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clinical research assistant, prn

clinical research coordinator

Gastro Health

<div>
 <strong>
  Gastro Health is seeking a Full-Time Clinical Research Coordinator to join our team!
  <br/>
  <br/>
 </strong>
 Gastro Health is a great place to work and advance in your career. You'll find a collaborative team of coworkers and providers, as well as consistent hours.
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 <br/>
 <strong>
  This Role Offers
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   A great work/life balance
  </li>
  <li>
   No weekends or evenings &ndash; Monday thru Friday
  </li>
  <li>
   Paid holidays and paid time off
  </li>
  <li>
   Rapidity growing team with opportunities for advancement
  </li>
  <li>
   Competitive compensation
  </li>
  <li>
   Benefits package
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Duties You Will Be Responsible For
  <br/>
  <br/>
 </strong>
 <strong>
  General Administrative
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Coordinates with Principal Investigator, local site, and Central Hub to help ensure that clinical research and related activities are performed in accordance with federal regulations and sponsoring agency policies and procedures.
  </li>
  <li>
   Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.
  </li>
  <li>
   Assists Principal Investigator to assure that all key personnel or persons &lsquo;engaged&rsquo; in the research project have met training requirements in accordance with federal regulations and university and sponsoring agency policies and procedures.
  </li>
  <li>
   Cooperates with compliance and monitoring efforts related to sponsored program administration and respond to any audit findings and implement approved recommendations.
  </li>
  <li>
   Coordinates and facilitates monitoring and auditing visits. Notifies appropriate institutional officials of external audits by FDA and sponsors.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Protocol Preparation &amp; Review
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Attends investigator meetings as required or requested by the PI.
  </li>
  <li>
   Collaborates with the Regulatory Specialist to prepare IRB and any other regulatory submission documents as required by the protocol.
  </li>
  <li>
   Prepares other study materials as requested necessary. These study materials include, but are not limited to, the informed consent document, source documents, enrollment logs, and drug/device accountability logs.
  </li>
  <li>
   Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Conduct of Research
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Reviews and comprehends the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.
  </li>
  <li>
   Assists PI in communication of study requirements to all individuals involved in the study. Provides appropriate training and tools for study team members. Documents date of training and signatures of study personnel trained on study specific training log.
  </li>
  <li>
   Develops and implement recruitment strategies in accordance with HRPO (IRB) requirements and approvals.
  </li>
  <li>
   Conducts or participates in the informed consent process and discussions with research participants, including answering any questions related to the study. Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.
  </li>
  <li>
   Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant&rsquo;s eligibility or exclusion.
  </li>
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   Registers each participant in CTMS to ensure billing of study procedures to the appropriate funding source.
  </li>
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   Coordinates participant tests and procedures.
  </li>
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   Collects data as required by the protocol. Assures timely completion of Source Documents.
  </li>
  <li>
   Maintains study timelines.
  </li>
  <li>
   Maintains adequate inventory of study supplies. If handling investigational drugs/devices, follows the sponsor protocol and/or Gastro Health Research Policy on Investigational Drug/Device Accountability.
  </li>
  <li>
   Completes study documentation and maintains study files in accordance with sponsor requirements and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.
  </li>
  <li>
   Retains all study records in accordance with sponsor requirements and Gastro Health Research policies and procedures.
  </li>
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   Maintains effective and ongoing communication with sponsor, research participants and PI during the course of the study.
  </li>
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   Works with the PI to manage the day to day activities of the study including problem solving, communication and protocol management.
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   <br/>
  </li>
 </ul>
 <strong>
  Project Closeout
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Assists the Principal Investigator and Regulatory Specialist in submission of accurate and timely closeout documents to applicable federal agencies, and the sponsoring agency in accordance with federal regulations and sponsoring agency policies and procedures.
  </li>
  <li>
   Arranges secure storage of study documents that will be maintained according to Gastro Health Research policy or for the contracted length of time, whichever is longer.
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   <br/>
  </li>
 </ul>
 <strong>
  Minimum Requirements
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  <br/>
 </strong>
 <ul>
  <li>
   Clinical research experience preferred
  </li>
  <li>
   Previous phlebotomy skills
  </li>
  <li>
   High School Diploma
   <br/>
   <br/>
  </li>
 </ul>
 Interested in learning more? Click here to learn more about the location.
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 <br/>
 Gastro Health is the one of the largest gastroenterology multi-specialty groups in the United States, with over 130+ locations throughout the country. Our team is composed of the finest gastroenterologists, pediatric gastroenterologists, colorectal surgeons, and allied health professionals. We are always looking for individuals that share our mission to provide outstanding medical care and an exceptional healthcare experience. We offer a comprehensive benefits package to our eligible employees.
 <br/>
 <br/>
 Gastro Health is proud to be an Equal Opportunity Employer. We do not discriminate based on race, color, gender, disability, protected veteran, military status, religion, age, creed, national origin, gender identity, sexual orientation, marital status, genetic information, or any other basis prohibited by local, state, or federal law.
 <br/>
 <br/>
 We thank you for your interest in joining our growing Gastro Health team!
</div>


