Research Contractors
DHR Health Institute for Research and Development
Edinburg, TXFull-time
86K a year
Behavioral Health Market Context
Apply Nowvia Tallo
Job Description
te / Remote:
Work onsite all of the time
Job Type:
Regular, Full Time (30 Hours or More), Permanent Employment Job Requirements and Properties
Help for Job Requirements and Properties. Work Onsite
Full Time Education
Bachelor's Degree Experience
24 Month(s) Schedule
Full Time Job Type
Regular Duration
Permanent Employment Public Transit
Available Help for . Clinical Research Contract Manager:
DHR Health Institute for Research & Development; Edinburg, TX 78539. Coordinate and monitor sponsored research accounts in accordance with study protocols and institutional guidelines. Ensure adherence to clinical trial billing practices and regulatory requirements, including federal, state, sponsor-specific, and institutional policies. Communicate sponsor guidelines, study protocols, and regulatory expectations to the research sta, and administrators to ensure proper conduct according to the contract language and budget. Track and evaluate expenditures and budget activity related to sponsored clinical research to ensure alignment with study budgets, funding agency requirements, and applicable regulations. Prepare and submit interim and final financial reports, in coordination with Research Institute administrators and sponsors, ensuring accuracy and timeliness. Promote effective research management practice by providing guidance and training to the team. Perform additional administrative and coordination duties related to the planning, implementation, and compliance of clinical research projects, as assigned. Requirements/Special Skills:
Bachelors degree in Healthcare Management or Healthcare Administration and 24 months of employment experience as Compliance Manager. 24 months as a Compliance Manager must include knowledge of local and state laws, legal codes, precedents, government regulations, executive orders, and agency rules. Knowledge of regulatory compliance applicable to biomedical and clinical research. This includes the U.S. Food and Drug Administration (FDA) regulations governing clinical trials, informed consent, and investigational products. Must possess knowledge of regulatory compliance of Institutional Review Board (IRB) regulations and human subject protection. Demonstrable ability in Good Clinical Practice guidelines and compliance, conflict-of-interest disclosures, and research integrity standards
Work onsite all of the time
Job Type:
Regular, Full Time (30 Hours or More), Permanent Employment Job Requirements and Properties
Help for Job Requirements and Properties. Work Onsite
Full Time Education
Bachelor's Degree Experience
24 Month(s) Schedule
Full Time Job Type
Regular Duration
Permanent Employment Public Transit
Available Help for . Clinical Research Contract Manager:
DHR Health Institute for Research & Development; Edinburg, TX 78539. Coordinate and monitor sponsored research accounts in accordance with study protocols and institutional guidelines. Ensure adherence to clinical trial billing practices and regulatory requirements, including federal, state, sponsor-specific, and institutional policies. Communicate sponsor guidelines, study protocols, and regulatory expectations to the research sta, and administrators to ensure proper conduct according to the contract language and budget. Track and evaluate expenditures and budget activity related to sponsored clinical research to ensure alignment with study budgets, funding agency requirements, and applicable regulations. Prepare and submit interim and final financial reports, in coordination with Research Institute administrators and sponsors, ensuring accuracy and timeliness. Promote effective research management practice by providing guidance and training to the team. Perform additional administrative and coordination duties related to the planning, implementation, and compliance of clinical research projects, as assigned. Requirements/Special Skills:
Bachelors degree in Healthcare Management or Healthcare Administration and 24 months of employment experience as Compliance Manager. 24 months as a Compliance Manager must include knowledge of local and state laws, legal codes, precedents, government regulations, executive orders, and agency rules. Knowledge of regulatory compliance applicable to biomedical and clinical research. This includes the U.S. Food and Drug Administration (FDA) regulations governing clinical trials, informed consent, and investigational products. Must possess knowledge of regulatory compliance of Institutional Review Board (IRB) regulations and human subject protection. Demonstrable ability in Good Clinical Practice guidelines and compliance, conflict-of-interest disclosures, and research integrity standards
Qualifications
- •Regular, Full Time (30 Hours or More), Permanent Employment Job Requirements and Properties
- •Bachelor's Degree Experience
- •24 Month(s) Schedule
- •Bachelors degree in Healthcare Management or Healthcare Administration and 24 months of employment experience as Compliance Manager
- •24 months as a Compliance Manager must include knowledge of local and state laws, legal codes, precedents, government regulations, executive orders, and agency rules
- •Knowledge of regulatory compliance applicable to biomedical and clinical research
- •This includes the U.S. Food and Drug Administration (FDA) regulations governing clinical trials, informed consent, and investigational products
- •Must possess knowledge of regulatory compliance of Institutional Review Board (IRB) regulations and human subject protection
- •Demonstrable ability in Good Clinical Practice guidelines and compliance, conflict-of-interest disclosures, and research integrity standards
Benefits
- •Full Time Education
- •Regular Duration
- •Permanent Employment Public Transit
Responsibilities
- •Coordinate and monitor sponsored research accounts in accordance with study protocols and institutional guidelines
- •Ensure adherence to clinical trial billing practices and regulatory requirements, including federal, state, sponsor-specific, and institutional policies
- •Communicate sponsor guidelines, study protocols, and regulatory expectations to the research sta, and administrators to ensure proper conduct according to the contract language and budget
- •Track and evaluate expenditures and budget activity related to sponsored clinical research to ensure alignment with study budgets, funding agency requirements, and applicable regulations
- •Prepare and submit interim and final financial reports, in coordination with Research Institute administrators and sponsors, ensuring accuracy and timeliness
- •Promote effective research management practice by providing guidance and training to the team
- •Perform additional administrative and coordination duties related to the planning, implementation, and compliance of clinical research projects, as assigned
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