medical research assistant

The Henry M. Jackson Foundation for the Advancement of Military Medicine

<div>Join the HJF Team!
HJF is seeking a Research Assistant I to perform research and/or development in collaboration with others for projects. The Research Assistant provides laboratory and technical support to senior technical and professional staff and solves less complex problems in carrying out research projects in a laboratory environment. This is the first of four levels within the Research Assistant series.
Serves as a Research Assistant I in the Department of Pharmacology and Molecular Therapeutics, to support the Kortum laboratory in the Department of Pharmacology at Uniformed Services University of the Health Sciences in Bethesda, MD. Responsible for initiating and carrying out research projects in collaboration with a research team.
The lab is working to determine the mechanisms that promote drug tolerant persister survival and identify biomarkers of tumor initiating cells that drive resistance to RTK-targeted therapies in RTK-mutated NSCLC.
The Henry M. Jackson Foundation for the Advancement of Military Medicine (HJF) is a nonprofit organization dedicated to advancing military medicine. We serve military, medical, academic and government clients by administering, managing and supporting preeminent scientific programs that benefit members of the armed forces and civilians alike. Since its founding in 1983, HJF has served as a vital link between the military medical community and its federal and private partners. HJF's support and administrative capabilities allow military medical researchers and clinicians to maintain their scientific focus and accomplish their research goals.</div>

Research Assistant I - Pharmacology and Molecular Therapeutics

Hennepin Healthcare Research Institute

<div>
 The Hennepin Healthcare Research Institute's (HHRI) Addiction Medicine department is seeking an experienced Research Assistant to support the research being conducted at Hennepin Healthcare
 
 
 This is an onsite position to work in downtown Minneapolis, MN on the HCMC campus.
 
 
 The Research Assistant would be supporting two clinical trials (CTN-0131 and CS-1036) funded by the National Institute of Drug Abuse (NIDA). CTN-0131's objective is to determine whether office-based methadone with pharmacy administration and/or dispensing or buprenorphine (BUP) results in greater treatment retention in patients with Opioid Use Disorder (OUD). The study will also identify implementation barriers, facilitators and acceptability at the patient, provider, and health-systems level for office-based methadone with pharmacy administration and/or dispensing. CS-1036 is a study investigating the efficacy of Wellbutrin and Naltrexone in reducing use and cravings for populations with methamphetamine use disorder (MUD).
 
 
 
 Position Summary
 
 
 
 The Research Assistant will screen, recruit patients, and determine patient eligibility for participation in study. The RA will also collect and interpret study data in an organized and precise fashion to maintain data integrity; disburse and track funds to study participants on a timely basis; provide comprehensive study support and contributes to successful project execution; and be responsible for protocol initiation, procedural adherence, and compliance.
 
 
 
 Essential Job Functions
 
 
 
 <ul>
 <li>
 Screens, recruits patients, and determines patient eligibility for participation in study via patient histories, test results, medical exams, etc.
 </li>
 <ul>
 <li>
 Willingly acts as a resource person to other medical staff regarding study protocol and interpretation.
 </li>
 </ul>
 <li>
 Responsible for protocol initiation, procedural adherence, and compliance.
 </li>
 <li>
 Obtains informed consent and administers and scores psychological, intellectual, and/or other medical assessments and tests.
 </li>
 <li>
 Obtains blood specimens by performing venipunctures, preparing specimens for laboratory testing, tracks collected specimens by initialing, dating, and noting times of collection.
 </li>
 <li>
 Documents and consistently maintains detailed records and research data files.
 </li>
 <li>
 Assist with data entry, data cleaning, and the preparation of reports.
 </li>
 <li>
 May accurately disburse and track funds to study participants and book transportation.
 </li>
 <li>
 Collects and interprets study data in an organized and precise fashion to maintain data integrity.
 </li>
 <ul>
 <li>
 Regularly schedules study related testing as required by protocols.
 </li>
 </ul>
 <li>
 Handle and protect confidential and sensitive data with integrity.
 </li>
 <li>
 Maintains and operates various scientific apparatus.
 </li>
 <li>
 Consult with PI and Study Coordinator on management of participant problems and concerns.
 </li>
 <li>
 Provide administrative coverage as an assistant to the Principal Investigator, project manager, and study coordinator as the need arises (general clerical: printing, copying, preparing correspondence, answering phones, inter-organization pick-up and delivery).
 </li>
 <li>
 Participate in Study team meetings
 
 </li>
 </ul>
 
 Education/Experience
 
 
 
 
 EMPLOYMENT STANDARDS:
 
 
 
 Any equivalent combination of education and experience that provides the required skills and knowledge is qualifying. Bachelor's degree is preferred or a combination of related education and work experience to equal at least four (4) years.
 
