clinical trial assistant

Planet Pharma

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  The Opportunity:
 </strong>
 Clinical Trial Assistant I
 <br/>
 <br/>
 This is a unique opportunity for an entry-level Clinical Operations Professional. As a Clinical Trial Assistant I (CTA I), you will be responsible for acting as an integral member of the clinical study team(s) and will be tasked to support the execution and management of clinical trials. Reporting into the Director (D) you will play a critical role in ensuring trials and studies align with all applicable standards.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Adhere to Clinical Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and International Conference on Harmonization (ICH) Guideline
  </li>
  <li>
   Assist in the development, review, distribution, and archiving of study specific documents and reports (e.g., essential documents, plans, training materials, study guides, manuals, etc.).
  </li>
  <li>
   Will lead the set-up and maintenance of the trial master files (TMF), if applicable, and work with the contract research organization (CRO) to audit and resolve discrepancies.
  </li>
  <li>
   Assist project team(s) with sample management and generate trial progress tracking systems.
  </li>
  <li>
   Tracks and prepare study-specific information utilizing databases, trackers, and other study tools.
  </li>
  <li>
   Assist in the preparation of meeting materials, including scheduling, developing agendas, and minute-taking for internal study team meetings.
  </li>
  <li>
   Gather investigator and site information to support study start-up, maintenance, and close-out activities.
  </li>
  <li>
   Assist in contacting investigator sites to provide study specific information.
  </li>
  <li>
   May serve as the point of contact for study sites and study monitors for clinical supplies, document collection, and preparation for close-out visits.
  </li>
  <li>
   Work with cross-functional study teams and vendors to assist in the coordination of clinical trial activities.
  </li>
  <li>
   Liaise with Clinical Supply and other cross functional teams with processing shipments, returns, and assists with in-house drug, specimen, and ancillary supply reconciliation.
  </li>
  <li>
   Support other clinical operations activities as appropriate.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Required Skills, Experience And Education
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in biological sciences or health-related field required.
  </li>
  <li>
   1-3 years relevant experience in the pharmaceutical or biotech industry, preferably in Clinical Operations or Clinical Research related experience.
  </li>
  <li>
   Has knowledge of GCP ICH Guidelines .
  </li>
  <li>
   Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.
  </li>
  <li>
   Excellent written/verbal communication and interpersonal skills.
  </li>
  <li>
   Demonstrate proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint); MS Project and/or Smartsheet a plus.
  </li>
  <li>
   Travel may be required (~10%).
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Preferred Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Has familiarity working with vendor systems/portals (e.g., eTMF, EDC, IRT, CTMS).
  </li>
  <li>
   Oncology experience preferred.
  </li>
  <li>
   Attention to detail.
   <br/>
  </li>
 </ul>
 The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
 <br/>
</div>


