clinical trial assistant

Boehringer Ingelheim

<div><p><b>We are IMETA
</b></p><p>ROPU IMETA is a Regional Operating Unit consisting of 6 mid-sized Operating Units: India, Turkey, Southern Africa (South Africa &amp; Sub Sahara Africa) Northeast &amp; West Africa, Near East &amp; UAE, Saudi Arabia, Gulf &amp; East Africa (SAGEA).
<br>
IMETA is home to more than 47 nationalities. We are a myriad of color and culture and embracing this diversity is one of our greatest opportunities.
<br>
We are a powerhouse of talent, and we work together to ensure that we grow, nurture, and retain our talent. Uniting and working together is the key to our success.<br>
</p><p></p><p><b>The Opportunity
</b></p><p><i>Are you an experienced professional who wants to be part of a truly innovative and revolutionary team! Join us if you want to make the difference.<br>
</i></p><p></p><p>We are hiring a Regional Clinical Trial Assistant (CTA), based at Dubai. The position reports directly to the Head of Clinical Development &amp; Operations IMETA.<br>
</p><p><br>
The CTA is a member of the regional trial team and is responsible to provide operational expertise and support to the trial team. The CTA is assigned to support the Clinical Trail Manager at Regional trial level, in all administrative tasks during the trial life cycle, including aspects of Trial Master File management and document management and in Clinical Trial Management System updates, among others.<br>
</p><p><br>
Additionally, CTA closely collaborates with the trial team and ensures that all trial related activities are done on time and according to SOPs, guidelines and internal and external standards.
</p><p><i>This is an outsourced role with a third party<br>
</i></p><p></p><p><b>Tasks &amp; Responsibilities:
</b></p><ul><li>Leads Trial Document Framework (TMF) &amp; Document management and completion
</li><li>Accountable for vendor related activities, vendor set-up, system access and training, account and report requests
</li><li>Responsible for management of meeting minutes of Trial Level Meetings
</li><li>Accountable for Clinical Trial Management System update and maintenance
</li><li>Support trial team in audits &amp; inspection and CAPA management<br>
</li></ul><p></p><p><b>Requirements:
</b></p><ul><li>Bachelors in Life Sciences
</li><li>Master&rsquo;s degree will be a plus
</li><li>Minimum 1 year of experience in Clinical Trial administration within pharmaceuticals / CRO
</li></ul><ul><li>Excellent knowledge in VEEVA systems
</li><li>Business fluent in English in its oral and written form
</li><li>Knowledge of additional languages within the region is a plus
</li><li>Should be based in Dubai, with a valid UAE resident visa<br>
</li></ul><br>
<p></p><p><b>What&rsquo;s Next?
</b></p><p>We are looking forward to receiving your application! We will then have a look at your profile. If we see a match, we will invite you for a screening interview.<br>
</p><p></p><p><b>Screening:
</b></p><p>To comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (&ldquo;SPL&rdquo;). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.</p></div>

