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patient care tech-transplant/hepatology 14e part-time nights Jobs in Chicago

clinical phlebotomist

Labcorp

<div><p>Labcorp is seeking a Phlebotomist to join our team at Laboratory, 233 E Erie St Ste. 307 Chicago, IL 60611.</p><p><b>
Work Schedule: </b>Monday - Friday 7:00am &ndash; 12pm</p><p><b>
Job Responsibilities:</b></p><ul><li><p>
Perform blood collections by venipuncture and capillary techniques for all age groups</p></li><li><p>
Collect specimens for drug screens, paternity tests, alcohol tests etc.</p></li><li><p>
Perform data entry of patient information in an accurate and timely manner</p></li><li><p>
Process billing information and collect payments when required</p></li><li><p>
Prepare all collected specimens for testing and analysis</p></li><li><p>
Maintain patient and specimen information logs</p></li><li><p>
Provide superior customer service to all patients</p></li><li><p>
Administrative and clerical duties as necessary</p></li><li><p>
Travel to additional sites when needed</p></li></ul><p><b>
Minimum Qualifications:</b></p><ul><li><p>
High school diploma or GED or equivalent</p></li><li><p>
Phlebotomy certification or completed training program or 3 months or more experience as a phlebotomist</p></li></ul><p><b>
Preferred Qualifications:</b></p><ul><li><p>
1 year or more of phlebotomy experience in a high paced environment</p></li></ul><p><b>
Additional Job Standards:</b></p><ul><li><p>
In lieu of work experience, a Phlebotomy certification or completed training program must come from an accredited agency</p></li><li><p>
Proven track record in providing exceptional customer service</p></li><li><p>
Strong communication skills; both written and verbal</p></li><li><p>
Ability to work independently or in a team environment</p></li><li><p>
Comfortable working under minimal supervision</p></li><li><p>
Reliable transportation</p></li><li><p>
Flexibility to work overtime as needed</p></li><li><p>
Able to pass a standardized color blindness test</p></li></ul><p>
At Labcorp we have a passion for helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step!</p><p>
Phlebotomist will work in either a Patient Service Center or Client office. In this role you will provide exceptional customer service, perform skilled specimen collections and be the face of the company. In addition, you will be provided opportunities for continuous growth within the organization.</p><p><b>
**Pay Range: </b><b>$17.50 - $24.50 per hour</b></p><p>
All job offers will be based on a candidate&rsquo;s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data</p><p>
Phlebotomist&rsquo;s may be eligible for participation in the PST Incentive Plan, which pays a quarterly bonus based on performance metrics.</p><p><b>
Benefits:</b> Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee</p><p>
Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please click here.</p><p><b>
If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!</b></p><p></p><p><b>
Labcorp is proud to be an Equal Opportunity Employer:</b></p><p>
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.</p><p></p><p><b>
We encourage all to apply</b></p><p>
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.</p></div><p></p>

