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Study Director Jobs in Colorado (NOW HIRING)

Inotiv

Study Director

Westminster, CO · On-site

Works with study sponsors to create study protocols * Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies

Inotiv, Inc.

Study Director

Westminster, CO · On-site

$80 - $120/hr

## Study DirectorApplyremote type: On-sitelocations: Westminster, COtime type: Full timeposted on: Posted 2 Days Agojob requisition id: JR101503**Summary**The position has responsibilities centered ...

Inotiv

Study Director

Westminster, CO · On-site

Works with study sponsors to create study protocols * Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies

INOTIV BOULDER LLC

Study Director

Boulder, CO · On-site

$75 - $95/hr

Works with study sponsors to create study protocols * Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies

Inotivco

Study Director

Westminster, CO · On-site

Works with study sponsors to create study protocols * Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies

Inotiv

Study Coordinator

Westminster, CO · On-site

$26 - $33/hr

Support and participate in company initiatives as directed * Maintain thorough knowledge of ... Maintain and submit study initiation materials * Order all applicable supplies for studies

Inotiv

Study Coordinator

Westminster, CO · On-site

$26 - $33/hr

Support and participate in company initiatives as directed * Maintain thorough knowledge of ... Maintain and submit study initiation materials * Order all applicable supplies for studies

Inotivco

Study Coordinator

Westminster, CO · On-site

$26 - $33/hr

Support and participate in company initiatives as directed * Maintain thorough knowledge of ... Maintain and submit study initiation materials * Order all applicable supplies for studies

SSR Mining, Inc.

Senior Project Engineer

Denver, CO

$101K - $132K/yr

Reporting to the Study Director, the Study Manager / Project Engineer will coordinate and manage technical workstreams associated with mining, processing, infrastructure, and capital project studies ...

SSR Mining, Inc.

Project Engineer (Growth)

Denver, CO

$120K - $135K/yr

Reporting to the Study Director, the Project Engineer will coordinate and manage technical workstreams associated with mining, processing, infrastructure, and capital project studies from scoping ...

SSR Mining Inc.

Project Engineer (Growth)

Denver, CO · On-site

$120 - $135/hr

Reporting to the Study Director, the Project Engineer will coordinate and manage technical workstreams associated with mining, processing, infrastructure, and capital project studies from scoping ...

SSR Mining Inc.

Senior Project Engineer

Denver, CO · On-site

$135 - $150/hr

Reporting to the Study Director, the Study Manager / Project Engineer will coordinate and manage technical workstreams associated with mining, processing, infrastructure, and capital project studies ...

SSR Mining, Inc.

Project Engineer (Growth)

Denver, CO · On-site

$120K - $135K/yr

Reporting to the Study Director, the Project Engineer will coordinate and manage technical workstreams associated with mining, processing, infrastructure, and capital project studies from scoping ...

Inotiv

Image Analyst/Morphometrist

Fort Collins, CO · On-site

Requests and organizes applicable data, as needed, from the Sponsor/Study Director in support of the Pathologist's evaluation of slides. * Prepares pathology report templates and data spreadsheets to ...

SSR Mining, Inc.

Senior Project Engineer

Denver, CO · On-site

$101K - $132K/yr

Reporting to the Study Director, the Study Manager / Project Engineer will coordinate and manage technical workstreams associated with mining, processing, infrastructure, and capital project studies ...

Inotiv

Image Analyst/Morphometrist

Fort Collins, CO · On-site

Requests and organizes applicable data, as needed, from the Sponsor/Study Director in support of the Pathologist's evaluation of slides. * Prepares pathology report templates and data spreadsheets to ...

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Study Director information

See Colorado salary details

$47.3K

$135K

$244.5K

How much do study director jobs pay per year?

As of Aug 30, 2026, the average yearly pay for study director in Colorado is $134,980.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,000.00 and $198,200.00 per year, depending on experience, location, and employer.

What is a study director?

A Study Director is the individual responsible for the overall conduct of a scientific study, particularly in regulated environments such as pharmaceuticals, chemicals, or environmental research. They oversee the planning, execution, and reporting of studies to ensure they comply with regulatory standards, such as Good Laboratory Practice (GLP). The Study Director acts as the main point of control and communication, coordinating among team members and ensuring that the study meets its scientific and regulatory objectives. Their role is critical for the integrity and quality of the data generated.

What does a study director do?

As a study director, your job is to manage studies, analyze results, and interpret reports so you can deliver a summary of the findings. This work has three categories. First, on the technical side, your job includes creating the plan for the study, coordinating with other scientists, and overseeing data collection. In the administrative role, you monitor junior employees and ensure each investigation finishes within budgetary constraints. In the compliance role, you ensure that each study happens under strict safety and ethics protocols. You may be asked to run multiple studies at the same time, adding to the complexity of this position.

How does a study director typically collaborate with cross-functional teams during a research project?

As a Study Director, you play a central role in coordinating research activities by regularly collaborating with scientists, technicians, quality assurance personnel, and regulatory teams. You are responsible for ensuring all team members are aligned on study objectives, timelines, and compliance requirements. Effective communication and leadership are essential, as you facilitate meetings, delegate tasks, and resolve issues that arise to keep the project on track. This collaborative environment not only fosters professional growth but also provides valuable exposure to various scientific and operational domains within the organization.