 
 
 Skill, Knowledge &amp; Ability (SKA)
 
 
 
 Requires interaction with a diverse population. Perform blood draws and processing. Demonstrate a working knowledge of basic computer applications. Basic knowledge of research design, protocols, and analysis a plus. Previous experience with participant study recruitment a plus. Ability to work independently, be self-directed and motivated. Demonstrated effective oral and written communication skills. Skilled in problem solving and keeping detailed records and files. Displays high standards of attendance, punctuality, maintains confidentiality, and manages time effectively.
 
 
 
 
 HHRI is an Equal Opportunity Employer
 
 
 
 
 Salary: $18.50 - $22.00 per hour
 
 
 
 Job Posted by ApplicantPro
 
</div>

Research Assistant - Addiction Medicine

Covenant Metabolic Specialists

Covenant Metabolic Specialists (CMS) is a leading medical practice dedicated to the clinical management and education of metabolic diseases, with a special focus on fatty liver disease and obesity. Founded in October 2019, CMS has rapidly emerged as a global leader in treating liver diseases through groundbreaking clinical care, research therapies and innovative treatments that are not available elsewhere. With over 200 years of combined clinical experience, our expert medical team delivers state-of-the-art therapies and lifestyle guidance to improve metabolic health for patients.Covenant is seeking a Research Assistant for our facility located in Ft Myers, Florida. This position will assist with our clinical operations by taking patient vital signs and other measurements, performing FibroScans, completing EDC entries, and other duties as needed.Responsibilities<ul><li>Use phlebotomy skills to collect lab specimens from patients.</li><li>Collect vital signs, weight, height, body measurements, EKG, etc. according to study requirements and documents appropriately in source document.</li><li>Upload EKGs to Sponsor specific portals, answer queries as needed, and reorder supplies.</li><li>Perform FibroScans on patients.</li><li>Restock patients&rsquo; rooms at the end of each week.</li><li>Enter data into EDC and answers queries as assigned.</li><li>Print and file study specific or patient specific documents.</li><li>Print labs daily from DocuSign as assigned and provide reports to the appropriate Clinical Research Coordinator (CRC).</li><li>Assist in the Lab.</li><li>Update or load documents into the Company&rsquo;s clinical trial management system as needed.</li><li>Update excel sheets as requested by CRCs.</li><li>Request medical records and follow up as needed.</li><li>Clean exam rooms.</li><li>Help CRCs with any other tasks as needed.</li><li>Other duties as assigned.</li></ul>Education and Experience<ul><li>Associate's degree in a related field (such as Medical Assisting, Nursing, Life Sciences, or Healthcare Administration), preferred.</li><li>Relevant certificates (e.g., Certified Medical Assistant, Emergency Medical Technician) or significant coursework in a related field.</li><li>1-2 years of experience in a clinical setting or in clinical research preferred.</li><li>Experience performing phlebotomy, EKGs, and other diagnostic procedures is desirable.</li><li>Experience with a Clinical Trial Management System (CTMS) is a plus.</li><li>Experience with specific technology, such as a FibroScan machine, is desirable</li></ul>Other Skills<ul><li>Proficient with Electronic Data Capture (EDC) or Electronic Medical Records (EMR) systems.</li><li>Basic office software (e.g., Microsoft Office Suite, especially Excel).</li><li>Excellent verbal and written communication skills to effectively interact with patients, staff, and sponsors.</li><li>Strong organizational and multitasking skills, with the ability to prioritize tasks in a fast-paced environment.</li><li>Bilingual (English/Spanish) preferred.</li><li>Certifications in CPR, Basic Life Support (BLS), or other relevant healthcare certifications</li><li>Ability to meticulously follow study protocols, document patient data accurately, and manage confidential information.</li><li>Demonstrated ability to work collaboratively in a team and support colleagues in achieving team goals.</li><li>Openness to learning new skills and adapting to changing procedures and protocols.</li><li>Understanding of patient privacy laws (HIPAA) and ethical considerations in clinical research.</li><li>Willingness to undergo background checks and necessary training for compliance with healthcare regulations.</li></ul>Covenant Metabolic Specialists, LLC is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, genetics, disability, age, veteran status, or any other characteristic protected by law.Pay: $40,000.00 - $50,000.00 per yearBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Education:<ul><li>Associate (Preferred)</li></ul>Experience:<ul><li>nursing or medical assistant: 1 year (Preferred)</li></ul>Work Location: In person

