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Clinical Study Manager Jobs in Reno, NV (NOW HIRING)

Communicates with physicians/Nurse Manager/co-workers, as appropriate about changes in patient's clinical condition including results of diagnostic studies and symptomatology. Is able to respond ...

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Clinical Study Manager information

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How much do clinical study manager jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for clinical study manager in Reno, NV is $62.33, according to ZipRecruiter salary data. Most workers in this role earn between $50.58 and $70.24 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

What are the most commonly searched types of Clinical Study jobs in Reno, NV?

The most popular types of Clinical Study jobs in Reno, NV are:

What are popular job titles related to Clinical Study Manager jobs in Reno, NV?

For Clinical Study Manager jobs in Reno, NV, the most frequently searched job titles are:

What job categories do people searching Clinical Study Manager jobs in Reno, NV look for?

The top searched job categories for Clinical Study Manager jobs in Reno, NV are:

What cities near Reno, NV are hiring for Clinical Study Manager jobs?

Cities near Reno, NV with the most Clinical Study Manager job openings:

Infographic showing various Clinical Study Manager job openings in Reno, NV as of August 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $129,653 per year, or $62.3 per hour.

Part-Time Clinical Research Coordinator

Actalent

Reno, NV

$25 - $33/hr

Part-time, Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New


Job description

Job Title: Clinical Research Coordinator

Job Description

This part-time Clinical Research Coordinator role in Reno, NV offers the opportunity to support a clinical trial focused on C. difficile (c. diff). You will play a key role in patient recruitment and enrollment, working closely with participants and research staff to ensure accurate pre-screening, informed participation, and strong retention throughout the study. The position is ideal for a coordinator with hands-on clinical research experience, excellent organizational skills, and the ability to communicate clearly and confidently with patients and multidisciplinary teams.

Responsibilities

  • Perform detailed chart reviews to assess potential participants against study inclusion and exclusion criteria.
  • Pre-screen potential participants using electronic medical records and other available data sources to determine eligibility.
  • Educate potential participants about the clinical trial, including study purpose, procedures, expectations, and visit schedules, in a clear and compassionate manner.
  • Conduct follow-up communications with enrolled participants to support retention and ensure adherence to study protocols.
  • Schedule in-person visits and follow-up appointments for participants, coordinating with clinical and research staff as needed.
  • Send appointment reminders and relevant study information to participants to support attendance and protocol compliance.
  • Collaborate with the research team to support overall enrollment efforts and help meet recruitment targets for the c. diff trial.
  • Maintain accurate and timely documentation of recruitment activities, pre-screening outcomes, and participant communications in the electronic medical record and study systems.
  • Apply Good Clinical Practice (GCP) and HIPAA training in all aspects of participant interaction, data handling, and documentation.

Essential Skills

  • Proven experience as a Clinical Research Coordinator.
  • At least 2 years of experience in patient recruitment for clinical research studies.
  • A minimum of 2 years of experience working with electronic medical records (EMR).
  • Hands-on experience conducting chart reviews to evaluate patient eligibility for clinical trials.
  • Demonstrated ability to pre-screen patients effectively for study participation.
  • Training in HIPAA regulations and patient privacy requirements.
  • Training in Good Clinical Practice (GCP) for clinical research.
  • Strong organizational skills with the ability to manage multiple participants, visits, and follow-up activities.
  • Clear and confident communication skills when interacting with patients and research staff.
  • High attention to detail in documentation, scheduling, and protocol adherence.

Additional Skills & Qualifications

  • Familiarity with patient recruitment strategies in a fast-paced clinical research environment.
  • Ability to build rapport with participants to encourage engagement and long-term study retention.
  • Comfort working within multidisciplinary research and clinical teams.
  • Strong time-management skills to balance chart review, pre-screening, education, and follow-up responsibilities.
  • Proficiency with EMR systems and basic office software used for scheduling and communication.

Work Environment

This position is part-time at approximately 24 hours per week, scheduled Monday through Friday during normal business hours. The work environment is fast paced and requires consistent attention to detail, particularly when reviewing charts, pre-screening participants, and coordinating visits. You will work primarily in a clinical research setting that relies heavily on electronic medical records and structured documentation. Collaboration with clinical and research staff is frequent, and the role involves regular interaction with patients in person and by phone or electronic communication.

Job Type & Location

This is a Contract position based out of Reno, NV.

Pay and Benefits

The pay range for this position is $25.00 - $33.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Reno,NV.

Application Deadline

This position is anticipated to close on Sep 7, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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