Clinical Research Coordinator

Nicklaus Children's Health System

<div><h2 class="jobSectionHeader"><div><b>Description</b></div></h2><p><b>
Job Summary</b></p>
<p>
Under direction of the Senior Manager of Clinical Trial Operations, the Clinical Research Coordinator (CRC) CTO manages and conducts the day-to-day activities of a research study. In general, the CRC ensures the study maintains in accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements. Beyond administrative duties, responsibilities of a CRC may include subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, collection and reviewing study data to enter it into the study and site systems, and correspondence with investigators, IRBs, sponsors, CRO's and regulatory authorities.</p>
<p><b>
Job Specific Duties</b></p>
<ul>
<li>Attends and participates in investigator meetings, pre-study visits, and initiation meetings or coordinator meetings as appropriate.<br>
</li>
<li>Collects and maintains accurate patient data for submission to Sponsor, maintaining proper patient records, coordinating the collection, and shipments of specimens as required by protocol.<br>
</li>
<li>Communicates study objectives/procedures to relevant hospital units involved with the study including the establishment of good rapport with the Principal Investigator &amp; providing required assistance.<br>
</li>
<li>Communicates with the Sponsor or their representatives, schedules and facilitates study monitor visits, and facilitates communication between Principal Investigator and Sponsor or Sponsor&rsquo;s Representatives.<br>
</li>
<li>Complies with the Research Finance Compliance policies and procedures including reporting requirements to research finance staff.<br>
</li>
<li>Interacts with patients and families to recruit (screen, consent, and enroll) study subjects and ensures compliance with the protocol.<br>
</li>
<li>Responsible for speedy and adequate patient enrollment as determined by Research Management and Principal Investigator in all assigned studies.<br>
</li>
<li>Demonstrates and utilizes Good Clinical Practices in the conduct of clinical trials as per established protocol.<br>
</li>
<li>Follows NCRI&rsquo;s Standard Operating Procedures, AAHRPP, HIPAA, and FDA guidelines for clinical research, and keeps updated in those procedures and/or guidelines.<br>
</li>
<li>Enters required data into CTMS in a timely manner, as stablished in department procedures.
<br>
</li><li>Provides new Protocols, Amendments, and study status updates to necessary research staff for digitization/entry into CTMS.<br>
</li>
<li>Keeps electronic patient files and required documents up-to-date within e-regulatory system.</li>
<li>Collaborates with study investigators to pre-screen and recruit patients to available clinical trials.</li>
</ul><h2 class="jobSectionHeader"><div><b>Qualifications</b></div></h2>
<ul><li></li></ul><p><b>
** Position is onsite in Miami **</b></p><p><b>
Minimum Job Requirements</b></p><ul><li>
Bachelor's degree and previous research experience (OR) Associate's degree and 2 years of research experience (OR) 3 years of research experience (OR) 5 years of healthcare experience</li></ul><p><b>
Knowledge, Skills, and Abilities</b></p><ul><li>
Experience in pediatric clinical research in a hospital setting highly preferred.<br>
</li><li>
Experience with relevant hospital equipment for each clinical trial project.<br>
</li><li>
Bilingual in English/Spanish preferred.<br>
</li><li>
Clinical research certification (CCRC, CCRP, CRA) and IATA certification preferred.<br>
</li><li>
Excellent communication skills in working with both children and adults.<br>
</li><li>
Excellent organizational skills, detail-oriented, people-oriented, flexible, and adaptable to change.<br>
</li><li>
Excellent time management skills.<br>
</li><li>
Knowledge of protocols and its process.<br>
</li><li>
Experience with software applications including word processing, scheduling and contact database, email, web browsing, hospital records, other database software and office equipment.<br>
</li><li>
Availability to work adjusted hours to accommodate subject visits.</li></ul><br>
<br>
<br>
<h2 class="jobSectionHeader"><div><b>Job:</b></div></h2>
Research<br>
<h2 class="jobSectionHeader"><div><b>
Department:</b></div></h2>
RI - ADMINISTRATION-2100-380950<br>
<h2 class="jobSectionHeader"><div><b>
Job Status:</b></div></h2>
Full Time</div>