Clinical Research Assistant

Virginia Commonwealth University

<div><div><div><div><div><ul><li>45001881
</li></ul></div><div><ul><li>907 Floyd Avenue, MCV Main Campus, Virginia, United States, 23284
</li><li>907 Floyd Avenue, VCU Main Campus, Virginia, United States, 23284
</li></ul></div><div><ul><li>Research
</li></ul></div><div><ul><li>Staff
</li></ul></div><div><ul><li>School Of Medicine MBU</li></ul></div></div><div> 
</div><div>Advertising Summary: Virginia Commonwealth University (VCU) School of Medicine is a premier academic medical center located in the heart of Richmond. Accounting for almost half of VCU&rsquo;s sponsored research, the School of Medicine is internationally recognized for patient care and education.

Unit: School Of Medicine MBU

Department: Pediatrics

Duties &amp; Responsibilities:

VCU's Department of Pediatrics invites all interested candidates to apply for our exciting Research Assistant position! At VCU, we Make it Real through learning, research, creativity, service and discovery - the hallmarks of the VCU experience. A premier, urban, public research university nationally recognized as one of the best employers for diversity, VCU is a great place to work. It's a place of opportunity, where your success is supported, and your career can thrive.

Position Primary Purpose and General Responsibilities

VCU's Department of Pediatrics invites all interested candidates to apply for our exciting Research Assistant position. Research Assistants perform a variety of routine, non-technical duties in assisting technical and professional personnel in a research clinical setting.

The Research Assistant will be expected to perform most components of data collection from human-subject volunteers required for multiple bio-behavioral and brain imaging research studies. The current position is to help us with data analysis on completed studies and subject recruitment and scheduling for active studies. The general responsibilities of this role are as follows:

Subject Recruitment - Participant/research subject recruitment, including placement of IRB-approved materials and media advertisements about research studies being conducted in the department, as well as collection and computer entry of responses and information furnished by potential research volunteers contacting the lab by phone, web or other means to identify possible participants. Scheduling of participants within protocol specific time frames.

Participant Consenting - Collection of informed consent and/or assent and permission from research volunteers, including describing the study to research participant candidates in simple language, and overseeing the signing of consent and assent forms.

Data Collection - Biological data collection, including collection and testing of urine and blood, saliva, and hair samples. Data collection from neuro-imaging studies will also be required, as well as vagal stimulation studies both from stimulating and recording devices for heart rate variability analysis.

Psychometric data collection, including administration, collection and scoring of paper-and-pencil or computer-driven questionnaires, as well as administration and recording of computer-driven cognitive performance tasks.

Maintain Study Data - Accurate and secure transmission and storage of study data, including to centralized databases or to physically secured case report forms for industry-sponsored clinical trials.

Participant Management - Accurate calculation of subject compensation. As part of the assessment, the employee will be expected to coordinate a busy study visit for the subjects, including escorting research volunteers to and from the different tasks and testing rooms and waiting rooms of the research facility

Other duties assigned by Lead Clinical Research Coordinator or Principal Investigator. Most work is done on-site with potentially some work done remotely.

