9,612 Study Start Up jobs in the United States

PCA Clinical Research Study PRN

45140 Loveland, Ohio Unavailable

Posted 1 day ago

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Job Description

Where You’ll Work

At CHI Health, we're dedicated to making a difference in people's lives every day.   We are offering a PRN opportunity on either day and night working on a clinical research study at Cincinnati Children's Hospital Medical Center.

  Job Summary and Responsibilities

Patient Care Assistant / Clinical Research Study on a PRN basis.

We currently are  seeking several quality, self-driven PCA's to work in  In-Patient Clinical Research Studies at Cincinnati Children's Hospital Medical Center in Cincinnati, OH.

  • Shifts are guaranteed and scheduling is very flexible.
  • $20 per hour paid weekly.
  • Part-time and up to 40 hours per week are available for this assignment. 
Job Requirements
  • Active State Tested Nurse Aide Certification issued by the Ohio Department of Health.

#RN_rx.

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RN Clinical Research Study PRN

45140 Loveland, Ohio CommonSpirit Health at Home

Posted 1 day ago

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Job Description

**Job Summary and Responsibilities**
Registered Nurse / Clinical Research Study on a PRN basis.
We currently are seeking several quality, self-driven RN's to work in In-Patient Clinical Research Studies at Cincinnati Children's Hospital Medical Center in Cincinnati, OH.
+ Shifts are guaranteed and scheduling is very flexible.
+ $38 per hour paid weekly.
+ Part-time and up to 40 hours per week are available for this assignment.
**Job Requirements**
+ Graduate of an accredited school of nursing
+ Currently licensed to practice in Ohio.
+ One year of RN nursing experience required
#RN_rx.
**Where You'll Work**
At CHI Health, we're dedicated to making a difference in people's lives every day. We are offering a PRN opportunity on either day and night working on a clinical research study at Cincinnati Children's Hospital Medical Center.
**Pay Range**
$8.00 - 38.00 /hour
We are an equal opportunity/affirmative action employer.
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PCA Clinical Research Study PRN

45140 Loveland, Ohio CommonSpirit Health at Home

Posted 6 days ago

Job Viewed

Tap Again To Close

Job Description

**Job Summary and Responsibilities**
Patient Care Assistant / Clinical Research Study on a PRN basis.
We currently are seeking several quality, self-driven PCA's to work in In-Patient Clinical Research Studies at Cincinnati Children's Hospital Medical Center in Cincinnati, OH.
+ Shifts are guaranteed and scheduling is very flexible.
+ $20 per hour paid weekly.
+ Part-time and up to 40 hours per week are available for this assignment.
**Job Requirements**
+ Active State Tested Nurse Aide Certification issued by the Ohio Department of Health.
#RN_rx.
**Where You'll Work**
At CHI Health, we're dedicated to making a difference in people's lives every day. We are offering a PRN opportunity on either day and night working on a clinical research study at Cincinnati Children's Hospital Medical Center.
**Pay Range**
$0.00 - 20.00 /hour
We are an equal opportunity/affirmative action employer.
View Now

PCA Clinical Research Study PRN

45140 Loveland, Ohio CommonSpirit Health at Home

Posted 6 days ago

Job Viewed

Tap Again To Close

Job Description

**Job Summary and Responsibilities**
Patient Care Assistant / Clinical Research Study on a PRN basis.
We currently are seeking several quality, self-driven PCA's to work in In-Patient Clinical Research Studies at Cincinnati Children's Hospital Medical Center in Cincinnati, OH.
+ Shifts are guaranteed and scheduling is very flexible.
+ $20 per hour paid weekly.
+ Part-time and up to 40 hours per week are available for this assignment.
**Job Requirements**
+ Active State Tested Nurse Aide Certification issued by the Ohio Department of Health.
#RN_rx.
**Where You'll Work**
At CHI Health, we're dedicated to making a difference in people's lives every day. We are offering a PRN opportunity on either day and night working on a clinical research study at Cincinnati Children's Hospital Medical Center.
**Pay Range**
$0.00 - 20.00 /hour
We are an equal opportunity/affirmative action employer.
View Now