Phlebotomist PST

Endeavor Health

<div><div>Hourly Pay Range:</div>
$19.31 - $28.00 - The hourly pay rate offered is determined by a candidate's expertise and years of experience, among other factors.<div></div><div>
Position Highlights:</div><ul><li>
Position: Phlebotomist II</li><li>
Location: Swedish Hospital</li><li>
Full Time/Part Time: Part time, 8 hours</li><li>
Hours: Monday-Friday, 10pm-6:30am, rotating weekends and holidays</li></ul><div></div><div>
What you will do:</div><ul><li>
Proficiently performs accurate venipuncture and capillary specimen collection for all inpatients and outpatients for all age groups.</li><li>
May be responsible for collection of body fluid or other samples including, nasal and throat swabs, and breath samples.</li><li>
Operates and utilizes the H.I.S and L.I.S. and other available resources to appropriately address the needs of the lab service areas and their clientele</li><li>
Prepares and assists in the processing of blood and body fluid samples per established guidelines.</li><li>
Assist in the orientation and training of phlebotomy staff and students.</li><li>
Applies skills and experience to identify and address problems as they arise and notifies lead/supervisory personnel as needed.</li><li>
Assists with inventory management duties as assigned.</li><li>
Ensures that all customer requests for Laboratory services are addressed in a timely and appropriate manner.</li><li>
Provides phone coverage and understands the importance of professional appearance and behavior in conducting oneself in a customer-oriented manner in accordance with the hospital&rsquo;s mission.</li></ul><div></div><div>
What you will need:</div><ul><li>
Education: High School diploma or GED equivalent required.</li><li>
Certification: Phlebotomy certification preferred but not required and CPR-BLS certification for Healthcare Provider (AHA) required</li><li>
Experience: One year of phlebotomy experience required.</li><li>
Unique or Preferred Skills: Good communication and organization skills, moderate computer skills needed, strong customer service skills</li></ul><div></div><div>
Benefits:</div><ul><li>
Premium pay such as shift, on call, holiday and more based on an employee&rsquo;s job</li><li>
Incentive pay for select positions</li><li>
Opportunity for annual increases based on performance</li><li>
Career Pathways to Promote Professional Growth and Development</li><li>
Various Medical, Dental, Pet and Vision options</li><li>
Tuition Reimbursement</li><li>
Free Parking</li><li>
Wellness Program Savings Plan</li><li>
Health Savings Account Options</li><li>
Retirement Options with Company Match</li><li>
Paid Time Off and Holiday Pay</li><li>
Community Involvement Opportunities</li></ul><div></div><div>
Endeavor Health is a fully integrated healthcare delivery system committed to providing access to quality, vibrant, community-connected care, serving an area of more than 4.2 million residents across six northeast Illinois counties. Our more than 25,000 team members and more than 6,000 physicians aim to deliver transformative patient experiences and expert care close to home across more than 300 ambulatory locations and eight acute care hospitals &ndash; Edward (Naperville), Elmhurst, Evanston, Glenbrook (Glenview), Highland Park, Northwest Community (Arlington Heights) Skokie and Swedish (Chicago) &ndash; all recognized as Magnet hospitals for nursing excellence. For more information, visit <div>www.endeavorhealth.org</div>.</div><div></div><div>
When you work for Endeavor Health, you will be part of an organization that encourages its employees to achieve career goals and maximize their professional potential.</div><div></div><div>
Please explore our website (<div>www.endeavorhealth.org</div>) to better understand how Endeavor Health delivers on its mission to &ldquo;help everyone in our communities be their best&rdquo;.</div><div></div><div>
Endeavor Health is committed to working with and providing reasonable accommodation to individuals with disabilities. Please refer to the main career page for more information.</div><div></div><div>
At Endeavor Health, we are united by a shared commitment to working together to create a culture of connection and belonging&mdash;each of us bringing different skills and experiences as we deliver safe, seamless, and personal care. Every person, every time. We are committed to fostering an environment where all team members can be their best, learn, and pursue excellence together.</div><div></div><div>
EOE: Race/Color/Sex/Sexual Orientation/ Gender Identity/Religion/National Origin/Disability/Vets, VEVRRA Federal Contractor.</div></div><div></div>