Clinical Trial Assistant I - CTA

Arizona Center for Cancer Care

<div>
 <strong>
  Description
  <br/>
  <br/>
 </strong>
 <strong>
  Job Summary
  <br/>
  <br/>
 </strong>
 The Clinical Research Assistant provides administrative and operational support for clinical research studies conducted by the organization. This position assists with document management, regulatory submissions, scheduling, and other activities essential to the coordination and execution of clinical trials. Under the supervision of the clinical program manager, the Clinical Research Assistant ensures that study-related documentation is accurate, organized, and compliant with applicable regulatory standards. The role requires strong attention to detail, effective communication skills, and the ability to perform routine support tasks within established guidelines. This position supports Clinical Research Coordinators (CRCs), investigators, and the broader research team to facilitate efficient trial conduct.
 <br/>
 <br/>
 <strong>
  Duties And Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Assists with study start-up activities, including the collection, organization, and preparation of study-related documents.
  </li>
  <li>
   Assists in maintaining regulatory binders and trial master files in compliance with sponsor and institutional requirements.
  </li>
  <li>
   Schedules participant visits and coordinates appointment logistics with clinical staff and investigators.
  </li>
  <li>
   Assists in preparing and submitting Institutional Review Board (IRB) documents, amendments, and continuing reviews under supervision.
  </li>
  <li>
   Knowledge and understanding of the laws, regulations, ICH/GCP guidelines, and ethical principles that guide the practice of clinical research.
  </li>
  <li>
   Knowledge and application of all privacy and safety standards as they relate to job responsibilities, human research subjects, staff, and the general operation of the facility.
  </li>
  <li>
   Tracks participant enrollment, screening outcomes, and visit completion to support study progress.
  </li>
  <li>
   Assists in maintaining study-related logs and trackers, such as delegation logs, screening logs, and training logs.
  </li>
  <li>
   Enters data into sponsor portals, electronic data capture (EDC) systems, and internal databases, ensuring accuracy and timeliness.
  </li>
  <li>
   Provides logistical and administrative support during site initiation visits (SIVs), monitoring visits, audits, and inspections.
  </li>
  <li>
   Assist in the receipt, inventory, and shipment of study supplies and laboratory kits.
  </li>
  <li>
   Supports Clinical Research Coordinators (CRCs) and investigators in daily clinical trial operations, following established procedures and protocols
  </li>
  <li>
   Other duties and responsibilities as delegated by clinical program manager.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Direct Reports
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   NA
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  EEO Statement
  <br/>
  <br/>
 </strong>
 Arizona Center for Cancer Care provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
 <br/>
 <br/>
 This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
 <br/>
 <br/>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <strong>
  Qualifications/Education Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   General Education Diploma or higher required, associate or bachelor&rsquo;s degree in healthcare, life sciences, or a related field preferred.
  </li>
  <li>
   Prior experience (approximately one year) in a clinical research or healthcare setting preferred.
  </li>
  <li>
   Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
  </li>
  <li>
   Must complete GCP (Good Clinical Practice) training and hold a certificate of completion within 30 days of hire (required).
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Licensure and Certifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Current CPR
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Working conditions
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Works in an office or clinical setting.
  </li>
  <li>
   Exposed to moderate noise levels.
  </li>
  <li>
   Emphasizes collaboration with various stakeholders.
  </li>
  <li>
   Necessitates effective communication and teamwork.
  </li>
  <li>
   Functions in a fast-paced environment.
  </li>
  <li>
   May require flexibility in working hours.
  </li>
  <li>
   Requires adherence to safety protocols and compliance with healthcare regulations.
  </li>
  <li>
   Valid driver&rsquo;s license and reliable transportation for travel between locations.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Physical Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Must be able to lift 25 lbs.
  </li>
  <li>
   Must be able to sit, stand and walk for extended periods of time
  </li>
  <li>
   Must be able to bend, kneel, crawl and twist as needed
  </li>
  <li>
   Must be able to see, hear, type, and speak
  </li>
  <li>
   Must be able to reach and pull
  </li>
 </ul>
</div>