Clinical Trial Administrator

<div><h3 class="jobSectionHeader"><b>We are the leading oncology CRO, developing novel treatments for patients that need them most. Our team is fully dedicated to oncology &ndash; it is all we do &ndash; combining innovation and expertise to quickly move medicines from preclinical development into clinical trials. Adaptive and forward-thinking &ndash; we guide our client's therapy through the most critical development milestones from the lab to planning their regulatory and clinical strategy. Our ultimate goal? To help patients.</b></h3><h4 class="jobSectionHeader"><b>
Position Summary:</b></h4><p>
The Clinical Trial Associate coordinates activities on clinical research projects by working with the appropriate clinical teams (e.g. Project Management, Clinical Monitoring, Data Management, Medical Monitoring) on project related activities.</p><h4 class="jobSectionHeader"><b>
Essential Functions:</b></h4><ul><li>
Draft project plans and create project documents for review prior to Sponsor review, as assigned.</li><li>
Act as a central contact and provides expert guidance to the clinical team for designated project communications, meeting coordination, meeting minutes, correspondence, and associated documentation.</li><li>
Coordinate activities on clinical trials, including active participation on weekly Sponsor and Investigator calls, maintaining project trackers, and communicating on behalf of the PM to the Sponsor, investigative sites, and vendors as appropriate.</li><li>
Schedule and maintain organization of all clinical project meetings.</li><li>
Accurately update and maintain clinical systems within the appropriate project timeline.</li><li>
Collect and submit documents for assigned Trial Master Files (TMF) per standard guidelines, to ensure continual TMF maintenance in an audit-ready state. Routinely perform TMF document Quality Checks (QCs).</li><li>
Prepare, handle, distribute, file, and archive clinical documentation and reports in a timely manner.</li><li>
Prepare and distribute agendas and minutes from Sponsor and Investigator for team meetings with review from the project management team for accuracy within established deadlines.</li><li>
Maintain accurate team contact lists for every assigned project, proactively gathering information, and updating the contact list. Ensure that the contact list is uploaded to the TMF, as required to meet Standard Operating Procedure timelines.</li><li>
Gather, track, and maintain project and site essential regulatory documents.</li><li>
Provide cross-functional project support to entire Clinical Project team.</li><li>
Prepare and compile trial related materials for investigative sites, including Investigator Site File (ISF) materials, site electronic binders, site instruction manuals, and trial templates, forms, and plans.</li><li>
Acts as Clinical Trial Associate back-up during absences as needed based on individual trial needs.</li><li>
Mentor and assist with training of Clinical Trial Associates.</li><li>
Assist with the development and implementation of clinical policies and procedures.</li><li>
Perform other related duties as assigned.</li></ul><h4 class="jobSectionHeader"><b>
Job Requirements:</b></h4><ul><li>
Associate degree in a life science or health related field required with Bachelor&rsquo;s degree preferred (experience working in clinical research may be substituted for education at TD2&rsquo;s discretion)</li><li>
Minimum of 4 years of experience in an administrative role.</li><li>
At least 3 years of experience in support of clinical research with preference to oncology research.</li></ul><h4 class="jobSectionHeader"><b>
Required Specialized/Technical Skills:</b></h4><ul><li>
Proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook.</li><li>
Advanced written and verbal communication skills</li><li>
Knowledge of GCP, ICH guidelines and clinical trial regulations</li><li>
Ability to work collaboratively in a team environment.</li><li>
Experience managing Trial Master Files and/or Investigative Site Files.</li><li>
Ability to take initiative and work independently with minimal guidance.</li></ul><p>
Born from the Translational Genomics Research Institute (TGen), TD2 was formed in 2003 as a subsidiary of TGen, and less than two years later, opened its doors on the campus of the Mayo Clinic in Scottsdale, Ariz. In our 17 years of business, we have helped more than 600 biotech and pharma companies, maintaining hundreds of client studies per year. Among them, our team has been involved in more than 600 first-in-man major oncology medicines, including numerous trials that have led to approvals in both rare and large indications.</p><p><i>
TD2 is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, creed, disability, veteran&rsquo;s status, gender, sexual orientation, gender identity, or gender expression.</i></p><p>
#LI-Remote</p><p>
#LI-TD2</p><br>
This is a remote position.</div>

