clinical project assistant

Innovo Research

<div>
 
 Description
 
 
 
 
 This position will be contract on a 3-4 month project.
 
 
 
 
 Job Summary
 
 
 
 A Clinical Research Assistant is an entry-level research position. This position is responsible for performing a variety of duties including coordinating aspects of clinical trial protocols including but not limited to study initiation, recruitment, study visits, monitor visits, regulatory compliance, and study close-out.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Act as a liaison between providers, study representatives, and patients.
 </li>
 <li>
 Maintain case report forms, source documents, and regulatory documents.
 </li>
 <li>
 Maintain stock of supplies needed to carry out protocols.
 </li>
 <li>
 Pack and ship patient labs and review lab results.
 </li>
 <li>
 Provide patient care and collect medical information during visits.
 </li>
 <li>
 Initiate and participate in the informed consent process.
 </li>
 <li>
 Conduct screening of prospective study participants and schedule appointments of patients interested in research studies.
 </li>
 <li>
 Identify potential research participant candidates utilizing various channels including medical records, databases, referrals, and community outreach to identify potential candidates for participation in clinical research studies.
 </li>
 <li>
 Obtain informed consent (if required and appropriately delegated) from eligible participants according to established guidelines and protocols, ensuring comprehension and compliance with ethical standards and regulatory requirements.
 </li>
 <li>
 Conduct thorough remote screenings and assessments to determine initial patient eligibility for participation in clinical trials, coordinating with healthcare professionals as needed to verify medical history and suitability.
 </li>
 <li>
 Maintain detailed and accurate records of patient interactions, recruitment efforts, and consent processes in accordance with regulatory standards and study protocols.
 </li>
 <li>
 Collaborate closely with interdisciplinary team members including investigators, research coordinators, healthcare providers, and administrative staff to facilitate seamless recruitment and enrollment processes.
 </li>
 <li>
 Adhere to all relevant regulatory guidelines, institutional policies, and ethical standards governing the conduct of screening, recruitment, and enrollment in clinical research, prioritizing patient safety, privacy, and confidentiality.
 </li>
 <li>
 Use employee calendars to schedule appointments for patients.
 </li>
 <li>
 Instruct patients regarding study protocols.
 </li>
 <li>
 Arrange for or perform phlebotomy.
 </li>
 <li>
 Perform related work as required.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 QUALIFICATIONS
 
 
 
 <ul>
 <li>
 High School Diploma or equivalent. Bachelor's Degree preferred.
 </li>
 <li>
 2-5 years of experience in a clinical setting is a plus.
 </li>
 <li>
 Phlebotomy experience/certification preferred.
 </li>
 <li>
 Certified Nurse Assistant Certificate and/or graduation from an accredited program for medical assistants is a plus.
 </li>
 <li>
 Knowledge of Good Clinical Practices for clinical research is a plus.
 </li>
 <li>
 Knowledge of OSHA and FDA regulations regarding clinical research a plus.
 </li>
 <li>
 Maintaining confidentiality is a must.
 </li>
 <li>
 Knowledge of medical terminology is a plus.
 </li>
 <li>
 Knowledge of electronic medical records and scheduling systems a plus.
 </li>
 <li>
 Experience in working with providers and other department staff.
 </li>
 <li>
 Ability to apply and modify professional research principles, methods, and techniques to provide ongoing patient care.
 </li>
 <li>
 Skilled in identifying problems and recommending solutions.
 </li>
 <li>
 Understand common safety hazards and precautions for maintaining a safe working environment.
 </li>
 <li>
 Prepare/maintain records, write reports, respond to correspondence, and respond to e-mails.
 </li>
 <li>
 High level of computer competency.
 </li>
 <li>
 Ability to maintain quality control standards.
 </li>
 <li>
 Ability to react calmly and effectively in all situations.
 </li>
 <li>
 Ability to work independently, prioritize, and work in a team environment.
 
 
 </li>
 </ul>
 
 BENEFITS (full Time)
 
 
 
 <ul>
 <li>
 Competitive salary
 </li>
 <li>
 Health Insurance
 </li>
 <li>
 Dental Insurance
 </li>
 <li>
 Disability Insurance
 </li>
 <li>
 Life insurance
 </li>
 <li>
 Paid Time Off
 </li>
 <li>
 Vision Insurance
 
 
 </li>
 </ul>
 
 WORKING CONDITIONS
 
 
 
 This job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites/clinics. This role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. It requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 50 pounds. Requires corrected vision and hearing to normal range.
 
