clinical trials nurse

Penn State Health

<div><div>Penn State Health - Hershey Medical Center
Location: US:PA: Hershey
 
Work Type: Full Time
 
FTE: 1.00
 
Shift: Day
 
Hours: 8:00a - 4:30p
 
Recruiter Contact: Denisse M. Rosado at drosado1@pennstatehealth.psu.edu
SUMMARY OF POSITION:
Under the direction of the Cancer Center Clinical Trials Office Administrative Director, the Clinical Research Cancer nurse will lead day-to-day operations of clinical research studies conducted by principal investigator(s) at Penn State Cancer Institute Clinical Trials Office. The RN Clinical Research nurse will perform a variety of duties involved in the collection, compilation, documentation, and analysis of clinical research data; introduced to the navigating process in the clinical research environment.
MINIMUM QUALIFICATION(S):
<ul><li>Currently licensed to practice as a Registered Nurse by state of employment or holds a multistate RN license through the interstate Nurse Licensure Compact or Associate Degree in Nursing. With Associates Degree, required to enroll to BSN within three (3) years of their start date Oncology clinical nursing experience at least two (2) years</li>
</ul>PREFERRED QUALIFICATION(S):
<ul><li>Bachelor's of Nursing Degree one (1) year Clinical Trials Research experience</li>
</ul>WHY PENN STATE HEALTH?
Penn State Health offers exceptional opportunities to learn and grow, exposure to a wide patient population, and the ability to provide individualized, innovative, and specialized care to patients in the community.
Penn State Health offers an exceptional benefits package including medical, dental and vision with no waiting period as well as a Total Rewards Program that highlights a few of the many additional offerings below:
<ul><li>Be Well with Employee Wellness Programs, and Fitness Discounts (University Fitness Center, Peloton).</li>
<li>Be Balanced with Generous Paid Time Off, Personal Time, and Paid Parental Leave.</li>
<li>Be Secured with Retirement, Extended Illness Bank, Life Insurance, and Identity Theft Protection.</li>
<li>Be Rewarded with Competitive Pay, Tuition Reimbursement, and PAWS UP employee recognition program.</li>
<li>Be Supported by the HR Solution Center, Learning and Organizational Development and Virtual Benefits Orientation, Employee Exclusive Concierge Service for scheduling.</li>
</ul>WHY PENN STATE HEALTH MILTON HERSHEY MEDICAL CENTER?
Penn State Hershey Medical Center is Central Pennsylvania&rsquo;s only Academic Medical Center, Level 1 Regional Adult and Pediatric Trauma Center, and Tertiary Care Provider. As a four-time Magnet-designated hospital, Hershey Medical Center values the hard work and dedication that our employees exhibit every day. Through our core values of Respect, Integrity, Teamwork, and Excellence, our employees are a team committed to compassionate care for our diverse patient population, our community and each other. As a valued team member, we promote continued professional development, specialty certification, continuing education, and career growth.
YOU TAKE CARE OF THEM. WE&rsquo;LL TAKE CARE OF YOU. State-of-the-art equipment, endless learning, and a culture of excellence &ndash; that&rsquo;s Penn State Health. But what makes our healthcare award-winning? That&rsquo;s all you.
This job posting is a general outline of duties performed and is not to be misconstrued as encompassing all duties performed within the position. Eligibility for shift differential pay based on the terms outlined in company policy or union contract. All individuals (including current employees) selected for a position will undergo a background check appropriate for the position's responsibilities.
Penn State Health is an Equal Opportunity Employer and does not discriminate on the basis of any protected class including disability or veteran status. Penn State Health&rsquo;s policies and objectives are in direct compliance with all federal and state constitutional provisions, laws, regulations, guidelines, and executive orders that prohibit or outlaw discrimination.
 Union: Non Bargained</div></div><div></div>

RN Registered Nurse Clinical Research Cancer - Hem Onc Clin Trials

CommonSpirit Health

<div>
 *Job Summary and Responsibilities*
 
 
 As our Clinician Research RN, you will leverage your clinical nursing expertise to critically support and execute clinical research studies, ensuring the highest standards of participant care, data integrity, and compliance within designated research areas.
 
 
 Every day you will actively participate in the lifecycle of clinical trials, which includes identifying and screening potential study participants, providing in-depth education about research protocols, and carefully monitoring participant well-being. Your responsibilities will involve performing essential clinical assessments, accurately collecting and documenting study data, and vigilantly observing for adverse events.
 
