clinical research assistant

University of Pittsburgh

<div><div><p><b>Clinical Research Assistant</b></p></div><div>
Med-Pediatrics - Pennsylvania-Pittsburgh - (26002023)</div><div></div><div><p><br>
This position for the division of Pediatric Hematology/Oncology. Equivalent relevant work experience may be substituted for degree requirement. This position is located at UPMC Children&rsquo;s Hospital of Pittsburgh in Lawrenceville. PA Child Abuse History Clearance, PA State Police Criminal Record Check, and FBI Criminal Record Check will be required prior to the start of employment. Also, a current TB test will be required as a condition of employment. EEO/AA/M/F/Vets/Disabled.</p></div><div><div><b>
Job Summary</b></div><p></p><p>
Conducts research assessments and procedures independently. Oversees operations when leadership is unavailable. Recruits and screens participants, reviews records and surveys, and maintains databases. Performs routine data analysis and prepares reports, data visualizations, and models.</p></div><p></p><div><div><b>
Essential Functions</b></div><ul><li>Conducts research assessments/procedures independently, including obtaining vital signs and brief medical histories, processing specimens using centrifuge, performing phlebotomy, preparing samples for shipment, and assisting with other clinical procedures as directed.</li><li>Oversees operations when leadership is unavailable; assigns work tasks and provides support.</li><li>Recruits, screens, and enrolls research participants. Follows up with study participants to schedule appointments and maintain study retention.</li><li>Reviews participants' medical records, collects and codes surveys, and verifies active status for participants.</li><li>Attends relevant meetings and prepares reports, data visualizations, and basic models identifying progress and trends.</li><li>Maintains and updates databases for registry assessments and clinical trial forms.</li><li>Orders supplies, maintains inventory, and organizes laboratory.</li><li>Performs data analysis involving routine procedures.</li><li>Assists in preparing standard operating procedures and manuals.</li></ul></div><div><div><b>
Physical Effort</b></div><p>
Light.</p></div><p></p><div><p><i><br>
The University of Pittsburgh is an equal opportunity employer / disability / veteran.</i></p><div><br>
</div></div><div><div><b>
Assignment Category</b></div> Full-time regular</div><div><div><b>
Job Classification</b></div> Staff.Clinical Research Assistant II</div><div><div><b>
Job Family</b></div> Research</div><div><div><b>
Job Sub-Family</b></div> Clinical Research</div><div><div><b>
Campus</b></div> Pittsburgh</div><div><div><b>
Minimum Education Level Required</b></div> Associate's Degree</div><div><div><b>
Minimum Years of Experience Required</b></div> 1</div><div><div><b>
Will this position accept substitution in lieu of education or experience? </b></div>Combination of education and relevant experience will be considered in lieu of education and/ or experience requirement.</div><div><div><b>
Work Schedule</b></div> This position will require flexibility with shift/hours.</div><div><div><b>
Work Arrangement</b></div> On-Campus: Teams that work on campus, in an office, or in a lab.</div><div><div><b>
Hiring Range</b></div> TBD Based Upon Qualifications</div><div><div><b>
Relocation Offered</b></div> No</div><div><div><b>
Visa Sponsorship Provided</b></div> No</div><div><div><b>
Background Check</b></div> For position finalists, employment with the University will require successful completion of a background check</div><div><div><b>
Child Protection Clearances</b></div> The following PA Act 153 clearances and background checks are required prior to commencement of employment and as a condition of continued employment: PA State Police Criminal Record Check, FBI Criminal Record Check, PA Child Abuse History Clearance.</div><div><div><b>
Required Documents</b></div> Resume</div><div><div><b>
Optional Documents</b></div> Cover Letter</div></div>

