clinical research technician

Michigan Medicine

<div>
 How to Apply
 <br/>
 <br/>
 A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.
 <br/>
 <br/>
 Mission Statement
 <br/>
 <br/>
 Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.
 <br/>
 <br/>
 <strong>
  Job Summary
  <br/>
  <br/>
 </strong>
 The Clinical Research Technician will support coordination and implementation of ongoing clinical research studies focused on hypertension treatment and stroke prevention. Responsibilities include participant recruitment, screening, enrollment, scheduling study visits, participant follow up, and maintenance of study documentation.
 <br/>
 <br/>
 Responsibilities*
 <br/>
 <br/>
 <ul>
  <li>
   Coordinate day-to-day activities for assigned clinical research studies
  </li>
  <li>
   Recruit, screen, and enroll study participants in accordance with protocol requirements
  </li>
  <li>
   Schedule and manage study visits, including follow-up activities
  </li>
  <li>
   Serve as a primary point of contact for study participants, ensuring clear communication and positive participant experience
  </li>
  <li>
   Maintain accurate and timely study documentation, including regulatory and source documents
  </li>
  <li>
   Assist with data collection and entry in study databases
  </li>
  <li>
   Support study teams and investigators with operational tasks related to study execution
  </li>
  <li>
   Collaborate with research staff and leadership to ensure adherence to study timelines and goals
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Required Qualifications*
 <br/>
 <br/>
 <ul>
  <li>
   Associate degree in Health Science or an equivalent combination of related education and experience is necessary.
  </li>
  <li>
   Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRA?s Definition of a Clinical Research Professional for qualifying experience prior to applying.)
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 or
 <br/>
 <br/>
 An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD.
 <br/>
 <br/>
 or
 <br/>
 <br/>
 Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
 <br/>
 <br/>
 Desired Qualifications*
 <br/>
 <br/>
 <ul>
  <li>
   Bachelor's degree in health sciences, public health, or related field, or equivalent combination of education and experience
  </li>
  <li>
   Strong organizational, communication, and interpersonal skills
  </li>
  <li>
   Ability to manage multiple tasks and priorities in a fast-paced research environment
  </li>
  <li>
   Experience interacting with human subjects or working in a clinical or research setting is preferred
  </li>
  <li>
   Prior experience coordinating clinical research studies
  </li>
  <li>
   Familiarity with participant recruitment and retention strategies
  </li>
  <li>
   Experience with data entry and research documentation systems (e.g., REDCap)
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Why Join Michigan Medicine?
 <br/>
 <br/>
 Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world's most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.
 <br/>
 <br/>
 <strong>
  What Benefits can you Look Forward to?
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Excellent medical, dental and vision coverage effective on your very first day
  </li>
  <li>
   2:1 Match on retirement savings
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Modes of Work
 <br/>
 <br/>
 Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes.
 <br/>
 <br/>
 Work Locations
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 <br/>
 Hurley Hospital, Flint, MI
 <br/>
 <br/>
 Underfill Statement
 <br/>
 <br/>
 This position may be underfilled at a lower classification depending on the qualifications of the selected candidate.
 <br/>
 <br/>
 Additional Information
 <br/>
 <br/>
 Work environment: This position works closely with a multidisciplinary research team and requires frequent interaction with study participants. The role may involve a combination of on-site and remote work, depending on study needs.
 <br/>
 <br/>
 <strong>
  Appointment Type:
 </strong>
 Full-Time, Term-Limited (1 year, with potential for extension based on funding)
 <br/>
 <br/>
 Application Deadline
 <br/>
 <br/>
 Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled any time after the minimum posting period has ended.
 <br/>
 <br/>
 U-M EEO Statement
 <br/>
 <br/>
 The University of Michigan is an equal employment opportunity employer.
</div>


Clinical Research Technician (Temporary)

Biotrial, Inc.