RN Clinical Research Study PRN

45140 Loveland, Ohio CommonSpirit Health at Home

Posted 14 days ago

Job Viewed

Tap Again To Close

Job Description

**Job Summary and Responsibilities**
Registered Nurse / Clinical Research Study on a PRN basis.
We currently are seeking several quality, self-driven RN's to work in In-Patient Clinical Research Studies at Cincinnati Children's Hospital Medical Center in Cincinnati, OH.
+ Shifts are guaranteed and scheduling is very flexible.
+ $38 per hour paid weekly.
+ Part-time and up to 40 hours per week are available for this assignment.
**Job Requirements**
+ Graduate of an accredited school of nursing
+ Currently licensed to practice in **Ohio.**
+ One year of RN nursing experience required
#RN_rx.
**Where You'll Work**
At CHI Health, we're dedicated to making a difference in peoples' lives every day. We are offering a PRN opportunity on either day and night working on a clinical research study at Cincinnati Children's Hospital Medical Center.
**Pay Range**
$8.00 - 38.01 /hour
We are an equal opportunity/affirmative action employer.
View Now

RN Clinical Research Study PRN Night Shift

45140 Loveland, Ohio CommonSpirit Health at Home

Posted 14 days ago

Job Viewed

Tap Again To Close

Job Description

**Job Summary and Responsibilities**
Registered Nurse / Clinical Research Study on a PRN basis.
We currently are seeking several quality, self-driven RN's to work in In-Patient Clinical Research Studies at Cincinnati Children's Hospital Medical Center in Cincinnati, OH.
+ Shifts are guaranteed and scheduling is very flexible.
+ Shift Hours: 7:00 PM - 7:30 AM
+ $38 per hour paid weekly.
+ Part-time and up to 40 hours per week are available for this assignment.
**Job Requirements**
+ Graduate of an accredited school of nursing
+ Currently licensed to practice in **Ohio.**
+ One year of RN nursing experience required
#RN_rx.
**Where You'll Work**
At CHI Health, we're dedicated to making a difference in people's lives every day. We are offering a PRN opportunity on night working on a clinical research study at Cincinnati Children's Hospital Medical Center.
**Pay Range**
$8.00 - 38.00 /hour
We are an equal opportunity/affirmative action employer.
View Now

Research Scientist – Clinical Study Management 

50501 $141000 annum Elanco

Posted 23 days ago

Job Viewed

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Job Description

Permanent

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Your Role: Research Scientist – Clinical Study Management 

The Research Scientist – Clinical Study Management position is responsible for the management of pivotal, regulated and non-pivotal studies at Elanco sites and Contract Research Organizations. You will work collaboratively to support experimental design and scientific interpretation of study results, and production of any materials for patents or publications.

Your Responsibilities: 

  • Oversee Study Design and Execution:  Lead the design and execution of clinical studies, including GLP, GCP, pivotal and non-pivotal studies, acting as Study Director for GLP safety studies and Study Investigator for clinical studies, ensuring overall conduct and scientific integrity.

  • Ensure Comprehensive Regulatory Compliance:  Maintain rigorous compliance with Good Laboratory Practice (GLP) - 21 CFR Part 58, Good Clinical Practices (GCP), and all applicable internal and external guidelines (e.g., SOPs, HSE, Animal Welfare, IACUC approvals), including managing protocol excursions and corrective actions.

  • Manage End-to-End Study Documentation:  Drive the development and completion of study protocols and final reports, support the creation and maintenance of all study-related SOPs, templates, and forms, and ensure the accurate interpretation, analysis, documentation, and secure archiving of all raw data and specimens.

  • Facilitate Cross-Functional Coordination & Communication:  Coordinate with study staff for protocol training and execution preparation, organize IVP supply management, and ensure continuous, clear communication between the Study Director, Sponsor Representative, Investigator, Clinical team, QA, and Study Monitor.

  • Contribute to Scientific Advancement & IP:  Support the generation of potential patents and publications based on study findings, leveraging study results to advance scientific knowledge and intellectual property within Elanco.

What You Need to Succeed (minimum qualifications): 

  • MS with 4+ years, BS with 7+ years of experience, or Doctorate level education (e.g., PhD, DVM, MD) with 2+ years in a relevant industry. 

  • Experience managing clinical study initiation, execution, and completion and thorough understanding in coordinating various clinical functional groups including regulatory, clinical laboratory, clinical execution, veterinary services, and animal care personnel.

