1

Clinical Research Project Manager Jobs in Indiana

Research Contracts Admin

Evansville, IN · On-site

$19.14 - $26.79/hr

Help Advance Clinical Research Through Strong Financial and Contract Management We are seeking a ... Experience managing multiple projects and deadlines simultaneously * Strong communication and ...

... clinical trials * Communicate with physicians, patients, sponsors, and internal research teams to facilitate enrollment * Request and secure sponsor study slots for qualified patients * Manage ...

Summary: The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations ... Study & Site Management * Serve as CRA for assigned complex clinical studies, providing expert ...

New

Showing results 41-60

Clinical Research Project Manager information

See Indiana salary details

$47.6K

$81.9K

$125.6K

How much do clinical research project manager jobs pay per year?

As of Aug 14, 2026, the average yearly pay for clinical research project manager in Indiana is $81,864.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,000.00 and $87,100.00 per year, depending on experience, location, and employer.

What is the difference between Clinical Research Project Manager vs Clinical Research Coordinator?

AspectClinical Research Project ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in health sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, and liaises with sponsorsConducts daily clinical trial activities, interacts directly with participants and site staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch hospitals, clinics, academic institutions

The Clinical Research Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, ensuring protocol adherence and participant safety. Both roles are essential but differ in scope and responsibilities.

What does a clinical research project manager do?

A Clinical Research Project Manager oversees the planning, execution, and management of clinical research studies. They coordinate teams, ensure regulatory compliance, manage budgets and timelines, and act as a liaison between stakeholders such as sponsors, investigators, and regulatory agencies. Their primary goal is to ensure that clinical trials are conducted efficiently, ethically, and according to protocol. This role requires strong organizational, leadership, and communication skills, as well as a deep understanding of clinical research processes.

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

Clinical Research Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance, and coordinating communication between diverse stakeholders. Balancing the needs of sponsors, research teams, and regulatory bodies requires strong organizational and problem-solving skills. Staying proactive with risk management and fostering clear, consistent communication can help address these challenges effectively. Leveraging project management tools and regularly scheduled check-ins also supports smoother project execution and team collaboration.

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

To thrive as a Clinical Research Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with tools such as CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications like PMP or ACRP-PM is highly valuable. Strong leadership, communication, and problem-solving skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial to ensure trials are conducted efficiently, ethically, and in line with regulatory standards.

What are the most commonly searched types of Clinical Research Project jobs in Indiana?

The most popular types of Clinical Research Project jobs in Indiana are:

What are popular job titles related to Clinical Research Project Manager jobs in Indiana?

For Clinical Research Project Manager jobs in Indiana, the most frequently searched job titles are:

What cities in Indiana are hiring for Clinical Research Project Manager jobs?

Cities in Indiana with the most Clinical Research Project Manager job openings:

Infographic showing various Clinical Research Project Manager job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $81,864 per year, or $39.4 per hour.

Clinical Research Support - IN

Versiti, Inc.

Indianapolis, IN

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago


Versiti rating

5.7

Company rating: 5.7 out of 10

Based on 46 frontline employees who took The Breakroom Quiz

783rd of 887 rated healthcare providers


Job description

OverviewVersiti is a fusion of donors, scientific curiosity, and precision medicine that recognize the gifts of blood and life are precious. We are home to the world-renowned Blood Research Institute, we enable life saving gifts from our donors, and provide the science behind the medicine through our diagnostic laboratories. Versiti brings together outstanding minds with unparalleled experience in transfusion medicine, transplantation, stem cells and cellular therapies, oncology and genomics, diagnostic lab services, and medical and scientific expertise. This combination of skill and knowledge results in improved patient outcomes, higher quality services and reduced cost of care for hospitals, blood centers, hospital systems, research and educational institutions, and other health care providers. At Versiti, we are passionate about improving the lives of patients and helping our healthcare partners thrive.Position SummaryUnder the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including processing specimens, entering data, maintaining files, etc. Proficiently performs phlebotomy, apheresis, collection of blood products and other biomaterials, and the protocols or studies under which subjects are consented and collected. Ensures a customer focused approach is implemented and systematically analyzes customer requests and information while adhering to all applicable compliance requirements. This position is responsible for handling these clearly delineated tasks/projects as delegated by and with guidance from department leadership.Total Rewards Package

