data coordinator

Optimasidata LLC

Data CoordinatorOptimasidata LLC &ndash; Doha, QatarPosition Summary: Optimasidata LLC is seeking a detail-oriented and organized Data Coordinator to support data management, processing, and quality assurance activities. The ideal candidate will ensure the accuracy, integrity, and timely flow of data across internal systems and client deliverables while supporting analytics and reporting functions.Key Responsibilities:<ul><li>Collect, organize, and validate data from multiple sources to ensure accuracy and consistency.</li><li>Maintain and update databases, spreadsheets, and data management systems.</li><li>Perform routine data quality checks and resolve discrepancies or missing information.</li><li>Support data entry, transformation, and cleansing processes.</li><li>Generate reports and summaries for internal teams and management.</li><li>Collaborate with IT, analytics, and operations teams to improve data workflows.</li><li>Ensure compliance with company data governance policies and confidentiality standards.</li><li>Assist in documentation of data processes and standard operating procedures (SOPs).</li><li>Support ad hoc data requests and project-based assignments.</li></ul>Requirements:<ul><li>Bachelor&rsquo;s degree in Information Technology, Computer Science, Statistics, Business Administration, or related field.</li><li>Proven experience in data coordination, data entry, or administrative data support roles.</li><li>Strong proficiency in Microsoft Excel and/or Google Sheets.</li><li>Familiarity with databases and data management tools is an advantage.</li><li>High attention to detail and strong analytical skills.</li><li>Ability to manage multiple tasks and meet deadlines.</li><li>Good communication and teamwork skills.</li><li>Knowledge of data privacy and confidentiality practices.</li></ul>Preferred Skills:<ul><li>Experience with BI tools (e.g., Power BI, Tableau).</li><li>Basic SQL knowledge.</li><li>Experience in a fast-paced or data-driven environment.</li></ul>Location: Doha, Qatar Company: Optimasidata LLCالراتب المدفوع: QAR٠٫٠٠&nbsp;لكل عامموقع العمل: بشكل شخصي

Data Coordinator

Data-and-Data LLC

Job Title: Data Coordinator Company: Data-and-Data LLC Location: Doha, QatarJob Overview: Data-and-Data LLC is seeking a detail-oriented and analytical Data Coordinator to manage, organize, and maintain accurate company data across multiple systems. The ideal candidate will ensure data integrity, support reporting needs, and assist teams in making informed, data-driven decisions.Key Responsibilities:<ul><li>Collect, organize, and maintain data from various internal and external sources</li><li>Ensure accuracy, consistency, and integrity of company databases</li><li>Update and manage records across CRM and data management systems</li><li>Generate reports and dashboards for management review</li><li>Support data entry, validation, and cleansing activities</li><li>Identify and resolve data discrepancies or inconsistencies</li><li>Collaborate with departments to understand data requirements and reporting needs</li><li>Assist in developing and improving data management processes and workflows</li><li>Ensure compliance with data privacy and security policies</li></ul>Qualifications:<ul><li>Bachelor&rsquo;s degree in Information Technology, Computer Science, Data Management, or related field</li><li>2&ndash;4 years of experience in data coordination, administration, or analytics support</li><li>Strong attention to detail and accuracy in data handling</li><li>Proficiency in Microsoft Excel and data management tools</li><li>Familiarity with databases and reporting systems (e.g., SQL, CRM platforms) is an advantage</li><li>Strong organizational and analytical skills</li><li>Good communication and teamwork abilities</li></ul>Preferred Skills:<ul><li>Experience with data visualization tools (e.g., Power BI, Tableau)</li><li>Knowledge of data governance and quality assurance practices</li><li>Ability to handle large datasets efficiently</li><li>Basic understanding of automation or data processing tools</li></ul>What We Offer:<ul><li>Competitive salary and benefits package</li><li>Opportunities for professional growth in data and analytics</li><li>Collaborative and technology-driven work environment</li><li>Training and skill development opportunities</li></ul>الراتب المدفوع: QAR٠٫٠٠&nbsp;لكل عامموقع العمل: بشكل شخصي