Clinical Research Coord - Psych (Full Time, Days)

Integrity Clinical Research

<p><b>Job Overview</b></p><p>We are seeking a dependable and detail-oriented Clinical Research Phlebotomist to join our growing clinical research team.</p><p>This position will begin with a primary focus on phlebotomy and laboratory procedures for approximately 90 days due to maternity coverage. After successful completion of this period, the role will transition into a Clinical Research Coordinator (CRC) position with expanded responsibilities.</p><p>This is a long-term opportunity for candidates interested in building a career in clinical research.</p><p><b>Responsibilities</b></p><p>Phase 1: Phlebotomy &amp; Lab Operations (First 90 Days)</p><ul><li>Perform venipuncture and timed PK blood draws</li><li>Process, centrifuge, aliquot, and prepare specimens per protocol</li><li>Maintain accurate and timely documentation</li><li>Ensure compliance with lab manuals and protocol requirements</li><li>Monitor specimen storage and shipping requirements</li><li>Assist with patient intake and vital signs</li></ul><p>Phase 2: Clinical Research Coordinator Duties</p><ul><li>Coordinate study visits and patient scheduling</li><li>Conduct informed consent process</li><li>Document and report adverse events (AE/SAE)</li><li>Maintain regulatory binders and source documentation</li><li>Communicate with sponsors and monitors</li><li>Ensure strict adherence to study protocols and timelines</li></ul><p><b>Required Skills &amp; Qualifications</b></p><ul><li>Minimum 1 year phlebotomy experience</li><li>Comfortable performing multiple blood draws daily</li><li>Strong attention to detail and documentation accuracy</li><li>Ability to follow strict protocol timelines</li><li>Professional communication skills</li><li>Ability to work in a fast-paced clinical environment</li></ul><p>Preferred:</p><ul><li>Clinical research experience</li><li>Medical Assistant certification</li><li>GCP training</li><li>Bilingual (English/Spanish)</li></ul><p><b>Who This Role Is Ideal For</b></p><ul><li>Medical Assistants looking to grow into research</li><li>Entry-level CRCs seeking hands-on experience</li><li>Foreign Medical Graduates seeking U.S. research experience</li><li>Candidates interested in long-term clinical research careers</li></ul><p>Pay: $18.00 - $19.00 per hour</p><p>Work Location: In person</p>

Clinical Research Phlebotomist (Growth to CRC)