Clinical Trial Associate

Children's Hospital of Philadelphia

<div><p>SHIFT:</p>
Day (United States of America)<p></p><p><b>
Seeking Breakthrough Makers</b><br>
<br>
Children&rsquo;s Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation.<br>
<br>
At CHOP, your experience is valued; your voice is heard; and your contributions make a difference for patients and families. Join us as we build on our promise to advance pediatric care&mdash;and your career.<br>
<br>
CHOP does not discriminate on the basis of race, color, sex, national origin, religion, or any other legally protected categories in any employment, training, or vendor decisions or programs. CHOP recognizes the critical importance of a workforce rich in varied backgrounds and experiences and engages in ongoing efforts to achieve that through equally varied and non-discriminatory means.<br>
<br>
<b>A Brief Overview</b><br>
The Division of Rheumatology at the Children&rsquo;s Hospital of Philadelphia is dedicated to improving the safety, quality, and health outcomes of children with rheumatic diseases. Led by Clinical Research Director, Pamela Weiss, MD, MSCE, the Rheumatology Research Core is seeking an entry-level Clinical Research Assistant to work alongside a team of two additional clinical research assistants and one clinical research coordinator. This position is full-time. The clinical research assistant will provide support in the day-to-day operations of recruiting and enrolling patients for active studies and clinical trials, providing regulatory support and oversight, and abstracting data into local and national databases.</p><p><b><br>
What you will do</b></p><ul><li>
Assists the Clinical Research Manager and Principal Investigators in all aspects of projects</li><li>
Assists in developing and overseeing IRB applications, including protocols, informed consent documents, trial registration, and HIPAA forms as well as modifications and renewals</li><li>
Recruits, screens, and enrolls subjects into the clinical studies and trials</li><li>
Maintains IRB regulatory documents for assigned protocols</li><li>
Participates in coordinating study visits, assures completion of all study questionnaires and coordinates participant incentives</li><li>
Conducts data abstraction from medical chart reviews, maintenance and storage of data, and analysis of subject information in both local databases and national registries</li><li>
Helps create and manage survey and data collection instruments on REDCap and other platforms as needed</li><li>
Attends weekly meetings of the Rheumatology Research Core and other pertinent project or division-related meetings</li></ul><p></p><p><b>
Education Qualifications</b></p><ul><li>
High School Diploma / GED - Required</li><li>
Bachelor's Degree in a related field - Preferred</li></ul><p></p><p><b>
Experience Qualifications</b></p><ul><li>
Previous relevant clinical research experience - Required</li><li>
At least one (1) year of relevant clinical research experience - Preferred</li></ul><p></p><p><b>
Skills and Abilities</b></p><ul><li>
Familiarity with IRB and human subject protection.</li><li>
Ability to perform assigned tasks while working under direct supervision.</li><li>
Able to work accurately and work well with others.</li><li>
Precision and great attention to detail when performing assigned responsibilities is required.</li><li>
Strong verbal and written communication skills to coordinate with subjects, team members, other departments, and outside institutions</li><li>
Effective problem solving/critical thinking skills.</li><li>
Highly motivated individual with great time management skills</li></ul><p><b><br>
To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community. As a condition of employment, CHOP employees who work in patient care buildings or who have patient facing responsibilities must receive an annual influenza vaccine. </b><b>Learn more.</b><br>
<br>
<b>EEO / VEVRAA Federal Contractor</b><b> | </b><b>Tobacco Statement
</b></p><p></p><p><b>SALARY RANGE:</b></p><p></p>
$20.55 - $25.69 Hourly<p></p><p>
Salary ranges are shown for full-time jobs. If you're working part-time, your pay will be adjusted accordingly.</p><p></p><p>
-</p><p></p><p>
At CHOP, we are committed to fair and transparent pay practices. Factors such as skills and experience could result in an offer above the salary range noted in this job posting. Click here for more information regarding CHOP's Compensation and Benefits.</p></div>