Veterans United Home Loans

<div>Whether you come from a background in data analytics, artificial intelligence and automated data systems, or information systems, you can be successful in this role. We don&rsquo;t require a specific degree or experience, but we&rsquo;re looking for translatable skills and relevant expertise. We will provide you with the training and development opportunities needed to build a career here!
About The Role:
As a Data Coordinator, you&rsquo;ll help make sure the data our Artificial Intelligence (AI) tools pull is spot-on. You&rsquo;ll review, double-check, and analyze AI-generated info to catch and fix any mistakes or missing pieces. Plus, you&rsquo;ll play a key role in helping our AI get smarter by sharing feedback and flagging any issues you find.
Compensation for this role is a fixed rate of $18.50/hour.
Here&rsquo;s a snapshot of what you&rsquo;d be doing:<ul><li>
Looking over data pulled from documents by AI, making sure it&rsquo;s accurate and complete, and fixing any errors, gaps, or mix-ups you spot.</li><li>
Using our guidelines and simple data checks to find missing or incomplete info in documents, then logging and sharing what you find so we can keep improving.</li><li>
Digging into any errors or odd spots you find, helping keep our data clean and reliable, and collaborating on projects that boost overall data quality.</li><li>
Pitching in wherever needed to help foster a supportive and collaborative team culture.</li></ul>
About You:<ul><li>
You know how to communicate your findings and suggestions in a way that makes sense to everyone.</li><li>
You&rsquo;re comfortable working on your own, figuring things out as you go, and thinking critically to solve whatever comes your way.</li><li>
Details matter to you, and you&rsquo;ve got an eye for catching the little things that make a big difference.</li><li>
Providing top-notch customer service comes naturally to you.</li><li>
You thrive in a fast-paced, results-driven environment and love working as part of a team.</li><li>
Spotting problems and fixing them quickly is something you excel at.</li><li>
You&rsquo;re comfortable with technology and can navigate basic computer systems with ease.</li><li>
You&rsquo;re good with numbers and know how to accurately pull meaning from large volumes of data.</li><li>
You show up consistently and can be counted on to get the job done.</li></ul>
About Us:
We&rsquo;re all about helping Veterans and military families become homeowners. In two short decades, we closed over 500,000 VA Loans and became the #1 VA lender for homebuyers in the nation. But to us, success isn&rsquo;t measured in numbers. Our success is measured in living our values every day: Be Passionate and Have Fun, Deliver Results with Integrity and Enhance Lives Every Day. We always strive to provide friendly service to military homebuyers and their families. And we always seek to lift up people and communities across the country.
We&rsquo;re so glad you&rsquo;re here checking out this opportunity! If this role gets you excited but you&rsquo;re worried you don&rsquo;t check every box &ndash; don't sweat it. We&rsquo;re more interested in what you can bring to the team than a perfect checklist. If you&rsquo;re passionate, driven, and ready to make a difference, we&rsquo;d love to hear from you. Come as you are, and together we&rsquo;ll create something amazing.
Interested? Apply Today!
Learn more about Veterans United on Glassdoor and our career site at vu.com/careers
Veterans United Home Loans and its affiliates are Equal Opportunity Employers that consider all qualified applicants regardless of race, color, religion, sex (including pregnancy, transgender status, and sexual orientation), national origin, age (40 or older), disability or genetic information.</div>