  • Background with both USDA and EU Regulatory guidelines preferred.

What will give you a competitive edge (preferred qualifications): 

  • Experience with clinical study management in the Animal Health industry is highly desired.

  • Strong organizational and time management skills.

  • Advanced ability to define problems, collect data, establish facts, and draw valid conclusions.

  • Experience with biological vaccines, small molecules, and large molecules.

  • Experience with or willing to gain experience with Pain and Dermatology models.

Additional Information: 

  • Travel: Up to 10% 

  • Location: Fort Dodge, Iowa

Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles! 

Elanco Benefits and Perks:   

We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:  

  • Multiple relocation packages  

  • Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)  

  • 8-week parental leave  

  • 9 Employee Resource Groups  

  • Annual bonus offering  

  • Flexible work arrangements  

  • Up to 6% 401K matching 

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Apply Now
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Research Study Manager

08901 New Brunswick, New Jersey Actalent

Posted 2 days ago

Job Viewed

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Job Description

Job Title: Research Study Manager
Job Description
We are seeking a dedicated and experienced Research Study Manager to oversee the day-to-day clinical research operations. This role requires a proactive leader with strong experience in oncology and clinical research coordination.
Responsibilities
+ Supervise and manage the workflow of coordinators in the assigned disease-specific group.
+ Communicate services that will support and enable the growth of clinical research, particularly in recruitment, retention, coordination of research, and data management.
+ Conduct quality assurance audits to ensure compliance with regulatory standards.
+ Partner with physicians to educate and assist them in selecting appropriate studies and explaining feasibility.
+ Work with research sites to oversee oncology research and ensure compliance with protocols.
+ Assist doctors in selecting trials and understand screening processes to improve site enrollment.
Essential Skills
+ Experience in supervising coordinators and managing workflow.
+ Prior experience in oncology and as a Clinical Research Coordinator (CRC).
+ Strong understanding of clinical operations and regulatory compliance.
+ Bachelor's Degree in a science discipline.
+ 3-5 years of oncology experience.
+ At least 1 year of supervisory experience.
Additional Skills & Qualifications
+ Experience as a Clinical Research Supervisor or Research Program Manager.
+ Familiarity with NCI Designated Cancer Institutes.
Job Type & Location
This is a Contract to Hire position based out of New Brunswick, New Jersey.
Pay and Benefits
The pay range for this position is $52.00 - $54.00/hr.
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 hybrid position in New Brunswick,NJ.
Application Deadline
This position is anticipated to close on Oct 14, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
View Now

Research Study Manager

08901 New Brunswick, New Jersey Actalent

Posted 9 days ago

Job Viewed

Tap Again To Close

Job Description

Job Title: Research Study Manager
Job Description
We are seeking a dedicated and experienced Research Study Manager to oversee the day-to-day clinical research operations. This role requires a proactive leader with strong experience in oncology and clinical research coordination.
Responsibilities
+ Supervise and manage the workflow of coordinators in the assigned disease-specific group.
+ Communicate services that will support and enable the growth of clinical research, particularly in recruitment, retention, coordination of research, and data management.
+ Conduct quality assurance audits to ensure compliance with regulatory standards.
+ Partner with physicians to educate and assist them in selecting appropriate studies and explaining feasibility.
+ Work with research sites to oversee oncology research and ensure compliance with protocols.
+ Assist doctors in selecting trials and understand screening processes to improve site enrollment.
Essential Skills
+ Experience in supervising coordinators and managing workflow.
+ Prior experience in oncology and as a Clinical Research Coordinator (CRC).
+ Strong understanding of clinical operations and regulatory compliance.
+ Bachelor's Degree in a science discipline.
+ 3-5 years of oncology experience.
+ At least 1 year of supervisory experience.
Additional Skills & Qualifications
+ Experience as a Clinical Research Supervisor or Research Program Manager.
+ Familiarity with NCI Designated Cancer Institutes.
Job Type & Location
This is a Contract to Hire position based out of New Brunswick, New Jersey.
Pay and Benefits
The pay range for this position is $52.00 - $54.00/hr.
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 hybrid position in New Brunswick,NJ.
Application Deadline
This position is anticipated to close on Oct 14, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
View Now
 

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