Qualifications:

Minimum Qualifications
<ul>
<li>Bachelor's of Science degree or equivalent in any of the science subspecialties or psychology.</li>
<li>Proficient in computer skills including word processing, data entry, spreadsheet, database management, and entry level statistical/programming skills required.</li>
<li>Strong interpersonal skills such as establishing rapport, maintaining participant motivation, empathic responding, ability to work effectively as part of a multidisciplinary team, and ability to use clinical judgment in (rare) emergency situations.</li>
<li>Strong organizational skills, including understanding of HIPAA regulations.</li>
<li>Demonstrated experience working in and fostering an environment of respect, professionalism and civility with a population of faculty, staff, and students from various backgrounds and experiences, or a commitment to do so as a staff member at VCU.</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience conducting research in pediatric or adolescent populations.</li>
<li>Experience recruiting, consenting, and carrying out study procedures with adult and youth participants</li>
<li>Qualitative research experience, including data collection, coding, analysis</li>
<li>Experience administering surveys in REDCap</li>
<li>Experience in conducting mental health surveys with adults and youth</li>
<li>Experience collecting biospecimens from research participants, including hair, saliva, blood, and urine</li>
<li>Experience in mentoring and training student research trainees, incorporating them into research teams</li>
</ul>
Salary Range: Commensurate with Experience (up to $55,000)

Benefits: All full-time university staff are eligible for VCU&rsquo;s robust benefits package that includes comprehensive health benefits, paid annual and holiday leave, generous tuition benefits, retirement planning and savings options, tax-deferred annuity and cash match programs, employee discounts, well-being resources, abundant opportunities for career development and advancement, and more.

FLSA Exemption Status: Non-Exempt 
 
Hours per Week: 40

Restricted Position: Yes

ORP Eligible: No

Flexible Work Arrangement: Hybrid

University Job Title: Clinical Research Assistant 1-3 (34001N, 34002N, 34003N)

Contact Name: Jewel Jefferson

Contact Email: jewel.jefferson@vcuhealth.org</div></div></div></div>

Clinical Research Assistant - SOM/Pediatrics

<div><div><div><ul><li>45001881
</li></ul></div><div><ul><li>907 Floyd Avenue, MCV Main Campus, Virginia, United States, 23284
</li><li>907 Floyd Avenue, VCU Main Campus, Virginia, United States, 23284
</li></ul></div><div><ul><li>SVP Health Sciences SML
</li></ul></div><div><ul><li>Research
</li></ul></div><div><ul><li>Staff
</li></ul></div><div><ul><li>Virginia Commonwealth University</li></ul></div></div><div> 
</div><div>Advertising Summary: Virginia Commonwealth University (VCU) School of Medicine is a premier academic medical center located in the heart of Richmond. Accounting for almost half of VCU&rsquo;s sponsored research, the School of Medicine is internationally recognized for patient care and education.

Unit: School Of Medicine MBU

Department: Pediatrics

Duties &amp; Responsibilities:

VCU's Department of Pediatrics invites all interested candidates to apply for our exciting Research Assistant position! At VCU, we Make it Real through learning, research, creativity, service and discovery - the hallmarks of the VCU experience. A premier, urban, public research university nationally recognized as one of the best employers for diversity, VCU is a great place to work. It's a place of opportunity, where your success is supported, and your career can thrive.

Position Primary Purpose and General Responsibilities

VCU's Department of Pediatrics invites all interested candidates to apply for our exciting Research Assistant position. Research Assistants perform a variety of routine, non-technical duties in assisting technical and professional personnel in a research clinical setting.

The Research Assistant will be expected to perform most components of data collection from human-subject volunteers required for multiple bio-behavioral and brain imaging research studies. The current position is to help us with data analysis on completed studies and subject recruitment and scheduling for active studies. The general responsibilities of this role are as follows:

Subject Recruitment - Participant/research subject recruitment, including placement of IRB-approved materials and media advertisements about research studies being conducted in the department, as well as collection and computer entry of responses and information furnished by potential research volunteers contacting the lab by phone, web or other means to identify possible participants. Scheduling of participants within protocol specific time frames.

Participant Consenting - Collection of informed consent and/or assent and permission from research volunteers, including describing the study to research participant candidates in simple language, and overseeing the signing of consent and assent forms.

Data Collection - Biological data collection, including collection and testing of urine and blood, saliva, and hair samples. Data collection from neuro-imaging studies will also be required, as well as vagal stimulation studies both from stimulating and recording devices for heart rate variability analysis.

Psychometric data collection, including administration, collection and scoring of paper-and-pencil or computer-driven questionnaires, as well as administration and recording of computer-driven cognitive performance tasks.

Maintain Study Data - Accurate and secure transmission and storage of study data, including to centralized databases or to physically secured case report forms for industry-sponsored clinical trials.

