clinical trial assistant

Tarsus Pharmaceuticals, Inc.

<div>
 
 About The Role
 
 
 
 Ensuring the most effective and efficient conduct of clinical research studies by providing administration, regulatory and project tracking support. The CTA will accept projects as assigned per the changing needs of the Clinical Operations Department. Experience with Trial Master File (TMF) maintenance is required.
 
 
 
 Let&rsquo;s talk about some of the key responsibilities of the role:
 
 
 
 <ul>
 <li>
 Organize and maintain clinical study documentation (e.g., Trial Master Study Files) including preparation for internal/external audits, final reconciliation and archival.
 </li>
 <li>
 Responsible for the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
 </li>
 <li>
 Assist Clinical Research Associates (CRAs) and the clinical teams with accurately updating and filing clinical documents from study visits and updating systems that track site compliance and performance within project timelines.
 </li>
 <li>
 Completes periodic review of study files for completeness and audit readiness.
 </li>
 <li>
 Assist Study Manager with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
 </li>
 <li>
 Assist with the tracking and management of study trial data, queries, and clinical data flow.
 </li>
 <li>
 Provide general administrative support to the Clinical Operations Department and Study Manager(s) as needed.
 </li>
 <li>
 Co-ordinate ordering/dispatch and tracking of trial materials (e.g. source, diary cards, lab supplies, drug supplies) as appropriate.
 </li>
 <li>
 Contact clinical sites for specific requests (e.g., enrolment updates, missing documentation, meeting arrangements, etc.).
 </li>
 <li>
 Assist in the tracking and distribution of safety reports.
 </li>
 <li>
 Co-ordinate document translation, if required.
 </li>
 <li>
 Attend clinical team meetings and generate meeting minutes.
 </li>
 <li>
 Assist in the production of PowerPoint slides, including graphics, as needed for project, departmental, sponsor and/or business development presentations.
 </li>
 <li>
 Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
 
 
 </li>
 </ul>
 
 Factors for Success:
 
 
 
 To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree, or an Associate degree with minimum of 2 years, working with study related regulatory files.
 </li>
 <li>
 Experience working with and maintaining, an electronic Trial Master File.
 </li>
 <li>
 Must be familiar with ICH/GCP guidelines and appropriate regulatory regulations.
 </li>
 <li>
 Strong organizational skills with the ability to manage multiple tasks with meticulous attention to detail.
 </li>
 <li>
 Excellent written and verbal communication skills.
 </li>
 <li>
 Computer literacy: e.g., Microsoft Word, Excel, PowerPoint, Outlook.
 </li>
 <li>
 Knowledge of clinical trials software (eDC systems).
 </li>
 <li>
 The ability to prioritize workload with minimal supervision.
 </li>
 <li>
 Decision Making - Demonstrates strong decision-making by applying structured analysis to complex challenges, balancing competing priorities and long-term impacts while engaging stakeholders and driving solutions aligned with organizational goals.
 </li>
 <li>
 Collaboration and Team Building - Promotes collaboration by aligning diverse teams around shared goals, fostering healthy debate to advance outcomes, and building strong networks that strengthen organizational effectiveness and cross-team learning.
 </li>
 <li>
 Outcome Driven - Demonstrates strong outcomes focus by aligning teams around shared priorities, proactively addressing risks and dependencies, and driving cross-functional accountability to sustain progress and deliver results.
 