 
 To be successful in this role, you will exhibit excellent organizational capabilities, meticulous attention to detail, and a commitment to ethical conduct in research. Your ability to effectively communicate with participants and collaborate within a research team will be key to contributing to meaningful research outcomes.
 
 
 <ul>
 <li>
 Demonstrates current knowledge of federal and state regulations, guidelines, and policies governing the conduct of clinical trials.
 </li>
 <li>
 Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB)
 </li>
 <li>
 Complies with licensure, contractual, protocol and policy requirements
 </li>
 <li>
 Directs intradepartmental and external resource activities relating to assigned studies
 </li>
 <li>
 Assists in the review and development of proposed study budgets
 </li>
 <li>
 Ensures compliance with all study billing process requirements
 
 
 </li>
 </ul>
 *Job Requirements**Required*
 
 
 <ul>
 <li>
 Bachelor's degree in related field
 </li>
 <li>
 One (1) year of clinical RN experience
 </li>
 <li>
 Licensed Registered Nurse: AZ
 
 
 </li>
 </ul>
 *Preferred*
 
 
 <ul>
 <li>
 Master's degree in related field
 </li>
 <li>
 One (1) year of RN experience within clinical research
 
 
 </li>
 </ul>
 Where You'll Work
 
 
 Hello Humankindness: Join a Legacy of Healing at Saint Joseph&rsquo;s Hospital and Medical Center (SJHMC) Ready to make a real difference? Join SJHMC in Phoenix AZ., a 571-bed nonprofit founded by the Sisters of Mercy over 125 years ago. We're more than a hospital; we're a global destination for life-changing care, embracing patients with humankindness. Here, your calling will flourish. We're not just a workplace; we're a community dedicated to a mission of service.
 
 
 
 Leaders In Specialized Care
 
 
 
 <ul>
 <li>
 Barrow Neurological Institute (BNI): A world-renowned center for groundbreaking neurological research and innovative treatments.
 </li>
 <li>
 Norton Thoracic Institute (NTI): A national leader in advanced thoracic care with pioneering surgical techniques.
 </li>
 <li>
 Level I Trauma Center: One of Arizona's busiest ERs, providing immediate, comprehensive care for critically injured patients 24/7.
 
 
 </li>
 </ul>
 Why SJHMC?
 
 
 <ul>
 <li>
 Culture of Excellence &amp; Well-being: We care for our people, fostering professional and personal growth.
 </li>
 <li>
 Community &amp; Collaboration: Be part of a network committed to global health and well-being.
 </li>
 <li>
 Join a Legacy, Shape a Future: Over 20% of our patients travel internationally for our specialized care.
 
 
 </li>
 </ul>
 This is an invitation to join a family of dedicated professionals at the forefront of medical innovation, united by the power of humankindness.
 