Clinical Research Assistant

Covenant Metabolic Specialists

<p><b>Covenant Metabolic Specialists (CMS)</b> is a leading medical practice dedicated to the clinical management and education of metabolic diseases, with a special focus on fatty liver disease and obesity. Founded in October 2019, CMS has rapidly emerged as a global leader in treating liver diseases through groundbreaking clinical care, research therapies and innovative treatments that are not available elsewhere. With over 200 years of combined clinical experience, our expert medical team delivers state-of-the-art therapies and lifestyle guidance to improve metabolic health for patients.</p><p>Covenant is seeking a <b>Research Assistant</b> for our facility located in Ft Myers, Florida. This position will assist with our clinical operations by taking patient vital signs and other measurements, performing FibroScans, completing EDC entries, and other duties as needed.</p><p><b>Responsibilities</b></p><ul><li>Use phlebotomy skills to collect lab specimens from patients.</li><li>Collect vital signs, weight, height, body measurements, EKG, etc. according to study requirements and documents appropriately in source document.</li><li>Upload EKGs to Sponsor specific portals, answer queries as needed, and reorder supplies.</li><li>Perform FibroScans on patients.</li><li>Restock patients&rsquo; rooms at the end of each week.</li><li>Enter data into EDC and answers queries as assigned.</li><li>Print and file study specific or patient specific documents.</li><li>Print labs daily from DocuSign as assigned and provide reports to the appropriate Clinical Research Coordinator (CRC).</li><li>Assist in the Lab.</li><li>Update or load documents into the Company&rsquo;s clinical trial management system as needed.</li><li>Update excel sheets as requested by CRCs.</li><li>Request medical records and follow up as needed.</li><li>Clean exam rooms.</li><li>Help CRCs with any other tasks as needed.</li><li>Other duties as assigned.</li></ul><p><b>Education and Experience</b></p><ul><li>Associate's degree in a related field (such as Medical Assisting, Nursing, Life Sciences, or Healthcare Administration), preferred.</li><li>Relevant certificates (e.g., Certified Medical Assistant, Emergency Medical Technician) or significant coursework in a related field.</li><li>1-2 years of experience in a clinical setting or in clinical research preferred.</li><li>Experience performing phlebotomy, EKGs, and other diagnostic procedures is desirable.</li><li>Experience with a Clinical Trial Management System (CTMS) is a plus.</li><li>Experience with specific technology, such as a FibroScan machine, is desirable</li></ul><p><b>Other Skills</b></p><ul><li>Proficient with Electronic Data Capture (EDC) or Electronic Medical Records (EMR) systems.</li><li>Basic office software (e.g., Microsoft Office Suite, especially Excel).</li><li>Excellent verbal and written communication skills to effectively interact with patients, staff, and sponsors.</li><li>Strong organizational and multitasking skills, with the ability to prioritize tasks in a fast-paced environment.</li><li>Bilingual (English/Spanish) preferred.</li><li>Certifications in CPR, Basic Life Support (BLS), or other relevant healthcare certifications</li><li>Ability to meticulously follow study protocols, document patient data accurately, and manage confidential information.</li><li>Demonstrated ability to work collaboratively in a team and support colleagues in achieving team goals.</li><li>Openness to learning new skills and adapting to changing procedures and protocols.</li><li>Understanding of patient privacy laws (HIPAA) and ethical considerations in clinical research.</li><li>Willingness to undergo background checks and necessary training for compliance with healthcare regulations.</li></ul><p><i>Covenant Metabolic Specialists, LLC is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, genetics, disability, age, veteran status, or any other characteristic protected by law.</i></p><p>Pay: $40,000.00 - $50,000.00 per year</p><p>Benefits:</p><ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Education:</p><ul><li>Associate (Preferred)</li></ul><p>Experience:</p><ul><li>nursing or medical assistant: 1 year (Preferred)</li></ul><p>Work Location: In person</p>