 
 </li>
 </ul>
 
 A Few Other Details Worth Mentioning:
 
 
 
 <ul>
 <li>
 The position will be based in our beautiful Irvine office, complete with onsite gym, pool, snacks, drinks, and occasional catered meals. We provide a hybrid work environment. [Remote work is an option.]
 </li>
 <li>
 We are passionate about our culture! Our Tarsans live our values of commitment to patients, empowerment to champion innovation, and teamwork to amplify impact! This position reports directly to our Manager II, Clinical Trials.
 </li>
 <li>
 Some travel may be required &ndash; up to 10%
 
 
 </li>
 </ul>
 At Tarsus, we understand the importance of attracting and retaining top talent. The expected base pay range for this position is $69,000 - $96,600 plus bonus, stock equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training. Our benefits include health, dental and vision insurance benefits to ensure your well-being. We believe in work-life balance and offer generous paid time off, including vacation, holidays, and personal days. For more details regarding Tarsus benefits, please visit: https://eb.alliant.com/26tarsusbenefitssnapshot.
 
 
 Tarsus Pharmaceuticals, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
 
 
</div>

Clinical Trial Assistant

IQVIA

<div>
 
 Essential Functions
 
 
 
 <ul>
 <li>
 Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
 </li>
 <li>
 Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
 </li>
 <li>
 Assist with periodic review of study files for completeness.
 </li>
 <li>
 Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
 </li>
 <li>
 Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
 </li>
 <li>
 Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
 </li>
 <li>
 May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor's Degree Required
 </li>
 <li>
 3 years administrative support experience.
 </li>
 <li>
 Equivalent combination of education, training and experience.
 </li>
 <li>
 Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
 </li>
 <li>
 Written and verbal communication skills including good command of English language.
 </li>
 <li>
 Effective time management and organizational skills.
 </li>
 <li>
 Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
 </li>
 <li>
 Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
 </li>
 <li>
 Knowledge of applicable protocol requirements as provided in company training.
 
 
 </li>
 </ul>
 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
 
 
 IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
 
 
 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
 
 
 The potential base pay range for this role, when annualized, is $34,400.00 - $118,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
</div>

University of Minnesota

<div>All required qualifications must be documented on application materials.
Required Qualifications:<ul><li>
Bachelor&rsquo;s degree in Life Sciences, Healthcare, or combination of education and relevant work experience to equal at least four years.</li> 
<li>
Basic understanding of medical terminology.</li><li>
Experience providing administrative support and interacting professionally with a wide range of people (i.e. executive leaders, faculty, clinical team members, patients, and visitors.</li><li>
Skills:<ul><li>
Proficiency with Microsoft Office and familiarity with data systems.</li><li>
Strong understanding of HIPAA and GCP guidelines.</li><li>
Exceptional organizational skills and &quot;eagle-eye&quot; attention to detail.</li></ul></li></ul> 
Preferred Qualifications:<ul><li>
2 years of clinical experience as a medical office assistant, Certified Medical Assistant, or Medical Appointment Scheduler</li><li>
Experience supporting complex electronic calendars.</li><li>
Experience prioritizing competing projects.</li><li>
Experience using MS Office Suite/Google/Epic/OnCore applications.</li><li>
Demonstrated commitment to strong customer service, detail oriented, and excellent communication and interpersonal skills.</li><li>
Excellent written and oral communication skills.</li><li>
Experience supporting more than one professional at a time and prioritizing work.</li><li>
Team player with excellent interpersonal skills; enjoys helping people and ability to adjust when project priorities change.</li><li>
Expert-level customer service skills, including both face-to-face and on the phone.</li><li>
Ability to work with a diverse population.</li><li>
Multitasking and working with details, managing workflow while dealing with expected interruptions and meeting deadlines.</li><li>
Excellent troubleshooting and problem-solving skills.</li><li>
Ability to make decisions in a timely manner.</li><li>
Experience with clinical research recruitment.</li></ul>
The Department of Dermatology Clinical Research Division is seeking a detail-oriented and motivated Clinical Trial Assistant (CTA) to join our research team. In this role, you will support our clinical research operations, ensuring that study protocol documents, scheduling and data are complete and accurate. The position will support both Investigator-Initiated Trials and Industry-sponsored protocols (Phases I&ndash;IV). The CRA will work closely with Clinical Research Coordinators (CRCs) and Principal Investigators (PIs) to facilitate the daily requirements of a diverse portfolio of clinical trials.
This position is based out of Minneapolis, MN and is eligible for hybrid work from home and/or on campus work dependent upon individual performance and organizational need, though some regular on-site work will be expected. Because the University of Minnesota is a land-grant institution that serves the state, residing in Minnesota is typically required. 
 
