Qureos Mentor

Caris Life Sciences

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary
The Specimen Processing Clerk I is responsible for supporting the department with all clerical and ancillary duties in creating and accessioning clinical cases for patient output. While maintaining job functions, the Specimen Processing Clerk is to progress in their learning of the regulations (CLIA, CAP and NYS) which the laboratory functions. This position works under the direction of the Supervisor and follows standard laboratory procedures and policies.
Job Responsibilities<ul><li>
Open packages and video receipt of all incoming specimens for clinical processing.</li><li>
Creates and manages patient cases including the setting up of new cases, updating current cases, entering of specimens in case, attaching relevant documents, Quality Control checking information for accuracy and other case management tasks.</li><li>
Opens and closes specimen and case discrepancies to ensure accurate information and processing of specimens in a timely fashion.</li><li>
Works cross-functionally with various departments including Customer Support, Molecular - Liquid Profiling, Compliance, Reporting, Patient Billing, PA's, Pharma Research Operations, and Biorepository.</li><li>
Responsible for filing, tracking, retrieval, and accurate record keeping.</li><li>
Maintains diagnostic viability of all specimens and ensures correct patient labeling of all materials. Routinely checks and verifies accuracy of all information in laboratory information system.</li><li>
Records in laboratory logs all specimens prepared. Logs appropriate information into the laboratory information system.</li><li>
Responsible for Quality Assurance (QA)/Quality Control (QC) for all cases, specimens and documentation.</li><li>
Maintains Supply Inventory, including package receiving and supply chain requests, and submitting orders to Purchasing department, in accordance with established policies and procedures.</li><li>
Assists as needed to perform other related duties and special projects to support the laboratory as required.</li><li>
Accepts other duties as assigned.</li></ul>
Required Qualifications<ul><li>
High School diploma or equivalent required.</li><li>
Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, and general working knowledge of Internet for business use.</li></ul>
Preferred Qualifications<ul><li>
One to three years of experience in general laboratory operations preferred.</li></ul>
Physical Demands<ul><li>
Will work at a computer some of the time as well as need to keep inventory and ordering records requiring the use of copiers, fax machines, and PDF scanners.</li><li>
Visual acuity and analytical skill to distinguish fine detail. Ability to pass a visual color discrimination test.</li><li>
Manual dexterity to use common laboratory equipment and perform sterile techniques as required.</li><li>
Must possess ability to sit and/or stand for long periods of time.</li><li>
Must possess ability to perform repetitive motion.</li><li>
Ability to lift up to 30 pounds.</li><li>
May have exposure to high noise levels in the data center, fumes and bio-hazardous material in the lab environment. Exposure to formaldehyde, xylene, DAB and alcohol which emit fumes. The formaldehyde, xylene, and DAB are carcinogenic.</li><li>
Required to handle blood-borne pathogens and general laboratory reagents.</li><li>
May have exposure to extreme temperatures, high noise levels, fumes and bio-hazardous material/chemicals including formalin in the lab environment.</li></ul>
Other<ul><li>
2nd Shift (2:00pm-10:30pm).</li><li>
This position may require periodic travel and some evenings, weekends and/or Holidays.</li></ul>
Required Training<ul><li>
All job specific, safety, and compliance training are assigned based on the job functions associated with this employee.</li></ul>
Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Specimen Processing Clerk (2nd Shift)