What skills and qualifications does a successful study director have?

To thrive as a Study Director, you need a solid background in scientific research methods, regulatory compliance, and study protocol development, usually supported by an advanced degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) standards, and project management tools is highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for managing cross-functional teams and ensuring study integrity. These competencies are vital to ensure regulatory adherence, data accuracy, and successful project outcomes in research environments.

What is the difference between Study Director vs Laboratory Manager?

AspectStudy DirectorLaboratory Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and relevant certificationsRequires relevant degrees and management experience, but not necessarily advanced research credentials
Work EnvironmentLeads specific research or regulatory studies, often in contract labs or pharmaceutical companiesOversees daily lab operations, staff, and compliance across multiple projects
Industry UsageCommonly used in GLP, clinical, and research settingsUsed broadly in laboratory settings across industries

The Study Director focuses on designing, overseeing, and ensuring the integrity of specific studies, often requiring scientific expertise. The Laboratory Manager handles overall lab operations, staff management, and compliance. Both roles are essential but differ in scope and responsibilities.

More about Study Director jobs

What are the most commonly searched types of Study jobs in Colorado?

The most popular types of Study jobs in Colorado are:

What are popular job titles related to Study Director jobs in Colorado?

For Study Director jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Study Director jobs in Colorado look for?

The top searched job categories for Study Director jobs in Colorado are:

What cities in Colorado are hiring for Study Director jobs?

Cities in Colorado with the most Study Director job openings:

Study Director jobs near you
Infographic showing various Study Director job openings in Colorado as of August 2026, with employment types broken down into 2% As Needed, 82% Full Time, 12% Part Time, 2% Temporary, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $134,980 per year, or $64.9 per hour.

Study Director

Westminster, CO • On-site

Inotiv
Scientific Research and Development Services • 201 - 500 employees

8.6

Company rating: 8.6 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

14th of 74 rated research

People enjoy working here

Good employer

Recommended by parents

Learn more about Inotivexternal

Full-time

Medical, Dental, Retirement, PTO

Re-posted 9 days ago

Job description

Summary
The position has responsibilities centered around the execution, planning, and management of assigned studies. The role will participate in vivo pharmacology research conducting biochemical screening models, proof-of-concept models for target validation, as well as disease efficacy models to evaluate development and discovery lead compounds. The ability to communicate succinctly with clients, coordinators, and technicians is key as well as a cross-functional, flexible, and collaborative spirit.
Responsibilities
  • Manages client correspondence and relationship
  • Works with study sponsors to create study protocols
  • Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies
  • Ensures all research technicians are properly trained to perform task and is ultimately responsible for all work performed on his/her study.
  • Performs disease-inducing procedures
  • Provides potential study sponsors with quotes for proposed studies
  • Ensures all tasks are performed on daily schedule
  • Performs surgical procedures
  • Performs research technicians' tasks, as needed
  • Prepares high quality and accurate data package for clients
  • Keeps track of project timelines for forecasting purposes
  • Oversees coordinating of all studies and allocates resources
  • Identifies and is accountable for driving ways to improve the efficiency and quality of processes and the resulting deliverables, influencing key stakeholders as applicable
  • Writes IACUC protocols
  • Other duties may be assigned

Qualifications
  • An individual with an in-depth understanding of in vivo models of multi-system rodent physiology and in vitro analyses of pathobiology and disease biomarkers.
  • Demonstrates strong organizational, communication (both oral and written), time management, and interpersonal skills in a cross-functional team.
  • Must actively participate and work well in a collaborative, team-oriented environment.
  • Experience with rodent cardiac survival surgeries and/or cardiac ultrasound is required.
  • Should be adept at data management and reduction.
  • Able to demonstrate strong skills in authoring and managing the production of scientific documents (e.g., pre-clinical study protocols, data package, technical reports, publications in peer-reviewed journals).
  • Proficient with Microsoft Excel, Word, and PowerPoint; familiarity with GraphPad Prism desired.
  • Shows flexibility and ability to apply his/her knowledge to new areas of study.
  • Commitment to safety and the humane treatment of laboratory animals is required.

Minimum Education / Experience Requirements:
  • A basic understanding of integrated physiology, pathophysiology, and pharmacology is required.
  • Previous pre-clinical in vivo laboratory experience including handling of research rodents is required.
  • Demonstrated ability to perform rodent cardiac survival surgeries and/or cardiac ultrasound is required.
  • Industry research experience is highly preferred.
  • Research experience in therapeutic area is highly preferred.
  • MS degree in related scientific discipline (e.g., Physiology, Pharmacology) and at least 3-8 years of related experience or an equivalent combination of education and experience is required.
  • Ph.D. degree in related scientific discipline (e.g., Physiology, Pharmacology) is highly preferred.

*This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level.
Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There's an opportunity for everyone at all phases of a career, each individual's unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world.
Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more!
Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.
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About Inotiv

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

201 - 500 Employees

Headquarters location

West Lafayette, IN, US

Year founded

1974

Social media

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