Key Responsibilities: 
1. Documentation &amp; Data Management-40%:<ul><li>
Source Documentation: Assist in the creation and maintenance of accurate source documents that capture all participant data during study visits.</li><li>
Case Report Forms (eCRFs): Accurately transcribe data from source documents into Electronic Data Capture (EDC) systems, ensuring all entries are timely and compliant with Good Clinical Practice (GCP).</li><li>
Clinical Trial Management (Oncore): Enter subject study visits accurately and in a timely manner.</li><li>
Data Entry &amp; Query Resolution: Perform routine data entry and work quickly to resolve any data queries or discrepancies identified by study monitors.</li></ul> 
2. Regulatory Compliance-10%:<ul><li>
Regulatory Binder Management: Maintain the Electronic Essential Documents Binder (eFlorence), ensuring all CVs, licenses are current and updated as necessary.</li><li>
Audit Readiness: Assist in preparing for site monitoring visits and potential audits by ensuring all files are organized and &quot;inspection-ready&quot; at all times.</li></ul>
3. Clinical &amp; Lab Support-50%:<ul><li>
Subject Recruitment: Assist the team in recruitment and screening to identify candidates for upcoming dermatology pipelines.</li><li>
Study Visit Facilitation: Support the clinical team in preparing for participant visits, including scheduling and confirming appointments, and ensuring all necessary supplies for the protocol are available.</li><li>
Laboratory Supply Inventory: Maintain adequate available lab kits and shipping supplies for each study. Document and dispose of expired kits.</li></ul>
Work Environment:<ul><li>
This position is primarily on-site to facilitate lab visits and physical document management.</li><li>
Must be comfortable handling biological samples and working in a fast-paced clinical setting.</li></ul>
The Department of Dermatology is committed to providing excellent patient care, conducting investigational research and training the next generation of dermatologist. We have world-renowned clinical programs, nationally recognized educational program, and pioneering clinical trials. We are dedicated to improving dermatological care not only for today, but also for the future.
For more information, please visit our website at https://med.umn.edu/dermatology.
Applications must be submitted online. To be considered for this position, please click the Apply button and follow the instructions. You will be given the opportunity to complete an online application for the position and attach a cover letter and resume.
Additional documents may be attached after application by accessing your &quot;My Job Applications&quot; page and uploading documents in the &quot;My Cover Letters and Attachments&quot; section.
To request an accommodation during the application process, please e-mail employ@umn.edu or call (612) 624-8647.
The University recognizes and values the importance of diversity and inclusion in enriching the employment experience of its employees and in supporting the academic mission. The University is committed to attracting and retaining employees with varying identities and backgrounds.
The University of Minnesota provides equal access to and opportunity in its programs, facilities, and employment without regard to race, color, creed, religion, national origin, gender, age, marital status, disability, public assistance status, veteran status, sexual orientation, gender identity, or gender expression. To learn more about diversity at the U: http://diversity.umn.edu
Any offer of employment is contingent upon the successful completion of a background check. Our presumption is that prospective employees are eligible to work here. Criminal convictions do not automatically disqualify finalists from employment.
The University of Minnesota, Twin Cities (UMTC)
The University of Minnesota, Twin Cities (UMTC), is among the largest public research universities in the country, offering undergraduate, graduate, and professional students a multitude of opportunities for study and research. Located at the heart of one of the nation's most vibrant, diverse metropolitan communities, students on the campuses in Minneapolis and St. Paul benefit from extensive partnerships with world-renowned health centers, international corporations, government agencies, and arts, nonprofit, and public service organizations.
At the University of Minnesota, we are proud to be recognized by the Star Tribune as a Top Workplace for 2021, as well as by Forbes as Best Employers for Women and one of America&rsquo;s Best Employers (2015, 2018, 2019, 2023), Best Employer for Diversity (2019, 2020), Best Employer for New Grads (2018, 2019), and Best Employer by State (2019, 2022).</div>