Participant Management - Accurate calculation of subject compensation. As part of the assessment, the employee will be expected to coordinate a busy study visit for the subjects, including escorting research volunteers to and from the different tasks and testing rooms and waiting rooms of the research facility

Other duties assigned by Lead Clinical Research Coordinator or Principal Investigator. Most work is done on-site with potentially some work done remotely.

Qualifications:

Minimum Qualifications
<ul>
<li>Bachelor's of Science degree or equivalent in any of the science subspecialties or psychology.</li>
<li>Proficient in computer skills including word processing, data entry, spreadsheet, database management, and entry level statistical/programming skills required.</li>
<li>Strong interpersonal skills such as establishing rapport, maintaining participant motivation, empathic responding, ability to work effectively as part of a multidisciplinary team, and ability to use clinical judgment in (rare) emergency situations.</li>
<li>Strong organizational skills, including understanding of HIPAA regulations.</li>
<li>Demonstrated experience working in and fostering an environment of respect, professionalism and civility with a population of faculty, staff, and students from various backgrounds and experiences, or a commitment to do so as a staff member at VCU.</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience conducting research in pediatric or adolescent populations.</li>
<li>Experience recruiting, consenting, and carrying out study procedures with adult and youth participants</li>
<li>Qualitative research experience, including data collection, coding, analysis</li>
<li>Experience administering surveys in REDCap</li>
<li>Experience in conducting mental health surveys with adults and youth</li>
<li>Experience collecting biospecimens from research participants, including hair, saliva, blood, and urine</li>
<li>Experience in mentoring and training student research trainees, incorporating them into research teams</li>
</ul>
Salary Range: Commensurate with Experience (up to $55,000)

Benefits: All full-time university staff are eligible for VCU&rsquo;s robust benefits package that includes comprehensive health benefits, paid annual and holiday leave, generous tuition benefits, retirement planning and savings options, tax-deferred annuity and cash match programs, employee discounts, well-being resources, abundant opportunities for career development and advancement, and more.

FLSA Exemption Status: Non-Exempt 
 
Hours per Week: 40

Restricted Position: Yes

ORP Eligible: No

Flexible Work Arrangement: Hybrid

University Job Title: Clinical Research Assistant 1-3 (34001N, 34002N, 34003N)

Contact Name: Jewel Jefferson

Contact Email: jewel.jefferson@vcuhealth.org</div></div>

RAYUS Radiology

<div>
 
 Job Summary
 
 
 
 
 RAYUS now offers DailyPay! Work today, get paid today!
 
 
 
 RAYUS Radiology is looking for a Clinical Research Assistant to join our team. We are challenging the status quo by shining light on radiology and making it a critical first step in diagnosis and proper treatment. Come join us and shine brighter together! As a Clinical Research Assistant, you will be responsible for assisting with the coordination of imaging scheduling and data uploading, maintaining relationships with local research sites and coordinators, and general administrative support.
 
 
 
 This is a full-time position working mid-shifts, 40 hours per week.
 
 
 
 
 Essential Duties And Responsibilities
 
 
 
 
 (90%) Research Assistance
 
 
 
 <ul>
 <li>
 Submit acquired research related scans to their corresponding imaging portals for sponsor &amp; PI review within 24 hours
 </li>
 <li>
 Provide clerical support such as sending and receiving faxes and scanning patient documentation
 </li>
 <li>
 Assist with maintaining current research binders for quarterly sponsor review
 </li>
 <li>
 Review and monitor any unresolved data clarification requests until resolved
 </li>
 <li>
 Schedule screening and follow up visits
 </li>
 <li>
 Educate study subjects about study requirements, appointment confirmations and procedure prep
 </li>
 <li>
 Work with research team and technologists with subject related tasks
 </li>
 <li>
 Maintain accurate records of services performed
 </li>
 <li>
 Ensure confidentiality of all health information as required by Florida Statues, HIPPA, and GCP guidelines
 
 
 </li>
 </ul>
 
 (10%) Other Duties as Assigned
 
 
 
 
 Remote Position
 
 
 
 No
 
 
 
 Status
 
 
 
 Full-time
 
 
 
 Requirements
 
 
 
 
 SUMMARY OF QUALIFICATIONS:
 
 
 
 
 Required
 
 
 
 <ul>
 <li>
 Highschool diploma, or equivalent
 </li>
 <li>
 Knowledge of clinical operations, protocols, safety regulations, and processes
 </li>
 <li>
 Proficient in Microsoft Office Suite; Outlook, Excel, Word, and PowerPoint
 
 
 </li>
 </ul>
 
 Preferred
 
 
 
 <ul>
 <li>
 Associate&rsquo;s degree in an applicable field
 
 
 </li>
 </ul>
 RAYUS is committed to delivering clinical excellence in communities across the U.S., driven by our passion for and superior service to referring providers and patients. RAYUS Radiology is built on our brilliant medicine, brilliant team, brilliant technology and services - all to provide the highest level of patient care possible.
 