 
 *Pay Range*
 
 
 $32.38 - $48.17 /hour
</div>

Clinical Research Nurse

Sunrise Research Institute

About 3Sync Research3Sync Research is a growing clinical research organization dedicated to advancing medicine through high-quality clinical trials. We partner with leading pharmaceutical companies, CROs, physicians, and healthcare professionals to bring innovative treatment options to diverse patient populations.Our office conducts outpatient clinical research across multiple therapeutic areas, including primary care, pediatrics, asthma/allergy, diabetes, endocrinology, infectious disease, vaccines, and other adult and pediatric studies. We are looking for a strong, experienced provider who is comfortable working directly with patients and supporting clinical trial oversight.Position OverviewWe are seeking a bilingual APRN / Nurse Practitioner to join our clinical research team as a Clinical Trial Sub-Investigator. This is an excellent opportunity for an experienced provider who is detail-oriented, and comfortable working with both adults and children.In this role, you will work closely with the Principal Investigator, site directors, operations leadership, recruitment team, clinical research coordinators, sponsors, CROs, and regulatory teams to support the safe and compliant conduct of clinical trials. The Sub-Investigator will conduct patient screening, eligibility review, physical exams, safety assessments, protocol compliance, clinical documentation, enrollment support, participant retention, and contribute to overall site performance.Key ResponsibilitiesAssist the Principal Investigator in the oversight and execution of clinical trialsConduct patient screening, enrollment, and ongoing study visit assessmentsPerform physical exams and clinical evaluations for adult and pediatric participantsReview medical history, medications, labs, vitals, inclusion/exclusion criteria, and study eligibilityMonitor participant safety throughout the studyIdentify, assess, document, and report adverse events and clinical concernsPerform or assist with blood draws, vital signs, and other protocol-required proceduresReview informed consent forms, source documents, lab reports, CRFs, and study records for accuracy and completenessSupport protocol compliance, data collection, and audit readinessCommunicate professionally with participants, parents/guardians, study staff, sponsors, CROs, and regulatory teamsSupervise and support clinical research staff when neededCollaborate closely with site directors, operations leadership, recruitment teams, coordinators, and the Principal Investigator to support successful study outcomes, strong enrollment, participant retention, protocol compliance, and overall site performanceServe as a team player within a fast-paced clinical research environment, helping ensure smooth communication between clinical, operational, and recruitment staffEnsure study activities are conducted in compliance with FDA regulations, ICH-GCP guidelines, HIPAA, protocol requirements, and site SOPsRequirementsActive and unrestricted License/Certification- Florida APRN / Nurse Practitioner License requiredMinimum of 5+ years of experience as an APRN / Nurse Practitioner(Bilingual English/Spanish )Must be comfortable working with both adult and pediatric patientsStrong clinical assessment, documentation, and decision-making skillsExperience with patient evaluation, medical history review, medication review, labs, and clinical proceduresPhlebotomy or blood sampling experience preferredFamiliarity with medical terminology, clinical documentation, and outpatient patient careAbility to work independently while collaborating with the Principal Investigator and research teamStrong attention to detail and ability to work in a fast-paced clinical environmentProfessional, dependable, organized, proactive, and team-orientedGCP certification preferred; training can be provided if neededAvailability to work occasional weekends as needed based on study requirementsPreferred ExperienceFamily MedicinePrimary CarePediatricsInternal MedicineUrgent CareAllergy / AsthmaEndocrinologyDiabetes CareInfectious DiseaseVaccinesClinical ResearchClinical Trial Sub-Investigator experienceIdeal CandidateThe ideal candidate is an experienced, bilingual provider who is comfortable making clinical assessments, asking the right questions, identifying safety concerns, and working with a wide range of patients. We are looking for someone who is confident in their clinical judgment, reliable, personable, and able to take ownership of patient evaluations in a research setting.This person should also be a strong team player who works well with site directors, operations leadership, recruitment teams, coordinators, and the Principal Investigator to help drive successful study outcomes, strong enrollment, participant retention, protocol compliance, and overall site performance.Why Join 3Sync ResearchOpportunity to work on innovative clinical trials and emerging treatmentsAdult and pediatric patient populationGrowing research organization with expanding study opportunitiesCollaborative team environmentExposure to multiple therapeutic areasFlexible schedule availableMeaningful role in supporting patient safety and advancing clinical researchBenefits:Health insuranceDental insuranceVision insurancePaid time offPay: $88,117.74 - $106,120.29 per yearBenefits:<ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Bilingual APRN / Nurse Practitioner

Civia Health

<div>
 
 Job Type:
 
 Full-time, on-site
 
 
 
 Reports to:
 
 Senior Manager, Site Management
 
 
 
 Join Us at Civia Health
 
 
 
 We&rsquo;re looking for a compassionate and experienced Nurse Practitioner to support our clinical research team in conducting Phase 2&ndash;4 trials, with a particular focus on metabolic conditions and GLP-1 therapies. If you thrive in a collaborative, patient-centered environment and are passionate about research-driven care, we&rsquo;d love to meet you.
 
 
 At Civia Health, you're not just taking a job: You're joining a mission to transform the way clinical research is done. Our purpose is bold: to bring clinical trials front and center in your community, make them accessible to everyday people, and empower underrepresented communities to participate.
 
 
 We&rsquo;re reinventing how clinical studies are run, delivering valid, scalable evidence with a consumer-first mindset. Too often, trials are expensive, fragmented, and overlook the experience of the participant. At Civia, we&rsquo;re changing that. Our leadership team are experienced industry leading, visionary professionals who know what&rsquo;s broken &mdash; and how to fix it.
 
 
 We treat participants like valued partners, not research subjects. That means supporting their agency, putting their needs, comfort, and enjoyment first &mdash; and rewarding them generously for their time and effort.
 
 
 
 What It Means To Work At Civia
 
 
 
 Every team member plays a crucial role in reshaping clinical research. You&rsquo;ll help make studies more human-centered, inclusive, and efficient. We're looking for people who are driven by purpose, inspired by innovation, and ready to roll up their sleeves to do meaningful work.
 