Clinical Research Assistant I-Rheumatology

Pinnacle Clinical Research

<div><div><b>Come join our team and make a difference as we blaze the way into the future of medical discovery through world-class clinical research.</b> <b>At Pinnacle Clinical Research, we are committed to driving innovation and advancing medical knowledge. Through our rigorous research studies, we strive to unlock breakthroughs that have the potential to transform patient care and improve lives. We pride ourselves on conducting high quality research as a complement to the medical care that our volunteers receive from their routine care center. Together, we will raise awareness about the importance of clinical research and its role in shaping the future of healthcare.</b></div>
<div></div><div><b>Be a part of the discovery!</b></div>
<div></div><div><b>Summary:</b> Assists the clinical research coordinator and the principal investigator with administering activities to facilitate clinical research, which may include working with an affiliate or collaborating research sites. Exercises judgment within the allowable limits defined within clinical trials protocols, standard operating procedures, and under the direction from the study Investigator and supervisor. Always maintains subject and document confidentiality, understands and complies with the appropriate sponsor requirements, regulations including the Food and Drug Administration (FDA), good clinical practice (GCP), International Conference on Harmonization (ICH), Health Insurance Portability and Accountability Act (HIPAA), Institutional Review Boards (IRB), and institutional policies and procedures by performing the following duties.</div>
<div><b>Duties and Responsibilities:</b></div>
<ul><li>Assists with the creation and completion of study related documents and new study preparation.</li>
<li>Assists with the completion of regulatory submissions and maintains regulatory files as directed.</li>
<li>Acts as a secondary liaison with sponsors.</li>
<li>Assists with the preparation for study monitor visits as directed.</li>
<li>Completes case report forms as directed.</li>
<li>Creates reports as requested.</li>
<li>Completes study directed assessments with patients to include, but not limited to adverse events, test article (TA) handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessment.</li>
<li>Assists with subject screening and recruitment as directed.</li>
<li>Updates Clinical Trial Management Software (CTMS) as directed.</li>
<li>Coordinates multiple projects with competing priorities and deadlines, as needed based on clinical trial protocol directives and study volume.</li>
<li>Interacts with internal and external personnel to include, but not limited to physicians, nurses, administration staff, industry sponsor representatives, central laboratory/imaging personnel, and clinical trial patients.</li>
</ul><div><b>Education/Experience:</b></div>
<div>High school diploma or general education degree (GED); or two to four years related experience and/or training; or equivalent combination of education and experience.</div>
<div><b>Certificates and Licenses:</b></div>
<ul><li>Clinical research certification preferred</li>
</ul><div><b>Knowledge, Skills, and Other Abilities:</b></div>
<ul><li>Ability to demonstrate competence in oral and written communication</li>
<li>Bilingual (English/Spanish) required</li>
<li>Must be organized, attentive to detail, and possess a positive, friendly, and professional demeanor</li>
<li>Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner</li>
<li>Medical knowledge, including medical terminology</li>
<li>Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization.</li>
<li>Must have knowledge of Microsoft Office Word, Microsoft Excel, Internet Explorer, Google Chrome, Mozilla Firefox, web-based enterprise solutions, and Electronic Case Report Form systems.</li>
</ul><div><b>Work Environment and Physical demands:</b></div>
<div>The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</div>
<ul><li>Work is performed in an office/laboratory and/or a clinical environment.</li>
<li>Exposure to biological fluids and/or bloodborne pathogens.</li>
<li>Personal protective equipment required such as protective eyewear, garments, and gloves.</li>
<li>Occasional travel may be required domestic and/or international.</li>
<li>Ability to work in an upright and/or stationary position for 6-10 hours per day.</li>
<li>Frequent mobility required.</li>
<li>Occasional squatting, kneeling, or bending.</li>
<li>Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs.</li>
</ul><div><b>Perks of working at Pinnacle Clinical Research:</b></div>
<ul><li><i>401k</i></li>
<li><i>Medical, dental, vision, long term disability, short term disability, FSA, and life insurance</i></li>
<li><i>3 weeks of paid time off</i></li>
<li><i>14 paid company holidays</i></li>
<li><i>Scrub voucher (specific positions apply)</i></li>
<li><i>And more!</i></li>
</ul><div>Pinnacle Clinical Research is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.</div></div>