<div><h2 class="jobSectionHeader"><div><b>Description</b></div></h2><p><b>
Job Summary</b></p>
<p>
The Clinical Research Nurse, CTO is part of a central team of specialized research professionals within the Nicklaus Children's Hospital Research Institute (NCH-RI). This research position reports directly to the NCH-RI Clinical Trials Office (CTO) Manager but works closely with Lead CRA's, Study Team (PI, Sub-I's, CRC', etc.), NCH-RI departments and Nicklaus Children's Hospital (NCH) department administrators, and other clinical research professionals to help ensure that clinical research and related activities are performed in accordance with all applicable Federal regulations, NCH/NCH-RI applicable policies and sponsor policies/requirements. This research position will also coordinate team activities to ensure studies are carried out according to protocol, standard operating procedures (SOPs) and applicable guidelines and regulations.</p>
<p><b>
Job Specific Duties</b></p>
<ul>
<li>Coordinates team activities to ensure studies are carried out according to protocol, standard operating procedures (SOPs) applicable guidelines and regulations, and within budget.<br>
</li>
<li>Plans logistical activity for procedures as per protocol and ensures thorough resource planning. Identifies risks on study and ensures that actions are implemented to mitigate risks identified.<br>
</li>
<li>Ensures study specific training materials, documents, and records are prepared and delivered or coordinate training, dry runs, simulations and tests as required.<br>
</li>
<li>Implements, monitors, and assesses the need for training programs to maintain staff skill proficiency, including annual validation and currency of required certifications and licenses.<br>
</li>
<li>Provides protocol-specific training to research study team and NCH hospital/department staff directly involved with the care/treatment of research patients.<br>
</li>
<li>Works with NCH-RI staff to assist with developing, updating and implementing new Research Standard Operating Procedures, guidance documents, standard work and work flows (related to early phase research).<br>
</li>
<li>Coordinates, plans, implements, and evaluates nursing care to clinical trial study participants including but not limited to Adverse Event reporting and other support activities.<br>
</li>
<li>Provides nursing-related care to clinical trial study participants as outlined (and applicable) in the study protocol.<br>
</li>
<li>Coordinates and executes the collection, compilation, and analysis of clinical research data from studies conducted by PIs and study teams at Nicklaus Children&rsquo;s and the NCH-RI.<br>
</li>
<li>Interacts with patients and families to recruit study subjects and ensures compliance with protocol guidelines and requirements of regulatory agencies.<br>
</li>
<li>Attends and participates in investigator meetings, pre-study visits/initiation or coordinator meetings. Produces quality documentation, including completion of assessments within the specified time.<br>
</li>
<li>Coordinates and responsible for the collection of blood samples (PK samples and other), cultures, tissues and other specimens as required by protocol.<br>
</li>
<li>Prepares oral presentations/written reports/data requests describing progress, trends and appropriate recommendations or conclusions as it relates to research at Nicklaus.
<br>
</li><li>Communicates with the Sponsor or representatives regarding scheduling and facilitation of study monitor visits and facilitates communication between PI and Sponsor or Sponsor&rsquo;s Representatives.<br>
</li>
<li>Reviews protocol and provides study feasibility input to the NCH-RI Leadership and Study Start-up Team. Works with QI/QA team to ensure quality standards are being met and reports adverse events, protocol deviations.<br>
</li>
<li>Ensures compliance of general and study specific regulatory related processes with SOPs, FDA, NIH, and applicable regulations for the reporting of events to regulatory agencies.<br>
</li>
<li>Assists with the design and implementation of protocols, forms/questionnaires and the preparation of amendments to protocols and/or modifications to study design as appropriate for local, Investigator Initiated studies.</li>
</ul><h2 class="jobSectionHeader"><div><b>Qualifications</b></div></h2>
<p><b>Minimum Job Requirements</b></p>
<ul>
<li>BSN &ndash; Bachelors of Science in Nursing<br>
</li>
<li>RN Licensure within the State of Florida or Multi-State Enhanced Nursing License Compact (eNLC) &ndash; maintain active and in good standing throughout employment<br>
</li>
<li>IATA certification completion required within 3 months of hire date<br>
</li>
<li>American Heart Association ACLS (Advanced Cardiovascular Life Support) certification required within 2 months of hire<br>
</li>
<li>American Heart Association PALS (Pediatric Advanced Life Support) certification completion required within 6 months of hire<br>
</li>
<li>American Heart Association BLS - maintain active and in good standing throughout employment<br>
</li>
<li>2-4 years of professional research or healthcare experience<br>
</li>
<li>1-3 years of Phase 1 clinical research experience</li>
</ul>
<p><b>Knowledge, Skills, and Abilities</b></p>
<ul>
<li>ARNP highly preferred<br>
</li>
<li>Clinical research certification (e.g., CCRC, CCRP, CRA) preferred<br>
</li>
<li>Bilingual in English/Spanish preferred<br>
</li>
<li>Pediatric Nursing experience in an acute care setting preferred<br>
</li>
<li>Experience in neurology, neurosurgery, or oncology preferred<br>
</li>
<li>Experienced with database management tools and/or REDCap preferred<br>
</li>
<li>In-depth knowledge of Phase I clinical trials<br>
</li>
<li>Demonstrated knowledge of clinical research trial design and execution<br>
</li>
<li>Experienced with electronic medical record and clinical trial management software applications<br>
</li>
<li>Strong written and verbal communication skills<br>
</li>
<li>Excellent interpersonal skills<br>
</li>
<li>Excellent problem-solving skills<br>
</li>
<li>Effective organizational and project management skills<br>
</li>
<li>Ability to pay close attention to detail<br>
</li>
<li>Ability to comprehend professional and scientific journals<br>
</li>
<li>Ability to apply principles of logical and scientific thinking to a wide variety of intellectual and practical problems<br>
</li>
<li>Ability to establish and maintain effective working relationships with coworkers, managers and clients<br>
</li>
<li>Proficiency in Microsoft Office including Access, Word, Excel, Outlook, and PowerPoint<br>
</li>
<li>Willing to work off-hours depending on the study requirements</li></ul><br>
<div></div>
<br>
<br>
<h2 class="jobSectionHeader"><div><b>Job:</b></div></h2>
Research<br>
<h2 class="jobSectionHeader"><div><b>
Department:</b></div></h2>
RI - ADMINISTRATION-2100-380950<br>
<h2 class="jobSectionHeader"><div><b>
Job Status:</b></div></h2>
Full Time</div>

