Clinical Research Associate II
Who We Are
elebrating 40+ years!
Theradex Oncology is a full-service CRO specializing in oncology. The company manages global oncology trials and programs. The company was founded in 1982 working with the National Cancer Institute, which led to its expansion to working with industry sponsors developing cancer therapeutics. As a service-based company we support both domestic and international sponsors in the conduct of both early and late phase trials.
What You'll Do
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 II
The primary responsibilities of this position include, but are not limited to, the following:
Act as the routine liaison between study site and the project team for study related issues.
Ensures protection of subjects, subjects' rights, and the integrity of data through monitoring of adherence to Good Clinical Practice, applicable regulatory requirements, Standard Operating Procedures and protocol compliance.
Conducts pre-qualification, initiation, routine monitoring, remote monitoring, and close-out visits in accordance with the relevant SOPs and the specific project scope of work to include but not limited to:
Source document review and comparison to CRF data
CRF review/retrieval and data corrections
IMP accountability
Maintenance of on-site investigator files
IEC/IRB documentation
Local laboratory documentation
Maintenance of investigational supplies
Reviews consent process for each subject (Informed Consent Form and source documentation)
Verify patient eligibility
Assess protocol compliance and deviations
Handling of safety and efficacy issues, including, but not limited to:
Serious adverse event reports
Adverse event trends
Treatment failures/outcomes
Conducts and documents onsite visits/contacts, including:
Pre-study visits
Initiation visits
Routine visits
Study completion visits/ Close-out visits
Telephone contact
Site visit report preparation within study specific timeframe
Responsible for all aspects of site management as described in the study plans
Proactively identify and resolve issues and potential site and study issues.
Assist with regulatory and study start-up activities including contract and budget negotiations, as required.
Ensure clinical data integrity and meet study timelines.
Provide ongoing updates and support to project management.
Mentor junior members of the team.
Prepare and deliver staff training sessions.
Clinical Review of individual patient listings
Initial clinical review of comprehensive patient data listings
Initial review of study start-up materials: SOPs, draft CRFs, completion manual, compliance forms, study prompters/calendars
Assist in the day to day running of projects assigned.
Assist in the preparation of project specific materials e.g., status reports, newsletters, templates, etc.
Participate in project administration as required e.g., photocopying, binder preparation, start-up pack preparation etc.
Maintain current knowledge related to cancer therapy, clinical trial design and conduct, and good clinical practice through literature reviews and other educational opportunities.
Perform other duties as assigned by management
What You Need
Level of Education
At minimum, Bachelor's degree (BSc, BA, or RN equivalent) in biological or science-related field or equivalent experience
Prior Experience
At least 2 years' experience as a Clinical Research Associate with a sound track record in managing clinical trial sites
Experience in monitoring oncology phase I-III studies is preferred
Skills and Competencies
Thorough knowledge of ICH Guidelines and GCP including an understanding of regulatory requirements.
Demonstrable multitasking and execution skills.
Good interpersonal skills, including communication, presentation, persuasion, and influence.
Good organizational skills, including efficiency, punctuality, and collaboration in a team environment.
Knowledgeable in the identification, anticipation, and reporting to appropriate management problems relating to study conduct, and effective in developing solutions to those problems
Effective knowledge of the drug development process and the Theradex organizational structure
Good communication skills: verbal and written
Proficient knowledge of Outlook, Word, Excel and PowerPoint; able to utilize remote meeting/teleconferencing platforms (such as Teams, Zoom, WebEx, GoToMeeting) effectively.
Additional Requirements
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 preferable.
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)
What We Offer
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 this position ranges from $90,000-$120,000 with bonus potential. The actual salary offer will be based on a number of factors, including but not limited to the candidate's qualifications, experience, skills, and competencies for the role.
This position is not eligible for company provided sponsorship or relocation.
Theradex is an Equal Opportunity Employer.
Clinical Research Associate II
Theradex Oncology
Princeton, NJ
Full Time
Bachelor's
Published on 08/05/2025
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Who We Are
elebrating 40+ years!