 
 Due to the nature of this position, employees are expected to work in person. This is an exempt position under the federal and state wage and hour laws, which means you are not eligible for overtime pay beyond your salary. Employees are expected to work 40 hours a week. Occasional evening and weekend work may be required as job duties demand.
 
 
 The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP's, working guidelines, policies, etc. Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Innovo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Innovo Research will not tolerate discrimination or harassment based on any of these characteristics. In addition, Innovo will provide reasonable accommodations for qualified individuals with disabilities.
 
 
 Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
</div>

Contract Clinical Research Assistant

Wayne State University

<div>Research Assistant/ Project Coordinator- CBHJ
Wayne State University is searching for an experienced Research Assistant/ Project Coordinator- CBHJ at its Detroit campus location.
Wayne State is a premier, public, urban research university located in the heart of Detroit, Michigan where students from all backgrounds are offered a rich, high-quality education. Our deep-rooted commitment to excellence, collaboration, integrity, diversity and inclusion creates exceptional educational opportunities which prepare students for success in a global society.
Essential functions (job duties):

The Center for Behavioral Health and Justice (CBHJ) is seeking a Project Coordinator to support its Assisted Outpatient Treatment and Courts initiative. The Project Coordinator will work closely with external partners and CBHJ team members to ensure successful program implementation and evaluation. The ideal candidate thrives in a dynamic environment, enjoys navigating systems, and is a natural at building relationships. Knowledge of criminal/legal and behavioral health systems and a passion for programming that supports justice-involved individuals is preferred.
Serve as primary liaison within state and county partners and maintain positive collaborative relationships among all involved partners and systems including law enforcement, jails, courts, dispatch, community mental health, emergency medical services, behavioral health providers, etc.
Implement technical assistance, evaluation design, and data collection methods as defined by Principal Investigator, Directors, and/or Project Manager including facilitations of interviews and community of practice meetings and management of data collection, process mapping, identification of data points, collection methods, and entry.
Apply critical thinking in completing tasks such as needs assessments, assisting county partners in determining the best programs and interventions for their region and developing implementation plans.
Work with partners to establish formal meeting schedule, determine attendees, and revise as needed; facilitate meetings, using innovative techniques for maximum participation.
Work closely with Project Manager and other Project Coordinators to ensure efficiency in performing duties and fidelity of processes and practices across counties.
Coordinate and balance goals and objectives of project with needs, abilities, and priorities of community partners.
Work with PI, Directors, Data Teams, and/or Project Manager to report findings to community partners and assist in interpreting data and determining next steps.
Provide support in writing reports and manuscripts, developing presentations, and creating other materials as needed.
Must have transportation for meetings in communities across the state. 
Qualifications:

Bachelor&rsquo;s degree or equivalent experience or Master of Social Work or related master&rsquo;s degree in related field including Public Health or Criminal Justice preferred.
Experience working in behavioral health and/or criminal/legal systems; preferred experience or knowledge of behavioral health and court processes.
Experience interfacing with project partners including courts, behavioral health, substance use, criminal/legal, jails, probation/parole, and/or law enforcement agencies. 
 
Experience implementing new programs or interventions preferred.
Excellent oral and written communication, problem-solving, and inter-personal skills. 
 
Ability to conceptualize and map processes within a system or agency to illustrate the flow of information or services and identify data collection points.
Self-motivated; ability to work remotely and independently.
Proficiency with Excel, Word, Outlook, and PowerPoint. 
School/College/Division:

H13 - School of Social Work
Primary department:
H1304 - Behavioral Health &amp; Justice Center
Employment type:
<ul><li>Regular Employee</li>
<li>Job type: Full Time</li>
<li>Job category: Research</li>
</ul>Funding/salary information:
<ul><li>Compensation type: Annual Salary 
</li>
<li>Salary minimum: $55,000</li>
<li>Salary hire maximum: $69,000</li></ul>
Job openings:
<ul><li>Number of openings: 1 
</li>
</ul>Background check requirements:
University policy requires certain persons who are offered employment to undergo a background check, including a criminal history check, before starting work. If you are offered employment, the university will inform you if a background check is required.</div>