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary
The Quality Control (QC) Specialist- Incoming is responsible for supporting the inspection of all inventory reagents, R&amp;D materials, consumables, finished goods and kits that are sent to customers meet the required quality standards in compliance with regulatory guidelines. This role involves performing detailed inspections and evaluations to confirm their conformity to established specifications. The QC Specialist ensures that all processes and products adhere to industry regulations, company policies and quality control protocols. Additionally, assists QC leadership in planning and conducting inspection activities in both the lab and receiving area.
Job Responsibilities<ul><li>
Performs QC inspection of reagents, consumables and R&amp;D materials by evaluating whether associated specifications/requirements meet the established acceptance criteria for production process.</li><li>
Performs inspection of manufactured products to verify that all components and labeling comply with applicable regulatory and quality requirements.</li><li>
Performs inspection of sample and test specific collection kits that will be sent to the customers.</li><li>
Responsible for the development and maintenance of inspection methodologies, along with creating SOP's and job aides for these processes.</li><li>
Responsible for initiating deviations in the eQMS when specifications are not met. Along with participating in CAPA investigations related to material to ensure compliance with quality standards.</li><li>
Performs inspections and maintains accurate records of inspection results and related documentation in a timely manner.</li><li>
Assists other QC functions in the organization in creating, maintaining documentation needed to comply with regulatory standards.</li><li>
Collaborates closely with supply chain, quality assurance and laboratory operations to facilitate seamless execution of business requirements while adhering to regulatory standards.</li><li>
Collaborates with cross-functional groups and supplier teams to address top quality issues for products or manufactured kits.</li><li>
Collaborates and coordinates with supplier quality teams to assist in developing performance metrics for vendors, ensuring alignment with quality standards and internal processes.</li><li>
Attention to detail and ability to catch discrepancies.</li><li>
Self-motivated with excellent communication and interpersonal skills.</li><li>
Identify and recommend opportunities for improving QC processes.</li><li>
Assist in training new QC staff and offering support to the team as needed.</li><li>
Other duties as assigned.</li></ul>
Required Qualifications<ul><li>
High school diploma with 1-2 years of experience in material management, quality control, or related field.</li><li>
Hands‑on experience performing Incoming Quality Control inspections.</li><li>
Working knowledge and understanding of Quality Systems (Document control, audits, Management Review).</li><li>
Ability to perform duties independently with minimal supervision in a regulated environment.</li><li>
Strong written and verbal communication skills.</li></ul>
Preferred Qualifications<ul><li>
Associate or Bachelor's degree.</li><li>
Knowledge of FDA regulated industry standards and regulations.</li><li>
Willingness to learn and adapt to new processes and technologies.</li><li>
Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook and general working knowledge of Internet for business use.</li><li>
Communication - Proficient verbal and written communication skills. Willingness to share and receive information and ideas from all levels of the organization to achieve the desired results.</li><li>
Teamwork - Commitment to the successful achievement of team and organizational goals through a desire to participate with and help other members of the team.</li></ul>
Physical Demands<ul><li>
Must possess ability to sit, stand, and/or work at a computer for long periods of time.</li><li>
Visual acuity and analytic skill to distinguish fine detail.</li><li>
Ability to pass a visual color discrimination test.</li><li>
Ability to lift up to 30 pounds.</li></ul> 
Required Training<ul><li>
All job specific, safety, and compliance training are assigned based on the job functions associated with this employee.</li></ul> 
Other
<ul><li>This position may require periodic travel and some evenings, weekends and/or holidays.</li></ul>
Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Quality Control Specialist

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary 
The Pathology Account Liaison serves as the key connection between pathology laboratories, ensuring smooth communication, specimen handling, and client satisfaction. This position is responsible for obtaining the specimen required to begin Caris&rsquo;s testing, communicating case updates to internal teams and pathology related escalations. Considerable independent judgment is required to carry out assignments that have a significant impact on client experience and case activation. 
 