Phlebotomist II

<div><div>Hourly Pay Range:</div>
$20.69 - $30.00 - The hourly pay rate offered is determined by a candidate's expertise and years of experience, among other factors.<div></div><div>
Position Highlights:</div><ul><li>
Position: Phlebotomist Lead</li><li>
Location: Swedish Hospital</li><li>
Full Time/Part Time: Full Time</li><li>
Hours: Monday-Friday,5am-1:30pm, rotating weekends and holidays</li></ul><div></div><div>
What you will do:</div><div>
Assigns and monitors work to ensure that laboratory customer service requests are met in an accurate, timely, and appropriate manner.</div><div></div><div>
Applies skills and experience to identify problems as they arise. Implements appropriate troubleshooting and follow through.</div><div></div><div>
Can proficiently operate and utilize the Data Management functions of the LIS to address the needs of the lab service areas and their clientele.</div><div></div><div>
Conducts all communication transactions in a professional and courteous manner, deferring to appropriate administrative personnel as needed.</div><div></div><div>
Proficient in all aspects of specimen preparation and processing procedures.</div><div></div><div>
Responsible for processing all reference lab testing and use of the associated electronic databases of the reference labs.</div><div></div><div>
Coordinates the orientation and training of phlebotomy staff and students.</div><div></div><div>
Is aware of and supports the Quality Assurance Program as it relates to the phlebotomy service areas, and reports possible infractions as they occur.</div><div></div><div>
Proficiently performs accurate venipunctures and capillary specimen collection for all inpatients and outpatients for all age groups.</div><div></div><div>
Responsible for the collection of body fluid or other samples including, nasal and throat swabs, stool, urine, semen, and breath samples.</div><div></div><div>
Other functions:</div><div>
Assists with inventory management duties as assigned.</div><div></div><div>
What you will need:</div><ul><li>
Education: High school diploma or GED preferred or equivalent work experience</li><li>
Certification: CPR-BLS certification for the Healthcare Provider required and PBT (ASCP) certification preferred</li><li>
Experience: 2 years of Phlebotomy training experience strongly preferred</li><li>
Unique or Preferred Skills: Good communication and organization skills, moderate computer skills needed, reliable transportation to travel between sites required, strong customer service skills.. Basic typing/keyboarding. Ability to process esoteric testing. Leadership, organizational and communication (verbal, written and telephone) skills and the ability to lead, work with and relate to personnel.</li></ul><div></div><div>
Benefits:</div><ul><li>
Premium pay such as shift, on call, holiday and more based on an employee&rsquo;s job</li><li>
Incentive pay for select positions</li><li>
Opportunity for annual increases based on performance</li><li>
Career Pathways to Promote Professional Growth and Development</li><li>
Various Medical, Dental, Pet and Vision options</li><li>
Tuition Reimbursement</li><li>
Free Parking</li><li>
Wellness Program Savings Plan</li><li>
Health Savings Account Options</li><li>
Retirement Options with Company Match</li><li>
Paid Time Off and Holiday Pay</li><li>
Community Involvement Opportunities</li></ul><div></div><div>
Endeavor Health is a fully integrated healthcare delivery system committed to providing access to quality, vibrant, community-connected care, serving an area of more than 4.2 million residents across six northeast Illinois counties. Our more than 25,000 team members and more than 6,000 physicians aim to deliver transformative patient experiences and expert care close to home across more than 300 ambulatory locations and eight acute care hospitals &ndash; Edward (Naperville), Elmhurst, Evanston, Glenbrook (Glenview), Highland Park, Northwest Community (Arlington Heights) Skokie and Swedish (Chicago) &ndash; all recognized as Magnet hospitals for nursing excellence. For more information, visit <div>www.endeavorhealth.org</div>.</div><div></div><div>
When you work for Endeavor Health, you will be part of an organization that encourages its employees to achieve career goals and maximize their professional potential.</div><div></div><div>
Please explore our website (<div>www.endeavorhealth.org</div>) to better understand how Endeavor Health delivers on its mission to &ldquo;help everyone in our communities be their best&rdquo;.</div><div></div><div>
Endeavor Health is committed to working with and providing reasonable accommodation to individuals with disabilities. Please refer to the main career page for more information.</div><div></div><div>
At Endeavor Health, we are united by a shared commitment to working together to create a culture of connection and belonging&mdash;each of us bringing different skills and experiences as we deliver safe, seamless, and personal care. Every person, every time. We are committed to fostering an environment where all team members can be their best, learn, and pursue excellence together.</div><div></div><div>
EOE: Race/Color/Sex/Sexual Orientation/ Gender Identity/Religion/National Origin/Disability/Vets, VEVRRA Federal Contractor.</div></div><div></div>