<p>BIOTRIAL is seeking a <b>Clinical Research Technician</b> <b>(EEG Technician and Medical Assistant) </b>to work full-time at its U.S. headquarters, a state-of-the art Clinical Pharmacology Unit in Newark, New Jersey.</p><p>The Clinical Research Technician will have responsibility for ensuring proper collection of biological samples from study participants according to protocol and will perform laboratory processing of samples and EEG testing based on study requirements. The position will report to the Clinical Unit Coordinator and work in close collaboration with the Clinical Research Team.</p><p><b>Responsibilities</b>:</p><p>The <b>Clinical Research Technician</b> will:</p><ul><li>Participate in screening examinations (urine drug screen, preparation, and management of the inclusion of biological results, transmission of results to volunteers).</li><li>Prepare sampling tubes (labeling, storing, etc.).</li><li>Draw and treat blood samples (centrifugation, pipetting, and performing platelets aggregation).</li><li>Manage blood and/or urine samples for studies.</li><li>Participate in monitoring measurements, i.e., cardiovascular (ECG) and psychometric tests.</li><li>Ensure proper use and control of clinical unit&rsquo;s equipment.</li><li>&middot; Positions patient on examination table and applies electrodes on predetermined measured positions on patient&rsquo;s head for optimum testing.</li><li>Checks EEG equipment performance and selects predetermined electrode combinations and special combinations as required by the protocol.</li><li>Operate EEG equipment to take EEG tracings.</li><li>Perform routine maintenance on EEG equipment. Identify malfunctions and report to management. Recommend more efficient working methods; participate in the development and implementation of new processes and operating procedures.</li><li>Ensure that work remains in compliance with regulatory guidelines, quality control standards, and the company&rsquo;s Standard Operating Procedures.</li><li>Work collaboratively with the principal investigator and clinical unit coordinator.</li><li>Maintain good communications and keep the Clinical Research Team fully informed.</li></ul><p><b>Requirements:</b></p><ul><li>Bachelor&rsquo;s Degree in scientific area of study preferred but not required.</li><li>EEG Certification.</li><li>Completion of Medical Assistant training that includes phlebotomy, vital signs, and ECG.</li><li>Phlebotomist Certification required.</li><li>1 years of experience in lab processing and lab procedures preferred.</li><li>Must be able to work a flexible schedule.</li></ul><p><i>Biotrial 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, genetics, disability, age, veteran status, or any other characteristic protected by law.</i></p><p>Job Type: Full time</p><p>Work Remotely</p><ul><li>No</li></ul><p>Job Type: Full-time</p><p>Pay: $32.00 - $38.00 per hour</p><p>Benefits:</p><ul><li>401(k) matching</li><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Referral program</li><li>Vision insurance</li></ul><p>Application Question(s):</p><ul><li>What days of the week and times are you available to work? Please be specific.</li><li>Are you looking for a full-time position?</li></ul><p>Experience:</p><ul><li>Phlebotomist and Medical Assistant: 1 year (Preferred)</li><li>EEG Testing: 1 year (Preferred)</li></ul><p>License/Certification:</p><ul><li>Medical Assistant certification (Preferred)</li><li>Phlebotomist Certification (Preferred)</li><li>EEG certification (Preferred)</li></ul><p>Work Location: In person</p>

Clinical Research Technician (EEG Technician and Medical Assistant) Full-time

UT Health Science Center at San Antonio

Job Description
<br>Under general supervision, provides routine technical assistance in performing assigned and delegated tasks in support of research projects. Responsibilities include assisting or conducting a variety of scientific experiments and research projects of limited complexity, collecting, evaluating and interpreting data for clinical and diagnostic research.
<br><div><ul>Responsibilities</ul></div>
<br><div><ul><li>Provides routine technical assistance in performing assigned and delegated tasks in support of research projects.
</li><li>Performs assigned clerical and technical duties in a research or clinical lab setting.
</li><li>Assists investigator or higher level technician with research studies, experiments and assays including collection of data, preparation of solutions and set-up and maintenance of equipment.
</li><li>Performs routine tests with direction from supervisor, manager or higher level technician.
</li><li>Assists in conducting a variety of scientific experiments and research projects of limited complexity, collecting, evaluating, and interpreting data.
</li><li>Carries out general laboratory maintenance.
</li><li>Performs all other duties as assigned.</li></ul></div>
<br><p></p><div><p><i>Qualifications</i></p></div>
<br><div><ul><li>Attention to detail by achieving thoroughness and accuracy when accomplishing a task through concern for all the areas involved.
</li><li>Ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner.
</li><li>Ability to monitor important and complex projects concurrently within a research environment or laboratory schedule.
</li><li>Ability to effectively communicate orally and in writing, to include writing and preparing memorandums, letters, and other official correspondence.
</li><li>Knowledge of Microsoft Word, Excel, PowerPoint, and Lotus Notes/other e-mail software.
</li></ul><p>Education:
</p>Bachelor's Degree in a basic science is required.<br>
<ul><li>
</li></ul><p></p><p>Experience:
</p>None<br>
<ul><li>
</li></ul><p></p><p><i>This position may require the ability to maintain the security and integrity of UT San Antonio and its infrastructure per Texas EO-GA-48.</i></p></div>
<br>Required Skills
<br><div></div><div><div>None</div><div>
SkillType</div><div>
null</div><div>
SkillId</div><div>
300001508005595</div><div>
SectionId</div><div>
300000006778627</div><div>
ContentItemId</div><div>
null</div></div><br><div></div>