 
 At Civia, your contributions aren&rsquo;t just transactional, they&rsquo;re
 
 
 transformational
 
 
 .
 
 
 
 What You&rsquo;ll Do
 
 
 
 <ul>
 <li>
 Conduct study visits including medical assessments, physical exams, and protocol-specific procedures.
 </li>
 <li>
 Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance.
 </li>
 <li>
 Engage participants with empathy&mdash;providing clear education, answering questions, and ensuring comfort throughout the trial process.
 </li>
 <li>
 Identify, document, and report adverse events per protocol and regulatory standards.
 </li>
 <li>
 Maintain accurate, timely, and high-quality documentation in source records and EDC systems.
 </li>
 <li>
 Contribute to continuous improvement of workflows and study execution with a team-first mindset.
 </li>
 <li>
 Occasional travel may be required for audits, site visits, or team meetings.
 
 
 </li>
 </ul>
 
 What You Bring
 
 
 
 <ul>
 <li>
 Active, unrestricted Nurse Practitioner license.
 </li>
 <li>
 2+ years of clinical research experience (Phase 2&ndash;4 trials preferred).
 </li>
 <li>
 Experience with GLP-1 therapies or metabolic/endocrine research highly preferred.
 </li>
 <li>
 Strong knowledge of GCP/ICH guidelines; certification is a plus.
 </li>
 <li>
 Excellent clinical judgment, attention to detail, and communication skills.
 </li>
 <li>
 A collaborative spirit and commitment to doing what&rsquo;s best for the patient and the team.
 
 
 </li>
 </ul>
 
 What We Offer
 
 
 
 <ul>
 <li>
 Competitive compensation
 </li>
 <li>
 Medical, dental, and vision insurance
 </li>
 <li>
 Generous PTO and paid holidays
 </li>
 <li>
 Flexible scheduling options
 </li>
 <li>
 Professional development and continuing education support
 </li>
 <li>
 A mission-driven team that values respect, inclusion, and innovation
 
 
 </li>
 </ul>
 
 Ready to Make an Impact?
 
 
 
 <ul>
 <li>
 Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact.
 </li>
 <li>
 Startup Energy, Proven Expertise: Work fast, adapt quickly, and help build something new; guided by seasoned visionary professionals who&rsquo;ve seen what needs to change.
 </li>
 <li>
 People First Culture: We care deeply about our patients, participants, and each other. Collaboration, transparency, and bold, straight-talking are core to how we work.
 </li>
 <li>
 Invested in Your Growth: We don&rsquo;t just hire for today; we&rsquo;re building the leaders and changemakers of tomorrow.
 
 
 </li>
 </ul>
 If you&rsquo;re ready to be part of something meaningful&mdash;and work with people who care deeply about doing good work&mdash;apply today by submitting your resume and cover letter to the link above. We&rsquo;re excited to learn more about you!
</div>

Nurse Practitioner/Sub-Investigator

Sarah Cannon Research Institute

<div>
 
 It&rsquo;s More Than a Career, It&rsquo;s a Mission.
 
 
 
 Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.
 
 
 
 Our Mission
 
 
 
 People who live with cancer &ndash; those who work to prevent it, fight it, and survive it &ndash; are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.
 
 
 The Clinical Trial Central Screener (CTCS) will be responsible for centralized clinical support for patient screening at SCRIs network of community-based medical oncology practices. The CTCS will partner with various SCRI departments (including but not limited to Personalized Medicine, Genospace, Therapeutic Development, Research Operations) for central screening services. The services will include 1) clinical trial patient identification 2) remote chart review for clinical appropriateness 3) communication with site personnel when appropriate clinical trial candidates are found.
 
 
 
 Duties include but are not limited to:
 
 
 
 <ul>
 <li>
 Clinical support for clinical trial central screening process
 </li>
 <li>
 Serve as a liaison between SCRI network sites and Personalized Medicine Operations team to provide feedback and make adjustments to processes and technology tools
 </li>
 <li>
 Aid in the enhancement of SCRI&rsquo;s precision medicine software platform, Genospace, to more efficiently match patients to clinical trials
 </li>
 <li>
 Escalate appropriate issues to supervisor to enable timely resolution of any issues during the central screening process
 </li>
 <li>
 Support the deployment, training, and utilization of Genospace at SCRI network sites
 </li>
 <li>
 Lead and facilite routine internal and external cross-functional meetings
 </li>
 <li>
 Build and maintain strategic relationships across the organization
 </li>
 <li>
 Other duties as assigned
 
 
 </li>
 </ul>
 
 Mandatory:
 
 
 The following are mandatory expectations of all SCRI employees.
 