Phlebotomist Lead

Altimeter Solutions

<div>The Patient Services Representative III-Floater (PSR III) represents the face of our company to patients who come in, both as part of their health routine or for insights into life-defining health decisions. The PSR III draws quality blood samples from patients and prepares those specimens for lab testing while following established practices and procedures. The PSR III has direct contact with patients and creates an atmosphere of trust and confidence while explaining procedures to patients and drawing blood specimens in a skillful, safe and accurate manner. The PSR III will demonstrate Leadership Behaviors while focusing on process excellence skills and sensitivity to confidentiality and accuracy to patient information. Successful applicants may be assigned to a doctor's office, a patient service center or as business needs dictate.<br>
<br>
Under the direction of the area supervisor, perform daily activities accurately and on time. Maintain a safe and professional environment. Performs with confidence, both the forensic and clinical specimen collection and processing duties following established practices and procedures. Perform verification of patient demographic info / initials including patient signature post-venipuncture to verify tubes were labeled in their presence and that the name on the label is correct. Maintains required records and documentation. Demonstrates organizational commitment and promotes a positive image to patients, clients, employees and the public in general.
<br>
<br>
Job Requirements:
<br>
<br>
Ability to provide quality, error free work in a fast-paced environment.
<br>
Ability to work independently with minimal on-site supervision.
<br>
Excellent phlebotomy skills to include pediatric and geriatric.
<br>
Flexible and available based on staffing needs, which includes weekends, holidays, on-call and overtime.
<br>
Committed to all Policies &amp; Procedures including Company dress code, Employee Health &amp; Safety, and Everyday Excellence Guiding Principles.
<br>
Must be able to make decisions based on established procedures and exercise good judgment. Must have reliable transportation, valid driver license, and clean driving record, if applicable.
<br>
Travel and flexible hours required to work multiple locations and required to cover at Patient Service Center/In-Office Phlebotomy locations with minimal notice.
<br>
Capable of handling multiple priorities in a high-volume setting.
<br>
Must demonstrate Superior Customer Focus; ability to communicate openly and transparently with peers, supervisors and patients; ability to accelerate and embrace change; and knowledge of our business.
<br>
<br>
Training locations may vary based on trainer availability.<br>
<br>
Required Education:
<br>
High school diploma or equivalent - REQUIRED<br>
Medical training: medical assistant or paramedic training preferred. Phlebotomy certification preferred. Required in California, Nevada, and Washington.
<br>
<br>
Work Experience:
<br>
Three years phlebotomy experience required, inclusive of pediatric, geriatric and capillary collections.
<br>
Minimum 2 years in a Patient Service Center environment preferred.
<br>
Customer service in a retail or service environment preferred. Keyboard/data entry experience.;
<br>
<br>
Comments:</div>

