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Global Study Manager Jobs in Utah (NOW HIRING)

Registered Nurse

Alta, UT · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Implements Provider directives through management of diagnostic and clinical treatment plans ... Studies level: License * Studies area: Nursing * BSN Degree-highly preferred * Studies level:

Physician Liaison - Healthcare Sales

Alta, UT · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

You'll enjoy the autonomy of managing your own territory with the support of experienced leadership ... Studies area: Marketing or other related field Position Requirements/Experience: * 2-3 years of ...

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Showing results 1-20

Global Study Manager information

See Utah salary details

$20.9K

$55.9K

$93.3K

How much do global study manager jobs pay per year?

As of Aug 20, 2026, the average yearly pay for global study manager in Utah is $55,852.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,100.00 and $62,800.00 per year, depending on experience, location, and employer.

How does a global study manager collaborate with cross-functional teams during a clinical trial?

A Global Study Manager plays a pivotal role in coordinating with cross-functional teams, such as clinical operations, data management, regulatory affairs, and safety teams, to ensure smooth execution of clinical trials. They facilitate regular meetings, provide clear communication on study timelines and deliverables, and address any issues that arise across different geographic regions. Effective collaboration is crucial for aligning global processes, maintaining data consistency, and meeting regulatory requirements, making strong interpersonal and project management skills essential for success in this role.

What are the key skills and qualifications needed to thrive as a global study manager, and why are they important?

To excel as a Global Study Manager, you need expertise in clinical trial management, regulatory requirements, and project leadership, often backed by a life sciences degree and experience in global studies. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Excellent organizational skills, cross-cultural communication, and problem-solving abilities are vital soft skills for this role. These skills ensure effective coordination of international studies, compliance with regulations, and the successful delivery of complex clinical projects.

What does a global study manager do?

A global study manager oversees the planning, execution, and management of clinical research studies across multiple regions or countries. They coordinate with cross-functional teams, ensure compliance with regulatory requirements, and monitor study progress using project management tools to meet deadlines and quality standards.

What are popular job titles related to Global Study Manager jobs in Utah?

For Global Study Manager jobs in Utah, the most frequently searched job titles are:

What job categories do people searching Global Study Manager jobs in Utah look for?

The top searched job categories for Global Study Manager jobs in Utah are:

What cities in Utah are hiring for Global Study Manager jobs?

Cities in Utah with the most Global Study Manager job openings:

Study Director II

Sotera Health Company

Salt Lake City, UT • On-site

$90 - $120/hr

Other

Re-posted 13 days ago


Job description

## Study Director IIApplylocations: Nelson Labs SLCtime type: Full timeposted on: Posted Yesterdayjob requisition id: R-2026-513The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health.Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry. With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality. We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.**Job Summary:** The Study Director has overall responsibility for the technical conduct of all assigned tests as well as for the review, interpretation, analysis, documentation, and reporting of results. The study director is the single point of study control. The study director ensures all assigned studies are completed on time. A Study Director II must have sufficient scientific knowledge and communication capabilities to build and maintain customer relationships. A Study Director II will represent well the testing they oversee both verbally and in writing. He/she may also be assigned supervisory responsibilities while in this role.**Essential Duties:** All responsibilities as outlined in the Study Director I job description in addition to the following: Scientific/General* Ensure final report templates (FRTs) are compliant with procedures.* Collaborate, review, and approve Customer Specification Sheets (CSS).* Collaborate on the test method and equipment validations.* Act as document owner for Standard Test Procedures (STP) as assigned.* Supervise and manage as assigned.Regulatory & Compliance* Resolve assigned Quality Events (QE).* Assist in hosting laboratory auditors and other visitors.* Professional Development* Review current technical and scientific information and contribute content to publications as assigned.Customer Service* Collaborate with Sales on project estimates and customized quotes as needed.* Communicate business strategy, product life cycle, and laboratory offerings to customers.* Communicate with sponsors regarding a resolution of service and testing issues (e.g., quality events, turnaround time, concerns, etc.)Project Management* Coordinate with sponsors and other sections regarding test requirements for routine and non-routine studies.Perform all other duties as assigned.**Competencies of this position** All requirements, as outlined in the Study Director I job description in addition to the following: Technical* Medical Device, Pharmaceutical, and Biomedical Industry knowledge as relates to section and testing offerings.* Understanding of company structure and imperatives.* Professional* Basic financial acumen and NL business understanding.* Conflict management skills* Presentation skills* Supervisory skills* Effective communication skills specific to technical concepts, problem identification, and solutions.* Demonstrated effective technical writing ability.**Work Environment:** This job operates in a professional laboratory environment. This role routinely uses standard office equipment and lab equipment including but not limited to computers keyboards, computer mouse, telephones, photocopiers, file cabinets, microscopes, micropipettes, pipette aids, various hand tools, and analytical equipment. The possibility exists for exposure to biological and chemical hazards, exposure to carcinogenic compounds, and other environmental aspects which may be considered unfavorable. Employees are expected to follow Biosafety and Chemical Hygiene policies, practices and procedures. **Travel:** Occasional local travel during the business day and occasional out of the area or overnight travel may be expected.**Physical requirements:** The physical demands described here are a representative of those that must be met to perform the essential job functions.* Requirements to stand and traverse to various office and lab locations and sit at a computer workstation will vary.* Bending, stooping, and crouching.* Occasional push and pull tasks with one or both hands.* Must be able to work while wearing personal protective equipment such as safety glasses, goggles, face shields, gloves, lab coats and personal protective equipment deemed necessary to protect testing and to protect employees from various solutions, wastes, etc.* Must be able to lift up to 45lbs.**Education and experience requirements:*** M.S. degree (life science strongly preferred) **or*** B.S. degree (life science strongly preferred), and a minimum of one year Study Director I experience **or*** A.A./A.S. or equivalent **and** three years NL laboratory experience as a Study Director I* Successful completion of Study Director Training #J-18808-Ljbffr