clinical research support specialist

Castle Biosciences, Inc.

<div>
 
 Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood!
 
 
 
 Learn more at www.CastleBiosciences.com
 
 
 
 Castle Biosciences Inc.
 
 is growing, and we are looking to hire a
 
 full-time Clinical Research, Clinical Research Assistant working from our Phoenix, AZ office location,
 
 with a start date of May 15, 2026.
 
 
 
 Why Castle Biosciences?
 
 
 
 
 Exceptional Benefits Package
 
 
 
 <ul>
 <li>
 Excellent Annual Salary + 20% Bonus Potential
 </li>
 <li>
 20 Accrued PTO Days Annually + 10 Paid Holidays
 </li>
 <li>
 401K with 100% Company Match up to 6%
 </li>
 <li>
 3 Health Care Plan Options + Company HSA Contribution
 </li>
 <li>
 Company Stock Grant Upon Hire
 
 
 </li>
 </ul>
 
 A DAY IN THE LIFE OF A Clinical Research Assistant
 
 
 
 The Clinical Research Assistant is an entry-level position that provides administrative support to the assigned study team. This role will spend the most time receiving, processing, and logging clinical specimens according to departmental standard operating procedures (SOPs) to ensure safety and quality standards. Under the guidance of the Clinical Research Project Manager, the Clinical Research Assistant will also maintain a database that records details of clinical trial shipments. In collaboration with the Clinical Research Associates, they will help plan, order, track, and distribute clinical trial supplies to study sites. Additionally, the role includes day-to-day tasks that support the organization of samples and kits, such as making, shipping, and distributing kits as needed, as well as maintaining and updating various databases and trackers. This position works closely with other Clinical Research Assistants to ensure smooth study operations and consistent support for the study team.
 
 
 
 Requirements
 
 
 
 <ul>
 <li>
 High School Diploma or GED, or equivalent experience required.
 </li>
 <li>
 Actively displays behaviors that support the mission, vision, and values of Castle Biosciences.
 
 
 </li>
 </ul>
 
 Preferred Requirements
 
 
 
 <ul>
 <li>
 Bachelor's degree in a related field (preferred) or demonstrated experience as evidence of competency
 </li>
 <li>
 Familiarity with research and development processes preferred.
 </li>
 <li>
 Previous experience receiving, processing, and sorting samples preferred.
 </li>
 <li>
 Please see the full job description at the end of the job ad.
 
 
 </li>
 </ul>
 
 SCHEDULE
 
 
 
 <ul>
 <li>
 Full-time 5 days a week in-office, Monday - Friday 40 hours a week. Based in our Phoenix, AZ office.
 </li>
 <li>
 Occasional travel up to 10%
 
 
 </li>
 </ul>
 
 READY TO JOIN OUR BIOTECH TEAM?
 
 
 
 We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our
 
 mobile-friendly application.
 
 We're excited to learn more about you and look forward to connecting soon!
 
 
 
 Castle Biosciences Awards and Research Developments!
 
 
 
 
 WORK AUTHORIZATION
 
 
 
 
 All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas.
 
 
 
 
 About Castle Biosciences Inc.
 
 
 
 At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes.
 
 
 Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both
 
 challenging and rewarding
 
 . We behave with
 
 integrity
 
 and treat our colleagues with
 
 respect and kindness
 
 . Our culture fosters an
 
 environment of trust, transparency, and collaboration
 
 . We prioritize and encourage
 
 internal growth
 
 and
 
 professional development
 
 .
 
 
 Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.
 
 
 If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail
 
 ReasonableAccommodationsRequest@castlebiosciences.com
 
 .
 
 
 This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.
 