Clinical Research Assistant

Medix™

<div>
 <p>
  <strong>
   <u>
    Clinical Research Assistant
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Must Haves:
  </strong>
  Must have experience as a Clinical Research Assistant, and experience with Oncology
 </p>
 <p>
  <strong>
   Hours:
  </strong>
  40 hours per week, Monday-Friday, onsite, normal business hours. Need someone flexible to come in earlier or stay later for patient needs.
 </p>
 <p>
  <strong>
   Contract Duration:
  </strong>
  Permanent position
 </p>
 <p>
  <strong>
   Benefits:
  </strong>
  Medical, Dental, Vision, time off, paid holidays off, bonus, 401k, growth opportunities, etc.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  The Research Assistant I is an essential team member in the conduct and execution of clinical research studies. The Research Assistant is to assist under direct supervision of the Site Director or Clinical Research Coordinator (CRC) in clinic supporting activities and perform duties and procedures related to the start-up, conduct and close-out phases of clinical research protocols. Under direct supervision and direction, to help obtain clean, objective, and accurate data within provided timelines while following applicable federal regulations, medical ethics, Good Clinical Practices (GCPs), Institutional Review Board (IRB) requirements, and in compliance with specific sponsor protocol requirements. All responsibilities should be completed in accordance with the companies Mission Statement and Employee Manual.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Required Skills
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   <strong>
    Education:
   </strong>
   Associate in Science degree or adequate experience within the field of clinical research to compensate. Bachelor's degree preferred.
  </li>
  <li>
   <strong>
    Experience:
   </strong>
   Preferably a
   <strong>
   </strong>
   minimum of 1-3+ years&rsquo; experience within the field of clinical research or biological research. Must have experience with Oncology.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Preferred Skills
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Exceptional knowledge of clinical research methods.
  </li>
  <li>
   Demonstrates core values &amp; all skills set required.
  </li>
  <li>
   Demonstrated ability to collaborate and align with all research department teams.
  </li>
  <li>
   Excellent oral and written communication skills.
  </li>
  <li>
   Excellent computer skills to include Office365 products.
  </li>
  <li>
   Is moral and ethical in decision-making and during interaction with patients, sponsor and IRB representatives, physicians and staff at satellite clinics, and other employees.
  </li>
  <li>
   Must be professional, have a strong work ethic, be motivated to identify tasks that need to be completed and to strive for accuracy and quality when completing assignments.
  </li>
  <li>
   ECG, phlebotomy skills, and any other technical skills related to the completion of a study visit as required by the protocol.
  </li>
  <li>
   Must be able to adapt and take on additional tasks as requested.
  </li>
  <li>
   Assists with key initiatives/process improvements in the department.
  </li>
  <li>
   Assists with training company new hires.
  </li>
  <li>
   Completes at least 80% of goals annually.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Apply Today!
 </p>
</div>