Research Assistant

Seattle Children's

<div><p>Assist the assigned division research team with in the organization, implementation and completion of clinical research trials. Maintain regulatory documents; assist the Principal Investigator in the planning of protocol implementation and site initiation visits and routine monitoring of clinical studies. Along with the PI, ensure that research projects are conducted in compliance with federal regulations, institutional policies/departmental guidelines, and standards of Good Clinical Practice. This position will also assist with research related procedures and clinical activities as outlines and permitted within the Medical Assistant scope of practice as defined by Washington State Department of Health and Seattle Children's policy.</p><p></p><b><br>
Required Education and Experience</b><br>
Bachelor&rsquo;s Degree in or related discipline, or equivalent combination of education and experience. Graduation from an ABHES or CAAHEP accredited Medical Assistant program. Prior experience in research or a related field/setting. Bilingual skills may be required for certain positions.<br>
<br>
<b>Required Credentials</b>
<br>
Current Medical Assistant &ndash; Certified designation by Washington Department of Health (DOH). Current Basic Life Support for Healthcare Providers (BLS). Current Certification as a Medical Assistant by the AAMA, AMT, NHA, or NCCT.<br>
<br>
<b>Preferred</b><br>
Pediatric research experience. Current Medical Assistant experience in Pediatrics, Urgent Care experience and/or Medical screening and immunization.<p></p><p><b>
Compensation Range</b></p>
$29.16 - $43.73 per hour<p></p><p><b>
Salary Information</b></p><p>
This compensation range was calculated based on full-time employment (2080 hours worked per calendar year). Offers are determined by multiple factors including equity, skills, experience, and expertise, and may vary within the range provided.</p><p></p><div><p><b>
Disclaimer for Out of State Applicants</b></p><p>
This compensation range is specific to Seattle, positions located outside of Seattle may be compensated differently depending on various factors<b>.</b></p><p></p><div><p><b>
Benefits Information</b></p><p>
Seattle Children&rsquo;s offers a generous benefit package, including medical, dental, and vision plans, 403(b), life insurance, paid time off, tuition reimbursement, and more. Additional details on our benefits can be found on our website www.seattlechildrens.org/careers/benefits.</p><p></p><div><p><b>
About Us</b></p><p><b>
Hope. Care. Cure. These three simple words capture what we do at Seattle Children&rsquo;s &ndash; to help every child live the healthiest and most fulfilling life possible. Are you ready to engage with a mission-driven organization that is life-changing to many, and touches the hearts of all? #HOPECARECURE</b></p><p></p><p>
As one of the nation's top five pediatric research centers, Seattle Children's Research Institute is dedicated to providing hope, care, and cures to help every child live the healthiest and most fulfilling life possible.</p><p></p><p>
Our investigators are involved in hundreds of projects that cover every phase of research, from studying how diseases work to improving investigational therapies. They have pioneered groundbreaking cystic fibrosis treatments and cutting-edge cancer therapies that help a child's immune system defeat cancer, and made other major contributions to pediatric medicine.</p><p></p><p>
Researchers work in close collaboration with one another, their colleagues at partner institutions including the University of Washington and Fred Hutch and our healthcare providers at Seattle Children's Hospital, one of U.S. News &amp; World Report&rsquo;s top children's hospitals. This collaboration is one of our key strengths, allowing our faculty to draw on a variety of disciplines and techniques as they pursue solutions to some of medicine's most complex problems.</p><p></p><p>
We are committed to not only treating disease but to eliminating it. Help us achieve our vision of being a worldwide leader in pediatric research aimed to improve the health and well-being of children. If you are interested in a challenging career aimed at groundbreaking research, Seattle Children's Research Institute is the place for you.</p><p><b><br>
Our Commitment
</b></p><p></p><p>Seattle Children&rsquo;s welcomes people of all experiences, backgrounds, and thoughts as this is what drives our spirit of inquiry and allows us to better connect with our patients and families. Our organization recruits, employs, trains, compensates, and promotes based on merit without regard to race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.</p><p>
The people who work at Seattle Children&rsquo;s are members of a community that seeks to respect and celebrate all the qualities that make each of us unique. Each of us is empowered to be ourselves.</p><p></p><p>
Seattle Children&rsquo;s is proud to be an Equal Opportunity Workplace and Affirmative Action Employer.</p></div></div></div></div>