Research Assistant

Segal Institute for Clinical Research

<p>The Mental Health Technician (MHT) at Segal Trials plays a vital role in overall maintenance of a therapeutic environment and ensures the safety of participants and staff on the research unit.</p><p><b>DUTIES AND ESSENTIAL JOB FUNCTIONS</b></p><ul><li>Ensures that clinical research and related activities are performed in accordance with Federal Regulatory guidelines and sponsor policies.</li><li>Develops a thorough working knowledge of all protocols assigned/delegated so that all study activities are completed accurately and completely.</li><li>Performs safety rounds at determined intervals while documenting findings.</li><li>Oversees general milieu while promoting a safe environment.</li><li>Incorporates non-violent crisis intervention de-escalation techniques to effectively manage the agitated Subject.</li><li>Understands and honors the established research unit rules, regulations, and Policy &amp; Procedures.</li><li>Answers telephone and communicates with other disciplines and facilities, including the coordination of patient transfers from community physicians/healthcare facilities.</li><li>Provides 1:1 observation for patients at risk of self-harm.</li><li>Charts patient observations, following delegated procedures and standards</li><li>Assists nursing with research study procedures including dosing, post dose monitoring and any study assessments as delegated by the research team.</li><li>Assists with any urgent/emergent issues on the unit</li></ul><p>Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.</p><p><b>REQUIREMENTS:</b></p><p>&middot; High School Diploma<br/>&middot; 2+ years of relevant work experience working in an inpatient setting.<br/>&middot; Certification in Behavioral Health Technician (CBHT) preferred.<br/>&middot; Proficiency in English required.<br/>&middot; Proficiency in English and Spanish preferred.</p><p><b>Who We Are?</b></p><p>Segal Trials, founded in 1998, is a privately held network of five research sites throughout South Florida, conducting phase I-IV research trials with a primary emphasis on psychiatry, neurology, addiction, insomnia, general medicine, vaccinations and more. With a team of over 150 professionals, Segal Trials remains agile and competitive.</p><p>Segal Trials is regarded as an innovator and a leader in the advancement of medicine with a strong dedication to the community it serves by spreading awareness about clinical trials as a potential care option.</p><p><b>Why Segal Trials?</b></p><p>When working at Segal Trials, you will be surrounded by passion, diversity, and likeminded individuals who are striving in the pursuit of excellence. We will foster your continued success and you will begin making a difference on your very first day!</p><p><b>For more information, visit www.segaltrials.com</b></p><p>Pay: Up to $20.00 per hour</p><p>Medical Specialty:</p><ul><li>Addiction Medicine</li></ul><p>Experience:</p><ul><li>Behavioral health: 2 years (Preferred)</li></ul><p>License/Certification:</p><ul><li>Driver's License (Preferred)</li><li>Certified Behavioral Health Technician (Preferred)</li></ul><p>Work Location: In person</p>

Part-Time Mental Health Technician (Friday & Saturday 8AM-8PM)

CenExel Clinical Research

<div><p>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.<br>
<br>
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.</p>
<p><b>
Job Summary:
</b></p><p>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.</p>
<p><b>
Schedule</b>: Full-Time (3:00 PM - 11:30 PM) + working every other weekend (Required)</p>
<p><b>
Compensation: </b>$20.00 - $22.00/hr (Depending on education, experience, and skillset)</p>
<p><b>
Essential Responsibilities and Duties:</b></p>
<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>
<p><b>Education/Experience/Skills:</b></p>
<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>
<p><b>Working Conditions
</b></p><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>
<p>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.</p><p>
Equal Opportunity Employer<br>
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.</p></div>