Clinical Research Assistant - 251480

GI ALLIANCE

<div><p><b>JOB TITLE: Research Assistant</b></p><p>
</p><p><b>FSLA STATUS: Exempt
</b></p><p></p><p><b>POSITION SUMMARY:</b></p><p>
</p><p>Experienced Medical Assistant or Research Assistant needed to contribute to Urology Austin&rsquo;s growing research department. Research Assistant (RA) roles often transition to Clinical Research Coordinator (CRC) roles and open the door to many other career opportunities within the industry. Research Assistants support the Clinical Research Team with subject recruitment, diagnostic testing, laboratory specimen collection, communications with patients, study sponsors, and investigators, and other interesting research related roles.
</p><p></p><p>You will work closely with our Study Coordinators, Clinical Research Director, Principal Investigators (PI) and Sub-Investigators (Sub-Is) on various clinical research studies.
</p><p></p><p><b>JOB RELATIONSHIPS:</b></p><p>
</p><ul><li>Reports to the Director of Clinical Research, VP of Clinical Research, Market President, and all the physicians at Urology Austin
</li><li>Able to collaborate with experienced patient navigators, IT, and data management teams</li></ul><p>
</p><p><b>ROLE QUALIFICATIONS: (experience, education, and skills)</b></p><p>
</p><ul><li>Must be willing to gain a thorough knowledge and follow strict adherence of all clinical study protocols.</li><li>
Develop an understanding of and demonstrate Good Clinical Practices (GCPs), learn and comply with all FDA clinical trial and IRB rules and regulations</li><li>
Must have &gt; 1 year experience as a medical assistant or research assistant.
</li><li>Urology based clinical experience preferred</li><li>
Should possess or develop proficiency in computer software use, including Microsoft Office, EMR and Practice Management systems, and study specific EDC and IVRS systems</li><li>
Effective time management and the ability to prioritize work</li><li>
Excellent communication skills and the ability to interact with all levels of management, staff, and physicians in person, virtually, and in writing</li><li>
Ability to be flexible with the day-to-day job requirements to facilitate a successful workflow in clinic</li></ul><p>
</p><p><b>ESSENTIAL JOB RESPONSIBLITIES:</b></p><p>
</p><ul><li>Review and follow Urology Austin Standard Operating Procedures</li><li>
Read and understand specific requirements of each study protocol and informed consent form</li><li>
Works with study coordinators and other research team members to complete protocol specific procedures and documentation</li><li>
Assists in clinic and protocol administration duties including but not limited to:<ul><li>
Explain the purpose, risks, and benefits of clinical trial participation</li><li>
Screen potential candidates in a timely and accurate manner</li><li>
Ensure that study patients understand the information presented and agree to the protocol requirements</li><li>
Obtain and maintain consent of patients prior to any study-related procedures being performed and with the highest ethical standards</li><li>
Provide instructions to patients to ensure proper protocol compliance</li><li>
Distribute study medications in compliance with protocol randomization requirements</li><li>
Learn and understand lab procedures and obtain and process study related lab specimens according to the study specific manuals (lab and procedural)</li><li>
Use approved source documents; obtain protocol-specific data to complete and maintain source documents and case report forms (including electronic data capture &ndash; EDC) in accordance with applicable regulations and sponsor requirements</li></ul></li><li><div><ul><li>
