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CTO Clinical Research Coordinator - Senior (Mays Cancer Center)

The UT Health Science Center at San Antonio

San Antonio, Texas • Today

Full-time

IT Director

Vaco by Highspring

Hybrid in San Antonio, Texas • Today

Easy Apply

Full-time

Depends on Experience

IT Director Quality Engineering

RBFCU

San Antonio, Texas • Today

Full-time

Chief Technology Officer (CTO), Artificial Intelligence (AI) Required, Work From Home - M

Next Step Systems

Remote • Today

Easy Apply

Full-time

$180,000 - $250,000

CTO Commissioning Specialist - Remote

Konecranes

Remote • Today

Full-time

Field CTO

3CLoud

Remote • Today

Full-time

Field Chief Technology Officer - Modern Workplace

SHI International Corporation

Remote or Texas • Today

Full-time

USD 250,000.00 - 350,000.00 per year

Chief Technology Officer - Databricks Data & AI Platform

EPAM Systems

Remote or New York, New York • Today

Full-time

Chief Technology Officer - Databricks Data & AI Platform

EPAM Systems

Remote • Today

Full-time

Field Chief Technology Officer - North America West

1Password

Remote or Canada, Kentucky • Today

Full-time

USD 228,000.00 per year

Field Chief Technology Officer - North America East

1Password

Remote or Canada, Kentucky • Today

Full-time

USD 228,000.00 per year

Field CTO, RSA ID Plus

RSA Security

Remote • Today

Full-time

USD 170,000.00 - 270,000.00 per year

Chief Technology Officer

AmeriSave Mortgage Corporation

Remote • Today

Full-time

USD 275,000.00 - 350,000.00 per year

IT Director, Payroll and Time & Attendance Technology

Stanley Black and Decker

Remote or Charlotte, North Carolina • Today

Full-time

USD 134,300.00 - 231,700.00 per year

Senior Tacton CPQ Consultant - Product Modeling & Administration

Miracle Software Systems, Inc.

Remote • Today

Easy Apply

Contract, Third Party

Depends on Experience

Senior SAP PLM Solution Architect

Shrive Technologies LLC

Remote • Today

Easy Apply

Contract, Third Party

$80 - $80

FTC Data Privacy Lead

Saicon Consultants Inc.

Remote • Today

Easy Apply

Third Party, Contract

Depends on Experience

Technical Director

Bounteous, Inc.

Remote • 6d ago

Easy Apply

Full-time

$160,000 - $200,000

IT Delivery Director

Randstad Digital

Remote or Plano, Texas • Today

Full-time

USD70 - USD80

Director of IT Enterprise

ScrumBytes

Remote • 5d ago

Easy Apply

Full-time

Depends on Experience

Director, IT & Cybersecurity

Revamp Engineering

Remote or Oakland, California • Today

Full-time

USD 160,000.00 - 220,000.00 per year

Director, Commercial IT Systems

Praxis Precision Medicines

Remote • Today

Full-time

USD 190,000.00 - 220,000.00 per year

Technical Director

Axiom Global Technologies, Inc.

Remote • 6d ago

Easy Apply

Contract, Third Party

Depends on Experience

Lead Security Engineer - AI

Microgreen Technologies LLC

Remote • 13d ago

Easy Apply

Contract

Depends on Experience

Chief Data & Technology Officer - Snowflake Services

Codeforce 360

Remote • Yesterday

Easy Apply

Full-time, Third Party

$180000 - $250000

SAP PLM Solution Architect

Akshaya Inc

Remote or Fremont, California • Yesterday

Easy Apply

Contract

Depends on Experience

SAP PLM Solution Architect

Akshaya Inc

Remote or Fremont, California • Today

Easy Apply

Contract

Depends on Experience

Senior SAP PLM Solution Architect :: 100% Remote

Prudent Technologies and Consulting

Remote • Yesterday

Easy Apply

Contract

70 - 80

SAP PLM Solution Architect / Principal Consultant

ICS Global Soft, Inc.

Remote • Yesterday

Easy Apply

Contract

Depends on Experience

Urgent requirement // Senior Enterprise Architect — Utility & Energy Sector // Remote 100%

Alliance IT

Remote • Yesterday

Easy Apply

Contract

90 - 100

Job Details

Skills

Supervision
Scheduling
Clinical Research
Pharmacy
Accountability
Corrective And Preventive Action
Regulatory Compliance
Forms
Decision-making
Communication
Finance
Effective Communication
Legal
Medical Records
HIPAA
Medical Terminology
Reporting
Documentation
EDC
Clinical Trials
Management
Clinical Trial Management System
Standard Operating Procedure
Screening
Recruiting
Conflict Resolution
Problem Solving
Critical Thinking
Collaboration
Teamwork
Research

Supervision
Scheduling
Clinical Research
Pharmacy
Accountability
Corrective And Preventive Action
Regulatory Compliance
Forms
Decision-making
Communication
Finance
Effective Communication
Legal
Medical Records
HIPAA
Medical Terminology
Reporting
Documentation
EDC
Clinical Trials
Management
Clinical Trial Management System
Standard Operating Procedure
Screening
Recruiting
Conflict Resolution
Problem Solving
Critical Thinking
Collaboration
Teamwork
Research

Summary

Job Description

Under limited supervision the Clinical Research Coordinator (CRC) - Senior champions patient safety and protocol integrity while upholding the highest standards of patient care. The CRC communicates effectively to support the successful conduct of clinical trials and ensure quality outcomes. Responsibilities include screening and scheduling patients, coordinating all on-study activities, and maintaining compliance with study requirements. The CRC also participates in study teleconferences with sponsors and clinical research organizations to promote clear communication and continuity of information.

Responsibilities

Independently identifies study objectives and outcome measures while ensuring adherence to all applicable federal, state, institutional, and Mays Cancer Center regulations, policies, and SOPs.
Maintains timely and accurate communication with the interdisciplinary team to support protocol compliance and the efficient conduct of study procedures.
Collaborates with the principal investigator, pharmacy, and other key personnel to ensure proper use and accountability of investigational products.
Provides protocol-specific education and guidance to clinical and research staff including review of protocol adherence for lower-level coordinators.
Coordinates, participates, and assists with leading meetings or teleconferences with sponsors, monitors, and auditors to ensure continuity of study information.
Ensures timely and accurate reporting of serious adverse events, unanticipated problems, deviations, and noncompliance to the IRB and study sponsor.
Assists in developing and implementing corrective and preventive action plans to address deviations, violations, and other compliance issues.
Ensures compliance with institutional policies and IRB requirements for the informed consent process, including use of the most current IRB-approved consent forms.
Collaborates with the physician investigator to conduct, document, and maintain ongoing informed consent and re-consent as required.
Identifies and addresses barriers to effective consent discussions and decision-making (e.g., literacy, language, capacity, distress, time constraints, therapeutic misconception).
Assesses and reinforces patient understanding of study information through ongoing communication and education.
Demonstrates knowledge of and adherence to tiered consent processes for optional correlative studies (e.g., biospecimen, quality of life, and patient-reported outcomes).
Verifies that informed consent is obtained and documented prior to initiating any study-specific procedures.
Assists in the review of lower-level Research Coordinators' work.
Collaborates with the investigator to assess and document patient eligibility for clinical trials according to protocol-specified criteria.
Provides education to patients and families regarding study participation, required procedures, and, if applicable, the clinical condition or disease process (directly if an RN, or in coordination with a nurse educator if not).
Coordinates and schedules all protocol-required events and assessments (e.g., pharmacokinetic/pharmacodynamic sampling, imaging, quality-of-life measures, and study visits) to ensure timely completion.
Evaluates and addresses physical, psychosocial, and financial factors that may impact patient adherence to study requirements.
Monitors patient adherence to self-administered study medications, ensuring accurate documentation and proper return of unused agents.
Collaborates with the investigator to assess disease response and determine treatment schedule or dosage modifications, communicating findings to the study team and care providers.
Promotes effective communication between research and clinical staff to ensure continuity of care and evidence-based symptom management in accordance with protocol parameters.
Documents all patient interactions in the legal medical record per institutional and licensure requirements and ensures proper source documentation for research data.
Obtains relevant outside records or laboratory results needed for study documentation and educates research and clinical staff on accurate data recording practices.
All other duties as assigned.

Qualifications

Education: Bachelors degree is required.

Advanced ability to communicate and liaise with research participants, research team members, and other relevant partner/key stakeholders.
Shown ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner.
Advanced ability to monitor important and complex projects concurrently.
Advanced knowledge of Federal regulations and ethical standards governing human subjects research (e.g., FDA, HIPAA, IRB processes).
Advanced understanding of Clinical trial design, methodology, and protocol requirements.
Knowledgeable in Medical terminology, anatomy, and disease processes relevant to assigned studies.
Advanced knowledge of adverse event reporting procedures and documentation standards.
Adept understanding of the principles of informed consent and patient rights.
Proven ability to use Electronic data capture (EDC) systems and clinical trial management systems (CTMS).
Shown ability to adhere to Institutional policies and standard operating procedures (SOPs).
Skilled at patient screening, recruitment, and informed consent processes.
Shown ability to conduct and document study visits according to protocol.
Advanced problem-solving and critical thinking for protocol deviations or logistical challenges.
Shown collaboration and teamwork in multidisciplinary clinical and research environments.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: RTX139cb4
Position Id: 54c0165ffc7102d615b68c03551f29c7
Posted 11 days ago

Fitment

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Clinical Trial Product Owner

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Job Details

Skills

Supervision
Scheduling
Clinical Research
Pharmacy
Accountability
Corrective And Preventive Action
Regulatory Compliance
Forms
Decision-making
Communication
Finance
Effective Communication
Legal
Medical Records
HIPAA
Medical Terminology
Reporting
Documentation
EDC
Clinical Trials
Management
Clinical Trial Management System
Standard Operating Procedure
Screening
Recruiting
Conflict Resolution
Problem Solving
Critical Thinking
Collaboration
Teamwork
Research

Supervision
Scheduling
Clinical Research
Pharmacy
Accountability
Corrective And Preventive Action
Regulatory Compliance
Forms
Decision-making
Communication
Finance
Effective Communication
Legal
Medical Records
HIPAA
Medical Terminology
Reporting
Documentation
EDC
Clinical Trials
Management
Clinical Trial Management System
Standard Operating Procedure
Screening
Recruiting
Conflict Resolution
Problem Solving
Critical Thinking
Collaboration
Teamwork
Research

Summary

Independently identifies study objectives and outcome measures while ensuring adherence to all applicable federal, state, institutional, and Mays Cancer Center regulations, policies, and SOPs.
Maintains timely and accurate communication with the interdisciplinary team to support protocol compliance and the efficient conduct of study procedures.
Collaborates with the principal investigator, pharmacy, and other key personnel to ensure proper use and accountability of investigational products.
Provides protocol-specific education and guidance to clinical and research staff including review of protocol adherence for lower-level coordinators.
Coordinates, participates, and assists with leading meetings or teleconferences with sponsors, monitors, and auditors to ensure continuity of study information.
Ensures timely and accurate reporting of serious adverse events, unanticipated problems, deviations, and noncompliance to the IRB and study sponsor.
Assists in developing and implementing corrective and preventive action plans to address deviations, violations, and other compliance issues.
Ensures compliance with institutional policies and IRB requirements for the informed consent process, including use of the most current IRB-approved consent forms.
Collaborates with the physician investigator to conduct, document, and maintain ongoing informed consent and re-consent as required.
Identifies and addresses barriers to effective consent discussions and decision-making (e.g., literacy, language, capacity, distress, time constraints, therapeutic misconception).
Assesses and reinforces patient understanding of study information through ongoing communication and education.
Demonstrates knowledge of and adherence to tiered consent processes for optional correlative studies (e.g., biospecimen, quality of life, and patient-reported outcomes).
Verifies that informed consent is obtained and documented prior to initiating any study-specific procedures.
Assists in the review of lower-level Research Coordinators' work.
Collaborates with the investigator to assess and document patient eligibility for clinical trials according to protocol-specified criteria.
Provides education to patients and families regarding study participation, required procedures, and, if applicable, the clinical condition or disease process (directly if an RN, or in coordination with a nurse educator if not).
Coordinates and schedules all protocol-required events and assessments (e.g., pharmacokinetic/pharmacodynamic sampling, imaging, quality-of-life measures, and study visits) to ensure timely completion.
Evaluates and addresses physical, psychosocial, and financial factors that may impact patient adherence to study requirements.
Monitors patient adherence to self-administered study medications, ensuring accurate documentation and proper return of unused agents.
Collaborates with the investigator to assess disease response and determine treatment schedule or dosage modifications, communicating findings to the study team and care providers.
Promotes effective communication between research and clinical staff to ensure continuity of care and evidence-based symptom management in accordance with protocol parameters.
Documents all patient interactions in the legal medical record per institutional and licensure requirements and ensures proper source documentation for research data.
Obtains relevant outside records or laboratory results needed for study documentation and educates research and clinical staff on accurate data recording practices.
All other duties as assigned.

Qualifications

Education: Bachelors degree is required.

Advanced ability to communicate and liaise with research participants, research team members, and other relevant partner/key stakeholders.
Shown ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner.
Advanced ability to monitor important and complex projects concurrently.
Advanced knowledge of Federal regulations and ethical standards governing human subjects research (e.g., FDA, HIPAA, IRB processes).
Advanced understanding of Clinical trial design, methodology, and protocol requirements.
Knowledgeable in Medical terminology, anatomy, and disease processes relevant to assigned studies.
Advanced knowledge of adverse event reporting procedures and documentation standards.
Adept understanding of the principles of informed consent and patient rights.
Proven ability to use Electronic data capture (EDC) systems and clinical trial management systems (CTMS).
Shown ability to adhere to Institutional policies and standard operating procedures (SOPs).
Skilled at patient screening, recruitment, and informed consent processes.
Shown ability to conduct and document study visits according to protocol.
Advanced problem-solving and critical thinking for protocol deviations or logistical challenges.
Shown collaboration and teamwork in multidisciplinary clinical and research environments.

Dice Id: RTX139cb4
Position Id: 54c0165ffc7102d615b68c03551f29c7
Posted 11 days ago

Fitment

Dice Job Match Score™

To see how well you match this job, please log in or create an account.

Once logged in, be sure to complete your profile to get the most accurate match score.

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

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