Psychiatric Care Tech - Clinical Research

<div><p>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.</p><br>
<p><b>
Job Summary:
</b></p><p>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.</p>
<p><b>
Schedule</b>: PRN, needed weekdays from 3:00 pm to 11:30 PM and weekends as needed</p>
<p><b>
Compensation: </b>$19.08 - $23.18/hr (Depending on education, experience, and skillset)</p>
<p><b>
Essential Responsibilities and Duties:</b></p>
<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>
<p><b>Education/Experience/Skills:</b></p>
<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>
<p><b>Working Conditions
</b></p><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>
<p>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.</p><p>
Equal Opportunity Employer<br>
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.</p></div>

Patient Care Tech - Per Diem - Clinical Research

Boston Children's Hospital

<div><div><div><div>85616BR</div>
</div><div><div>Neurology</div>
</div><div><p><b>Job Posting Description</b></p>
<div><b>Position Summary:
</b><br>
The Rosamund Stone Zander and Hansjoerg Wyss Translational Neuroscience Center (TNC) is comprised of translational investigators and clinical experts focused on neurogenetic and neurodevelopmental disorders. The TNC has been selected to join a multi-site longitudinal natural history study aims to map the trajectory of autism and related neurodevelopmental disorders (NDDs). This initiative aims to deeply phenotype these populations and identify future clinical trial outcome measures. The clinical research assistant will work closely with TNC research staff and physician researchers to execute this study.<br>
<br>
Under immediate supervision, the clinical research assistant will coordinate the daily operation activities of this initiative. They will be responsible for screening, consenting, recruiting, and selecting participants. They will prepare IRB documentation and IRB submissions in conjunction with the Principal Investigator and/or other members of the research team. They will conduct data collection activities, complete data entry, maintain regulatory binders, and support research activities as required.<br>
<br>
<b>Key Responsibilities:</b><ul><li>
Consents and recruit participants through personal interviews and written communications with patients/families. Provides detailed background information regarding the study to families, communicates all policies and procedures, and responds to all inquiries. Evaluates suitability of prospective study candidates and makes selections based upon clinical knowledge of each study.</li><li>
Serves as liaison to the families/participants in the research studies, conducted at both on-site and off-site locations, guiding and advising them throughout each phase of the study. Coordinates follow-up visits as necessary. Acts as a resource to study participants, addressing any concerns they may have. Troubleshoots resolution of any issues that may arise throughout the study.</li><li>
Coordinates and prepares the necessary documentation for Institutional Review Board (IRB) and Committee on Clinical Investigations (CCI) submissions, together with the Principal Investigator of the study.</li><li>
Creates and prepares data collection statistical reports and analytical summaries for distribution to study research team for review and analysis.</li><li>
Participates in the training of newly hired research study assistants, as required.</li>
Coordinates activities between the hospital and research laboratories to ensure correct testing/processing and sends out instructions specific to the study. Communicates project policies and procedures to personnel. Monitors and reviews data collection, data entry, and informed consent procedures <li>- ensuring consistency of application for all participants.</li><li>
Performs other miscellaneous administrative duties as assigned or required.</li></ul><br>
<b>
Minimum Qualifications</b><br>
<b>Education:</b><ul><li>
The knowledge of theories, principles, and concepts acquired through completion of a Bachelor's degree in STEM or psychology.</li></ul><b>
Experience:</b><ul><li>
Work requires the analytical skills to gather and interpret data in which the information or problems are moderately complex to complex.</li><li>
Work requires well-developed communication skills in order to provide critical information to patients, effectively deal with conflicting views or issues, and the ability to mediate fair solutions. Work also requires advanced writing skills.</li><li>
Fluency in English and Spanish preferred.</li><li>
2 year commitment is preferred.</li></ul></div>
</div><div><p><b>Status</b></p>
<div>Full-Time</div>
</div><div><p><b>Regular, Temporary, Per Diem</b></p>
<div>Regular
</div></div><div><p><b>Standard Hours per Week</b></p>
<div>40
</div></div><div><p><b>Pay Range</b></p>
<div>$41246.40-$61339.20 Annual</div>
</div><div><p><b>Office/Site Location</b></p>
<div>Brookline</div>
</div><div><p><b>Job Posting Category</b></p>
<div>Research</div>
</div><div><p><b>Remote Eligibility
</b></p><div>Part Remote/Hybrid</div></div></div></div><div></div>

Clinical Research Assistant - Translational Neuroscience Center (TNC)

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