Perform study-specific readings and measurements including but not limited to:
</li></ul></div></li></ul><ul><li>Vital signs</li><li>
ECG</li><li>
Urine Pregnancy Test</li><li>
Uroflow, TRUS, urinalysis, cystoscopy</li><li>
Photography and videography</li></ul><ul><li>
Reports irregular readings and measurements to Investigator and Lead Study Coordinator</li><li>
Package and ship laboratory specimens to study-specific destinations</li><li>
Complete applicable training requirements and ongoing education as required</li></ul><ul><li>
Maintain certifications in, and continually update knowledge of, FDA, GCP, ICH, federal and state regulations, etc.</li><li>
Communicate with and support patients and their families as necessary.</li><li>
Work with the EMR and data management systems to complete EDC, eCRFs, find patients, maintain records</li><li>
Effectively communicate with potential candidates for trials and collect metrics to track progress
</li><li>Must have or gain knowledge of relevant software/programs</li></ul><p>
</p><ul><li>Work closely with IRB and study sponsors, PIs and Sub-Is. Attend necessary meetings and calls</li><li>
Assist with the development of source documents and phone screen tools</li><li>
Manage ancillary supply inventory and assist with drug accountability
</li><li>Maintain HIPAA compliant communication and confidentiality, at all times</li><li>
Participate in site visits (site initiation visits, interim monitoring visits, close-out visits, etc.</li><li>
Assist study coordinators with necessary study close-out procedures and documentation</li><li>
Performs other duties as assigned</li></ul><p>
</p><p><b>PERFORMANCE REQUIREMENTS:</b></p><p>
</p><p><i>Knowledge</i></p><ul><li>
Knowledge of health care field; medical practice clinical and administrative systems, departments, and practices, including clinical financial policies and reimbursement payment requirements.</li><li>
Understanding of medical terminology.
</li></ul><p><i>Skills
</i></p><ul><li>Ability to use multi-line phone systems and basic computer systems.</li><li>
Interpersonal and communication both with internal staff and external customers.</li><li>
Skill in evaluating and implementing study protocols and budgets.</li><li>
Skill in reading medical chart terminology.</li><li>
Time Management.</li></ul><p><i>
Abilities</i></p><ul><li>
Ability to communicate effectively with patients, staff, and external contacts via phone, in person, and through electronic mail.</li><li>
Elicit appropriate information for patients to clinic staff.</li><li>
Ability to read and understand information and ideas presented in writing.</li><li>
Ability to apply general rules to specific problems to produce answers that make sense &ndash; deductive reasoning.</li></ul><p>
</p><p><b>REPORTING TO THIS POSITION</b>: No direct reports at this time, can change as department grows</p><p>
</p><p><b>PHYSICAL DEMANDS AND WORK ENVIRONMENT</b><b>:</b></p><p>
</p><p>The physical demands and work environment characteristics described here are the representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions:</p><ul><li><i>
Physical demands</i>: Involves sitting approximately 90 percent of the day, walking or standing for the remainder. Work may require stooping and bending to access files, supplies, mobility to complete errands, and lifting up to 20 pounds.
</li><li><i>Work environment</i>: Primarily office setting. Noise level in the work environment is usually moderate. Clean, well-lighted office environment.</li></ul></div>