Clinical Research Nurse (Full Time, Days)

New Horizon Research Center

<p>A Recruiter position is available for a Clinical Research Site in the Kendall area. Our office is located near the Florida Turnpike / Bird Road exit. This is a part-time or full-time position, Monday-Friday from 9:00 AM or 7:00am to 3:30 PM.</p><p>A qualified candidate will be primarily be responsible for recruiting patients for current and upcoming clinical trials through the use of several tools. Upon notice of a selected study, a Clinical Research Recruiter must thoroughly understand the Protocol and Inclusion/Exclusion criteria of the study, determine the specific patient population which needs to be reached, and develop a recruitment plan with the help of the research team.</p><p>A Recruiter must be able perform several duties including but not limited to patient chart reviews for eligibility for any of the ongoing trials, database review for patients interested in clinical trials, prescreen patients and disposition unqualified candidates, schedule appointments for pre-qualified eligible candidates, maintain and update the patient database.</p><p>Requirements:<br/>- Must speak fluent Spanish and English<br/>- Friendly, positive attitude<br/>- Able to make phone calls throughout the day and find potential subjects<br/>- High School diploma<br/>- Experience in a recruiting position or telemarketing preferred<br/>- Medical terminology and clinical research experience preferred</p><p>Benefits:</p><ul><li>Commission (if agreed)</li></ul><p>If you feel like you would be a good fit for this position, please send your resume and we will reach out to you as soon as possible.</p><p>Job Types: Full-time, Part-time</p><p>Pay: $14.00 - $15.00 per hour</p><p>Experience:</p><ul><li>Recruiting: 1 year (Preferred)</li><li>Clinical Research: 1 year (Preferred)</li></ul><p>Language:</p><ul><li>Spanish (Preferred)</li></ul><p>Work Location: In person</p>

