Top 12 Clinical data manager Jobs in Las Vegas Nv

Clinical Research Manager
Thermo Fisher Scientific —Las Vegas, NV
- Full-time
- Mid-level
- Clinic
- Bachelor's degree
2d
Software Project Manager
Siemens Healthineers —Las Vegas, NV
- $89,220 - $122,672 a year
- Full-time
- Remote
- Microsoft Excel
- Current TB test
- Mid-level
- Disability insurance
- Health insurance
2d
Site Network Manager (North America)
Alimentiv —Las Vegas, NV
- $97,500 - $163,000 a year
- Full-time
- Remote
- Nursing
- 7 years
- Bachelor's degree
Quick Apply
Psychology Program Manager, Psychology Training Program Director
US Veterans Health Administration —Las Vegas, NV
- $159,322 - $207,137 a year
- Online Application
- Background check
- Doctoral degree
- Writing skills
- Paid parental leave
- Paid holidays
9d
Air Force Clinical Social Worker (FATM) - Nellis AFB, NV
IVA'AL Solutions, LLC —Las Vegas, NV
- $78,000 - $86,000 a year
- Full-time
- Background check
- Computer literacy
- Licensed Clinical Social Worker
- Paid holidays
- Disability insurance
Counselor
WESTCARE NEVADA INC —Las Vegas, NV
- $20.40 - $24.00 an hour
- Full-time
- Writing skills
- Mid-level
- Office
Quick Apply
Mental Health Therapist (Part-Time, W-2)
Two Chairs —Las Vegas, NV
- $58.50 an hour
- Part-time
- Remote
- LMFT
- Licensed Clinical Social Worker
- HIPAA
- Continuing education credits
- 401(k)
Quick Apply
Clinical Director – Adolescent Behavioral Health (LCSW, LMFT, or Psychologist)
Silver State Adolescent Treatment Center —Las Vegas, NV
- $85,000 - $105,000 a year
- Full-time
- LMFT
- Licensed Clinical Social Worker
- HIPAA
Quick Apply

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Project Manager, Implementation
Aristocrat Interactive —Las Vegas, NV
Conduct weekly project meetings either onsite or via conference calls. Coordinate installation of Aristocrat software and hardware products at customer…
$64,400 - $146,928 a year
3d
Software Project Manager
Siemens Healthineers —Las Vegas, NV
These requirements vary by client and may include, but are not limited to: Proof of valid identification (photo, driver's license, SSN) Criminal background…
$89,220 - $122,672 a year
2d

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Clinical Research Monitor - CTSI
The Ohio State University Wexner Medical Center —Columbus, OH
The study monitor will review and provide feedback on study related documents, such as the study protocol, consent form, case report forms, and the clinical…
9d
Data Entry Clerk
Evolution Research Group —Columbus, OH
Track to ensure that data entry is complete for subjects including completed study visits and related forms. The Data Entry Clerk is responsible for the overall…
Quick Apply

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Clinical Research Manager

Thermo Fisher Scientific -
Las Vegas, NV

Apply Now

Job Details

Full-time
2 days ago

Qualifications

Fiscal management
Managing healthcare project budgets
Informed consent
Clinical trial risk management
Mid-level
Project communication management
Patient safety
ICH guidelines
Bachelor's degree
Informed consent procedures implementation
Managing clinical research teams
Forecasting
Desktop applications
Vendor relationship management
Vendor communication
Clinical trial standard operating procedures
Implementing research protocols
Communication with regulatory authorities for clinical trials
Productivity software
Clinical quality assurance standards
Data collection
Project contract management
Research budget management
Clinical program risk management
Research and development project management
Project Development
Clinical consent forms
Ethical review application preparation
Project leadership
Standard operating procedures (SOPs)

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance

Job Description

Join Us as a Clinical Research Manager - Make an Impact at the Forefront of Innovation
The Clinical Research Manager manages all aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings. The role involves acting as liaison between functions (i.e. PM, investigator, research team, etc.) The Clinical Research Manager ensures client requirements and specifications are communicated to the research teams and any issues/questions raised by the research team or investigators are communicated back to the project leads and client (as needed) for resolution.

What You'll Do:

Serve as a primary point of contact for the project team and the business unit for clinical site related aspects of the study.
Collaborate with internal departments to ensure deliverables are met as defined within the contract and study timeline.
Manage all clinical and administrative aspects of a clinical project, including site level study set-up, recruitment, conduction and data collection.
Manage IRB submissions including creation of study specific informed consent forms, SAE notifications and maintenance of the regulatory file and documents.
Collect feedback from various departments to create a risk register for each study and maintains and updates the register throughout the study. Work with the Principal Investigator to ensure that a risk mitigation plan (RMP) is finalized and reviewed by the safety committee prior to study conduct.
Work closely with finance department to manage fiscal aspects of study conduct while meeting sponsor requirements and adhering to the protocol, SOPs and contract.
Provide vendor oversight when services are contracted.

Education & Experience Requirements:

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).

Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.

Knowledge, Skills, Abilities:

Knowledge of Phase I processes and strong knowledge of clinical study operations
Knowledge of FDA regulations and ICH GCP guidelines
Solid computer skills with working knowledge of Microsoft Office applications
Good time management and multi-tasking skills
Solid written and verbal communication skills
Strong organizational and prioritization skills with the ability to prioritize workload and adapt to changing study needs
Favorable consulting skills with t to act as a liaison between external and internal groups
Knowledge of budgeting/forecasting/planning projects.

Working Conditions and Environment:

Work is performed in an office/ laboratory and/or a clinical environment.
Exposure to biological fluids with potential exposure to infectious organisms.
Exposure to electrical office equipment.
Personal protective equipment required such as protective eyewear, garments and gloves.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Apply Now

Refine Your Search

clinical data manager jobs in las vegas nv

Clinical Research Manager

Software Project Manager

Site Network Manager (North America)

Psychology Program Manager, Psychology Training Program Director

Air Force Clinical Social Worker (FATM) - Nellis AFB, NV

Counselor

Mental Health Therapist (Part-Time, W-2)

Clinical Director – Adolescent Behavioral Health (LCSW, LMFT, or Psychologist)

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