Metro Infectious Disease Consultants

<div><p>Metro Infusion Center/Metro Infectious Disease Consultants is seeking a <b>Full-Time Clinical Research Assistant</b> who will be responsible for providing non-clinical support in the operations and monitoring of clinical trials. The Research Assistant will analyze and evaluate clinical data gathered during research while ensuring compliance with protocols and overall clinical objectives. Responsibilities assigned to individuals can and will change at any time at the discretion of management or the supervisor</p><p><b>
Schedule</b>: Monday-Friday 8:30am-5:00 pm,<b> in-person</b>
</p><p><b>Duties:</b></p><ul><li>
Enter data proficiently and accurately into a data capture system for sponsors and contract research organizations to monitor.</li><li>
Request or acquire the equipment and supplies necessary for each project.</li><li>
Set up, calibrate, and maintain laboratory and/or field research equipment, as specified by the requirements of the study.</li><li>
Assist Clinical Research Associates that are monitoring each study (on and off-site).</li><li>
Invoice for payments associated with the clinical trial budget.</li><li>
Ship lab samples while following regulations and protocols when needed.</li><li>
Attend project meetings and communicate with fellow staff through email and phone calls.</li><li>
Perform ECG's</li><li>
Upload study documents to EMR chart</li><li>
Track specimen shipments</li><li>
Responsibilities may evolve depending on protocol specific requirements</li></ul><br>
<b>
Requirements</b><br>
<ul>
<li>High school diploma required</li>
<li>Bachelor's Degree preferred</li>
<li>Proof of current vaccinations, including recommended boosters, commonly required for those working with immunocompromised patients, including measles, mumps, rubella, varicella, hepatitis A &amp; B, influenza.</li>
</ul><p>Requests for accommodations/exceptions will be considered on a case-by-case basis, consistent with applicable laws.</p><b><br>
Benefits</b><br>
<ul><li>
401(k)</li><li>
Dental insurance</li><li>
Health insurance</li><li>
Life insurance</li><li>
Paid time off</li><li>
Referral program</li><li>
Vision insurance</li><li>
$50,000-$53,000 ($20/hour + monthly bonus)</li></ul></div>

