Rochester, MN · Remote
$150 - $400/day
Conduct in-home visits with clinical trial participants according to study schedules * Perform ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...
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Rochester, MN · Remote
$150 - $400/day
Conduct in-home visits with clinical trial participants according to study schedules * Perform ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...
Rochester, MN · On-site
$150 - $400/day
Conduct in-home visits with clinical trial participants according to study schedules * Perform ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...
Rochester, MN · On-site
$150 - $400/day
Conduct in-home visits with clinical trial participants according to study schedules * Perform ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...
Rochester, MN · On-site
$110K - $143K/yr
... or recurrence, clinical trial participation, and end-of-life care. The colorectal patient ... Assistant program with current PA certification by NCCPA and registration as a PA by the Minnesota ...
Rochester, MN · On-site
$110K - $143K/yr
... or recurrence, clinical trial participation, and end-of-life care. The colorectal patient ... Assistant program with current PA certification by NCCPA and registration as a PA by the Minnesota ...
$110K - $143K/yr
... or recurrence, clinical trial participation, and end-of-life care. The colorectal patient ... Assistant program with current PA certification by NCCPA and registration as a PA by the Minnesota ...
$110K - $143K/yr
... or recurrence, clinical trial participation, and end-of-life care. The colorectal patient ... Assistant program with current PA certification by NCCPA and registration as a PA by the Minnesota ...
Rochester, MN · On-site
$14.75 - $19.50/hr
... Clinical Trial Management System (CTMS). How You'll Create Impact * Assist in testing and maintaining clinical software applications under the guidance of experienced developers and analysts.
Rochester, MN · On-site
$14.75 - $19.50/hr
... Clinical Trial Management System (CTMS). How You'll Create Impact * Assist in testing and maintaining clinical software applications under the guidance of experienced developers and analysts.
$110K - $143K/yr
... or recurrence, clinical trial participation, and end-of-life care. The colorectal patient ... Assistant program with current PA certification by NCCPA and registration as a PA by the Minnesota ...
$110K - $143K/yr
... or recurrence, clinical trial participation, and end-of-life care. The colorectal patient ... Assistant program with current PA certification by NCCPA and registration as a PA by the Minnesota ...
$110K - $143K/yr
... or recurrence, clinical trial participation, and end-of-life care. The colorectal patient ... Assistant program with current PA certification by NCCPA and registration as a PA by the Minnesota ...
$110K - $143K/yr
... or recurrence, clinical trial participation, and end-of-life care. The colorectal patient ... Assistant program with current PA certification by NCCPA and registration as a PA by the Minnesota ...
Rochester, MN · On-site
It does not include clinical trial operations or regulatory ownership. Core Responsibilities A ... Support execution of scanner experiments as needed. * Assist with validation of OGSE and FLORET ...
Rochester, MN · On-site
It does not include clinical trial operations or regulatory ownership. Core Responsibilities A ... Support execution of scanner experiments as needed. * Assist with validation of OGSE and FLORET ...
Rochester, MN · On-site
It does not include clinical trial operations or regulatory ownership. Core Responsibilities A ... Support execution of scanner experiments as needed. * Assist with validation of OGSE and FLORET ...
Rochester, MN · On-site
It does not include clinical trial operations or regulatory ownership. Core Responsibilities A ... Support execution of scanner experiments as needed. * Assist with validation of OGSE and FLORET ...
The candidate must also be able to assist with clinical trial activities, manuscript writing, and grant writing. A Research Fellow position in Life Sciences (LS) will require knowledge of either ...
The candidate must also be able to assist with clinical trial activities, manuscript writing, and grant writing. A Research Fellow position in Life Sciences (LS) will require knowledge of either ...
The candidate must also be able to assist with clinical trial activities, manuscript writing, and grant writing. A Research Fellow position in Life Sciences (LS) will require knowledge of either ...
The candidate must also be able to assist with clinical trial activities, manuscript writing, and grant writing. A Research Fellow position in Life Sciences (LS) will require knowledge of either ...
The candidate must also be able to assist with clinical trial activities, manuscript writing, and grant writing. A Research Fellow position in Life Sciences (LS) will require knowledge of either ...
The candidate must also be able to assist with clinical trial activities, manuscript writing, and grant writing. A Research Fellow position in Life Sciences (LS) will require knowledge of either ...
Rochester, MN · On-site
$94K - $121K/yr
... assist and support the full spectrum of clinical trial operations and translation of research findings to practice. The duties of this position will include but not limited to the administration ...
Rochester, MN · On-site
$94K - $121K/yr
... assist and support the full spectrum of clinical trial operations and translation of research findings to practice. The duties of this position will include but not limited to the administration ...
Rochester, MN · On-site
$94K - $121K/yr
... assist and support the full spectrum of clinical trial operations and translation of research findings to practice. The duties of this position will include but not limited to the administration ...
Rochester, MN · On-site
$94K - $121K/yr
... assist and support the full spectrum of clinical trial operations and translation of research findings to practice. The duties of this position will include but not limited to the administration ...
... assist and support the full spectrum of clinical trial operations and translation of research findings to practice. The duties of this position will include but not limited to the administration ...
... assist and support the full spectrum of clinical trial operations and translation of research findings to practice. The duties of this position will include but not limited to the administration ...
Rochester, MN · On-site
$94K - $121K/yr
... assist and support the full spectrum of clinical trial operations and translation of research findings to practice. The duties of this position will include but not limited to the administration ...