Research Assistant/ Project Coordinator- CBHJ

Meucci & Company

Job Description: Operations &amp; Project Assistant InternMeucci &amp; Company (Meucci) is a consultancy focused on STEM education, digital development, digital resiliency and its transformative power relative to equity/inclusion; gainful employability; future of work; problem solving; and civil society. The company's areas of expertise include training and capacity building; stakeholder engagement, outreach and communication; strategic planning; insights, measurement and adaptive learning; program design and project management. Meucci &amp; Company brings over 20 years&rsquo; experience leading STEM education, EdTech and digital development projects in partnership with corporations, state and local government agencies, K-12 and higher education institutions, DoD, DoL and non-profit clients.Job DescriptionMeucci is seeking an organized, initiative-taker for the role of Operations &amp; Project Assistant Intern. This person should have a strong professional acumen, eager to learn and be excited about STEM education, EdTech and digital development. Top candidates will also possess excellent writing and verbal communication skills and be able to juggle multiple tasks.In addition, the selected intern should be prepared to propose a concept or interest area for a professional development output that they would like to achieve by the end of the internship. Upon approval, Meucci will provide the necessary resources and ongoing mentoring to help achieve the output.ResponsibilitiesProvide administrative support as directed by senior management in the following areas.<ul><li>Participate in meetings as a record keeper and disseminate talking points</li><li>Maintain knowledge management systems</li><li>Draft BD and organizational communications content</li><li>Manage updates to Meucci professional networking and social media accounts</li><li>Proof-read and light editing of content for proposals, presentations and other project documents. Requirement: Candidates must be able to demonstrate</li><li>Due diligence research to support business development, projects, strategic planning and other insight needs</li><li>Document formatting. Requirement: Candidates must be able to demonstrate intermediate level (at a minimum) formatting skills</li><li>Provide administrative support for trainings, project and events</li><li>Other administrative and project support duties as assigned</li></ul>Requirements:<ul><li>Recent College/University Bachelor&rsquo;s degree graduate, or senior currently pursuing a 4-year degree</li><li>Proficiency in Microsoft Office (Word, Excel &amp; PowerPoint)</li><li>Excellent Document Formatting Skills. Requirement: Candidates must be able to demonstrate intermediate level (at a minimum) formatting skills via a required test.</li><li>Previous relevant experience</li><li>Strong technical writing skills. Candidate will be required to take a required writing test.</li><li>Critical thinking skills</li><li>Self-directed and output oriented</li><li>Excellent time management and organizational skills</li><li>Prepared to propose a professional development concept</li><li>Creative and innovative thinker who seeks challenges</li></ul>Work Hours:<ul><li>16 hours per week, between Monday and Friday</li><li>Flexible schedule.</li></ul>Salary: Competitive per hourWorking requirement: Onsite Office in Downtown Washington, DC. Dupont Circle and Farragut North Metro Accessible. This is NOT a remote position. Only local candidates will be considered. Please DO NOT respond if you are NOT locally based.Please respond to Recruit@meucciandco.comJob Types: Part-time, Temporary, InternshipPay: $18.00 per hourBenefits:<ul><li>Flexible schedule</li></ul>Compensation Package:<ul><li>Hourly pay</li></ul>Work Location: In person

Operations & Project Assistant Intern

Children's Hospital of Philadelphia

<div>SHIFT:
Day (United States of America)
Seeking Breakthrough Makers 
 
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. 
 
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. 
 
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. 
About the Department: 
Clinical Research Assistant I will work in the Craig-Dalsimer Division of Adolescent Medicine at the Children&rsquo;s Hospital of Philadelphia and PolicyLab in the Research Institute. The Children&rsquo;s Hospital of Philadelphia Research Institute is an interdisciplinary institution dedicated to conducting basic, clinical and translational research on conditions and diseases that affect children, and is part of The Children's Hospital of Philadelphia and University of Pennsylvania research community. 
Position Description:
The Clinical Research Assistant I will be aiding the Research Team and the Principal Investigator in clinical, behavioral, policy, health technology, and community-engaged research. Through research, the team strives to better understand and improve the health of adolescents living with HIV/AIDS and other marginalized youth including LGBT and homeless adolescents. Research interests focus on improving adherence to antiretroviral therapy and secondary prevention for adolescents living with HIV using youth-friendly technology, improving routine HIV/STI screening and sexual health education for adolescents, understanding risk and protective factors to improve health outcomes and access for LGBT youth, and addressing policy issues that affect health inequities experienced by these youth. 
A Brief Overview 
Under the direct supervision of the Principal Investigator and/or other study team members, this role provides support in the conduct of clinical research. 
 