 
 
 <ul>
 <li>
 Practices and adheres to the &ldquo;Code of Conduct&rdquo; philosophy and &ldquo;Mission and Value Statement.&rdquo;
 </li>
 <li>
 During your employment with SCRI, you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.
 
 
 </li>
 </ul>
 
 Knowledge:
 
 
 A body of information needed to perform tasks; May be obtained through education, training or experience.
 
 
 
 <ul>
 <li>
 Knowledge of pharmaceutical industry, regulatory process, clinical trials and medical terminology
 </li>
 <li>
 Business Experience &ndash; Experience working in a clinical research environment (within a SMO, CRO, sponsor, site) and a deep understanding of the oncology clinical research setting is strongly preferred.
 </li>
 <li>
 Knowledge and interpretation of clinical research protocols, and experience in a clinical setting analyzing patient charts is required.
 
 
 </li>
 </ul>
 
 Skills:
 
 
 The proficiency to perform a certain task.
 
 
 
 <ul>
 <li>
 Attention to detail, solid execution, meeting aggressive timelines, strong interpersonal skills and team player. Excellent verbal and written communication skills.
 </li>
 <li>
 Documented training, knowledge and application of current FDA Regulations, GCP and ICH guidelines in clinical trials.
 </li>
 <li>
 Ability to collaborate effectively with the study team, cross functional team members and external partners (including investigators and site staff) using collaborative negotiation skills.
 </li>
 <li>
 Excellent organizational and priority management skills.
 </li>
 <li>
 Strong computer skills including knowledge of Microsoft Excel, Word, PowerPoint and Outlook.
 </li>
 <li>
 Ability to work within established timelines, in a fast-paced environment.
 
 
 </li>
 </ul>
 
 Abilities:
 
 
 An underlying, enduring trait useful for performing duties.
 
 
 
 <ul>
 <li>
 Problem solving skills in fast-paced environment
 </li>
 <li>
 Interpersonal skills and detailed-oriented
 </li>
 <li>
 Detail-oriented and meticulous
 </li>
 <li>
 Demonstrate ability to positively influence others in a team environment
 
 
 </li>
 </ul>
 
 Minimum Qualifications:
 
 
 
 <ul>
 <li>
 Bachelor's Degree in Nursing or Licensed Registered Nurse
 </li>
 <li>
 3+ years of experience as a research nurse, preferably within clinical research
 </li>
 <li>
 Experience in clinical trials required
 </li>
 <li>
 Must be able to read a protocol and match patients with a protocol
 
 
 </li>
 </ul>
 
 About Sarah Cannon Research Institute
 
 
 
 Sarah Cannon Research Institute (SCRI) is one of the world&rsquo;s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI&rsquo;s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S. Please click here to learn more about our research offerings.
 
 
 We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That&rsquo;s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here.
 
 
 As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.
 
 
 McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson&rsquo;s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:
 
 
 McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.
 
 
 McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.
 
 
 McKesson job postings are posted on our career site: careers.mckesson.com.
 
 
 
 We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
 
</div>

Clinical Trial Central Screener

CenExel Clinical Research

<div>CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process. 

Job Summary:
With moderate oversight the Psychiatric Technician I PRN position interacts directly with psychiatric patients participating in clinical trials. The psychiatric technician demonstrates knowledge of the principles of growth and development appropriate to adults with psychiatric disorders and has basic competency in applying these principles when providing individualized care for specific research subjects.

Schedule: PRN, needed weekdays from 3:00 pm to 11:30 PM and weekends as needed

Compensation: $19.08 - $23.18/hr (Depending on education, experience, and skillset)