Temple University

<div>
 The Temple University's Lewis Katz School of Medicine's TMS-Pulm/Critical Care/SleepMed Department is searching for a
 <strong>
  Part-Time Clinical Research Assistant
 </strong>
 to join our team!
 <br/>
 <br/>
 <strong>
  Become a part of the Temple family and you will have access to the following:
  <br/>
  <br/>
 </strong>
 Full medical, dental, vision coverage
 <br/>
 <br/>
 Paid time off
 <br/>
 <br/>
 11 Paid Holidays
 <br/>
 <br/>
 Tuition remission - eligible employees and their dependents can obtain a degree TUITION FREE
 <br/>
 <br/>
 A generous retirement plan and so much more!
 <br/>
 <br/>
 <strong>
  Salary Grade: T23
  <br/>
  <br/>
 </strong>
 Learn more about the "T" salary structure
 <br/>
 <br/>
 <strong>
  Salary Range: Up to $8,000 per year
  <br/>
  <br/>
 </strong>
 A variety of important factors are reviewed by HR when considering salary, including job duties, the applicant's education and experience, all relevant internal equity considerations, department budget, and funding source.
 <br/>
 <br/>
 <strong>
  Job Details
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   This position will be on-site
  </li>
  <li>
   This position requires the following background checks: PII/Cash Handling
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Position Summary
  <br/>
  <br/>
 </strong>
 The Clinical Research Assistant works under the direct supervision of the Principal Investigator and/or other Research Coordinators and will assist with specific research tasks associated with clinical research projects or clinical trials. The Clinical Research Assistant is mentored by coordinators, managers and/or the PI. Decisions are made within the limits of clearly established policies, procedures or instructions. This is a grant-funded position and requires a background check.
 <br/>
 <br/>
 At Temple University's Lewis Katz School of Medicine, you will be part of a nationally recognized, state-of-the-art research community that is driving innovation in patient care. Our clinical research programs span a wide range of disciplines and provide coordinators with the opportunity to contribute to groundbreaking studies that directly impact the health and well-being of diverse populations. With access to advanced resources, collaborative teams, and a strong commitment to excellence, Temple offers an ideal environment for Clinical Research Coordinators to grow their careers while shaping the future of medicine.
 <br/>
 <br/>
 <strong>
  Required Education And Experience
  <br/>
  <br/>
 </strong>
 Zero to 6 months of related experience is required, or an equivalent combination of education and experience may be considered. The position requires a strong interest in learning about Clinical Research.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 The Clinical Research Assistant performs study coordination tasks under the direct supervision, following established protocols and procedures. This position does not require prior experience in clinical research specifically, however, analytical thinking and attention to detail are necessary with responsibilities that may include performing repetitive tasks such as consenting patients.
 <br/>
 <br/>
 <ul>
  <li>
   Assist with screening, enrollment and tracking patients in clinical trials and other research studies for the Lewis Katz School of Medicine at Temple University
  </li>
  <li>
   May participate in the enrollment of human subjects for clinical trials. Obtain informed consent, schedule subjects for visits, perform basic clinical assessments and collect and enter study data.
  </li>
  <li>
   Perform various research, database, and clerical tasks to support clinical trials, aiding investigators in organizing, gathering, and compiling clinical research data.
  </li>
  <li>
   Organize and maintain documentation required for clinical trials and/or other research projects.
  </li>
  <li>
   Inform the Principal Investigator or other designated individuals about any issues regarding patient responses to treatment, medication, or adverse effects.
  </li>
  <li>
   Assist the Principal Investigator with Institutional Review Board (IRB) filings and annual reviews.
  </li>
  <li>
   Offer clerical and technical support to ensure adherence to research protocols and maintain the quality of information received.
  </li>
  <li>
   Adheres with FDA, IRB, Pennsylvania, and other applicable regulations.
  </li>
  <li>
   Performs other duties as assigned
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Required Skills And Abilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Interest in learning about Clinical Research.
  </li>
  <li>
   Demonstrated computer skills, and proficiency with MS Office Suite software programs.
  </li>
  <li>
   Aptitude in professionalism.
  </li>
  <li>
   Excellent written and oral communication skills.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Information
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   This position requires PII/Cash Handling Clearance prior to the commencement of service
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Temple University
 </strong>
 is committed to a policy of equal opportunity for all in every aspect of its operations, including employment, service, and educational programs. The University has pledged not to discriminate on the basis of age, color, disability, marital status, national origin or ethnic origin, race, religion, sex (including pregnancy), sexual orientation, gender identity, genetic information or veteran status.
 <br/>
 <br/>
 <strong>
  Compliance Statement:
 </strong>
 In the performance of their functions as detailed in the position description employees have an obligation to avoid ethical, legal, financial and other conflicts of interest to ensure that their actions and outside activities do not conflict with their primary employment responsibilities at the institution. Employees are also expected to understand and be in compliance with applicable laws, University and employment policies and regulations, including NCAA regulations for areas and departments which their essential functions cause them to interact.
 <br/>
 <br/>
 <strong>
  Temple University's Annual Security and Fire Safety Report
 </strong>
 contains statistics, policies, and procedures related to campus safety. Go here to review.
 <br/>
 <br/>
 You may request a copy of the report by calling
 <strong>
  Temple University's Department of Public Safety at 215-204-7900
 </strong>
 .
</div>