Job Responsibilities<ul><li>
Timely and accurately facilitates the resolution of 125 or more discrepancies per day.
</li><li>Responsible for adhering to the email turnaround time expectations</li><li>
Quality check case work with a quality average of 96% of better.</li><li>
Responsible for incoming attachments, timely discrepancy documentation and resolution
</li><li>Meets compliance good documentation standards
</li><li>Assist other team members with work as needed to ensure full completion of daily caseloads.</li><li>
Meets all deliverables and goals set by the department leadership</li><li>
Provides support to Caris Lab for quick resolution of specimen issues.</li><li>
Builds strong customer relationships through client focus, professional demeanor, reliability, and timely responsiveness.</li><li>
Responds to client emails, calls or fax inquiries regarding the tissue request letter, missing documents or specimen ordering requirements.</li><li>
Provides attention to detail and problem-solving skills to quickly resolve specimen concerns</li><li>
Utilizes the case manager system and other internal software to enter, gather and analyze data.</li><li>
Evaluates client concerns, complaints, and specimen turnaround trends to recommend changes for improvement</li><li>
Meets all regulatory agency requirements as they pertain to job function.</li><li>
Executes other tasks and projects assigned by management.</li></ul> 
Required Qualifications<ul><li>
High School diploma or equivalent required.</li><li>
1-3 years of experience in a client services role where deductive reasoning is necessary and compelling evidence of related service skillsets is required.</li><li>
Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, and general working knowledge of Internet for business use.</li></ul> 
Preferred Qualifications<ul><li>
1-3 years of experience working in a customer support environment preferred.</li><li>
1-3 years of Laboratory experience.</li><li>
Bachelor&rsquo;s degree preferred.</li><li>
1-3 years of experience in a physician office environment, hospital environment or other patient healthcare setting highly preferred.</li><li>
Proficiency in healthcare and medical terminology required.</li><li>
Knowledge of HIPAA provisions and importance of privacy of patient data.</li></ul> 
Physical Demands<ul><li>
Must possess ability to sit and/or stand for long periods of time.</li><li>
Must possess ability to perform repetitive motion.
</li><li>Ability to lift up to 30 pounds.</li></ul> 
Training<ul><li>
All job specific, safety, and compliance training are assigned based on the job functions associated with this employee.</li></ul> 
Other<ul><li>
This position requires periodic travel and some evenings, weekends and/or holidays.</li><li>
Potential for hybrid work schedule after 3 months of service and meet the eligibility requirements.</li><li>
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time.</li><li>
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</li></ul>
Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Pathology Account Liaison

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary
The Clinical Data Coordinator is responsible for clinical data entry activities for the Caris Medical Affairs protocols and projects at the Caris Precision Oncology Alliance sites. The position will ensure the highest standards for clinical data integrity and quality are maintained in alignment with critical research efforts aimed to improve the treatment, health and medical outcomes for oncology patients. Responsible for the collection and review of clinical protocol research data; Interpretation of data (including appropriate source documentation) for entry into computerized databases; Good understanding of data definitions and case report forms and other information related to data collection for clinical research. Must respond to queries in a timely fashion. Schedule on-site visits to perform data review and EDC data entry.
Job Responsibilities<ul><li>
Abstract clinical data from subject source documentation.</li><li>
Enter clinical data into the study specific EDC case report forms.</li><li>
Clean the clinical data to verify accuracy.</li><li>
Update the EDC following verification of subject data, including the resolution of data queries.</li><li>
Track site goals and case report form completion.</li><li>
Prioritize site cases for analysis.</li><li>
Maintain study specific documentation.</li><li>
Perform QC audits of the clinical database.</li><li>
Support and adhere to Good Clinical Practices (GCP) guidelines, FDA, Institutional Review Board (IRB) and HIPAA regulations, Site Operating Procedures and ethical standards for the conduct of research clinical trials.</li><li>
Work closely with onsite team to confirm appropriate consenting is being performed and documented prior to data abstraction.</li><li>
Maintain to Caris and Site requirements for source document management and request for information.</li><li>
Act as site designated entry person.</li><li>
Willingness to travel to multiple investigative sites if required.</li><li>
Communicate effectively with the research team, investigator(s), Clinical Research Associate(s), study sponsor and ancillary staff.</li></ul>
Required Qualifications<ul><li>
Position requires 3-5 years of experience in data collection activities within a GCP/clinical research regulatory environment.</li><li>
Knowledgeable in critical elements for success in clinical trials. GCPs, ICH, and Code of Federal Regulations.</li><li>
Clinical study experience in the field of Oncology.</li><li>
Strong medical terminology understanding.</li><li>
Experience in both small and large scale project planning and reporting with strong communication and presentation skills.</li><li>
Experience in providing training for both internal and external staff with a mentorship approach for less experienced colleagues.</li><li>
Experience with EDC systems.</li><li>
Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, and general working knowledge of Internet for business use.</li></ul>
Physical Demands<ul><li>
Must possess ability to sit and/or stand for long periods of time.</li></ul>
Training<ul><li>
All job specific, safety, and compliance training are assigned based on the job functions associated with this employee.</li></ul>
Other<ul><li>
This position may require occasional evenings and overtime.</li></ul>
Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Clinical Data Coordinator I

