Clinical Research Associate (CRA) – All levels (I/II/Senior)
About the position
As part of Theradex Oncology, you will have the opportunity to work with one of the largest professional teams focused solely on the development of cancer therapies. Cancer research continues to evolve as new therapies and therapeutic approaches are discovered, as part of the team you will the work to support our sponsors in the development of these therapies. Theradex Oncology is an environment for highly motivated individuals who want to make a difference.
Opportunity
Clinical Research Associate (CRA) – All levels (I/II/Senior)
We are expanding our team and are looking to hire CRAs for onsite and remote monitoring of phase l-lll oncology studies.
The primary responsibilities of this position include, but are not limited to, the following:
Conduct Site Monitoring:
Site Qualification visits
Site Initiation visits
Routine Monitoring visits
Close-out visits
All aspects of site management as described in the study plans
Source document verification:
Verify patient eligibility
Reviews consent process for each subject (Informed Consent Form and source documentation)
Assess protocol compliance and deviations
CRF review and data corrections
IMP accountability
Maintenance of on-site investigator files
IEC/IRB documentation
Local laboratory documentation
Maintenance of investigational supplies
Identify and assess safety issues and reporting (SAEs/AEs)
Site Management:
Ensure protection of participants and participants' rights
Proactively identify and resolve actual and potential site and study issues
Ensure clinical data integrity and adherence to study timelines
Clinical Review of individual patient listings
Assist in the preparation of project specific materials e.g., status reports, newsletters, templates, etc.
Act as the routine liaison between study site and the project team for study related issues
Perform other duties as assigned by management
Responsibilities
• Conduct Site Monitoring
• Site Qualification visits
• Site Initiation visits
• Routine Monitoring visits
• Close-out visits
• All aspects of site management as described in the study plans
• Source document verification
• Verify patient eligibility
• Reviews consent process for each subject (Informed Consent Form and source documentation)
• Assess protocol compliance and deviations
• CRF review and data corrections
• IMP accountability
• Maintenance of on-site investigator files
• IEC/IRB documentation
• Local laboratory documentation
• Maintenance of investigational supplies
• Identify and assess safety issues and reporting (SAEs/AEs)
• Site Management
• Ensure protection of participants and participants' rights
• Proactively identify and resolve actual and potential site and study issues
• Ensure clinical data integrity and adherence to study timelines
• Clinical Review of individual patient listings
• Assist in the preparation of project specific materials e.g., status reports, newsletters, templates, etc.
• Act as the routine liaison between study site and the project team for study related issues
• Perform other duties as assigned by management
Requirements
• At minimum, Bachelor's degree in biological or science-related field (BSc, BA, or RN equivalent) or equivalent experience.
• As a Clinical Research Associate with experience managing clinical trial sites, the number years and type of monitoring experience will determine CRA level.
• Knowledge of ICH/GCP Guidelines, and Regulatory requirements
• Ongoing development of cancer therapy knowledge, clinical trial design and conduct, and drug development process through work experience, literature reviews and other educational opportunities
• Proficient in Excel, PowerPoint, Word, and Outlook
• Skilled remote collaboration and teleconferencing platforms
• Strong organizational skills, including efficiency, punctuality, and collaboration in a team environment.
• Effective communication skills: verbal and written
• Strong interpersonal skills including presentation, persuasion, and influence
• This position involves travel as needed to meet study requirements. Ability to travel up to 50% may involve overnight stays.
• Valid Driver’s License required and Passport preferred
• Successfully pass background clearance checks which may be run on a periodic basis due to 3rd party contractual obligation requirements.
• Fluent in English (written and verbal)
Nice-to-haves
• Experience in monitoring early phase oncology studies is preferred.
Benefits
• At Theradex we offer a supportive culture that puts people first. Our employees are eligible to participate in our comprehensive benefits package which includes medical, dental and vision coverage; life insurance, disability insurance (STD/LTD), company matched 401(k), very competitive tuition reimbursement, generous vacation/sick plans, flexible work schedules, employee discounts and other company provided benefits. The annual base salary for our CRA positions range from $75,000-$145,000 with bonus potential.