State of Maine

<div><h2 class="jobSectionHeader">If you are a current State of Maine employee, please submit your application through the internal application process using the Find Jobs report in PRISM. Seasonal employees who do not have PRISM access should apply through the State&rsquo;s career page and indicate on the application that they have previously worked for the State.
</h2>.
Department of Health and Human Services (DHHS)
Medical Care Coordinator
Opening Date: April 22, 2026
Closing Date: May 5, 2026
Job Class Code: 5055
Grade: 16 (Professional and Technical)
Salary: $17.69 - $24.27 per hour
Position Number: 02000-2404
Location: Augusta
This position allows for partial telework with management approval.
Currently, this position is not eligible for visa sponsorship or STEM OPT extensions.
Core Responsibilities:
Join the Maine CDC Breast and Cervical Health Program (MBCHP) and play a vital role in ensuring underserved individuals have access to life-saving cancer screening and diagnostic services. As a Medical Care Coordinator, you will be at the center of a mission-driven team working to reduce health disparities and improve early detection outcomes statewide.
This role is ideal for someone detail-oriented, analytical, and motivated by meaningful public health work. You&rsquo;ll have the opportunity to collaborate with healthcare providers, support patient care coordination, and contribute to a program that directly impacts lives.
You will:
<ul><li>Manage and maintain accurate clinical records, ensuring timely collection and entry of screening and diagnostic data
</li><li>Review and validate clinical information to ensure compliance with program guidelines and coverage criteria
</li><li>Analyze claims and clinical data reports to support program operations
</li><li>Process medical claims and resolve billing issues for clients, providers, and internal staff
</li><li>Partner with patient navigators to communicate abnormal screening results, supporting timely follow-up care
</li><li>Monitor provider compliance with data reporting
</li><li>Serve as a subject matter resource for providers by delivering guidance on MBCHP billing processes
</li><li>Use independent judgment to prioritize tasks, solve problems, and ensure high-quality, accurate work
 </li></ul>Preferred candidates will also have:
<ul><li>Strong attention to detail and the ability to manage complex data with accuracy
</li><li>Proven organizational skills and the ability to manage multiple priorities in a deadline-driven environment
</li><li>A collaborative, team-oriented mindset with a commitment to customer service
</li><li>Experience working with patients, clinical, or health-related data systems preferred
</li><li>Ability to handle sensitive and confidential information with professionalism and discretion
</li><li>Comfort working in a role connected to cancer care and women&rsquo;s health
</li></ul>Minimum Qualifications:
A four (4) year combination of education and experience in medical eligibility programs and/or experience which demonstrates interviewing and data gathering skills as needed to form basis for judgments in eligibility determinations, claims resolutions, and payment authorization.
Thinking about applying?
Research shows that people from historically excluded communities tend to apply to jobs only when they check every box in the posting. If you&rsquo;re currently reading this and hesitating to apply for that reason, we encourage you to go for it! Let us know how your experience and passion set you apart.
Agency information:
The Department of Health and Human Services (DHHS) is dedicated to promoting health, safety, resilience, and opportunity for Maine people. The Department provides health and social services to approximately a third of the State's population, including children, families, older Mainers, and individuals with disabilities, mental illness, and substance use disorders. The Department also promotes public health, operates two state psychiatric hospitals, and provides oversight to health care providers.
Application Information:
For questions about this position, please contact Eric Frohmberg at eric.j.frohmberg@maine.gov
Please submit all documents or files in PDF or Word format.
To request a paper application, please contact Mandy.Hernandez@Maine.gov
Benefits of working for the State of Maine:
No matter where you work across Maine state government, you find employees who embody our state motto&mdash;&quot;Dirigo&quot; or &quot;I lead&quot;&mdash;as they provide essential services to Mainers every day. We believe in supporting our workforce's health and wellbeing with a valuable total compensation package, including:
<ul><li>Work-Life Fit &ndash; Rest is essential. Take time for yourself using 13 paid holidays, 12 days of sick leave , and 3+ weeks of vacation leave annually. Vacation leave accrual increases with years of service, and overtime-exempt employees receive personal leave.
</li><li>Health Insurance Coverage &ndash; The State of Maine pays 85%-100% of employee-only premiums ($12,845.82 - $15,112.76 annual value), depending on salary. Use this chart to find the premium costs for you and your family, including the percentage of dependent coverage paid by the State.
</li><li>Health Insurance Premium Credit &ndash; Participation decreases employee-only premiums by 5%. Visit the Office of Employee Health and Wellness for more information about program requirements .
</li><li>Dental Insurance &ndash; The State of Maine pays 100% of employee-only dental premiums ($395.72 annual value).
</li><li>Retirement Plan &ndash; The State contributes the equivalent of 14.11% of the employee's pay towards the Maine Public Employees Retirement System (MainePERS).
</li><li>Parental leave is one of the most important benefits for any working parent. All employees who are welcoming a child&mdash;including non-birthing and adoptive parents&mdash;receive six weeks of fully paid parental leave . Additional, unpaid leave may also be available, under the Family and Medical Leave Act .
</li></ul>State employees are eligible for an extensive and highly competitive benefits package , covering many aspects of wellness. Learn about additional wellness benefits for State employees from the Office of Employee Health and Wellness .
Note: Benefits may vary somewhat according to specific collective bargaining agreements and are prorated for anything less than full-time.
There's a job and then there's purposeful, transformative work. Our aim is to create a workplace where you can learn, grow, and continuously refine your skills. Applicants demonstrate job requirements in differing ways, and we appreciate that many skills and backgrounds can make people successful in this role.
As an Equal Opportunity employer, Maine State Government embraces a culture of respect and awareness. We are committed to creating a strong sense of belonging for all team members, and our process ensures an inclusive environment to applicants of all backgrounds including diverse race, color, sex, sexual orientation or gender identity, physical or mental disability, religion, age, ancestry, national origin, familial status or genetics.
If you&rsquo;re looking for a great next step, and want to feel good about what you do, we&rsquo;d love to hear from you. Please note reasonable accommodations are provided to qualified individuals with disabilities upon request.
.
If you are unable to complete the online application, please contact the Human Resources representative listed on the job opening you are interested in applying for. They will work with you for an alternative method of submitting.</div>