Rochester, MN · On-site
$94K - $121K/yr
... assist and support the full spectrum of clinical trial operations and translation of research findings to practice. The duties of this position will include but not limited to the administration ...
The candidate must also be able to assist with clinical trial activities, manuscript writing, and grant writing. A Research Fellow position in Life Sciences (LS) will require knowledge of either ...
The candidate must also be able to assist with clinical trial activities, manuscript writing, and grant writing. A Research Fellow position in Life Sciences (LS) will require knowledge of either ...
The procedural support assistant assists with other aspects of patient care including patient ... Must be willing to adjust work schedules in response to department or clinical needs. Certification:
The procedural support assistant assists with other aspects of patient care including patient ... Must be willing to adjust work schedules in response to department or clinical needs. Certification:
Responsibilities The procedural support assistant is an integral member of the procedural team in ... Must be willing to adjust work schedules in response to department or clinical needs. Certification:
Responsibilities The procedural support assistant is an integral member of the procedural team in ... Must be willing to adjust work schedules in response to department or clinical needs. Certification:
May perform technical duties related to clinical and experimental research as directed and under the supervision of other study personnel. May order materials/supplies and assist with general office ...
May perform technical duties related to clinical and experimental research as directed and under the supervision of other study personnel. May order materials/supplies and assist with general office ...
$11.73 - $17.02
4% of jobs
$17.02 - $22.30
15% of jobs
$24.95 is the 25th percentile. Wages below this are outliers.
$22.30 - $27.59
13% of jobs
$27.59 - $32.88
8% of jobs
The median wage is $35.81 / hr.
$32.88 - $38.16
19% of jobs
$38.16 - $43.45
13% of jobs
$45.56 is the 75th percentile. Wages above this are outliers.
$43.45 - $48.74
10% of jobs
$48.74 - $54.02
5% of jobs
$54.02 - $59.31
11% of jobs
$59.31 - $64.60
1% of jobs
$64.60 - $69.88
1% of jobs
$11
$38
$69
A clinical trial assistant is responsible for monitoring the medical and administrative procedures during a clinical trial. In this career, you prepare patients for tests, take blood, perform laboratory work, prep for medical treatments, and collect data for research. You work with project managers and research associates throughout the beginning, implementation, and closeout of the trial. You also handle paperwork, file records, prepare reports, label medication, track progress, and fulfill other duties that arise during medical studies. You may assist with appointment schedules, plan meetings, and communicate with external sources and investigators as well.
| Aspect | Clinical Trial Assistant | Clinical Research Coordinator |
|---|---|---|
| Responsibilities | Supports trial logistics, manages documentation, assists with regulatory compliance | Oversees study conduct, recruits participants, manages site operations |
| Credentials | Typically requires a bachelor's degree in health or life sciences | Often requires a bachelor's or master's degree in health sciences or related fields |
| Work Environment | Research sites, sponsor offices, clinical trial centers | Clinical sites, hospitals, research institutions |
| Industry Usage | Commonly employed in pharmaceutical companies, CROs, research institutions | Primarily in hospitals, clinics, research centers |
The Clinical Trial Assistant primarily supports trial logistics and documentation, working closely with the research team. In contrast, the Clinical Research Coordinator manages the overall conduct of the study, including participant recruitment and site management. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.
$150 - $400/day
Contractor
Posted 15 days ago
We are seeking a skilled and compassionate Mobile Clinical Research Phlebotomist to support clinical research studies by conducting in-home visits with study participants. In this role, you will perform blood draws, collect biological specimens, and complete study procedures according to clinical research protocols.
This position is ideal for phlebotomists who are comfortable working independently, traveling to patient homes, and providing a professional, patient-centered experience while supporting important clinical research.
ResponsibilitiesConduct in-home visits with clinical trial participants according to study schedules
Perform venipuncture and collect blood specimens following study protocols and safety guidelines
Process, label, and prepare specimens for shipment to central laboratories
Accurately document study procedures and visit details
Maintain compliance with study protocols and Good Clinical Practice (GCP) guidelines
Maintain proper chain of custody for biological specimens
Ensure participant safety, privacy, and comfort during home visits
Communicate with clinical research coordinators and study teams as needed
Manage and maintain phlebotomy and specimen collection supplies
Follow all infection control and safety procedures
High school diploma or equivalent
Phlebotomy certification from an accredited program
Minimum 1–2 years of phlebotomy experience
Demonstrated experience performing venipuncture on diverse patient populations
Reliable transportation and ability to travel to participant homes
Valid driver’s license with a clean driving record
Strong interpersonal and communication skills
Ability to work independently and manage a flexible schedule
Comfortable using electronic documentation systems
Experience working in clinical research or clinical trials
Knowledge of clinical trial protocols and documentation requirements
Familiarity with specimen processing and shipment procedures
Experience providing mobile or home-based healthcare services
Certification in Good Clinical Practice (GCP)
Ability to travel to participant homes within the assigned region
Ability to lift and carry specimen kits and medical supplies
Ability to stand, bend, and safely perform venipuncture procedures
Ability to use a tablet or computer for documentation
Home visit setting (travel to participant residences)
Collaboration with clinical research teams and study coordinators
Flexible scheduling based on participant availability
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.To view our privacy policy and terms of use, please use the links below. Privacy Policy: https://hawthornehealth.com/privacy-policy/Terms of Use: https://hawthornehealth.com/terms-of-use/