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary
The experienced Senior Data Scientist will support our precision medicine and biomarker discovery initiatives. This role will contribute to target and drug discovery efforts through advanced analytics, machine learning, and large-scale data processing across multi-omics and clinical datasets, and brings a strong quantitative and scientific background, excellent programming skills, and the ability to translate complex biological questions into robust analytical solutions. This role also involves technical leadership, cross-functional collaboration, and ownership of end-to-end analytics and machine learning workflows.
Job Responsibilities<ul><li>
Lead and contribute to scientific research efforts using advanced statistical, machine learning, and AI methodologies.</li><li>
Manipulate, integrate, and analyze large, multi-source and multi-omics datasets.</li><li>
Design, develop, validate, deploy, and monitor data processing and machine learning pipelines.</li><li>
Develop, implement, refine, and test algorithms and workflows to meet specific project objectives.</li><li>
Provide statistical support for experimental design, assay development, biomarker discovery, and diagnostic product development.</li><li>
Build and deploy scalable analytics solutions, APIs, and data applications using cloud and/or HPC environments.</li><li>
Author and review statistical analysis plans, protocols, and technical reports for clinical and non-clinical studies.</li><li>
Collaborate closely with data engineers, data scientists, software engineers, and R&amp;D scientists to build and maintain analytics platforms.</li><li>
Lead or contribute to cross-functional and cross-team research initiatives.</li><li>
Provide general informatics and analytical support for laboratory research, technology development, and clinical studies.</li><li>
Respond to ad hoc data analysis requests with accuracy, rigor, and timeliness.</li><li>
Adhere to coding, documentation, and quality standards; manage technical deliverables for assigned projects.</li><li>
Provide technical mentorship and guidance to junior team members, as appropriate.</li></ul>
Required Qualifications<ul><li>
Ph.D. in Mathematics, Computer Science, Engineering, Bioinformatics, Computational Biology, or a related quantitative field with strong domain knowledge in molecular biology and genomics.</li><li>
Proficiency in Python (and/or R) for data analysis, statistical modeling, and machine learning in a scientific computing environment.</li><li>
Hands-on experience with AWS cloud computing platform.</li><li>
5+ years of relevant experience applying quantitative, statistical, and computational approaches in biotech, life sciences, or translational research.</li><li>
Demonstrated experience in computational biology, including analysis and interpretation of high-throughput biological data such as genomics, transcriptomics, proteomics, epigenomics, or other multi-omics modalities.</li><li>
Hands-on experience working with molecular, cellular, clinical, and/or multi-omics datasets, including data QC, normalization, integration, and downstream analysis.</li><li>
Strong ability to translate biological and clinical research questions into statistically sound and computationally efficient analytical solutions.</li><li>
Working knowledge of bioinformatics tools, pipelines, and data formats (e.g., FASTQ, BAM/CRAM, VCF, GTF, HDF5, or equivalent).</li><li>
Proficiency with Linux and command-line workflows commonly used in bioinformatics and computational research.</li><li>
Experience querying and working with complex relational and non-relational databases.</li><li>
Strong verbal and written communication skills, with the ability to clearly explain complex biological and computational concepts to multidisciplinary audiences.</li><li>
Team-oriented mindset with a passion for personalized medicine, data-driven discovery, and scientific innovation.</li></ul>
Preferred Qualifications<ul><li>
Experience in cancer biology, molecular biology, biomarker discovery, or diagnostic development.</li><li>
Proven experience developing and validating predictive models using machine learning, deep learning, LLM and/or Agentic AI techniques.</li><li>
Experience designing and maintaining relational (e.g., MySQL, PostgreSQL) and non-relational (e.g., MongoDB) databases.</li><li>
Experience developing data-driven or analytics-enabled applications.</li><li>
Familiarity with modern software engineering best practices, including CI/CD, containerization, microservices, and system architecture.</li><li>
Knowledge of DevOps, MLOps, and/or DataOps concepts and tooling.</li><li>
Demonstrated success working in multidisciplinary, cross-functional teams.</li></ul>
Physical Demands<ul><li>
Will work at a computer most of the time, with some time spent collaborating with subject matter experts and business group leaders either in person or through remote conferencing.</li></ul>
Training<ul><li>
All job-specific, safety, and compliance training are assigned based on the job functions associated with this employee.</li></ul>
Other<ul><li>
Job may require after-hours response to emergency issues.</li></ul>
Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Senior Data Scientist