Adams Clinical

<div><p><b>Join Us in Shaping the Future of Clinical Research</b><br>
Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values&mdash;Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration&mdash;we create an environment where meaningful work drives meaningful change.</p>
<p>
At Adams Clinical, you'll find:</p>
<ul>
<li>A culture of respect, transparency, and continuous improvement</li>
<li>Opportunities for professional growth and learning</li>
<li>A team dedicated to improving lives through innovation and integrity</li>
</ul>
<p>If you're passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we'd love to have you on our team.</p>
<p><b>
Overview
</b><br>
Adams Clinical is a rapidly growing research site network specializing focused on late phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions, supporting both inpatient and outpatient studies. Adams Clinical Site Network has locations in Watertown, MA; Boston, MA; Harlem, NY; Bronx, NY; Philadelphia, PA; and Dallas, TX.</p>
<p>
We are seeking entry-level applicants for the Clinical Research Assistant role at our Dallas location (Zipcode: 75115). This role is ideal for entry-level candidates interested in learning clinical research operations, contributing to study execution, and developing foundational skills in patient interaction, data management, and regulatory compliance.</p>
<p>
The Clinical Research Assistant (RA) provides foundational support in the conduct of clinical trials at the site level. Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with operational, administrative, and participant-facing tasks to ensure studies run smoothly and in accordance with ICH-GCP, regulatory requirements, and protocol guidelines. This role is an ideal entry point for individuals seeking to gain hands-on experience in clinical research.</p>
<p><b>
Key Responsibilities
</b></p><ul><li>Support study start-up activities, including supply inventory, document preparation, and site initiation readiness.</li>
<li>Assist with participant screening workflows as delegated, including scheduling screening visits and collecting basic information such as demographics, medical history, and other study-relevant details to support eligibility assessment.</li>
<li>Schedule and prepare for participant visits, including source prep, lab kits, and CRFs.</li>
<li>Serve as a participant liaison&mdash;confirm appointments, coordinate transportation, and maintain ongoing communication.</li>
<li>Escort and assist participants during on-site visits; perform vital signs, ECGs, and specimen collection/processing as trained.</li>
<li>Complete accurate, ALCOA+-compliant source documentation for delegated procedures.</li>
<li>Perform data entry into EDC systems and assist with query resolution.</li>
<li>Maintain study binders, charts, and logs; support supply management.</li>
<li>Ensure accurate capture and upload of paper source documents into eSource systems in accordance with site processes and regulatory requirements, supporting long-term retention and audit readiness.</li>
<li>Obtain, track, and manage medical releases, as well as medical and pharmacy records from external providers as needed, in accordance with site SOPs and protocol requirements.</li>
<li>Support CRCs during monitoring visits and assist with preparing documentation and materials to ensure audit and inspection readiness.</li>
<li>Assist with investigational product (IP) accountability tasks as needed and where applicable, gaining exposure to IP handling, tracking, and documentation under the direct supervision of CRC staff, while ensuring adherence to protocol and site SOPs.</li>
<li>Develop proficiency in site SOPs, institutional policies, and GCP requirements to build foundational knowledge in compliant research practices.</li>
<li>Assist in collecting and entering study data into trackers, logs, and EDC systems, focusing on accurate and timely data collection.</li>
<li>Support CRCs in maintaining accurate records and updating study metrics.</li>
</ul>
<p><b>Qualifications
</b></p><ul><li>Minimum requirement of a high school diploma or GED equivalent; Bachelor's degree preferred.</li>
<li>No prior clinical research experience is necessary; training will be provided. Basic understanding of clinical research principles is a plus.</li>
<li>Strong attention to detail, organization, and communication skills.</li>
<li>Proficiency in Microsoft Office.</li>
<li>Willingness to perform phlebotomy and clinical procedures as trained.</li></ul><br>
<p></p>
<p><b>
Pay</b>: $40,000 - 48,000 per year</p>
<div><b>
Benefits</b>:</div>
<ul><li>401(k) matching</li>
<li> Medical, Dental &amp;Vision insurance</li>
<li> Employee assistance program</li>
<li> Flexible spending account</li>
<li> Health insurance</li>
<li> Health savings account</li>
<li> Life insurance</li>
<li> Paid time off</li>
<li> Parental leave</li>
<li> Professional development assistance</li></ul><br>
<p></p>
<p>
Adams Clinical is committed to being an equal opportunity and affirmative action employer. We focus on hiring and nurturing top talent. All employment decisions, including recruitment, hiring, promotion, compensation, transfer, training, discipline, and termination, are made based on the candidate's or employee's qualifications relevant to the position. These decisions are made without regard to age, sex, sexual orientation, gender identity or expression, genetic information, race, color, creed, religion, ethnicity, national origin, citizenship, disability, marital status, military status, pregnancy, or any other legally protected status.</p>
<p>
In compliance with federal law, all individuals hired must, as a condition of employment, provide documentation verifying their identity and authorization to work in the United States and complete Form I-9 within the required timeframe. Adams Clinical participates in E-Verify to confirm employment eligibility.</p></div>