Clinical Research Coordinator 1, MA Certified

University of Arkansas

<div><h2 class="jobSectionHeader"><b>Current University of Arkansas System employees, including student employees and graduate assistants, need to log in to Workday via </b><b>MyApps.Microsoft.com </b><b>, then access Find Jobs from the Workday search bar to view and apply for open positions. Students at University of Arkansas System two-year institutions will also view open positions and apply within Workday by searching for &ldquo;Find Jobs for Students&rdquo;.
</b><br>
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<b>All Job Postings will close at 12:01 a.m. CT on the specified Closing Date (if designated).
</b></h2><h2 class="jobSectionHeader"><br>
<b>If you close the browser or exit your application prior to submitting, the application process will be saved as a draft. You will be able to access and complete the application through &ldquo;My Draft Applications&rdquo; located on your Candidate Home page.<br>
</b><br>
</h2><p><br>
<b>Closing Date:
</b></p>12/11/2025
<h2 class="jobSectionHeader"><br>
<b>Type of Position:
</b></h2>Researchers
<h2 class="jobSectionHeader"><br>
<b>Job Type:
</b></h2>Regular
<div><div><div><div><div><div><div><h2 class="jobSectionHeader"><br>
<b>Work Shift:
</b></h2></div></div></div></div></div></div></div><p></p><div><div><div><div><div><div><div><p><b>Sponsorship Available:
</b></p></div></div></div></div></div></div></div>No
<h2 class="jobSectionHeader"><br>
<b>Institution Name:
</b></h2>University of Arkansas for Medical Sciences<br>
<p><br>
The University of Arkansas for Medical Sciences (UAMS) has a unique combination of education, research, and clinical programs that encourages and supports teamwork and diversity. We champion being a collaborative health care organization, focused on improving patient care and the lives of Arkansans.<br>
<br>
</p><p><b>UAMS offers amazing benefits and perks </b>( available for benefits eligible positions only ):
</p><ul><li>Health: Medical, Dental and Vision plans available for qualifying staff and family
</li><li>Holiday, Vacation and Sick Leave
</li><li>Education discount for staff and dependents (undergraduate only)
</li><li>Retirement: Up to 10% matched contribution from UAMS
</li><li>Basic Life Insurance up to $50,000
</li><li>Career Training and Educational Opportunities
</li><li>Merchant Discounts
</li><li>Concierge prescription delivery on the main campus when using UAMS pharmacy
</li></ul><p></p><p>Below you will find the details for the position including any supplementary documentation and questions you should review before applying for the opening.
</p><p></p>The University of Arkansas is an equal opportunity institution. The University does not discriminate in its education programs or activities (including in admission and employment) on the basis of any category or status protected by law, including age, race, color, national origin, disability, religion, protected veteran status, military service, genetic information, sex, sexual orientation, or pregnancy. Questions or concerns about the application of Title IX, which prohibits discrimination on the basis of sex, may be sent to the University&rsquo;s Title IX Coordinator and to the U.S. Department of Education Office for Civil Rights.
<p></p><p>Persons must have proof of legal authority to work in the United States on the first day of employment.
</p><p></p><p>All application information is subject to public disclosure under the Arkansas Freedom of Information Act.<br>
<br>
</p><p>For general application assistance or if you have questions about a job posting, please contact Human Resources at askrecruitment@uams.edu .<br>
</p><h2 class="jobSectionHeader"><br>
<b>Department:
</b></h2>COM | PSY CAR &amp; WMH Administration<br>
<p><br>
<b>Department's Website:<br>
</b></p><h2 class="jobSectionHeader"><br>
<b>Summary of Job Duties:
</b></h2>The Research Assistant I (RA) serves as a member of a close-knit research team conducting clinical trials investigating the efficacy of pharmacotherapies for the treatment of psychostimulant use disorders and/or opioid use disorder. The RA will oversee and perform research clinic activities, perform recruitment activities, including assessing subject's eligibility for research projects, conducts informed consent, processes specimen samples, prepare and conduct research intakes and research assessments of the participants, prepare research/clinic materials, monitor enrolled subject's physical and emotional condition throughout the study, and perform data entry/data management activities. This position works with oversight by the study coordinator and under the supervision of the Principal Investigator (PI), and will work closely with the study physicians to bring potential medical issues to the study physicians for further evaluation. After initial training, this RA will work with other members of the research team with latitude for independent judgment.
<h2 class="jobSectionHeader"><br>
<b>Qualifications:
</b></h2><ul><li><p>Bachelor's degree in behavioral sciences (psychology, sociology, health sciences, or related field) or medical sciences, plus three (3) years of research-related experience required.
</p></li><li><p>Certified Research Specialist (CRS) or equivalent to be completed within two years of hire date.
</p></li></ul><p></p><p><b>Knowledge, Skills &amp; Abilities:
</b></p><ul><li><p>Computer program experience: Microsoft Office software, particularly Excel and Outlook. Experience with electronic data capture (EDC) systems preferred.
</p></li><li><p>Commitment to clinical research and willingness/ability to work with research participants who are substance users and at high risk for infection with HIV/other infectious diseases.
</p></li><li><p>Attention to detail.
</p></li><li><p>Strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments, and outside institutions.
</p></li><li><p>Ability to multitask in a fast-paced environment while working with a diverse subject population.
</p></li><li><p>Ability to follow Good Clinical Practice Guidelines, HIPAA, and the Protection of Human Research Subjects.<br>
</p></li></ul><p><br>
<b>Additional Information:
</b></p><p></p><p><b>Responsibilities:
</b></p><ul><li><p>Assists in the recruitment of participants, including placing ads.
</p></li><li><p>Assists with the phone, returns screening phone calls, schedules, and performs informed consent and screening procedures.
</p></li><li><p>Keeps screening logs up to date and performs outreach activities.
</p></li><li><p>Recruits and enrolls potential participants according to study protocol and standard operating procedures.
</p></li><li><p>Conducts the informed consent process and, as appropriate, obtains authorization(s) for release of information.
</p></li><li><p>With the study physicians, screens participants for study eligibility and randomizes eligible participants.
</p></li><li><p>Schedules participants for study visits.
</p></li><li><p>Serves as the participant tracker.
</p></li><li><p>Performs routine outreach (phone calls, mailings, in-person reminders) to ensure that participants attend study visits and coordinates ride-share services to/from clinic visits.
</p></li><li><p>Keeps in close touch with participants, including tracking and meeting with participants in the community if they have stopped coming to the clinic.
</p></li><li><p>Encourages participants to re-contact the treatment program and resume treatment.
</p></li><li><p>Collects extensive locator information at screening and regularly during the trial to assist in locating and following participants into the community if they fail to return for scheduled visits.
</p></li><li><p>Performs other duties as assigned.<br>
</p></li></ul><p><br>
<b>Salary Information:
</b></p>Commensurate with education and experience<br>
<p><br>
<b>Required Documents to Apply:
</b></p>Resume<br>
<div><div><div><div><div><div><div><p><br>
<b>Optional Documents:<br>
</b></p></div></div></div></div></div></div></div><h2 class="jobSectionHeader"><br>
<b>Special Instructions to Applicants:<br>
</b></h2><div><div><div><div><div><div><div><p><br>
<b>Recruitment Contact Information:
</b></p></div></div></div></div></div></div></div><p>Please contact askrecruitment@uams.edu for any recruiting related questions.<br>
</p><p><br>
<i>All application materials must be uploaded to the University of Arkansas System Career Site </i><i>https://uasys.wd5.myworkdayjobs.com/UASYS
</i></p><p><i>Please do not send to listed recruitment contact.<br>
</i></p><h2 class="jobSectionHeader"><br>
<b>Pre-employment Screening Requirements:
</b></h2>Criminal Background Check<br>
<p><br>
This position is subject to pre-employment screening (criminal background, drug testing, and/or education verification). A criminal conviction or arrest pending adjudication alone shall not disqualify an applicant except as provided by law. Any criminal history will be evaluated in relationship to job responsibilities and business necessity. The information obtained in these reports will be used in a confidential, non-discriminatory manner consistent with state and federal law.<br>
</p><h2 class="jobSectionHeader"><br>
<b>Constant Physical Activity:
</b></h2>N/A
<h2 class="jobSectionHeader"><br>
<b>Frequent Physical Activity:
</b></h2>Feeling, Hearing, Sitting, Standing, Talking, Walking
<h2 class="jobSectionHeader"><br>
<b>Occasional Physical Activity:
</b></h2>Climbing, Crawling, Crouching, Kneeling, Lifting, Pulling, Pushing, Reaching, Sharps
<h2 class="jobSectionHeader"><br>
<b>Benefits Eligible:
</b></h2>Yes</div>