Phlebotomist III - Floater (US Citizen)- Chicago, Illinois - 18618

Advocate Aurora Health

<div><p><b>Major Responsibilities:</b></p><ul><li>
Verifies positive patient identification to ensure patient safety. Assesses patient reactions to specimen procurement.</li><li>
Performs venipuncture and collects other specimens from newborn, pediatric, and adult patients according to established protocol. Obtains medical assistance when judged necessary.</li><li>
Obtains specimens according to priority and scheduled draw times. Ensures completion of specimen collection functions according to protocol. Ensures that specimens are properly labeled and suitable for testing. Resolves specimen identification and/or requisition problems and clarifies requests.</li><li>
Performs limited testing under Clinical Laboratory Improvement Amendments (CLIA), 1988 guidelines according to established policies and procedures.</li><li>
Answers and screens telephone calls. Assists with inventory and maintains supplies and/or equipment. Provides assistance in support of Billing and other business functions.</li><li>
Accepts specimens from a variety of internal and external customers. Receives and sorts specimens. Packages and tracks specimens for transport. Processes specimens for testing, including aliquoting, pre-analytical steps, and loading instruments, while maintaining proper specimen identification. Responds to additional specimen procurement requests via pager or other means.</li><li>
Orders and verifies test requests. Documents appropriate information for quality assurance/improvement according to established protocol. Runs quality control checks. Takes appropriate action to notify providers of stat, critical and other abnormal results as defined by policy and procedure.</li><li>
Performs laboratory result entry in the computer system.</li><li>
Performs internal and external proficiency testing in the same manner as patient samples. Reviews various pending and management reports. Generates and distributes reports.</li><li>
Instructs employees and students in phlebotomy, data entry and specimen processing functions.</li><li>
Must be able to demonstrate knowledge and skills necessary to provide care appropriate to the age of the patients served.</li></ul><p><b><br>
Licensure, Registration, and/or Certification Required:</b></p><ul><li>
n/a</li></ul><p><b><br>
Education Required:</b></p><ul><li>
High school diploma or equivalent</li></ul><p><b><br>
Experience Required:</b></p><ul><li>
1 year phlebotomy experience, preferred</li></ul><p><b><br>
Knowledge, Skills &amp; Abilities Required:</b></p><ul><li>
Demonstrates knowledge and experience in phlebotomy or related laboratory function.</li><li>
Basic computer skills including experience using computer software applications.</li><li>
Keyboarding and typing skills.</li><li>
Excellent verbal and written communication skills. Good listening skills.</li><li>
Ability to work in a fast paced environment and to handle multiple tasks simultaneously.</li><li>
Demonstrated customer service skills to interface effectively with physicians, patients, visitors, and other healthcare employees.</li></ul><p><b><br>
Physical Requirements and Working Conditions:</b></p><ul><li>
Operates all equipment necessary to perform the job.</li><li>
Frequently lifts up to 10 lbs. Occasionally lifts up to 50 lbs.</li><li>
Must be able to sit, stand, walk and bend the majority of the workday.</li><li>
May be exposed to mechanical, electrical, chemical, radioactive and/or infectious agents.</li><li>
Will be exposed to human blood and body fluids.</li><li>
Must wear appropriate lab coat, gloves, gowns and eye and face protection as needed.</li></ul><p><i><br>
This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the incumbent. Incumbent may be required to perform other related duties.</i></p></div>

Phlebotomist/Part-Time/Days/Trinity

Impact Tactic Solutions

<p><b>About Us:</b><br/>At ITS, we provide nationwide on-site health screenings and wellness solutions to businesses. We are looking for experienced medical professionals to join our team in conducting health screenings and wellness events.</p><p><b>Summary:</b></p><p>Impact Tactic Solutions is seeking experienced, reliable phlebotomists to support onsite biometric screening events across Illinois. This role is ideal for clinicians who enjoy flexible scheduling, professional work environments, and consistent event based opportunities.</p><p>Phlebotomists play a critical role in delivering high quality wellness services including blood collection, participant interaction, and accurate documentation. Events are typically held at corporate locations during standard business hours.</p><p><b>Responsibilities:</b></p><ul><li>Perform venipuncture and capillary blood draws following established protocols</li><li>Confirm participant identity and ensure proper specimen labeling</li><li>Maintain a clean, organized, and compliant screening area</li><li>Provide a positive and professional experience for participants</li><li>Accurately complete all required documentation and reporting</li><li>Adhere to HIPAA, OSHA, and company standards at all times</li></ul><p><b>Qualifications:</b></p><ul><li>Current phlebotomy certification required</li><li>Active Illinois license</li><li>Minimum of one year hands on phlebotomy experience preferred</li><li>Strong venipuncture skills with adult populations</li><li>Excellent professionalism, communication, and bedside manner</li><li>Reliable transportation and ability to travel locally</li><li>CPR certification preferred</li></ul><p><b>Why Join Us?</b></p><ul><li>Competitive compensation.</li><li>Opportunity to work in a variety of environments and settings.</li><li>Gain valuable experience in the health and wellness industry.</li><li>Be part of a dedicated team committed to improving workplace health</li></ul><p>We believe in offering competitive compensation to our team, considering these factors while ensuring our rates align with industry standards. We typically discuss and lock in an hourly rate with our potential staff when there is an upcoming event in their area prior to assigning them into the event.</p><p>Job Types: Contract, PRN, Per diem</p><p>Pay: $18.00 - $25.00 per hour</p><p>Benefits:</p><ul><li>Flexible schedule</li></ul><p>Work Location: On the road</p>