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>

Evolution Research Group

<div><p><b>About us:</b></p><p>
ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug development. With 20 wholly owned clinical sites and 4 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 400+ in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep disorders, addictions, Acute and Chronic Pain, diabetes, and other illnesses as well as normal healthy volunteers who participate in trials for the advancement of medicine. With access to over 32 million patients/subjects and 5000 + completed trials, ERG continues to grow its capabilities and expand into indications where there are tremendous unmet medical needs in the United States and globally.</p><p><b>
Job Description:</b></p><p>
The Patient Care Technician assists with the conduct of clinical trials through overseeing the care of clinical trial subjects while housed on unit. Assist with the collection of biological samples, perform venipuncture, electrocardiograms, tube labeling, sample processing, documenting in subject charts, and other related tasks in accordance with the doctor&rsquo;s written orders. In executing these responsibilities, the Patient Care Technician is guided by Good Clinical Practices (GCP), International Conference on Harmonization (ICH) guidelines, Health Insurance Portability and Accountability Act (HIPAA) and company standard operating procedures and policies.</p><p><b>
This role will be for nights/weekends, but flexibility is preferred to cover shifts if needed.</b></p><p><b>
Responsibilities:</b></p><ul><li>
Perform regular safety and status checks on clinical trial subjects housed on unit as determined by physician orders.</li><li>
Perform appropriate research protocol procedures as delegated which may include but are not limited to vital signs, blood collection and processing, ECGs, and point of care laboratory tests.</li><li>
Perform basic lab procedures as delegated including but not limited to preparation of specimen tubes and labels, blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-ups.</li><li>
Ensure that biological specimens are disposed of appropriately.</li><li>
Maintain a clean, safe work environment for both fellow employees and clinical trial subjects.</li><li>
Engage the clinical trial subjects in group activities or one-on-one activities while housed on unit.</li><li>
Assure subjects have linens, toiletry items, and other sundries needed while the subject is housed on the unit.</li><li>
Serve meals and provide snacks to clinical trial subjects while subjects are housed on unit.</li><li>
Study, learn and comply with ERG site standard operating procedures, and other policies, practices and regulations where applicable.</li><li>
Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG&rsquo;s objectives.</li></ul><p><b>
Skills and Qualifications:</b></p><ul><li><b>
Education and experience</b><ul><li>
High school Degree or equivalent</li><li>
One (1) year of clinical experience preferred.</li><li>
CPR Certification required.</li><li>
Phlebotomy certification (national) preferred.</li><li>
Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines.</li><li>
Able to communicate with providers, co-workers, and others in a collaborative and courteous manner.</li><li>
Knowledgeable in medical terminology so as to communicate with physician office and staff.</li><li>
Able to initiate or modify behavior to achieve desired outcomes despite environmental factors, priorities, or problems that might not be well defined or that are subject to change.</li></ul></li><li><b>
Requirements</b><ul><li>
Ability to work independently and as a team player.</li><li>
Ability to organize and prioritize within a changing environment.</li><li>
Use safety/universal precautions to protect self, subjects and staff.</li><li>
Able to appropriately implement protocol and regulatory requirements in study conduct.</li><li>
Proficient in venipuncture, centrifugation, sample storage and performing electrocardiogram.</li><li>
Excellent documentation practices</li><li>
Good organizational and interpersonal skills</li><li>
Attentive to detail, good initiative and able to work with changing priorities.</li></ul></li></ul></div>