Clinical Research Patient Recruiter

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>
<div>
<p>Bring clinical research to your community on your schedule.</p>
<p>
Join the Future of Medicine program at Care Access, where we're bringing clinical research directly into local communities. As a <b>Clinical Research Assistant, PRN</b>, you'll play a key role in delivering life-changing research opportunities to participants but with the flexibility to work when and where it fits your life.</p>
</div>
<div><h3 class="jobSectionHeader"><b>How You'll Make An Impact</b></h3>
<div>
<p>In this event-based role, you'll:</p>
<ul>
<li>Support participant care and event operations, including phlebotomy, specimen handling, and documentation (paper or electronic).</li>
<li>Help set up and manage clinical research events to ensure they run smoothly, safely, and compliantly.</li>
<li>Be part of a mobile, mission-driven team advancing the future of healthcare access.</li>
</ul>
<p>This is not your traditional part-time job. It is flexible, purpose-driven work that fits your schedule. You'll opt into local events through our scheduling system and log actual hours worked after each one. Whether you want to pick up one event a month or several a week, you'll be helping make clinical research more accessible for everyone.</p>
<ul>
<li><b>Clinical &amp; Participant Care</b>: Perform venipuncture and capillary collections (as applicable) while maintaining aseptic technique and participant comfort. Handle and prepare biospecimens with care &mdash; labeling, processing, packaging, and transferring or shipping under proper chain-of-custody and temperature controls. Communicate clearly and promptly escalate any safety or quality concerns to onsite leadership.</li>
<li><b>Study Operations &amp; Data Management:</b> Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA). Follow established SOPs to help keep each event audit-ready and compliant.</li>
<li><b>Participant Experience &amp; Event Operations</b>: Welcome participants and help guide them through event flow. Set up and break down event stations, prepare kits and supplies, and maintain a safe, organized, and professional workspace that reflects Care Access' high standards.</li>
<li><b>Site &amp; Administrative Support</b>: Assist with light administrative and inventory tasks that keep the event running smoothly, from restocking supplies to supporting team coordination.</li>
</ul></div><h3 class="jobSectionHeader"><b>The Expertise Required</b></h3>
<div><ul><li>Clinical Expertise: Proficiency in venipuncture and specimen handling best practices, with strong attention to labeling, documentation, and chain-of-custody integrity.</li>
<li>Participant Care: Clear, compassionate communication skills and professionalism when engaging with participants and community partners.</li>
<li>Tech Readiness: Comfort using mobile apps and e-source tools for real-time logging and documentation.</li>
<li>Dependability &amp; Adaptability: Reliable, punctual, and team-oriented &mdash; able to thrive in dynamic event environments and work independently under event-day guidance.</li>
<li>Mission Mindset (optional addition): Motivated by bringing clinical research to local communities and expanding access to the future of medicine.</li>
</ul></div><div><h3 class="jobSectionHeader"><b>Certifications/Licenses, Education, and Experience</b></h3>
</div><div><ul><li>Experience: Minimum of 1 year performing phlebotomy and specimen handling activities.</li>
<li>Active, unrestricted RN license in the state of practice.</li>
<li>Active and unrestricted State Board of Nursing license in good standing</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 less than 10% travel requirements. Occasional planned travel may be required as part of the role.</li>
<li><b>Physical demands associated with this position Include</b>: The ability to use keyboards and other computer equipment.
<ul><li>Walking - 20%</li>
<li>Standing - 40%</li>
<li>Sitting - 30%</li>
<li>Lifting (up to 25 lbs, over 25lbs, and overhead) - 10%</li>
<li>Driving - &lt;10%</li>
<li>Exposure to bloodbourne pathegons - 50% (variable by station supporting)</li>
</ul>
</li></ul><p>The expected salary range for this role is $19.00 - $44.00 USD per hour for full time team members.</p>
</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>
<p>
Care Access is unable to sponsor work visas at this time.</p>
<p>
If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.com</p>
<p>
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>