 
 We bring brilliance to health and wellness. Join our team and shine the light on Radiology Services! RAYUS Radiology is an EO Employer/Vets/Disabled.
 
 
 We offer benefits (based on eligibility) including medical, dental and vision insurance, 401k with company match, life and disability insurance, tuition reimbursement, adoption assistance, pet insurance, PTO and holiday pay and many more! Visit our career page to see them all www.rayusradiology.com/careers.
 
 
 DailyPay implementation is contingent upon initial set-up period.
</div>

<div><div>RAYUS now offers DailyPay! Work today, get paid today!</div>
<div>
</div><div>RAYUS Radiology is looking for a Clinical Research Assistant to join our team. We are challenging the status quo by shining light on radiology and making it a critical first step in diagnosis and proper treatment. Come join us and shine brighter together! As a Clinical Research Assistant, you will be responsible for assisting with the coordination of imaging scheduling and data uploading, maintaining relationships with local research sites and coordinators, and general administrative support.
</div>This is a full-time position working mid-shifts, 40 hours per week.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
(90%) Research Assistance
<ul><li>Submit acquired research related scans to their corresponding imaging portals for sponsor &amp; PI review within 24 hours</li></ul>
<ul><li>Provide clerical support such as sending and receiving faxes and scanning patient documentation</li></ul>
<ul><li>Assist with maintaining current research binders for quarterly sponsor review</li></ul>
<ul><li>Review and monitor any unresolved data clarification requests until resolved</li></ul>
<ul><li>Schedule screening and follow up visits</li></ul>
<ul><li>Educate study subjects about study requirements, appointment confirmations and procedure prep
</li></ul><ul><li>Work with research team and technologists with subject related tasks</li></ul>
<ul><li>Maintain accurate records of services performed</li></ul>
<ul><li>Ensure confidentiality of all health information as required by Florida Statues, HIPPA, and GCP guidelines</li></ul>
(10%) Other Duties as Assigned
Requirements:
<div>SUMMARY OF QUALIFICATIONS:

Required:
<ul><li>Highschool diploma, or equivalent</li></ul>
<ul><li>Knowledge of clinical operations, protocols, safety regulations, and processes</li></ul>
<ul><li>Proficient in Microsoft Office Suite; Outlook, Excel, Word, and PowerPoint</li></ul>
Preferred:
<ul><li>Associate's degree in an applicable field</li></ul>
<div>RAYUS is committed to delivering clinical excellence in communities across the U.S., driven by our passion for and superior service to referring providers and patients. RAYUS Radiology is built on our brilliant medicine, brilliant team, brilliant technology and services - all to provide the highest level of patient care possible.</div>
<div>
</div><div>We bring brilliance to health and wellness. Join our team and shine the light on Radiology Services! RAYUS Radiology is an EO Employer/Vets/Disabled.</div>
<div>
</div><div>We offer benefits (based on eligibility) including medical, dental and vision insurance, 401k with company match, life and disability insurance, tuition reimbursement, adoption assistance, pet insurance, PTO and holiday pay and many more! Visit our career page to see them all www.rayusradiology.com/careers.</div>
<div>
</div><div></div><div>DailyPay implementation is contingent upon initial set-up period.</div></div></div>

Search 10000+ Medical research assistant jobs near you this April. New roles added regularly across leading industries. Apply today.

10000 medical research assistant jobs Near Me

Research Assistant I - Pharmacology and Molecular Therapeutics

Research Assistant - Addiction Medicine

Clinical Research Assistant

Clinical Research Assistant - SOM/Pediatrics

Clinical Research Assistant - SOM/Pediatrics

Clinical Research Assistant

Clinical Research Assistant