Patient Care Technician (PCT)- FT Nights

UC Irvine Health

<div>Overview:
<div>
Founded in 1965, <b>UC Irvine</b> is a member of the prestigious Association of American Universities and is ranked among the nation&rsquo;s top 10 public universities by U.S. News &amp; World Report. The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs. It&rsquo;s located in one of the world&rsquo;s safest and most economically vibrant communities and is Orange County&rsquo;s second-largest employer, contributing $7 billion annually to the local economy and $8 billion statewide.<br>
<br>
To learn more about UC Irvine, visit www.uci.edu.</div><div></div><div><br>
The UCI Alpha Clinic provides the necessary infrastructure, clinical and operational expertise to accelerate cell and gene therapies at UCI and throughout our communities. To accomplish our mission, we are working to achieve the following five goals:
<br>
1. Creating a Center of Excellence for cell-based therapeutics that addresses the unique challenges of testing and delivering novel cell therapies by integrating and building upon the extensive experience and many strengths of UCI and our partners.
<br>
2. Building interactive and highly trained teams and electronic data sharing systems to accelerate and translate discovery to improve human health.
<br>
3. Transforming the delivery of cell and gene therapeutics through our proven Good Manufacturing Practice (GMP) manufacturing.
<br>
4. Advancing, expanding, and integrating educational opportunities to inform patients, families, communities, and clinicians of the full range of scientifically sound and medically appropriate, regulated cell and gene therapy clinical trials while providing objective information about potentially dangerous and unproven procedures.
<br>
5. Serving as a regional, national and international resource for evidence-based best practices in cell and gene treatments.<br>
</div><div></div><br>
<br>
Responsibilities:
<div>
Under the direction of the Principal Investigator and the Clinical Research Coordinator, the incumbent will assist in the setup, execution, and data collection of clinical studies. The incumbent is expected to collect medical data from participants. The incumbent will also be responsible for recruitment, assisting in performing informed consent, and interview of study subjects if needed. Must ensure accuracy and completeness of patient files in accordance with protocol requirements and compile research data for input into patient database and various reports. In addition, this individual must accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies.</div>
Qualifications:
<div><b>
Required:</b></div><ul><li>
Willingness to work as a supportive, cooperative member of an interdisciplinary team</li><li>
Demonstrated problem solving capabilities to resolve concerns that arise unexpectedly</li><li>
Demonstrated ability to research, properly evaluate information, and prepare concise, well organized reports, summaries, and correspondence</li><li>
Demonstrated ability to organize and prioritize a complex and dynamic workload</li><li>
Ability to multitask and meet deadlines, despite interruptions</li><li>
Ability to independently exercise discretion and sound judgment</li><li>
Ability to work collegially and cooperatively in a small office and to establish and maintain cooperative working relationships</li><li>
Demonstrated skill in interacting with persons of various social, cultural, economic and educational backgrounds</li><li>
Ability to prioritize assignments and achieve high productivity/quality with short time frames, under rigid deadlines, and /or in environments with frequent workload changes and competing demands</li><li>
Skill in working independently, taking initiative and following through on assignments</li><li>
Ability to think critically, compiles data from various sources, analyze data, and prepare reports.</li><li>
Strong attention to detail</li><li>
HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities.</li><li>
Bachelor's degree and 1-3 years of experience or equivalent experience.</li></ul><div><b><br>
Preferred:</b></div><ul><li>
Excellent communication skills: Demonstrated high-level communication skills to convey information in a clear and concise way, synthesizing information and presenting it to others</li><li>
Strong and proven organization and administrative skills: scheduling, data/file management, word processing (Microsoft Word), spreadsheets (EXCEL), copying, phone skills, data entry</li><li>
Access to transportation to off-site research locations</li></ul><div><b><br>
Special Conditions:</b></div><ul><li>
Must be willing to occasionally work early or late hours, or on weekends as necessary per clinical study protocols.</li></ul><div></div><div><b><br>
Total Rewards</b></div><div>
In addition to the salary range listed below, we offer a wealth of benefits to make working at UCI even more rewarding. These benefits may include medical insurance, sick and vacation time, retirement savings plans, and access to a number of discounts and perks. Please utilize the links listed here to learn more about our compensation practices and benefits.</div><div><b><br>
Conditions of Employment:</b></div><div>
The University of California, Irvine (UCI) seeks to provide a safe and healthy environment for the entire UCI community. As part of this commitment, all applicants who accept an offer of employment must comply with the following conditions of employment:</div><ul><li>
Background Check and Live Scan</li><li>
Employment Misconduct*</li><li>
Legal Right to work in the United States</li><li>
Vaccination Policies</li><li>
Smoking and Tobacco Policy</li><li>
Drug Free Environment</li><li><i>Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.
</i></li></ul><div>The following additional conditions may apply, some of which are dependent upon business unit or job specific requirements.</div><ul><li>
California Child Abuse and Neglect Reporting Act</li><li>
E-Verify</li><li>
Pre-Placement Health Evaluation</li></ul><div>
Details of each policy may be reviewed by visiting the following page - https://hr.uci.edu/new-hire/conditions-of-employment.php</div><div><b><br>
Closing Statement:</b>
</div><div>The University of California is 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, age, protected veteran status, or other protected categories covered by the UC Anti-Discrimination Policy.
<br>
<br>
We are committed to attracting and retaining a diverse workforce along with honoring unique experiences, perspectives, and identities. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable, and welcoming.
<br>
<br>
UCI provides reasonable accommodations for applicants with disabilities upon request. For more information, please contact Human Resources at (949) 824-0500 or eec@uci.edu.</div></div>

Assistant Clinical Research Coordinator

Search 6927+ Clinical trial assistant jobs near you this June. New roles added regularly across leading industries. Apply today.

6927 clinical trial assistant jobs Near Me

Clinical Trial Assistant I - CTA

Clinical Research Assistant

Clinical Research Assistant

Clinical Research Assistant

Clinical Research Assistant

Patient Care Technician (PCT)- FT Nights

Assistant Clinical Research Coordinator