Clinical Research Assistant, PRN

IQVIA

<div><div><div>Miami, United States of America | Full time | Home-based | R1530825</div><div><div><b>
Job available in additional locations</b></div></div></div><p></p><div><h2 class="jobSectionHeader"><b><br>
Our </b><b>MedTech Project Coordinator</b><b> will support the SDS organization within our Medication Management Solutions (MMS) Business Unit by managing field action deliverables in compliance with our quality and regulatory requirements. These deliverables include supporting customer remediation for recalls (where applicable), preparing the remediation team for new recalls, contacting customers to schedule remediation efforts, and support financial reporting for Dispensing field actions.
</b></h2><h2 class="jobSectionHeader"><b>The Project Coordinator will have solid project management skills, attention to detail as well as strong process execution and analytical skills. As part of a remote team, the Project Coordinator will be expected to set his/her own work direction and complete tasks with minimal supervision. The Project Coordinator will be responsible for managing customer remediation associated with Field Actions, as well as other small projects, as needed.</b></h2><h2 class="jobSectionHeader"><b>
Job Responsibilities:</b></h2><ul><li><b>Plan, coordinate, and execute small project, as assigned</b></li><li><b>Manage customer remediation for all applicable field actions</b></li><li><b>Monitor and report on field action budget, both expense to date and forecast</b></li><li><b>Attain required expertise in all databases that house product data for the platform (SAP, SharePoint)</b></li><li><b>Attain a thorough knowledge of all BD processes for field actions/recalls</b></li><li><b>Assist Senior Project Managers with preparing the remediation team for new field actions</b></li><li><b>Contact customers to schedule remediation projects with the customer, including building out detailed remediation project schedules with customers.</b></li></ul><h2 class="jobSectionHeader"><b>
Schedule:</b></h2><ul><li><h2 class="jobSectionHeader"><b>
[Insert overview of schedule/travel/needed availability here]</b></h2></li></ul><h2 class="jobSectionHeader"><b>
Required Qualifications:</b></h2><ul><li><b>HS Diploma minimum is required or higher degree is preferred.</b></li><li><b>Excellent writing skills and the ability to communicate accurately and concisely in English
</b></li><li><b>Ability to gain new technical skills quickly</b></li><li><b>Strong customer service skills and positive attitude</b></li><li><b>Ability to communicate complex technical concepts in layman&rsquo;s terms</b></li><li><b>Advanced skills with Microsoft Office products and Salesforce</b></li><li><b>Ability to meet tight deadlines and handle changing priorities</b></li></ul><h2 class="jobSectionHeader"><b>
 </b><b>Travel Requirement:
</b></h2><ul><li><b>This is a Remote; work from home position that requires Internet and the ability to be flexible in different time zones. The ideal candidate will be located physically on the East or West Coast working EST or PST.</b></li></ul><h2 class="jobSectionHeader"><b>
Preferred Qualifications:</b></h2><ul><li><b>Bachelor&rsquo;s Degree in Engineering, Technology, or Life Sciences preferred.</b></li><li><b>Two or more years of experience in project management, preferred</b></li><li><b>Prior experience within a regulated industry (e.g., medical device, pharma, automotive, aerospace), preferred</b></li><li><b>Managed/supported projects cross-functionally in an iterative, fast paced environment</b></li><li><b>Excellent verbal and written communication skills required</b></li><li><b>Strong analytical, problem-solving, and interpersonal skills
</b></li><li><b>High attention to detail while managing multiple complex deliverables and stakeholder groups required</b></li><li><b>Ability to learn quickly, deal with ambiguity, take initiative and achieve results required</b></li></ul><h2 class="jobSectionHeader"><b>
IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities.</b></h2><h2 class="jobSectionHeader"><b>
Benefits:</b></h2><ul><li><h2 class="jobSectionHeader"><b>
This position is not eligible for our Medical Benefits.</b></h2></li></ul><h2 class="jobSectionHeader"><b>
Vaccine/Immunization/Hospital Credentialing Requirement:</b><b> A required function of this job requires individuals to enter various healthcare facilities. Thus, upon selection, individuals must complete healthcare facility credentialing process. To obtain credentials, individuals must meet the immunization requirements specified by the facility. Individuals are typically required to have completed/up to date: Measles, Mumps &amp; Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria &amp; Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons. However, our client&rsquo;s requirements may supersede this.
</b></h2><h2 class="jobSectionHeader"><b>Note: This role is not eligible for visa sponsorship. Candidates must have authorization to work in the US without the need for sponsorship.</b></h2><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div><div>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div>
The potential base pay range for this role is $27-$29 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div></div><div></div>

MedTech Field Action Remediation Project Coordinator

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