Phlebotomist-Illinois

ProPharma

<div>
 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality &amp; compliance, pharmacovigilance, medical information, and R&amp;D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners&rsquo; most high-profile drug and device programs.
 <br/>
 <br/>
 <strong>
  Position Overview
  <br/>
  <br/>
 </strong>
 This position is responsible for executing, managing and conducting projects associated with the company clinical study plans. The Contract Clinical Research Associate (CCRA) is responsible for site management deliverables on assigned protocols and may support other CRAs on the team.
 <br/>
 <br/>
 <strong>
  Essential Duties
  <br/>
  <br/>
 </strong>
 Include, but are not limited to, the following:
 <br/>
 <br/>
 <ul>
  <li>
   Establish and maintain primary Sponsor communication with clinical sites for in-house and outsourced studies.
  </li>
  <li>
   Conduct oversight visits for outsourced studies to promote study engagement, enrollment and foster sponsor/site relationships.
  </li>
  <li>
   Serve as a point of contact for investigators and site staff. Maintain regular contact with study sites to ensure GCP/ICH/Protocol compliance, assessment of accrual rates.
  </li>
  <li>
   Facilitate communication between the project team and site personnel to ensure that they are appropriately trained, remain current with project requirements, and have a thorough understanding of study milestones and deliverables.
  </li>
  <li>
   Conduct thorough site qualifications visits. Ensure all required information concerning site/staff qualifications is clearly documented and communicated to project teams.
  </li>
  <li>
   Conduct efficient and comprehensive site initiation visits. Ensure all assigned site staff are trained appropriately, have access to the required electronic systems, and are informed of data collection, GCP, protocol and reporting requirements.
  </li>
  <li>
   Ensure monitoring visits are scheduled and performed per the Monitoring Plan and according to the performance of the clinical site and the project team needs. Maintain a flexible monitoring schedule (as appropriate) and assist in co-monitoring or monitoring support of clinical sites/studies.
  </li>
  <li>
   Conduct study specific training for new study coordinators (protocol, ICH/GCP and regulatory guidelines and study specific requirements). Ensure all clinical site staff actively participating in the study are appropriately trained. Identify if any untrained staff are participating in Clinical trial activities, document and communicate the issues and suggested resolutions to the Clinical site and project team.
  </li>
  <li>
   Conduct device/product accountability responsibilities at clinical sites; Identify, clearly communicate and document issues to the clinical site and project team. Assist clinical site in resolving issues, if appropriate.
  </li>
  <li>
   Participate in all aspects of site close-out activities (i.e., evaluation of site readiness for final IMV, preparation for Database lock, etc.). Communicate status of Site management activities on a routine basis to the Clinical Project team and management.
  </li>
  <li>
   Actively participate as an extended team member of the clinical study team including participating in study-specific meetings, teleconferences and investigator meetings, clear and timely communication with cross functional partners and CRA team members.
  </li>
  <li>
   Implement and execute the clinical study Monitoring Plan to ensure compliance with the plan and all assigned tasks throughout the study.
  </li>
  <li>
   Ensure clear and efficient written communication to clinical sites (confirmation letter, site visit report, follow up letter, requests for remediation or action) and project team members.
  </li>
  <li>
   Communicate project specific information to/from trial sites through teleconferences, newsletters, etc.
  </li>
  <li>
   Work with clinical project manager to assure investigator payments are appropriate and paid on a timely basis.
  </li>
  <li>
   Document monitoring activities in monitoring visit reports and follow-up letters.
  </li>
  <li>
   Communicate serious issues to appropriate parties, in a timely manner.
  </li>
  <li>