 
 <ul>
 <li>
 No third-party recruiters, please
 </li>
 </ul>
</div>

Clinical Research, Clinical Research Assistant (PHX)

The Ohio State University Wexner Medical Center

<div>Job Description Summary
To provide assistance in support of clinical research studies being done within the College of Medicine (COM) Department of Internal Medicine, Division of Immunology and Rheumatology in partnership with the COM Center for Clinical Research Management (CCRM); assists with implementation and coordination of studies; participates in recruitment of study participants; performs behavioral or diagnostic testing; assists with collection maintenance &amp; reporting of clinical research data.
Minimum Education Requirement
Bachelor&rsquo;s Degree in Biological Sciences, Health Sciences or medical field, or equivalent combination of education experience required.
Experience Required
0 years of relevant experience required.
Preferred Experience
2-4 years of relevant experience preferred. Experience in research capacity desired; knowledge or experience in specialty may be desired; experience in phlebotomy may be desired; experience performing basic laboratory procedures to process biological specimens may be desired; computer skill required with knowledge of database software applications desired.
FUNCTION/SUBFUNCTION: Research and Scholarship/Clinical Research
CAREER BAND: Individual Contributor-Technical
CAREER LEVEL: T2
This position is located at Outpatient Care East; however, some travel to main campus or other outpatient locations may be required. Other locations within the Columbus metropolitan area are Dublin, New Albany, Powell, Grandview.
Regular 40 First Shift</div>

Clinical Research Assistant-2

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. 
 
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>

Clinical Research Assistant I - Resuscitation Science Center

Eastern Nephrology Associates, PLLC

<div>
 
 
 &nbsp;
 
 
 Summary
 
 
 
 
 
 To serve as a clinical research assistant during the conduct of clinical research at the investigative site. Provides administrative and clinical support for the implementation and conduct of clinical trials under the direct supervision of the Principal Investigator and other site personnel as applicable. &nbsp;
 
 
 
 Responsible for the collection and submission of regulatory documents, performance of study specific procedures, regulatory reporting requirements as instructed by the Principal Investigator and governed by Good Clinical Practice and International Council for Harmonization and assisting with ongoing study activity
 
 .
 
 
 
 
 In-office presence is an essential function due to the need for real-time collaboration with providers, direct interaction with patients and caregivers, and secure handling of health data in compliance with HIPAA. &nbsp;
 
 
 
 
 
 Qualification Requirements
 
 
 
 
 
 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 accommodation may be made to enable individuals with disabilities to perform the essential functions.
 
 
 <ul>
 
 <li>
 High School Diploma or equivalent
 </li>
 
 <li>
 Healthcare and/or Research experience preferred.
 </li>
 
 <li>
 Skilled in the use of personal computers and related software applications to include Microsoft Office Applications and email. &nbsp;
 </li>
 
 <li>
 Valid drivers&rsquo; license and reliable transportation to allow individuals to provide support to offsite locations, as necessary.
 </li>
 
 <li>
 
 The ability to provide a minimum of a 4 week notice in the event resignation is tendered.
 
 </li>
 
 </ul>
 
 
 
 
 Minimum Qualifications
 
 
 
 
 <ul>
 
 <li>
 Excellent record maintenance skills.&nbsp;
 </li>
 
 <li>
 Ability to communicate effectively both orally and written.
 </li>
 
 <li>
 Proactive individuals with the ability to be a self-starter with strong independent decision-making skills and attention to detail.
 </li>
 
 </ul>
 
 
 
 
 Knowledge, Skills and Abilities
 
 
 &nbsp;
 
 
 <ul>
 
 <li>
 Demonstrated human relations and effective communication skills are required.
 </li>
 
 <li>
 Ability to understand the ethics of confidentiality and the ability to maintain confidentiality of sensitive information.&nbsp;
 </li>
 
 <li>
 The ability to function independently and enjoy a fast paced, challenging, changing environment; possesses the energy and commitment to help the organization move forward.
 </li>
 
 <li>
 Maintain a positive and professional attitude in all aspects of work from patient care to interaction with co-workers and physicians.
 </li>
 