Care Access

<div><div><p><b>About Care Access</b></p>
<p>
Care Access is working to make the future of health better for all. <b>With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. </b>We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, <b>and contribute to the medical breakthroughs of tomorrow.</b></p>
<p>
With programs like <i>Future of Medicine</i>, which makes advanced health screenings and research opportunities accessible to communities worldwide, and <i>Difference Makers</i>, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.</p>
<p>
To learn more about Care Access, visit www.CareAccess.com.</p></div><h3 class="jobSectionHeader"><b>
How This Role Makes a Difference</b></h3>
<p>
The <b>Clinical Research </b><b>Assistant </b>is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator. This position has potential growth and advancement within the Care Access Research organization.</p>
<div>
<h3 class="jobSectionHeader"><b>How You'll Make An Impact</b></h3>
<ul><li>Ability to understand and follow institutional SOPs</li>
<li>Participate in recruitment and pre-screening events (may be at another location)</li>
<li>Assist with preparation of outreach materials</li>
<li>Identify potential participants by reviewing medical records, study charts and subject database</li>
<li>Assist with recruitment of new participants by conducting phone screenings</li>
<li>Request medical records of potential and current research participants</li>
<li>Schedule visits with participants, contact with reminders</li>
<li>Obtain informed consent per Care Access Research SOP, under the direction of the CRC</li>
<li>Complete visit procedures as required by protocol, under the direction of the CRC</li>
<li>Collect, process and ship specimens as directed by protocol, under the direction of the CRC</li>
<li>Record data legibly and enter in real time on paper or e-source documents</li>
<li>Request study participant payments</li>
<li>Update all applicable internal trackers and online recruitment systems</li>
<li>Assist with query resolution</li>
<li>Assist with administrative tasks such as copying, scanning, filing, mailing, emailing, etc.</li>
<li>Assist with maintaining all site logs</li>
<li>Assist with inventory and ordering equipment and supplies</li>
<li>Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.</li>
<li>Maintain effective relationships with study participants and other care Access Research personnel.</li>
<li>Interact in a positive, professional manner with patients/participants, sponsor representatives, Investigators and Care Access Research personnel and management.</li>
<li>Communicate clearly verbally and in writing.</li>
<li>Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.</li>
</ul><h3 class="jobSectionHeader"><b>The Expertise Required</b></h3>
<div><ul><li>Bilingual in Spanish required</li>
<li>Ability and willingness to work independently with minimal supervision</li>
<li>Ability to learn to work in a fast-paced environment</li>
<li>Excellent communication skills and a high degree of professionalism with all types of people</li>
<li>Excellent organizational skills with strong attention to detail</li>
<li>A working knowledge of medical and research terminology</li>
<li>A working knowledge of federal regulations, Good Clinical Practices (GCP)</li>
<li>Critical thinker and problem solver</li>
<li>Friendly, outgoing personality with the ability to maintain a positive attitude under pressure</li>
<li>Contribute to team and site goals</li>
<li>Proficiency in Microsoft Office Suite</li>
<li>High level of self-motivation and energy</li>
<li>An optimistic, &quot;can do&quot; attitude</li>
</ul></div><div><div><b>Certifications/Licenses, Education, and Experience:</b></div>
</div><div><ul><li>A minimum of 1-year recent working experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist.
</li><li>Phlebotomy Experience and Proficiency Required</li>
<li>Some Clinical Research experience preferred</li>
<li>California based roles require National phlebotomy certification by an organization approved by the California Department of Public Health</li>
<li>Louisiana based roles require National phlebotomy certification by an organization approved by the Louisiana State Board of Medical Examiners</li>
<li>Washington based roles require National phlebotomy certification by an organization approved by the Washington State Department of Health</li>
<li>Nevada based roles require Laboratory Assistant certification by the Division of Public and Behavioral Health</li>
</ul></div><h3 class="jobSectionHeader"><b>How We Work Together</b></h3>
<ul><li><b>Location</b>: This is an on-site position with regional commute requirements. Regularly planned travel within the region will be required as part of the role. Overnight travel will be minimal (&lt;10%).</li>
<li><b>Physical demands associated with this position Include</b>: The ability to use keyboards and other computer equipment.</li>
</ul>
<p>The expected salary range for this role is $19.00 - $33.00 USD per hour for full time team members.</p>
<div></div>
<h3 class="jobSectionHeader"><b>Benefits &amp; Perks (US Full Time Employees)</b></h3>
<ul><li>Paid Time Off (PTO) and Company Paid Holidays</li>
<li>100% Employer paid medical, dental, and vision insurance plan options</li>
<li>Health Savings Account and Flexible Spending Accounts</li>
<li>Bi-weekly HSA employer contribution</li>
<li>Company paid Short-Term Disability and Long-Term Disability</li>
<li>401(k) Retirement Plan, with Company Match</li>
</ul>
</div><div><p><b>Diversity &amp; Inclusion</b></p>
<p>
We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission.</p>
<p>
We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.</p>
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Care Access is unable to sponsor work visas at this time.</p>
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If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.com</p>
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Mandatory Employer Disclosures:<br>
<b>Notice to Illinois applicants:</b> Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.<br>
<b>Notice to Connecticut applicants:</b> Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.<br>
<b>Notice to Arizona, Georgia, Indiana, and North Dakota applicants:</b> Care Access complies with applicable laws prohibiting smoking in and around places of employment.<br>
<b>Notice to Massachusetts applicants:</b> It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.<br>
<b>Notice to Rhode Island applicants: </b>Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29&ndash;38 of Title 28 of the Rhode Island General Laws.<br>
<b>Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100.</b></p></div></div>