CompensationThe target salary is based on internal averages. Versiti sets salary ranges aligned to local markets in which the job is performed. Compensation decisions take into account internal salary averages and differentiation based on education, experience, skills, and performance. Specific salary and benefits information is shared at the time of the phone screening based on your location and qualifications.BenefitsVersiti provides a comprehensive benefits package based on your job classification. Full-time regular employes are eligible for Medical, Dental, and Vision Plans, Paid Time Off (PTO) and Holidays, Short- and Long-term disability, life insurance, 7% match dollar for dollar 401(k), voluntary programs, discount programs, others.

Responsibilities
  • Collects biospecimens using a variety of methods, including phlebotomy with or without automation, for use in research and further manufacturing. Uses independent judgement to adjust processes to optimize efficiency and accommodate specific requirements for a wide variety of contract collections and/or specific research protocols (including processing, labeling, storage and shipments).
  • Organize, prioritize, problem solve and accurately complete project tasks and responsibilities so that the critical project goals and timelines that are inherent in research studies are met
  • Under general supervision, may process specimens as directed which may include receiving, storing, shipping, tracking, collection, and/or specified technical procedures
  • Completes a variety of administrative tasks to support the research team, such as scheduling visits, handling telephones and voicemail, lab walk-throughs, errands, etc.
  • Communicates effectively with team members, health care workers, collaborating professionals, Principal Investigators, etc.
  • Assists the department leadership in day-to-day operations of the project(s)
  • Completes thorough, accurate and timely data entry
  • Maintains thorough, accurate and current files
  • Assists the department leadership with meeting and event set-up tasks as assigned
  • Maintains confidentiality of all subject-related records including written and verbal communications
  • Completes all projects and tasks in an accurate, thorough, and timely manner to meet project goals and communicates any concerns or questions to department leadership
  • Participates in process improvement activities
  • Attends and contributes to meetings
  • Provides effective input into team project planning and problem solving
  • Performs other duties as required or assigned which are reasonably within the scope of the duties in this job classification
  • Understands and performs in accordance with all applicable regulatory and compliance requirements
  • Complies with all standard operating policies and procedures
QualificationsEducation
  • High School Diploma or equivalent required
  • Bachelor's Degree preferred
Experience
  • Experience in a health care or research setting preferred
Knowledge, Skills and Abilities
  • Good customer service and interpersonal skills, including verbal and written communication skills. required
  • Ability to work effectively with study subjects and sponsors, investigators, health care workers, and collaborating professionals. Familiarity with regulations associated with human subject research preferred. required
  • Effective organizational, prioritization, and problem-solving skills with the ability to meet stringent deadlines. required
  • Attention to detail to ensure accuracy of data related to laboratory results, subject health history, and data collection and reporting. Takes pride in and is committed to delivering high quality data required
  • Proficiency in Microsoft Office products such as, Word, Excel, Powerpoint, and Outlook. Typing skills required to prepare business correspondence and reports with speed and accuracy. Proficiency with data entry. required
  • Valid driver's license and access to a vehicle required
  • Works cooperatively and is a supportive member of the team required
  • Acquires job skills and learns company policies and procedures to complete routine tasks. Typically encounters repetitive situations requiring choice of things learned. Asks questions as needed required
Tools and Technology
  • Personal Computer (desk top, lap top, tablet) required
  • General office equipment (computer, printer, fax, copy machine) required
  • Microsoft Suite (Word, Excel, PowerPoint) required
  • EPIC medical record system required
  • Electronic Data Capture systems such as Velos, Redcap, Medidata, Inform, etc. required
Employment Type: FULL_TIME

What Versiti employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom