- Attends appropriate departmental meetings and institutional continuing education programs.
- Plans, designs, and conducts complex professional and ancillary education sessions to ensure dissemination of new information and policies.
- Demonstrates excellent oral and written communication skills when contacting other institutions, patients and agencies (i.e. NCI, pharmaceutical companies, sponsoring agencies, etc.) by phone, email and/or face to face interactions. Assimilates pertinent information in order to compose written correspondence.
- Maintains working knowledge of current Code of Federal Regulation and Good Clinical Practice guidelines as well as a comprehensive understanding of the research trial process, including but not limited to eligibility and disease processes.
- Requisition ID: 167141
- Employment Status: Full-Time
- Employee Status: Regular
- Work Week: Days
- Minimum Salary: US Dollar (USD) 55,500
- Midpoint Salary: US Dollar (USD) 69,500
- Maximum Salary : US Dollar (USD) 83,500
- Fund Type: Soft
- Work Location: Hybrid Onsite/Remote
- Pivotal Position: No
- Referral Bonus Available?: No
- Relocation Assistance Available?: No
- Science Jobs: Yes
-
Clinical Studies Coordinator
1 week ago
University of Texas M.D. Anderson Houston, United StatesThe primary purpose of the Clinical Studies Coordinator is to provide all study related coordination for a position supporting Melanoma Medical Oncology and Nephrology, including but not limited to data management, patient coordination, and regulatory management for a clinical re ...
-
Clinical Studies Coordinator
1 week ago
University of Texas M.D. Anderson Houston, United StatesJOB SPECIFIC COMPETENCIES · Coordination of Study initiation and Operations of Clinical Research Protocols · * Under supervision of the protocol primary investigator (PI), the research nurse manager and/or clinical studies supervisor, assumes responsibility for the overall effect ...
-
Coordinator, Clinical Studies
2 weeks ago
University of Texas M.D. Anderson Houston, United StatesThe Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol compliance, quality assurance and communicating with staff regarding protocol information. · KEY FUNCTIONS · Designs, implements, moni ...
-
Coordinator, Clinical Studies
1 week ago
University of Texas M.D. Anderson Houston, United StatesCoordinator, Clinical Studies · MISSION STATEMENT · The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and prevention, and through educat ...
-
Coordinator, Clinical Studies
1 week ago
MD Anderson Houston, United StatesCoordinator, Clinical Studies · MISSION STATEMENT · The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and prevention, and through educat ...
-
Coordinator, Clinical Studies
2 weeks ago
University of Texas M.D. Anderson Houston, United StatesCoordinator, Clinical Studies · MISSION STATEMENT · The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and prevention, and through educat ...
-
Coordinator, Clinical Studies
2 weeks ago
University of Texas M.D. Anderson Houston, United StatesCoordinator, Clinical Studies - Genitourinary Medical Oncology · Summary · The Coordinator, Clinical Studies - Regulatory - ensures regulatory compliance for the Department of Genitourinary Medical Oncology clinical trials, assists with the institutional and federal approval proc ...
-
Coordinator, Clinical Studies
1 week ago
MD Anderson Cancer Center Houston, United StatesThe University of Texas MD Anderson Cancer Center in Houston is one of the world's most respected centers focused on cancer patient care, research, education, and prevention. It was named the nation's No. 1 hospital for cancer care in U.S. News & World Report's rankings. It is on ...
-
Coordinator, Clinical Studies
2 weeks ago
University of Texas M.D. Anderson Houston, United StatesSummary · The Coordinator, Clinical Studies ensures regulatory compliance for the Department of Genitourinary Medical Oncology clinical trials, assists with the institutional and federal approval procedures for research lab and clinical trials and provides education relevant to r ...
-
Clinical Studies Coordinator
3 weeks ago
MD Anderson Cancer Center Houston, United States Paid WorkThe primary purpose of the Clinical Studies Coordinator is to provide all study related coordination for a position supporting Melanoma Medical Oncology and Nephrology, including but not limited to data management, patient coordination, and regulatory management for a clinical re ...
-
Coordinator, Clinical Studies
3 weeks ago
University of Texas MD Anderson Cancer Center Houston, United States OTHERCoordinator, Clinical Studies · MISSION STATEMENT · The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and prevention, and through educa ...
-
Clinical Studies Coordinator
3 weeks ago
MD Anderson Cancer Center Houston, United StatesThe Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol compliance, quality assurance and communicating with staff regarding protocol information. · **Key Functions** · **Designs, implements ...
-
Clinical Studies Coordinator
2 weeks ago
MD Anderson Houston, United StatesThe Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol compliance, quality assurance and communicating with staff regarding protocol information. · Key Functions · Designs, implements, moni ...
-
Coordinator, Clinical Studies
2 weeks ago
MD Anderson Houston, United StatesCoordinator, Clinical Studies · MISSION STATEMENT · The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and prevention, and through educat ...
-
Coordinator, Clinical Studies
1 week ago
MD Anderson Houston, United StatesCoordinator, Clinical Studies - Finance - GU Medical Oncology · Summary · The Coordinator, Clinical Studies ensures regulatory compliance for the Department of Genitourinary Medical Oncology clinical trials, assists with the institutional and federal approval procedures for resea ...
-
Coordinator, Clinical Studies
2 weeks ago
University of Texas M.D. Anderson Houston, United StatesCoordinator, Clinical Studies - Finance - GU Medical Oncology · Summary · The Coordinator, Clinical Studies ensures regulatory compliance for the Department of Genitourinary Medical Oncology clinical trials, assists with the institutional and federal approval procedures for resea ...
-
Coordinator, Clinical Studies
1 week ago
University of Texas M.D. Anderson Houston, United StatesThe University of Texas MD Anderson Cancer Center in Houston is one of the world's most respected centers focused on cancer patient care, research, education, and prevention. It was named the nation's No. 1 hospital for cancer care in U.S. News & World Report's rankings. It is on ...
-
Coordinator, Clinical Studies
6 days ago
University of Texas M.D. Anderson Cancer Center Houston, United StatesThe Coordinator, Clinical Studies ensures regulatory compliance for the Department of Gastrointestinal Medical Oncology clinical trials, assists with the institutional and federal approval procedures for research lab and clinical trials and provides Clinical, Clinical Research, C ...
-
Coordinator, Clinical Studies
2 weeks ago
MD Anderson Houston, United StatesSummary · The Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol compliance, quality assurance and communicating with staff regarding protocol information. · Key Functions · Designs, implem ...
-
Coordinator, Clinical Studies
3 weeks ago
University of Texas M.D. Anderson Houston, United StatesSummary · The Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol compliance, quality assurance and communicating with staff regarding protocol information. · Key Functions · Designs, implem ...
Clinical Studies Coordinator - Houston, United States - University of Texas M.D. Anderson
Description
The primary purpose of the Coordinator, Clinical Studies position is to collaborate with the research team and Principal Investigator (PI) to coordinate clinical trial subject accrual and data management activities for departmental clinical research, specifically for the Minimal Risk Team.
Under the guidance of the Supervisor, Clinical Studies, the Coordinator, Clinical Studies will also assist with ensuring that departmental clinical research is conducted in compliance with institutional policies, the Code of Federal Regulations, and Good Clinical Practice Guidelines.
KEY FUNCTIONS:
ADMINISTRATIVE:
Assures that policies/procedures of the institution and department are communicated to staff formally and informally by written and/or verbal means.
CLINICAL TRIAL MANAGEMENT
In consultation with the physician and research nurse, assesses patients for eligibility through personal interviews and medical record review. Responsible for accurate and successful patient recruitment to assigned protocols.
Reads protocol and develops systems for screening patients. Assists with the development of source document templates and other documents as needed for protocols.
In collaboration with the Principal Investigator (PI), responsible for ensuring the consent is understood, signed, and processed appropriately.
Consults with principal investigator (PI) regarding ongoing clinical trial assignments. Ensures consistency between protocol database and source documentation; includes generating written queries for missing/deficient source documentation. As needed, obtains patient charts and outside documents required for protocol compliance.
Responsible for accurate and timely transcription of study data to paper and/or electronic Case Report Form (CRF), retrieving information from electronic record, chart, and/or phone call.
Knowledge of protocol databases and electronic applications; proficient in the use of Microsoft office applications and departmental electronic data systems.
Provides sufficient, appropriate, and timely responses to sponsor queries. Participates with activities ensuring preparedness for industry, institutional, and federal clinical trial audits.
MAINTAINS A LEVEL OF PROFESSIONAL EXPERTISE
EDUCATION:
Required:
Bachelor's degree.
Preferred:
Master's degree.
EXPERIENCE:
Required:
Three years experience in area of research study or direct patient care obtained from nursing, data gathering or other related experience.
May substitute required education degree with additional years of equivalent experience on a one to one basis. With preferred degree, one year of required experience.Experience Preferred - Research Consenting and Patient Management Experience.
It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law.