   Ensure operational and regulatory integrity of assigned studies and participate in FDA or other regulatory authority inspections, as needed.
  </li>
  <li>
   Participate in Investigator Meetings, and other study trainings and meetings as required.
  </li>
  <li>
   Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
  </li>
  <li>
   Support and comply with the company&rsquo;s Quality Management System policies and procedures.
  </li>
  <li>
   Maintain regular and reliable attendance.
  </li>
  <li>
   Ability to act with an inclusion mindset and model these behaviors for the organization.
  </li>
  <li>
   Ability to work designated schedule.
  </li>
  <li>
   Ability to work nights and/or weekends, as needed.
  </li>
  <li>
   Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.
  </li>
  <li>
   Ability to work on a computer and phone simultaneously.
  </li>
  <li>
   Ability to use a telephone through a headset.
  </li>
  <li>
   Ability to travel 50% of working time away from work location may include overnight/weekend travel.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Minimum Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s Degree in field as outlined in essential duties or
  </li>
  <ul>
   <li>
    Associate degree with a minimum of 6 years of monitoring experience or equivalent experience.
   </li>
   <li>
    Highschool Diploma with a minimum 8 years of monitoring experience or equivalent experience.
   </li>
  </ul>
  <li>
   4+ years clinical research monitoring experience or equivalent experience.
  </li>
  <li>
   No other results from the Motor Vehicle Report (MVR) check that exposes Exact Sciences to what Exact Sciences deems to be an unacceptable level of liability.
  </li>
  <li>
   Proficiency in data management, including progressive experience in data entry, validation, and cleaning. Familiarity with Electronic Data Capture (EDC) systems.
  </li>
  <li>
   Effective communication skills and ability to collaborate with investigators, site staff, and team members. Demonstrated ability to work well within a team and convey information effectively.
  </li>
  <li>
   Understanding of regulatory compliance to ensure adherence to applicable regulations and requirements. Knowledge and experience in informed consent procedures, adverse event reporting, documentation, and record-keeping practices.
  </li>
  <li>
   Meticulousness with a focus on accuracy and precision in all tasks and activities.
  </li>
  <li>
   Extensive experience in clinical trial monitoring, including site initiation visits, routine monitoring visits, and close-out visits. Proficiency in monitoring plans, protocol adherence, and GCP guidelines. Conducting source data verification, resolving queries, and ensuring site compliance and data accuracy.
  </li>
  <li>
   Demonstrated ability to perform the essential duties of the position with or without accommodation.
  </li>
  <li>
   Authorization to work in the United States without sponsorship.
   <br/>
  </li>
 </ul>
 <strong>
  Preferred Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Experience or knowledge in In Vitro Diagnostics (IVD).
  </li>
  <li>
   Certifications related to clinical research.
  </li>
  <li>
   Working knowledge of the FDA submission process including IDE, PMA, and 510(k).
  </li>
  <li>
   Strong on-site monitoring experience in clinical trials, including:
  </li>
  <ul>
   <li>
    Site initiation.
   </li>
   <li>
    Routine monitoring visits.
   </li>
   <li>
    Site closeout.
   </li>
  </ul>
  <li>
   Knowledge of electronic trial master file (eTMF) systems and document management processes.
  </li>
  <li>
   This position requires the CRA to be based in either Chicago, IL or Dallas, TX and be fluent in Spanish.
   <br/>
  </li>
 </ul>
 We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
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 <br/>
 All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
 <br/>
 <br/>
 Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.
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 <br/>
 ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
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</div>


Clinical Research Associate (Spanish Speaking)

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