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary
The Clinical Data Coordinator is responsible for clinical data entry activities for the Caris Medical Affairs protocols and projects at the Caris Precision Oncology Alliance sites. The position will ensure the highest standards for clinical data integrity and quality are maintained in alignment with critical research efforts aimed to improve the treatment, health and medical outcomes for oncology patients. Responsible for the collection and review of clinical protocol research data; Interpretation of data (including appropriate source documentation) for entry into computerized databases; Good understanding of data definitions and case report forms and other information related to data collection for clinical research. Must respond to queries in a timely fashion. Schedule on-site visits to perform data review and EDC data entry.
Job Responsibilities
<ul><li>Abstract clinical data from subject source documentation.
</li><li>Enter clinical data into the study specific EDC case report forms.
</li><li>Clean the clinical data to verify accuracy.
</li><li>Update the EDC following verification of subject data, including the resolution of data queries.
</li><li>Track site goals and case report form completion.
</li><li>Prioritize site cases for analysis.
</li><li>Maintain study specific documentation.
</li><li>Perform QC audits of the clinical database.
</li><li>Support and adhere to Good Clinical Practices (GCP) guidelines, FDA, Institutional Review Board (IRB) and HIPAA regulations, Site Operating Procedures and ethical standards for the conduct of research clinical trials.
</li><li>Work closely with onsite team to confirm appropriate consenting is being performed and documented prior to data abstraction.
</li><li>Maintain to Caris and Site requirements for source document management and request for information.
</li><li>Act as site designated entry person.
</li><li>Willingness to travel to multiple investigative sites if required.
</li><li>Communicate effectively with the research team, investigator(s), Clinical Research Associate(s), study sponsor and ancillary staff.
</li></ul>Required Qualifications
<ul><li>Position requires 3-5 years of experience in data collection activities within a GCP/clinical research regulatory environment.
</li><li>Knowledgeable in critical elements for success in clinical trials. GCPs, ICH, and Code of Federal Regulations.
</li><li>Clinical study experience in the field of Oncology.
</li><li>Strong medical terminology understanding.
</li><li>Experience in both small and large scale project planning and reporting with strong communication and presentation skills.
</li><li>Experience in providing training for both internal and external staff with a mentorship approach for less experienced colleagues.
</li><li>Experience with EDC systems.
</li><li>Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, and general working knowledge of Internet for business use .
</li></ul>Physical Demands
<ul><li>Must possess ability to sit and/or stand for long periods of time.
</li></ul>Training
<ul><li>All job specific, safety, and compliance training are assigned based on the job functions associated with this employee.
</li></ul>Other
<ul><li>This position may require occasional evenings and overtime.
</li></ul>Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions ) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Join Caris Life Sciences and explore 6   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Caris Life Sciences

About Company

Specimen Processing Clerk (2nd Shift)

Quality Control Specialist

Pathology Account Liaison

Clinical Data Coordinator I

Senior Data Scientist

Clinical Data Coordinator I