering and maintaining research supplies. Responsible for assisting in the investigational drug accountability process. Maintains research records in a confidential manner according to practice policies, sponsor confidentiality agreements, HIPAA guidelines, and any other applicable regulations. May lead and mentor other data coordinators at the site/location May be responsible for coordinating patient billing and research payout/payment tracking.
Other Functions And Responsibilities
This job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
COMPETENCIES
Patient & Customer Focus Ethical Conduct Flexibility Initiative Personal Effectiveness/Credibility Stress Management/Composure EDC Platforms: RAVE, imedidata, Inform, Medrio
Qualifications
Required
Associates of Science Degree (or related field) Bachelor's Degree preferred
Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
Job function Research, Analyst, and Information Technology Industries Medical Practices Referrals increase your chances of interviewing at Urology San Antonio by 2x Sign in to set job alerts for “Clinical Data Coordinator” roles.
Clinical Research Coordinator 2 (Recent Grads)- San Antonio, TX - Office Based
Clinical Research Coordinator 2 - San Antonio, TX - Office Based
San Antonio, Texas Metropolitan Area $80,000.00-$120,000.00 2 weeks ago Research Coordinator (Emergency Medicine- Regulatory)
PRN Research Technician - San Antonio, TX - Office Based **New Grads Welcome**
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr