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Work Study Jobs in Zimmerman, MN (NOW HIRING)

You will work under the direction and closely with the Clinical Research Manager to satisfy applicable regulatory standards and Medtronic internal requirements for clinical studies. The Structural ...

You will work under the direction and closely with the Clinical Research Manager to satisfy applicable regulatory standards and Medtronic internal requirements for clinical studies. The Structural ...

You will work under the direction and closely with the Clinical Research Manager to satisfy applicable regulatory standards and Medtronic internal requirements for clinical studies. The Structural ...

Perform one of the following END study: EEG, Evoked Potentials or TCD. Sets-up patient for ... work/technical sheet, including a technical description of the modality recorded, with emphasis on ...

Perform one of the following END study: EEG, Evoked Potentials or TCD. • Sets-up patient for ... work/technical sheet, including a technical description of the modality recorded, with emphasis on ...

Perform one of the following END study: EEG, Evoked Potentials or TCD. • Sets-up patient for ... work/technical sheet, including a technical description of the modality recorded, with emphasis on ...

Perform one of the following END study: EEG, Evoked Potentials or TCD. • Sets-up patient for ... work/technical sheet, including a technical description of the modality recorded, with emphasis on ...

Showing results 41-60

Work Study information

See Zimmerman, MN salary details

$23K

$130.8K

$215K

How much do work study jobs pay per year?

As of Sep 6, 2026, the average yearly pay for work study in Zimmerman, MN is $130,768.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,700.00 and $163,900.00 per year, depending on experience, location, and employer.

What is a work study?

Work study jobs are part-time positions offered to students, typically through a federal or institutional financial aid program, to help them earn money while attending school. These jobs are often located on campus or with approved off-campus employers and are designed to be flexible with students' class schedules. Work study positions can include roles in administrative offices, libraries, research labs, or community service organizations, and they provide valuable work experience while helping to offset educational expenses.

How do work study positions typically balance job responsibilities with academic schedules?

Work study positions are designed to accommodate students' academic commitments, with supervisors often offering flexible scheduling and reduced hours during exam periods. Students are generally expected to communicate their class schedules and workload in advance to ensure shifts do not conflict with academic requirements. While workload varies by department, most roles emphasize efficient time management and prioritize academics, fostering a supportive environment for student employees. Many work study roles also provide opportunities to develop professional skills and network within the institution.

What are the key skills and qualifications needed to thrive as a work study, and why are they important?

To succeed as a Work Study, you generally need strong organizational skills, time management, and the ability to balance academic and work responsibilities, often with eligibility based on financial aid requirements. Familiarity with basic office software, campus systems, and sometimes data entry tools is typically required. Reliability, professionalism, and effective communication help students stand out in diverse campus work environments. These skills are essential for meeting job expectations, supporting campus operations, and maintaining academic performance.

What is the difference between Work Study vs Intern?

AspectWork StudyIntern
CredentialsUsually requires enrollment in a college or universityMay require enrollment or recent graduation
Work EnvironmentOn-campus or related to academic institutionVaries; can be on-site or remote in various industries
Employer & IndustryEducational institutions, government, some nonprofitsBusinesses, organizations across multiple industries
PurposeFinancial aid and work experience for studentsGaining work experience, networking, or exploring careers

Work Study positions are primarily designed for students enrolled in college, offering financial aid and relevant work experience within academic or related environments. Internships are broader, often targeted at students or recent graduates seeking industry experience across various sectors. While both provide valuable work exposure, Work Study is more focused on supporting education costs, whereas internships emphasize career development.

What are typical work-study jobs?

Work-study jobs are part-time positions offered to students through their college or university, often in administrative offices, libraries, or campus facilities. These jobs typically involve tasks such as data entry, customer service, or event support and help students earn money while gaining work experience. Scheduling is usually flexible to accommodate class schedules, and some positions may require basic skills like computer literacy or communication abilities.

What cities near Zimmerman, MN are hiring for Work Study jobs?

Cities near Zimmerman, MN with the most Work Study job openings:

Infographic showing various Work Study job openings in Zimmerman, MN as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 19% Part Time, and 3% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $130,768 per year, or $62.9 per hour.

Clinical Trial Operations Specialist II

Boston Scientific Gruppe

Maple Grove, MN • On-site

$68 - $129/hr

Other

Posted 5 days ago


Job description

Additional Location(s): US-MA-Marlborough; US-MN-Maple Grove

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit- High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

About the role:

Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.

At Boston Scientific Urology, we are committed to developing innovative technologies that improve the lives of patients with urologic and pelvic health conditions. As a Clinical Trial Operations Specialist II, you will support clinical research programs that generate the evidence needed to advance therapies across areas such as neuromodulation, pelvic floor disorders, stone management, benign prostatic hyperplasia, and prosthetic urology.

In this role, you will work closely with cross-functional teams to support the planning, execution, and oversight of global clinical studies that evaluate the safety, effectiveness, and real-world impact of innovative medical technologies. This position offers an excellent opportunity to build foundational clinical researchexpertisewhile contributing toevidencegeneration that informs regulatory submissions, scientific publications, healthcare provider education, and patient access to life-changing therapies

At Boston Scientific, we value collaboration andsynergy. This role follows a hybrid work model requiring employees to be in our localofficeMaple Grove,MNor Marlborough, MAat least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for thispositionat this time.Relocation assistance is not available for this position at this time.

Your responsibilities will include:

Support the project team in planning,executing,and managing operational aspects of global clinical trials.

Participatewith supervision, in the execution of clinical studiesin accordance withproject plans, budgets and resource allocations while following applicable regulatory requirements and standard operating procedures.

Track the development of project materials and collaborate with cross-functional team members on internal and external study materials, processes, manuals, plans,committees,and study systems.

Support-required sponsor regulatory submissions, as applicable.

Maintain documentation and processes that support a continuous state of audit readiness.

Collaborate with the project teamtoidentify,assess,and manage clinical study risks.

Partner effectively with departmental and cross-functional stakeholders to support clinical study and programobjectives.

Required qualifications:

Minimum bachelor's degree in biology, life sciences, nursing, biomedical engineering, public health, clinical research, or related field and 2 years of clinical research experience, for example, Clinical Research Coordinator, Clinical Trial Assistant, Clinical Operations Associate, Research Assistant, Regulatory Coordinator, or internship/co-op in clinical research.

Basic understanding of clinical research or healthcare environment.

Experience working with multiple stakeholders to complete projects, coordinate activities, and meet established timelines.

Demonstrated ability to organize andmaintainproject documentation, track deadlines, follow up on action items, and manage multiple assigned tasks simultaneously.

Abilityto work within established procedures, projectplans,and quality requirements.

Strong written and verbal communication skills.

Strong project management skills and experienced with Microsoft Office Suite

Demonstrated knowledge of Trial Master Files and essential clinical and regulatory documents

Preferredqualifications:

Proven experience supporting clinical studies, clinicalresearchor clinical trial operations, especially in medical devices

Working knowledge of Good Clinical Practice (GCP) principles; familiarity with ICH-GCP, ISO 14155, and applicable FDA clinical research regulations preferred.

Exposure to EDC, CTMS, eTMF or electronic medical records

Familiarity with clinical study documentation, studysystems,and regulatory processes.

Understanding clinical research quality requirements and audit-readiness practices.

Experience supporting global or cross-functional projectspreferred.

PreferredAssociation of Clinical Research Professionals (ACRP) accreditation.

Requisition ID:633925

Minimum Salary:$68100

Maximum Salary: $129400

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com— will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life byprovidinga broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological,neurologicaland urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn .

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specificprohibited substancetest requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.


Nearest Major Market: Minneapolis
Job Segment: Clinical Research, Medical Research, EMR, Compliance, Urology, Healthcare, Legal

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