 <li>
 Maintains confidentiality of patients and their medical information.
 </li>
 
 <li>
 Maintains confidentiality of research activities as required by study sponsor confidentiality agreements and mandates.
 </li>
 
 <li>
 Must be able to meet deadlines for multiple concurrent projects.
 </li>
 
 <li>
 Ability to understand and follow policies, procedures and direction.
 </li>
 
 <li>
 Ability to foster a cooperative work environment. Possess a willingness to accept orders and to perform repetitive tasks.&nbsp;
 </li>
 
 <li>
 Strong interpersonal and communication skills and the ability to work effectively with a wide range of constituencies in a diverse community. &nbsp;
 </li>
 
 <li>
 Ability to function well while involved in multiple task assignments. &nbsp;
 </li>
 
 <li>
 Ability to concentrate on details and deal with constant interruption. &nbsp;
 </li>
 
 <li>
 Skill in organizing resources and establishing priorities.&nbsp;
 </li>
 
 <li>
 Ability to travel to attend off-site meetings as necessary and as directed.
 </li>
 
 <li>
 Ability to accept delegated tasks from Clinical Research Coordinators as applicable.
 </li>
 
 </ul>
 
 
 
 
 Supervisory Responsibilities:&nbsp;
 
 
 None
 
 
 
 
 
 Essential Functions %&nbsp;
 
 
 
 
 
 
 
 All essential functions listed below are expected to be performed on-site. &nbsp;ENA has determined that these duties cannot be effectively or securely executed in a remote environment without compromising patient care, data privacy, or operational standards.
 
 
 &nbsp;
 
 
 
 
 &nbsp;
 
 
 <ul>
 
 <li>
 Provides administrative and clinical support to help coordinate and facilitate day-to-day operations of the Clinical Research department- 90%
 </li>
 
 <li>
 Other duties as assigned -10%
 </li>
 
 </ul>
 
 
 
 
 Physical Demands
 
 
 
 
 <ul>
 
 <li>
 The employee may be required to assist in patient transfer and should use appropriate techniques and equipment to safely transfer patients.
 </li>
 
 <li>
 Hearing, visual acuity, depth perception, balancing, handling, and talking and requires full range of body motion.&nbsp;
 </li>
 
 <li>
 Reaching, grabbing, holding &ndash; fine motor skills&nbsp;with dexterity and eye-hand coordination
 </li>
 
 <li>
 Extended periods in a stationary or standing position&nbsp;
 </li>
 
 <li>
 Repetitive motion such as entering data into computer-based programs&nbsp;
 </li>
 
 <li>
 Lift or move up to 30 pounds. Employees are expected to use appropriate ergonomics and tools such as hand carts for heavier loads.&nbsp;
 </li>
 
 </ul>
 
 
 
 
 Work Environment
 
 
 
 
 <ul>
 
 <li>
 Work is normally performed in a typical interior/office work environment. &nbsp;
 </li>
 
 <li>
 The noise level is usually moderate.&nbsp;
 </li>
 
 <li>
 This position requires visual acuity eyesight (corrected or uncorrected).
 </li>
 
 <li>
 Moderate risk of exposure to blood borne pathogens and OPIM.
 </li>
 
 </ul>
 
 
 The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties and skills required for the position. &nbsp;All employees may have other duties assigned at any time.
 
 
 
 This position falls under a 180-day evaluation review period.&nbsp;
 
 
 
 &nbsp;
 
