ZipRecruiter

Log In

1

Clinical Trial Operations Manager Jobs in Indiana

DaVita

Then you might be a great fit for our Operations Analyst I position with DaVita Clinical Research ... RAVE, Medidata), Clinical Trial Management Systems required; 3 or more years of experience ...

Priority OnDemand

Operations Manager

Indianapolis, IN · On-site

A "high-quality unit hour" may be summarized as a clinically competent, neat appearing, well ... The Operations Manager participates in and/or undertakes any special projects as required by the ...

previous pagenext page

Showing results 21-40

All JobsClinical Trial Operations JobsClinical Trial Operations Manager JobsClinical Trial Operations Manager Jobs in Indiana

Clinical Trial Operations Manager information

See Indiana salary details

$27

$59

$91

How much do clinical trial operations manager jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical trial operations manager in Indiana is $59.49, according to ZipRecruiter salary data. Most workers in this role earn between $48.27 and $67.02 per hour, depending on experience, location, and employer.

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

Clinical Trial Operations Managers often encounter challenges such as ensuring regulatory compliance across multiple sites, managing tight timelines, and coordinating diverse teams. Effective communication and proactive planning are essential to address these difficulties. Leveraging project management tools and fostering strong relationships with investigators and site staff can also help streamline operations and reduce risks of delays or protocol deviations.

What is the difference between Clinical Trial Operations Manager vs Clinical Research Coordinator?

AspectClinical Trial Operations ManagerClinical Research Coordinator
CredentialsBachelor's degree; often advanced degrees or certifications in clinical research or managementBachelor's degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentOversees multiple trials, manages teams, and coordinates with stakeholders in clinical settingsWorks directly with participants, manages trial documentation, and supports daily trial activities
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinics, research institutions

The Clinical Trial Operations Manager focuses on overseeing entire clinical trial processes, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at the trial site, working closely with participants and supporting trial documentation. Both roles require relevant certifications and are essential in the clinical research industry, but they differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as a clinical trial operations manager, and why are they important?

To thrive as a Clinical Trial Operations Manager, you need a strong background in clinical research, regulatory compliance, project management, and a relevant degree such as in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications like ACRP or SOCRA are highly valued. Leadership, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These competencies ensure clinical trials are conducted efficiently, ethically, and in accordance with regulatory requirements.

What does a clinical trial operations manager do?

A Clinical Trial Operations Manager oversees the planning, execution, and completion of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate with cross-functional teams, manage budgets and timelines, and handle any issues that arise during the trial process. This role is crucial for ensuring that new drugs or medical devices are tested safely and effectively before reaching the market.
What are popular job titles related to Clinical Trial Operations Manager jobs in Indiana? For Clinical Trial Operations Manager jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Operations Manager jobs in Indiana look for? The top searched job categories for Clinical Trial Operations Manager jobs in Indiana are:
What cities in Indiana are hiring for Clinical Trial Operations Manager jobs? Cities in Indiana with the most Clinical Trial Operations Manager job openings:
Clinical Trial Operations Manager jobs near you

Hybrid Registered Nurse (Oncology)

Actalent

Indianapolis, IN • On-site

$40 - $45/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Job description

Hybrid - Registered Nurse - Oncology (Phase I Trials)
*Clinical research experience NOT required*
Job Description
This clinical research nurse role focuses on supporting phase I oncology clinical trials by providing direct patient care during study visits. The nurse conducts patient visits, obtains vital signs, collects and processes specimens, and ensures timely delivery of samples to the appropriate laboratories. The position emphasizes hands-on clinical work in a collaborative environment, without responsibility for regulatory documentation or patient recruitment. The nurse uses EPIC for charting and works across multiple disease groups, sharing the workload with a multidisciplinary team.
Responsibilities
  • Conduct patient visits for phase I clinical trials, seeing approximately 5-7 patients per day across multiple studies.
  • Perform patient vital sign assessments and document findings accurately in EPIC.
  • Collect specimens, including blood draws, and ensure proper labeling, handling, and timely transport to the appropriate laboratory.
  • Participate in pre-screening of patients as required by study protocols.
  • Provide oncology-focused nursing care to patients enrolled in clinical trials, ensuring patient safety and comfort throughout visits that may range from 1 to 8 hours.
  • Collaborate with the clinical research team to divide and coordinate daily patient visits and share workload across all disease groups.
  • Complete clinical charting and documentation in EPIC, while not being responsible for data management, regulatory documentation, or patient recruitment activities.
  • Attend required team meetings, including the Friday morning meeting, and contribute to discussions on workflow, patient care, and trial operations.
  • Travel between designated cancer center locations as needed to support trial operations and patient care.
  • Adhere to clinical trial protocols, institutional policies, and professional nursing standards in all aspects of patient care and specimen handling.
Essential Skills
  • Current nursing license for the state of Indiana.
  • Oncology nursing experience, with the ability to provide specialized care to oncology patients.
  • Experience taking patient vital signs and documenting clinical assessments accurately.
  • Proficiency in performing blood draws and handling specimens in a clinical setting.
  • Experience pre-screening patients in a healthcare or clinical research environment.
  • Familiarity with clinical research processes, particularly within oncology trials.
  • Ability to use EPIC or similar electronic medical record systems for charting and documentation.
  • Strong teamwork skills and the ability to share workload across multiple disease groups.
  • Reliability in following clinical protocols and maintaining high standards of patient safety.
Additional Skills & Qualifications
  • Oncology Nursing experience with interest in or exposure to clinical research.
  • Certified chemotherapy nurse (chemotherapy certification).
  • Prior clinical research experience, particularly in oncology or phase I trials, is a plus.
  • Willingness to learn and develop research-specific skills, with training provided for oncology nurses transitioning into research.
  • Strong organizational and time management skills to handle patient visits ranging from 1 to 8 hours.
  • Effective communication skills to collaborate with a multidisciplinary team and support patients throughout their visits.

Work Environment
The role is based within cancer center facilities and involves working closely with a collaborative clinical research team. This position is required 4 days per week onsite.
Job Type & Location
This is a Contract to Hire position based out of Indianapolis, IN.
Pay and Benefits
The pay range for this position is $40.00 - $45.00/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 fully onsite position in Indianapolis,IN.
Application Deadline
This position is anticipated to close on Aug 13, 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 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 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 the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall 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 applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
Actalent logo

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

Social media

Facebook

View All Actalent Jobs

Apply