Essential Responsibilities and Duties:
<ul>
<li>Presents an understanding of components of care and how the role of psychiatric technician fits into the delivery of services.</li>
<li>Observes and reports personality and/or behavior changes in subjects to the charge person or charge nurse.</li>
<li>Completes responsibilities as delegated by the charge person or charge nurse for the shift.</li>
<li>Interacts closely with clients to assist them in problem solving and to de-escalate subjects who become upset or belligerent.</li>
<li>Assists with completing a group activity during each shift worked.</li>
<li>Communicates appropriately with subjects while assisting them with ADL&rsquo;s, supplying them with cigarette breaks as allowed in the protocol.</li>
<li>Provides the subjects with meals and snacks as allowed in the study, ensuring subjects adhere to the protocol specific dietary and smoking restrictions.</li>
<li>Assist the subjects with meal prep, meal ordering, meal choices, and delivers meals depending on location.</li>
<li>Assists subjects with laundry and housekeeping tasks as needed.</li>
<li>Assists with nightly room and equipment checks.</li>
<li>Assists with dispensing medications (if properly certified) as instructed by MD or Medication Administration Record. Communicates with MD in person or over the phone to receive PRN or STAT medication changes as needed for subjects.</li>
<li>Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.</li>
<li>Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.</li>
</ul>
Education/Experience/Skills:
<ul>
<li>Must be able to effectively communicate verbally and in writing.</li>
<li>1 - 2 years experience working with the persons with major mental illnesses (schizophrenia, bipolar disorder, depression) as a psych tech in inpatient/acute care settings is preferred.</li>
<li>High School graduate or equivalent.</li>
<li>Prior medical experience is preferred but not required.</li>
<li>Must maintain professional boundaries with subjects.</li>
</ul>
Working Conditions
<div><ul><li>Indoor, Clinic environment.</li></ul>
<ul><li>Essential physical requirements include sitting, typing, standing, and walking.</li></ul>
<ul><li>Lightly active position, occasional lifting of up to 20 pounds.</li></ul>
<ul><li>Reporting to work, as scheduled, is essential.</li></ul>
<ul><li>On-site work arrangement.</li></ul>
</div>
CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer 
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.</div>

Patient Care Tech - Per Diem - Clinical Research

<div>CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process. 
 
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Job Summary:
With moderate oversight the Psychiatric Technician I position interacts directly with psychiatric patients participating in clinical trials. The psychiatric technician demonstrates knowledge of the principles of growth and development appropriate to adults with psychiatric disorders and has basic competency in applying these principles when providing individualized care for specific research subjects.

Schedule: Full-Time (3:00 PM - 11:30 PM) + working every other weekend (Required)

Compensation: $20.00 - $22.00/hr (Depending on education, experience, and skillset)

Essential Responsibilities and Duties:
<ul>
<li>Presents an understanding of components of care and how the role of psychiatric technician fits into the delivery of services.</li>
<li>Observes and reports personality and/or behavior changes in subjects to the charge person or charge nurse.</li>
<li>Completes responsibilities as delegated by the charge person or charge nurse for the shift.</li>
<li>Interacts closely with clients to assist them in problem solving and to de-escalate subjects who become upset or belligerent.</li>
<li>Assists with completing a group activity during each shift worked.</li>
<li>Communicates appropriately with subjects while assisting them with ADL&rsquo;s, supplying them with cigarette breaks as allowed in the protocol.</li>
<li>Provides the subjects with meals and snacks as allowed in the study, ensuring subjects adhere to the protocol specific dietary and smoking restrictions.</li>
<li>Assist the subjects with meal prep, meal ordering, meal choices, and delivers meals depending on location.</li>
<li>Assists subjects with laundry and housekeeping tasks as needed.</li>
<li>Assists with nightly room and equipment checks.</li>
<li>Assists with dispensing medications (if properly certified) as instructed by MD or Medication Administration Record. Communicates with MD in person or over the phone to receive PRN or STAT medication changes as needed for subjects.</li>
<li>Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.</li>
<li>Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.</li>
</ul>
Education/Experience/Skills:
<ul>
<li>Must be able to effectively communicate verbally and in writing.</li>
<li>1 - 2 years experience working with the persons with major mental illnesses (schizophrenia, bipolar disorder, depression) as a psych tech in inpatient/acute care settings is preferred.</li>
<li>High School graduate or equivalent.</li>
<li>Prior medical experience is preferred but not required.</li>
<li>Must maintain professional boundaries with subjects.</li>
</ul>
Working Conditions
<div><ul><li>Indoor, Clinic environment.</li></ul>
<ul><li>Essential physical requirements include sitting, typing, standing, and walking.</li></ul>
<ul><li>Lightly active position, occasional lifting of up to 20 pounds.</li></ul>
<ul><li>Reporting to work, as scheduled, is essential.</li></ul>
<ul><li>On-site work arrangement.</li></ul>
</div>
CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer 
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.</div>

Psychiatric Care Tech - Clinical Research

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