Temple University Health System

<div></div><div><div><p>The Temple University&rsquo;s Lewis Katz School of Medicine&rsquo;s Center for Neural Development and Repair is searching for a <b>Clinical Research Assistant</b> to join our team!</p><p><b>
Become a part of the Temple family and you will have access to the following:</b><br>
<i>Full medical, dental, vision coverage</i><br>
<i>Paid time off</i><br>
<i>11 Paid Holidays</i><br>
<i>Tuition remission - eligible employees and their dependents can obtain a degree TUITION FREE</i><br>
<i>A generous retirement plan and so much more!</i><br>
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<b>Salary Grade: T23</b><br>
Learn more about the &ldquo;T&rdquo; salary structure</p><p><b>
Salary Range: Up to $45,000.00 per year</b><br>
<i>A variety of important factors are reviewed by HR when considering salary, including job duties, the applicant&rsquo;s education and experience, all relevant internal equity considerations, department budget, and funding source.</i></p><div><b>
Job Details:</b><br>
<ul><li>This position will be on-site</li><li>This position requires the following background checks: Cash Handling</li></ul></div><p><b>
Position Summary:</b><br>
The Clinical Research Assistant works under the direct supervision of the Principal Investigator and/or other Research Coordinators and will assist with specific research tasks associated with clinical research projects or clinical trials. The Clinical Research Assistant is mentored by coordinators, managers and/or the PI. Decisions are made within the limits of clearly established policies, procedures or instructions.</p><p>
At Temple University&rsquo;s Lewis Katz School of Medicine, you will be part of a nationally recognized, state-of-the-art research community that is driving innovation in patient care. Our clinical research programs span a wide range of disciplines and provide coordinators with the opportunity to contribute to groundbreaking studies that directly impact the health and well-being of diverse populations. With access to advanced resources, collaborative teams, and a strong commitment to excellence, Temple offers an ideal environment for Clinical Research Coordinators to grow their careers while shaping the future of medicine.</p><p>
This is a grant-funded position and requires a background check. Clinical Research Coordinators may be hired for a specific department or as a pooled coordinator. Hybrid work options may be considered depending on study and departmental needs.</p><div><b>
Required Education and Experience:</b><br>
<ul><li>Zero to 6 months of related experience is required, or an equivalent combination of education and experience may be considered. The position requires a strong interest in learning about Clinical Research.</li></ul></div><p><b>
Responsibilities:</b><br>
The Clinical Research Assistant performs study coordination tasks under the direct supervision, following established protocols and procedures. This position does not require prior experience in clinical research specifically, however, analytical thinking and attention to detail are necessary with responsibilities that may include performing repetitive tasks such as consenting patients.</p><ul><li>Assist with screening, enrollment and tracking patients in clinical trials and other research studies for the Lewis Katz School of Medicine at Temple University</li><li>May participate in the enrollment of human subjects for clinical trials. Obtain informed consent, schedule subjects for visits, perform basic clinical assessments and collect and enter study data.</li><li>Perform various research, database, and clerical tasks to support clinical trials, aiding investigators in organizing, gathering, and compiling clinical research data.</li><li>Organize and maintain documentation required for clinical trials and/or other research projects.</li><li>Inform the Principal Investigator or other designated individuals about any issues regarding patient responses to treatment, medication, or adverse effects.</li><li>Assist the Principal Investigator with Institutional Review Board (IRB) filings and annual reviews.</li><li>Offer clerical and technical support to ensure adherence to research protocols and maintain the quality of information received.</li><li>Adheres with FDA, IRB, Pennsylvania, and other applicable regulations.</li><li>Performs other duties as assigned</li></ul><div><b>
Required Skills and Abilities:</b><br>
<ul><li>Interest in learning about Clinical Research.</li><li>Demonstrated computer skills, and proficiency with MS Office Suite software programs.</li><li>Aptitude in professionalism.</li><li>Excellent written and oral communication skills.</li></ul></div><div><b>
Additional Information:</b><br>
<ul><li>This is a grant-funded position and requires PII/Cash Handling Clearance prior to the commencement of service</li><li>Clinical Research Coordinators may be hired for a specific department or as a pooled coordinator.</li></ul></div><p><b>
Temple University</b> is committed to a policy of equal opportunity for all in every aspect of its operations, including employment, service, and educational programs. The University has pledged not to discriminate on the basis of age, color, disability, marital status, national origin or ethnic origin, race, religion, sex (including pregnancy), sexual orientation, gender identity, genetic information or veteran status.</p><p><b>
Compliance Statement:</b> In the performance of their functions as detailed in the position description employees have an obligation to avoid ethical, legal, financial and other conflicts of interest to ensure that their actions and outside activities do not conflict with their primary employment responsibilities at the institution. Employees are also expected to understand and be in compliance with applicable laws, University and employment policies and regulations, including NCAA regulations for areas and departments which their essential functions cause them to interact.<br>
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<b>Temple University's Annual Security and Fire Safety Report </b>contains statistics, policies, and procedures related to campus safety. Go here to review.<br>
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You may request a copy of the report by calling Temple University&rsquo;s <b>Department of Public Safety at 215-204-7900</b>.</p></div></div><p></p>

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