Planet Pharma

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

Clinical Trial Assistant I  - CTA

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

Clinical Trial Assistant I - CTA

Headlands Research

<div><div>At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.</div><h3 class="jobSectionHeader"> 
</h3>
<h2 class="jobSectionHeader">About the Opportunity</h2>

We're always interested in connecting with individuals who are curious about, experienced in, or eager to grow their careers in clinical research.

This general interest posting is designed for Clinical Research Assistants (RAs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide.

Research Assistants play a critical role in supporting clinical trials and bridging the gap between research and patient care. This is an ideal opportunity for individuals with patient-care, lab, academic, or research experience who are looking to transition into a clinical research role and gain hands-on clinical exposure.<h2 class="jobSectionHeader"> 
</h2>
<h2 class="jobSectionHeader">Our Process</h2>

When you apply to this posting, your profile is reviewed by our Talent Acquisition team and kept on file for current and upcoming Research Assistant opportunities. As new roles open, we proactively match candidates based on location preference, education, experience, and career interests. If there's a strong fit, a member of our team will reach out to start the conversation.<h2 class="jobSectionHeader"> 
</h2>
<h2 class="jobSectionHeader">What Research Assistant Roles Look Like at Our Company</h2>

Research Assistants support the execution of clinical trials by assisting with study visits, preparing study materials, collecting and organizing data, and helping ensure studies run smoothly and in compliance with protocols.

This role offers direct exposure to patient interactions, clinical workflows, and regulatory processes. Research Assistants work closely with Clinical Research Coordinators, investigators, and patients, gaining valuable experience that can serve as a strong foundation for advancement into Clinical Research Coordinator roles and beyond.

Responsibilities may vary depending on experience level and site needs but are designed to provide meaningful, hands-on learning and growth opportunities.<h2 class="jobSectionHeader"> 
</h2>
<h2 class="jobSectionHeader">Who We're Looking For</h2>

We welcome interest from candidates who bring:
<ul>
<li>A bachelor's or master's degree involving 1+ year of laboratory classes, preferably within a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or</li>
<li>Hands-on experience in lab work, research projects, or clinical environments</li>
<li>Strong attention to detail and the ability to follow structured protocols</li>
<li>Excellent organizational and time management skills</li>
<li>Clear communication skills and a desire to work directly with patients and care teams</li>
<li>A positive team-based attitude and approach</li>
<li>Prior clinical research experience is a plus</li>
</ul>
<h2 class="jobSectionHeader">Why Start or Grow Your Career in Clinical Research with Us</h2>
<ul><li>A strong entry point into clinical research with exposure to both research and patient care</li>
<li>Hands-on experience supporting clinical trials and working alongside experienced CRCs and investigators</li>
<li>Opportunities to learn Good Clinical Practice (GCP), regulatory processes, and study operations</li>
<li>Clear pathways for growth into Clinical Research Coordinator and other roles</li>
<li>The opportunity to contribute to developing new treatments that improve patient outcomes</li>
</ul>
<h2 class="jobSectionHeader">Ready to Start the Conversation?</h2>

Whether you're coming from a lab, academic research, or early clinical background and are looking to take the next step into a more patient-focused role, we'd love to connect.

Apply here to be considered for current and future Research Assistant opportunities. Our Talent Acquisition team will reach out as roles become available that align with your background and interests.</div>

Clinical Research Assistant Opportunities – Multiple Locations Nationwide

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Clinical Trial Assistant I - CTA

Clinical Trial Assistant I - CTA

Clinical Research Assistant Opportunities – Multiple Locations Nationwide