</div>

Clinical Research Assistant

Eastern Nephrology Associates

<div>Summary
To serve as a clinical research assistant during the conduct of clinical research at the investigative site. Provides administrative and clinical support for the implementation and conduct of clinical trials under the direct supervision of the Principal Investigator and other site personnel as applicable.
Responsible for the collection and submission of regulatory documents, performance of study specific procedures, regulatory reporting requirements as instructed by the Principal Investigator and governed by Good Clinical Practice and International Council for Harmonization and assisting with ongoing study activity.
In-office presence is an essential function due to the need for real-time collaboration with providers, direct interaction with patients and caregivers, and secure handling of health data in compliance with HIPAA.
Qualification Requirements
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 accommodation may be made to enable individuals with disabilities to perform the essential functions.<ul><li>
High School Diploma or equivalent</li><li>
Healthcare and/or Research experience preferred.</li><li>
Skilled in the use of personal computers and related software applications to include Microsoft Office Applications and email.</li><li>
Valid drivers&rsquo; license and reliable transportation to allow individuals to provide support to offsite locations, as necessary.</li><li>
The ability to provide a minimum of a 4 week notice in the event resignation is tendered.</li></ul>
Minimum Qualifications<ul><li>
Excellent record maintenance skills.</li><li>
Ability to communicate effectively both orally and written.</li><li>
Proactive individuals with the ability to be a self-starter with strong independent decision-making skills and attention to detail.</li></ul>
Knowledge, Skills and Abilities<ul><li>
Demonstrated human relations and effective communication skills are required.</li><li>
Ability to understand the ethics of confidentiality and the ability to maintain confidentiality of sensitive information.</li><li>
The ability to function independently and enjoy a fast paced, challenging, changing environment; possesses the energy and commitment to help the organization move forward.</li><li>
Maintain a positive and professional attitude in all aspects of work from patient care to interaction with co-workers and physicians.</li><li>
Maintains confidentiality of patients and their medical information.</li><li>
Maintains confidentiality of research activities as required by study sponsor confidentiality agreements and mandates.</li><li>
Must be able to meet deadlines for multiple concurrent projects.</li><li>
Ability to understand and follow policies, procedures and direction.</li><li>
Ability to foster a cooperative work environment. Possess a willingness to accept orders and to perform repetitive tasks.</li><li>
Strong interpersonal and communication skills and the ability to work effectively with a wide range of constituencies in a diverse community.</li><li>
Ability to function well while involved in multiple task assignments.</li><li>
Ability to concentrate on details and deal with constant interruption.</li><li>
Skill in organizing resources and establishing priorities.</li><li>
Ability to travel to attend off-site meetings as necessary and as directed.</li><li>
Ability to accept delegated tasks from Clinical Research Coordinators as applicable.</li></ul>
Supervisory Responsibilities: None
Essential Functions %
All essential functions listed below are expected to be performed on-site. ENA has determined that these duties cannot be effectively or securely executed in a remote environment without compromising patient care, data privacy, or operational standards.<ul><li>
Provides administrative and clinical support to help coordinate and facilitate day-to-day operations of the Clinical Research department- 90%</li><li>
Other duties as assigned -10%</li></ul>
Physical Demands<ul><li>
The employee may be required to assist in patient transfer and should use appropriate techniques and equipment to safely transfer patients.</li><li>
Hearing, visual acuity, depth perception, balancing, handling, and talking and requires full range of body motion.</li><li>
Reaching, grabbing, holding &ndash; fine motor skills with dexterity and eye-hand coordination</li><li>
Extended periods in a stationary or standing position</li><li>
Repetitive motion such as entering data into computer-based programs</li><li>
Lift or move up to 30 pounds. Employees are expected to use appropriate ergonomics and tools such as hand carts for heavier loads.</li></ul>
Work Environment<ul><li>
Work is normally performed in a typical interior/office work environment.</li><li>
The noise level is usually moderate.</li><li>
This position requires visual acuity eyesight (corrected or uncorrected).</li><li>
Moderate risk of exposure to blood borne pathogens and OPIM.</li></ul>
The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties and skills required for the position. All employees may have other duties assigned at any time.
This position falls under a 180-day evaluation review period.</div>

CenExel Clinical Research

<div>About Us:
Each of CenExel&rsquo;s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early-phase trials, and all our sites have inpatient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full-time employees after 30 days of employment, including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Hourly Range: $21.00 - $23.00/hr (Depending on education, experience, and skillset)

Schedule: Full-Time - Monday - Friday 40 Hours/ Week - 8:00 am - 4:30 pm

Job Summary:
Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.

