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Position Title: Senior Project Manager Classification: Full-Time – Exempt Reports to: Director of Evidence and Strategic Initiatives Salary: $82,000 - $92,000 based on experience Position available: Immediately in …
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Capital Creek Medical
Arthrex Area Manager: Boulder
Boulder, Colorado, United States · On-site
Senior
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State Government Growth & Regulatory Board Partnerships (Remote, US)
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Propelus® simplifies workforce compliance management across healthcare. Our innovative technology and strategic partnerships empower millions of professionals, their employers, and regulators to work together, creating a…
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Skills: Sales, New logo acquisition, Enterprise sales, Healthcare SaaS, Pipeline management
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Responsibilities and Duties The ACT is responsible for providing exceptional animal care to the research animals at Inotiv. This includes performing daily husbandry and care and of laboratory animals in a research enviro…
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Propelus® simplifies workforce compliance management across healthcare. Our innovative technology and strategic partnerships empower millions of professionals, their employers, and regulators to work together, creating a…
Description At Academy Mapleton Hill, we craft all of our dishes from scratch in our La Cucina Raffinata—Italian for refined cuisine. Our kitchen was recently honored with the 2026 Snail of Approval Award, which celebrat…
Manufacturing Technician II Monday – Friday 8:30am – 4:30pm
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$21/hr–$24/hr
Entry level$8.0B raised
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Emergency Credentialed Veterinary Technician (Shift Lead) - Boulder, CO
Boulder, Colorado, United States · On-site
$25/hr–$51/hr
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Full-time
bachelor degree
Health coverage, Dental coverage, Short-term disability, Long-term disability, Paid time off, Paid parental leave
Posted 15d ago
~40 hrs/week
Responsibilities
The Study Coordinator manages study initiation materials, schedules activities, and ensures compliance with regulatory standards like GLP and USDA. They are responsible for preparing protocols, reviewing raw data, and maintaining study files for archival.
Requirements
Candidates must have a Bachelor's degree in life sciences and at least three years of experience in a pharmaceutical setting. Additionally, a minimum of one year of experience with animal handling is required.
Full job description
Responsibilities and Duties
Corporate
Follow all SOPs and other applicable company policies and procedures
Maintain confidential information
General
Interact and communicate with clients, vendors, other employees, and the community in a professional manner
Support and participate in company initiatives as directed
Maintain thorough knowledge of facility SOPs, policies, protocols, etc.
Adhere to all safety regulations and procedures
Provide assistance or support to other Inotiv sites as necessary
Perform other duties as assigned
Specific
Maintain and submit study initiation materials
Order all applicable supplies for studies
Communicate with other coordinators to schedule study activities
Ensure creation of data sheets
Confirm laboratory math for test article and disease induction formulation
Communicate with formulations team regarding timeline and materials needed
Assist with in-life study conduct, as needed, and as trained
Complete training requirements as assigned and maintain appropriate training documentation
Perform periodic review of all applicable SOPs to ensure accuracy and confirm procedures are being performed according to SOPs. Participate in SOP writing, reviews, and revisions, as needed
Maintain compliance with all policies and procedures
Ensure compliance with USDA, AAALAC, OLAW, GLPs and other applicable regulations
Perform quality checks, reviews, and formatting on all Inotiv documents (e.g. protocols, amendments, deviations, reports, tables, etc.)
Develop and maintain study protocol, report, and data table master templates
Provide back-up support for Study Directors as needed
Aid in protocol and any protocol amendment or deviation preparation and distribution
Prepare and review raw data collection forms and review for adherence to protocol, both prior to study start and after study completion
Review raw data collection and in-life study conduct
Assist to prepare a complete study file for archival following finalization of report
Assist to ensure that study samples and test articles are shipped appropriately, on schedule, and documented in the study file
Perform other duties as assigned
Position Requirements
Education and experience
At a minimum, the Study Coordinator must have a Bachelor's degree in life sciences or other directly related field or degree with comparable coursework and a minimum of three years in a relevant pharmaceutical setting
The Study Coordinator must have a minimum of one year experience with animals and animal handling
Skills and abilities
A working knowledge and awareness of general laboratory procedures
Customer focused, results driven, communicative, and collaborative enabling effective customer satisfaction, including problem solving, fostering positive relationships, and proactive communication
Ability to adhere to and manage in accordance with the Code of Federal Regulations procedures
Experience in the use of computer software applications (e.g., Word, Outlook, Excel)
Possess strong skills for editing the format, style and language of draft protocols, spreadsheets and reports
Excellent written and verbal communication skills
An attitude for quality, an eye for detail and the ability to read and follow written instructions
Ability to interact with scientific staff at all levels
Performance Requirements
General
Ability to read, write, speak, and understand English
Able and willing to work a flexible schedule according to study needs
Physical activity
Moderate physical activity:
Prolonged periods of sitting at a desk and working on a computer
May occasionally lift and/or move objects
Able to wear PPE (Personal Protection Equipment) as required
Working Conditions
Work is normally performed in a typical interior office or laboratory environment
Work may require use of PPE due to exposure to potentially dangerous materials and situations
Noise level is usually moderate as commensurate with a typical office environment
Salary Range: $26.00-$33.00 per hour, adjusted according to the level of the role and the candidate’s relevant experience and/or education. Salary will be commensurate with experience and responsibilities.
Benefits: Health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401(k), and more.
Position Status: Open until filled.
#LI-JM1
#LI-Onsite
*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.
At Inotiv, our work helps advance the development of new medicines and therapies that can improve people's lives. As a leading global contract research organization (CRO), we partner with researchers to tackle complex scientific challenges, drive innovation, and help build a healthier, safer world. Bringing together scientists, researchers, technical experts, and business professionals, we provide the expertise and collaboration needed to move research forward. Our people make this work possible, and we value the knowledge, ideas, and contributions each person brings to the team. Whether you are starting your career or bringing years of experience, Inotiv offers opportunities to learn, grow, and play a meaningful role in advancing treatments for patients around 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.
WHERE INSIGHTS LEAD TO ANSWERS
Expect More
In choosing a partner for discovery, development and research models, expect more: more attention, more insight, and a superlative experience. You’ve worked hard to get this far, and you deserve a provider seamlessly aligned to your needs and goals.
Through scientific leadership and ongoing investments, Inotiv delivers a comprehensive range of services and products that will exceed your expectations. Benefit from our long and impeccable regulatory history, world class team of scientists, and track record of providing attentive, decisive service.
Answering the right questions on time and with high-quality data is the key to achieving your objectives. At Inotiv, that is our focus: to provide you with both the broad scope and right-size solutions essential to your success.
Gain the insights you deserve to get the answers you need. Expect more — with Inotiv.
Inotiv is a Top Workplaces 2023 Winner.
Offices: 2701 Kent Ave., West Lafayette, IN 47906, US
How many Healthcare jobs are open in Boulder, CO right now?
There are currently 223 open healthcare positions in Boulder, CO listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Healthcare roles in Boulder, CO?
Companies currently hiring include KBI Biopharma, CorrHealth, PACS, Brookdale, Clinica Family Health, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Healthcare jobs in Boulder, CO?
Yes — 28 of the 223 open healthcare positions offer remote or hybrid work (13 remote, 15 hybrid).
How do I apply for Healthcare jobs in Boulder, CO?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.