Theradex Oncology is a full-service CRO specializing in oncology. The company manages global oncology trials and programs. The company was founded in 1982 working with the National Cancer Institute, which led to its expansion to working with industry sponsors developing cancer therapeutics. As a service-based company we support both domestic and international sponsors in the conduct of both early and late phase trials.
What You'll Do
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 II
The primary responsibilities of this position include, but are not limited to, the following:
Act as the routine liaison between study site and the project team for study related issues.
Ensures protection of subjects, subjects' rights, and the integrity of data through monitoring of adherence to Good Clinical Practice, applicable regulatory requirements, Standard Operating Procedures and protocol compliance.
Conducts pre-qualification, initiation, routine monitoring, remote monitoring, and close-out visits in accordance with the relevant SOPs and the specific project scope of work to include but not limited to:
Source document review and comparison to CRF data
CRF review/retrieval and data corrections
IMP accountability
Maintenance of on-site investigator files
IEC/IRB documentation
Local laboratory documentation
Maintenance of investigational supplies
Reviews consent process for each subject (Informed Consent Form and source documentation)
Verify patient eligibility
Assess protocol compliance and deviations
Handling of safety and efficacy issues, including, but not limited to:
Serious adverse event reports
Adverse event trends
Treatment failures/outcomes
Conducts and documents onsite visits/contacts, including:
Pre-study visits
Initiation visits
Routine visits
Study completion visits/ Close-out visits
Telephone contact
Site visit report preparation within study specific timeframe
Responsible for all aspects of site management as described in the study plans
Proactively identify and resolve issues and potential site and study issues.
Assist with regulatory and study start-up activities including contract and budget negotiations, as required.
Ensure clinical data integrity and meet study timelines.
Provide ongoing updates and support to project management.
Mentor junior members of the team.
Prepare and deliver staff training sessions.
Clinical Review of individual patient listings
Initial clinical review of comprehensive patient data listings
Initial review of study start-up materials: SOPs, draft CRFs, completion manual, compliance forms, study prompters/calendars
Assist in the day to day running of projects assigned.
Assist in the preparation of project specific materials e.g., status reports, newsletters, templates, etc.
Participate in project administration as required e.g., photocopying, binder preparation, start-up pack preparation etc.
Maintain current knowledge related to cancer therapy, clinical trial design and conduct, and good clinical practice through literature reviews and other educational opportunities.
Perform other duties as assigned by management
What You Need
Level of Education
At minimum, Bachelor's degree (BSc, BA, or RN equivalent) in biological or science-related field or equivalent experience
Prior Experience
At least 2 years' experience as a Clinical Research Associate with a sound track record in managing clinical trial sites
Experience in monitoring oncology phase I-III studies is preferred
Skills and Competencies
Thorough knowledge of ICH Guidelines and GCP including an understanding of regulatory requirements.
Demonstrable multitasking and execution skills.
Good interpersonal skills, including communication, presentation, persuasion, and influence.
Good organizational skills, including efficiency, punctuality, and collaboration in a team environment.
Knowledgeable in the identification, anticipation, and reporting to appropriate management problems relating to study conduct, and effective in developing solutions to those problems
Effective knowledge of the drug development process and the Theradex organizational structure
Good communication skills: verbal and written
Proficient knowledge of Outlook, Word, Excel and PowerPoint; able to utilize remote meeting/teleconferencing platforms (such as Teams, Zoom, WebEx, GoToMeeting) effectively.
Additional Requirements
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 preferable.
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)
What We Offer
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 this position ranges from $90,000-$120,000 with bonus potential. The actual salary offer will be based on a number of factors, including but not limited to the candidate's qualifications, experience, skills, and competencies for the role.
This position is not eligible for company provided sponsorship or relocation.
Theradex is an Equal Opportunity Employer.
Clinical Research Associate II
Theradex Oncology
Princeton, NJ
Full Time
Bachelor's
Published on 08/05/2025
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Job ID: 488983689
Originally Posted on: 8/11/2025
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