Research Assistant I

Fortrea

<div><p><b>Apprenticeship Summary:</b></p><p>
The Apprentice participates in and executes the entry level department functions (Designation of Apprentice) in accordance with Fortrea and/or sponsor Standard Operating Procedures (SOPs)</p><ul><li>
Assist and Support the Centralized Delivery Team in delivering for Global Clinical Operations and Project Delivery team in Reviewing reports, Process Prep packs for CRA&rsquo;s, Study support and access management tasks, Startup tasks, eTMF tasks, Process Investigator Payment as instructed, etc.&hellip;</li><li>
Support and assist team in completing the day-to-day tasks ensuring quality and productivity</li><li>
Assist in maintaining project and technical documentation in an appropriate manner</li><li>
Help team visualize data into valuable analytics and insights for more informed decision making</li><li>
Support and assist the team in performing quality checks and escalation</li><li>
Provide support and assistance for administration activities of functional and Line management.</li></ul><p><b>
Education/Qualifications/Skills:</b></p><ul><li><b>
Bachelor of Engineering (B.E.) or Bachelor of Technology (B. Tech) in Biotechnology or Master of Science (M.Sc.) in Life Sciences</b></li><li>
Has experience delivering multiple projects in an academic or professional setting</li><li>
Has analytical and scientific curiosity in understanding of Clinical Research aspects</li><li>
Ability to collaborate with various stakeholders and internal/external colleagues</li><li>
Embraces diverse ways of thinking through various forms of collaboration and partnership</li></ul><p></p><p><b>
Work Experience:</b></p><ul><li>
0-11 Months of work experience working in any Clinical Development areas Clinical Operations preferred, across CROs, Pharmaceutical or Biotech companies.</li></ul><p></p><p><b>
Job Location :</b></p><ul><li>
Bangalore (Office based)</li></ul><p></p><p>
Learn more about our EEO &amp; Accommodations request here.</p></div>

Apprentice-Centralized Delivery

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