Clinical Data Coordinator

Pinnacle Clinical Research

<div>Summary: The Clinical Research Data Coordinator (CRDC) will abstract clinical data and research data from electronic medical records and other sources and enter this data into an electronic data capture system utilized for the clinical research protocol. The CRDC will be responsible for entering quality data for multiple clinical trials and conducting data activities in an efficient manner and in accordance with regulations. The ideal candidate will be responsive, thoughtful, self-motivated, highly organized, and a team player. This role reports directly to the Clinical Operations Manager.
Specifically, the Clinical Research Data Coordinator will be responsible for:<ul><li>
Maintain subject and document confidentiality at all times, understand and comply with the appropriate sponsor requirements and regulations which includes the Food and Drug Administration, Good Clinical Practices, International Conference on Harmonization, Health Insurance Portability and Accountability Act, institutional review boards, and institutional policies and procedures</li><li>
Obtain and abstract complex clinical information from multiple sources (medical records, research records, etc.) for research subjects. Verify all records are readable, accurate, and complete</li><li>
Responsible for CTMS (CRIO) and EDC data management which is essential for daily business operations</li><li>
Record information into various study-specific data-capture systems (both electronic and paper-based). Ensure that all adverse events, concomitant medications, and medical histories are transcribed accurately</li><li>
Perform daily query resolution with minimal errors</li><li>
Assist in the creation of data management process for quality control and assurance</li><li>
Perform auditing and review of CTMS and EDC entries to ensure compliance standards are maintained</li><li>
Assist in preparing for Regulatory Agency inspections and sponsor audits</li><li>
Maintain awareness of details of clinical data to identify missing or inaccurate data; track data inconsistencies for Clinical Research Operations team to review and report accordingly</li><li>
Act as primary contact with sponsor&rsquo;s data management team to resolve and review any data management issues</li><li>
Exercise independent judgment on query resolutions</li><li>
Create reports to track data and quality metrics</li><li>
Collaborate with internal site staff and external personnel such as physicians, nurses, administration, industry sponsor representatives, central laboratory and imaging personnel to resolve queries to ensure clinical data quality and compliance</li><li>
Coordinate multiple complex projects with competing priorities and deadlines as needed based on clinical trial protocol directives and study volume</li><li>
Collaborate with study staff in the preparation of study audits, quality reviews, and monitor visits</li><li>
Provide cross-coverage support on study and site activities as assigned</li><li>
Create source document development per data capture requirements per protocol</li><li>
Assist with the implementation of quality assurance data management plans and other auditing processes as needed</li></ul>
 Duties, responsibilities, and activities may change, or new ones may be assigned at any time.
Qualifications:<ul><li>
Bachelor&rsquo;s Degree in scientific area of study or equivalent combination of education, training, and experience</li><li>
Previous experience in a clinical research environment or equivalent work environment</li><li>
1-2 years of previous data entry experience as a clinical research coordinator, clinical research assistant or data entry specialist for therapeutic clinical trials</li><li>
Knowledge of regulations governing clinical research (CFR, GCP, HIPAA) required</li><li>
Proficiency in all Microsoft Office applications (Word, Excel, Outlook, PowerPoint)</li><li>
Familiarity with clinical trial management system software, preferably Clinical Research IO</li><li>
Basic medical knowledge, including medical terminology</li><li>
Demonstrated competence in oral and written communication</li><li>
Must complete CITI and GCP training certification</li><li>
Demonstrated organizational skills and outstanding time management, including keen attention to detail</li><li>
Possess impeccable integrity and personal and professional values that are consistent with PCR&rsquo;s high standards and mission</li><li>
Comply with the company policies, code of ethics, and guiding values at all times</li></ul>
Competencies:<ul><li>
Strong analytical and problem-solving skills</li><li>
Detail oriented with the ability to perform at a high level of accuracy</li><li>
Proactive at identifying and addressing issues in real time</li><li>
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner</li><li>
Must handle confidential matters and sensitive information with discretion and judgment</li><li>
Ability to manage small projects personally and work independently</li><li>
Ability to understand and interpret clinical research protocols and other applicable sponsor documents</li></ul>
 Other benefits include:<ul><li>
 401k</li><li>
Medical, dental, vision and more</li><li>
3 weeks of paid time off</li><li>
13 paid company holidays</li><li>
Scrub voucher (specific positions apply)</li><li>
And more!</li></ul>
Summit Pinnacle Clinical Research is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.</div>

Clinical Research Data Coordinator

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 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 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>

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Clinical Research Data Coordinator

Clinical Data Coordinator I

Clinical Data Coordinator I