Job responsibilities may include human subject research activities including but not limited to subject enrollment, data/sample collection, data entry, and regulatory submissions support. 
 
What you will do<ul><li>
Provide technical and administrative support in the conduct of clinical research:</li><li>
Patient/research participant scheduling</li><li>
Patient/Research Participant screening for inclusion/exclusion criteria or case history</li><li>
Data collection</li><li>
Data entry</li><li>
Data management</li><li>
Laboratory sample processing</li><li>
Clinical research study procedures or questionnaire administration</li><li>
Organization of research records and/or other study related documentation</li><li>
Research Study Compliance</li><li>
Adhere to IRB approved protocols and compliance with HIPAA and handling confidential materials</li><li>
Comply with Institutional policies, SOPs and guidelines</li><li>
Comply with federal, state, and sponsor policies</li><li>
Additional Responsibilities may include:</li><li>
Consent subjects, with appropriate authorization and training</li><li>
Document and report adverse events</li><li>
Maintain study source documents</li><li>
Complete case report forms (paper and electronic data capture)</li><li>
Assist with IRB/regulatory submissions</li><li>
Complete case report forms or other study documentation (paper and electronic data capture)</li><li>
Follow-up care</li><li>
Order materials/supplies</li><li>
Schedule research meetings</li></ul>
Education Qualifications<ul><li>
High School Diploma / GED Required</li><li>
Bachelor's Degree Preferred</li></ul>
Experience Qualifications<ul><li>
Previous relevant clinical research experience Required</li><li>
At least one (1) year of relevant clinical research experience Preferred</li></ul>
Skills and Abilities<ul><li>
Familiarity with IRB and human subject protection.</li></ul> 
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. Learn more. 
 
EEO / VEVRAA Federal Contractor | Tobacco Statement
SALARY RANGE:
$20.55 - $25.69 Hourly
Salary ranges are shown for full-time jobs. If you're working part-time, your pay will be adjusted accordingly.
-
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.</div>

Full-Time Clinical Research Assistant I (HIV/STI & GSDP)

ProPharma

<div>
 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality &amp; compliance, pharmacovigilance, medical information, and R&amp;D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners&rsquo; most high-profile drug and device programs.
 
 
 
 Job Summary
 
 
 
 The Central Study Coordinator/Research Assistant position is responsible for the coordination and support of remote site activities for assigned projects.
 
 
 
 Essential Functions
 
 
 
 <ul>
 <li>
 Serve as point of contact for day-to-day Site communications, document submissions and activity coordination.
 </li>
 <li>
 Support pre-screening, screening and recruitment activities, as assigned.
 </li>
 <li>
 Responsible for subject re-consenting, acquiring medical records, conducting protocol activities, as directed by the Principal Investigator.
 </li>
 <li>
 Perform data-entry, evaluate and respond to system queries and monitor clinical databases as assigned.
 </li>
 <li>
 Establish and maintain timely Site communication as assigned.
 </li>
 <li>
 Maintain documentation which complies with IRB/FDA policies.
 </li>
 <li>
 Assist with study closeout.
 </li>
 <li>
 Assist site with other study-related activities as directed.
 
 
 </li>
 </ul>
 
 Necesary Skills And Abilities
 
 
 
 <ul>
 <li>
 Ability to manage technology and web-based research platforms on PC (Microsoft OS) laptop in the remote workspace;
 </li>
 <li>
 Study Team experience is ideal
 </li>
 <li>
 Critical thinking skills
 </li>
 <li>
 Strong communication Skills (verbal and written)
 </li>
 <li>
 Ability to work independently, and collaboratively with other CSCs to delegate tasks as needed
 </li>
 <li>
 Working location that has the ability to maintain privacy
 </li>
 <li>
 Current knowledge of and the ability to apply ICH / GCP and applicable regulations and guidelines.
 </li>
 <li>
 Competent in the application of standard business procedures including but not limited to SOPs, global regulations.
 </li>
 <li>
 Well organized and able to multitask.
 </li>
 <li>
 Able to work independently and as a team member.
 </li>
 <li>
 Able to take initiative while following directives.
 