Essential Responsibilities and Duties:
<ul>
<li>Creating and maintaining patient charts for all assigned studies.</li>
<li>Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.</li>
<li>Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.</li>
<li>Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.</li>
<li>Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.</li>
<li>Communicating with study participants, caregivers, third party vendors and laboratories as needed.</li>
<li>Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.</li>
<li>Aiding Coordinators in the facilitation of study monitoring visits.</li>
<li>Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.</li>
<li>Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.</li>
</ul>
Education/Experience/Skills:
<ul>
<li>Medical Assistant Certification (Required)</li>
<li>Phlebotomy and ECG experience (Required)</li>
<li>Interest in and knowledge of specific study indications.</li>
<li>Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).</li>
<li>Skilled in organization and record maintenance.</li>
<li>Skilled in developing and maintaining effective working relationships with supervisors and co-workers.</li>
<li>Strong personal initiative and attention to detail.</li>
<li>Ability to react calmly and effectively in emergencies.</li>
<li>Ability to interpret, adapt, and apply guidelines and procedures.</li>
<li>Ability to clearly communicate both orally and verbally.</li>
</ul>
Working Conditions
<div><ul><li>Indoor, Office environment.</li></ul>
<ul><li>Essential physical requirements include sitting, typing, standing, and walking.</li></ul>
<ul><li>Lightly active position, occasional lifting of up to 20 pounds.</li></ul>
<ul><li>Reporting to work, as scheduled, is essential.</li></ul>
</div>
CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.</div>

Medical Assistant - (Clinical Research)

Denali Health

<div>
 
 Denali Health is offering a path for candidates to break into clinical research. No&nbsp;prior experience required. Just a strong work ethic and a willingness to learn!
 
 
 
 
 
 
 Why this role matters
 
 
 
 Every visit you support keeps a study safe, compliant, and on schedule. Your work turns complex protocols into steady, compassionate care. When you draw a tube, run an ECG, or log a result, a therapy moves one step closer to people who need it.
 
 
 
 
 
 
 About Denali
 
 
 
 Denali Health is a fast-growing integrated site organization focused on getting therapies to market faster. We foster a culture of trust and talent to deliver industry-leading results for the trials we support.
 
 
 
 
 
 
 What you&rsquo;ll do
 
 
 <ul>
 <li>
 
 Set up visit rooms
 
 &nbsp;and packets: print source, labels, and schedule; lay out kits and PPE so the team is ready at start time.
 </li>
 <li>
 
 Welcome participants
 
 &nbsp;and guide check-in; verify IDs, update demographics, and offer a calm, clear overview of the visit flow.
 </li>
 <li>
 
 Handle reminders &amp; follow-ups:
 
 &nbsp;send confirmations, arrange transportation as needed, and make post-visit check-in calls using approved scripts.
 </li>
 <li>
 
 Assist clinical procedures
 
 &nbsp;after training: prepare supplies for draws, hand off tubes, time spins, and complete chain-of-custody; perform phlebotomy only after competency sign-off.
 </li>
 <li>
 
 Support measurements
 
 &nbsp;under supervision: record vitals and help with ECG/EKG or spirometry setup/cleaning; log device temps/calibration.
 </li>
 <li>
 
 Document carefully:
 
 &nbsp;transcribe notes to source/eSource, upload/scans to the eISF, and enter data in eCRFs as delegated, following ICH-GCP/HIPAA.
 </li>
 <li>
 
 Tackle data quality tasks:
 
 &nbsp;pre-fill templates, check identifiers, time-stamp entries, and flag discrepancies or queries for the CRC to review.
 </li>
 <li>
 
 Coordinate the day:
 