As part of Theradex Oncology, you will have the opportunity to work with one of the largest professional teams focused solely on the development of cancer therapies. Cancer research continues to evolve as new therapies and therapeutic approaches are discovered, as part of the team you will the work to support our sponsors in the development of these therapies. Theradex Oncology is an environment for highly motivated individuals who want to make a difference.
Opportunity
Clinical Research Associate (CRA) – All levels (I/II/Senior)
We are expanding our team and are looking to hire CRAs for onsite and remote monitoring of phase l-lll oncology studies.
The primary responsibilities of this position include, but are not limited to, the following:
Conduct Site Monitoring:
Site Qualification visits
Site Initiation visits
Routine Monitoring visits
Close-out visits
All aspects of site management as described in the study plans
Source document verification:
Verify patient eligibility
Reviews consent process for each subject (Informed Consent Form and source documentation)
Assess protocol compliance and deviations
CRF review and data corrections
IMP accountability
Maintenance of on-site investigator files
IEC/IRB documentation
Local laboratory documentation
Maintenance of investigational supplies
Identify and assess safety issues and reporting (SAEs/AEs)
Site Management:
Ensure protection of participants and participants' rights
Proactively identify and resolve actual and potential site and study issues
Ensure clinical data integrity and adherence to study timelines
Clinical Review of individual patient listings
Assist in the preparation of project specific materials e.g., status reports, newsletters, templates, etc.
Act as the routine liaison between study site and the project team for study related issues
Perform other duties as assigned by management
Responsibilities
• Conduct Site Monitoring
• Site Qualification visits
• Site Initiation visits
• Routine Monitoring visits
• Close-out visits
• All aspects of site management as described in the study plans
• Source document verification
• Verify patient eligibility
• Reviews consent process for each subject (Informed Consent Form and source documentation)
• Assess protocol compliance and deviations
• CRF review and data corrections
• IMP accountability
• Maintenance of on-site investigator files
• IEC/IRB documentation
• Local laboratory documentation
• Maintenance of investigational supplies
• Identify and assess safety issues and reporting (SAEs/AEs)
• Site Management
• Ensure protection of participants and participants' rights
• Proactively identify and resolve actual and potential site and study issues
• Ensure clinical data integrity and adherence to study timelines
• Clinical Review of individual patient listings
• Assist in the preparation of project specific materials e.g., status reports, newsletters, templates, etc.
• Act as the routine liaison between study site and the project team for study related issues
• Perform other duties as assigned by management
Requirements
• At minimum, Bachelor's degree in biological or science-related field (BSc, BA, or RN equivalent) or equivalent experience.
• As a Clinical Research Associate with experience managing clinical trial sites, the number years and type of monitoring experience will determine CRA level.
• Knowledge of ICH/GCP Guidelines, and Regulatory requirements
• Ongoing development of cancer therapy knowledge, clinical trial design and conduct, and drug development process through work experience, literature reviews and other educational opportunities
• Proficient in Excel, PowerPoint, Word, and Outlook
• Skilled remote collaboration and teleconferencing platforms
• Strong organizational skills, including efficiency, punctuality, and collaboration in a team environment.
• Effective communication skills: verbal and written
• Strong interpersonal skills including presentation, persuasion, and influence
• This position involves travel as needed to meet study requirements. Ability to travel up to 50% may involve overnight stays.
• Valid Driver’s License required and Passport preferred
• Successfully pass background clearance checks which may be run on a periodic basis due to 3rd party contractual obligation requirements.
• Fluent in English (written and verbal)
Nice-to-haves
• Experience in monitoring early phase oncology studies is preferred.
Benefits
• At Theradex we offer a supportive culture that puts people first. Our employees are eligible to participate in our comprehensive benefits package which includes medical, dental and vision coverage; life insurance, disability insurance (STD/LTD), company matched 401(k), very competitive tuition reimbursement, generous vacation/sick plans, flexible work schedules, employee discounts and other company provided benefits. The annual base salary for our CRA positions range from $75,000-$145,000 with bonus potential.