 
 </li>
 </ul>
 
 Central Study Coordinator Position Requirements
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree or equivalent experience defined as a minimum of 2 years related, combined experience in education, knowledge and skills that will allow one to perform the tasks of the role proficiently.
 </li>
 <li>
 Minimum 2 years of study coordinator experience .
 
 
 </li>
 </ul>
 
 Research Assistant Position Requirements
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree or equivalent experience defined as a minimum of 1 year related, combined experience in education, knowledge and skills that will allow one to perform the tasks of the role proficiently.
 </li>
 <li>
 Research experience preferred.
 
 
 </li>
 </ul>
 We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
 
 
 All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
 
 
 ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
 
 
</div>

On-site Central Study Coordinator/Research Assistant - Buenos Aires, Argentina

Boston Children's Hospital

<div><div><div><div>84679BR</div>
</div><div><div>Orthopedic Surgery and Research
</div></div><div>Job Posting Description
<div>Position Summary: 
This is a CRA opportunity in Translational research. This is a competitive 2-year initiative for recent college graduates aspiring to leadership roles in medicine. It provides hands-on training in clinical practice, research, and leadership within the Orthopedics &amp; Sports Medicine department. Participants will have the opportunity to work alongside renowned orthopedic surgeons and researchers. 
 
Key Responsibilities:
<ul><li>Clinical Research: Involves subject recruitment, IRB submissions, data analysis, and manuscript preparation.</li><li>
Study Design &amp; Analytics: Exposure to research methodology, statistics, and clinical science study design.</li><li>
Research Ethics: Training in human subjects, protections and management of multicenter registries.</li><li>
Clinical Exposure Scribe Role: Participate in patient visits, documentation, and learn clinical decision-making and physical exam techniques.</li><li>
Shadowing &amp; Mentorship: Collaborate with leading orthopedic surgeons; attend lectures, case reviews, and conferences.</li><li>
Educational Opportunities Daily Lecture Series: Covers orthopedic topics and research skills.</li><li>
Weekly &amp; Quarterly Events: Includes case reviews, journal clubs, and visiting professor seminars.</li><li>
Research Engagement: Opportunities for co-authorship on publications and presentations at regional/national conferences.</li><li>
Mentorship and Scholar Support Mentorship: One-on-one guidance from top faculty, with regular career coaching and project feedback. This program emphasizes building futures and advancing knowledge through dedicated faculty support.</li></ul>
 
Minimum Qualifications 
Education:<ul><li>
A Bachelor&rsquo;s Degree is required.</li></ul>
Experience:<ul><li>
Analytical skills to gather and interpret data, excellent organizational skills and attention to detail.</li><li>
Effective communication and writing skills to provide critical information to team members, patients, and families with ability to triage and escalate concerns to appropriate leadership.</li><li>
Problem-solving, troubleshooting abilities and resourcefulness.</li></ul></div>
</div><div>Status
<div>Full-Time</div>
</div><div>Regular, Temporary, Per Diem
<div>Regular
</div></div><div>Standard Hours per Week
<div>40
</div></div><div>Pay Range
<div>$41246.40-$61339.20 Annual</div>
</div><div>Office/Site Location
<div>Boston</div>
</div><div>Job Posting Category
<div>Research</div>
</div><div>Remote Eligibility
<div>Part Remote/Hybrid</div></div></div></div><div></div>

Clinical Research Assistant - MCD Scholar

Brown University Health

<div><ul><li>Job ID: JR-107849
</li><li>Entity: Rhode Island Hospital
</li><li>Location Name: Rhode Island Hospital
</li><li>City, State: Providence, RI
</li><li>Work Type: PER DIEM
</li><li>Hours Per Week: Variable
</li><li>Shift: Day
</li><li>Posted Date: 4/9/2026
</li></ul><div><h2 class="jobSectionHeader">SUMMARY</h2>

Under the general supervision of the Principal Investigator(s) and Clinical Research Coordinator, assist in acquisition and analysis of patient information for multiple clinical research projects. Interviews patients to gather information, prepares and maintains study record, enters data via computer, performs statistical analyses of resultant data. Participates in qualitative/quantitative analyses of resultant data. Reviews relevant literature to gather information; may participate in development of research protocols. May perform EKG&rsquo;s and take vital signs during research-based monitoring tests. May also perform blood spinning and shipment of blood and tissue samples as required by protocol. Brown University Health employees are expected to successfully role model the organization's values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another.