 &nbsp;manage the visit tracker, keep the schedule moving, and communicate changes to CRCs, PIs, labs, and couriers.
 </li>
 <li>
 
 Pitch in wherever needed
 
 &nbsp;to keep visits safe, on time, and participant-centered.
 </li>
 </ul>
 
 
 
 
 
 You&rsquo;re a good fit if you are&hellip;
 
 
 <ul>
 <li>
 
 Clinically inclined
 
 </li>
 <li>
 
 Detail-Oriented
 
 </li>
 <li>
 
 Hardworking &amp; reliable
 
 </li>
 <li>
 
 Ownership mindset
 
 </li>
 <li>
 
 Coachable
 
 </li>
 <li>
 
 Growth-oriented
 
 </li>
 </ul>
 
 
 
 
 
 Must-haves
 
 
 <ul>
 <li>
 High school diploma or GED.
 </li>
 <li>
 Strong technology proficiency (typing, EHR basics, Excel/Word); quick to learn new systems.
 </li>
 <li>
 Professionalism, reliability, and clear written documentation habits.
 </li>
 </ul>
 
 
 
 
 
 Nice-to-haves
 
 
 <ul>
 <li>
 Medical Assistant training/certification or prior patient-care experience.
 </li>
 <li>
 Exposure to clinical research (eSource/eCRF; Medidata Rave or REDCap).
 </li>
 <li>
 Familiarity with ICH-GCP, SOPs, CLIA.
 </li>
 <li>
 Bilingual (especially Spanish/English).
 </li>
 </ul>
 
 
 
 
 
 How we will support your growth
 
 
 <ul>
 <li>
 30-60-90 day onboarding with hands-on checklists and frequent feedback.
 </li>
 <li>
 Paid ICH-GCP training/renewals and device competency sign-offs.
 </li>
 <li>
 Mentorship from senior CRCs and the PI; shadowing on complex visits.
 </li>
 <li>
 
 Clear ladder:&nbsp;Research Assistant &rarr;&nbsp;&nbsp;CRC in ~12&ndash;18 months, with milestone reviews and pay steps.
 
 </li>
 </ul>
 
 
 
 
 
 Why Denali?
 
 
 <ul>
 <li>
 
 Do work that matters:
 
 &nbsp;help bring&nbsp;tomorrow&rsquo;s therapies to patients sooner&mdash;your effort shows up in real lives.
 </li>
 <li>
 
 Learn from the best:
 
 &nbsp;collaborate daily with experienced PIs, CRCs who coach, not micromanage.
 </li>
 <li>
 
 Grow fast on purpose:
 
 &nbsp;structured onboarding, paid trainings, and clear milestones that move you up.
 </li>
 <li>
 
 Choose your lane (and change it):
 
 &nbsp;opportunities across clinic operations, data/QA, regulatory, and patient engagement.
 </li>
 <li>
 
 Own meaningful work:
 
 &nbsp;small, trusted teams where you get responsibility early&mdash;and the support to do it right.
 </li>
 <li>
 
 Be recognized:
 
 &nbsp;competitive pay and benefits, thoughtful feedback, and visible wins that build your career story.
 </li>
 <li>
 
 Thrive in our culture:
 
 &nbsp;low-ego, high-standards, and steady teamwork so you can do your best work&mdash;consistently.
 </li>
 </ul>
 
 
 
 
 
 If you are interested, please email your CV to&nbsp;hr@denali-health.com&nbsp;with a cover letter on how you might excel in this position.
 
 
</div>

Research Assistant

Search 10000+ Clinical research support specialist jobs near you this March. New roles added regularly across leading industries. Apply today.

10000 clinical research support specialist jobs Near Me

Clinical Research, Clinical Research Assistant (PHX)

Clinical Research Assistant-2

Clinical Research Assistant I - Resuscitation Science Center

Clinical Research Assistant

Clinical Research Assistant

Medical Assistant - (Clinical Research)

Research Assistant