In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include:
<ul>
<li>Instill Trust and Value Differences</li>
<li>Patient and Community Focus and Collaborate</li>
</ul><h2 class="jobSectionHeader">RESPONSIBILITIES</h2>

Provides assistance to Principal Investigators to coordinate clinical research activities related to department&rsquo;s field of study and investigators specific study. Assists research physician in identification and follow up of patients meeting criteria for inclusion in clinical research studies; ensures protocol eligibility requirements are met. Establishes and/or maintains study record for each participant. Interviews patient and/or family to explain nature of study, elicit cooperation and gather information to complete study questionnaire. Facilitates obtaining informed consent. May schedule patient appointments and call patients to complete documentation. May review medical records to abstract information necessary to complete forms. May request and follow up on missing data such as laboratory test results and the like. Monitors adherence to protocol; alerts physician when laboratory tests ordered have not been performed, medication protocol not followed, etc. May perform research-based EKG&rsquo;s, vital signs, blood spinning and shipping of blood and tissue products, in accordance with protocol specifications. Collects and organizes patient data into appropriate format to facilitate data entry. Operates computer to enter study information into database. Using pre-packaged software and according to needs of research supervisor, performs computer-assisted statistical analysis such as multiple antecedent variables, linear regression, frequencies, cross tabulations and the like. May write non-complex programs using computer and software-compatible language to reformat information, create new files, etc. Maintains computer equipment, arranges for internal/external service as necessary to effect repairs and maintenance. Prepares related graphs and charts or results of data gathered. Participates in quantitative and qualitative analyses of resultant information. May assist in planning research protocols. Coordinates activities of others assigned to research project to interview patients, complete forms or perform other tasks. Reviews literature pertaining to research being conducted in order to better understand project and gather relevant information.
<h2 class="jobSectionHeader">
MINIMUM QUALIFICATIONS</h2>

BASIC KNOWLEDGE: Bachelor&rsquo;s Degree in Applied or Life Sciences or related area, including courses in research methodologies and microcomputer systems.

EXPERIENCE:
<ul>
<li>Three to six months on-the-job experience to become familiar with specific research studies.</li>
<li>Knowledge of theory and techniques of research methodology.</li>
<li>Organizational skills to organize and prioritize own efforts on multiple projects and to gather research information, format appropriately for computer data entry, prepare and maintain records and reports, etc.</li>
<li>Interpersonal skills to effectively interact with patients, families and Hospital professionals to gather and exchange information.</li>
<li>Analytical skills to participate in developing research protocols, perform statistical analyses and participate in qualitative/quantitative analyses of research data.</li>
<li>Technical ability to operate and maintain computer system.</li>
<li>Demonstrated knowledge and skills necessary to provide care to patients with consideration of aging processes, human development stages and cultural patterns in each step of the care process.</li>
</ul>
WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS: Often works within a specific department to identify, enroll and follow up on research patients. May spend much of the time standing and walking between departments, offices, Medical Records, etc.

INDEPENDENT ACTION: Perform independently within the department&rsquo;s policies and practices. Refers specific complex problems to the supervisor when clarification of the departmental policies and procedures are required.

SUPERVISORY RESPONSIBILITY: None.
<h2 class="jobSectionHeader">
PAY RANGE</h2>

$19.97-$32.96
<h2 class="jobSectionHeader">
LOCATION</h2>

Rhode Island Hospital - 593 Eddy Street Providence, Rhode Island 02903
<h2 class="jobSectionHeader">
WORK TYPE</h2>

m-f 8:00am to 5:00pm
<h2 class="jobSectionHeader">
WORK SHIFT</h2>

Day
<h2 class="jobSectionHeader">
DAILY HOURS</h2>

Per Diem - As required
<h2 class="jobSectionHeader">
DRIVING REQUIRED</h2>

No

Brown University Health is committed to providing equal employment opportunities and maintaining a work environment free from all forms of unlawful discrimination and harassment.</div></div>

Clinical Research Assistant NES

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