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Remote Cro Jobs in Utah (NOW HIRING)

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... a sponsor, CRO, or as an independent consultant. * Demonstrated proficiency in authoring or ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... a sponsor, CRO, or as an independent consultant. * Demonstrated proficiency in authoring or ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... a sponsor, CRO, or as an independent consultant. * Demonstrated proficiency in authoring or ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... a sponsor, CRO, or as an independent consultant. * Demonstrated proficiency in authoring or ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

Biostatistician

Provo, UT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

Medical Writing Manager

Provo, UT · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent ...

Showing results 21-40

Remote Cro information

See Utah salary details

$15

$19

$21

How much do remote cro jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for remote cro in Utah is $19.57, according to ZipRecruiter salary data. Most workers in this role earn between $16.39 and $20.77 per hour, depending on experience, location, and employer.

What is a remote CRO?

A Remote CRO, or Remote Conversion Rate Optimization specialist, is a professional who works remotely to analyze, test, and improve the effectiveness of websites or digital marketing campaigns to increase the percentage of visitors who take a desired action, such as making a purchase or filling out a form. They use data analysis, user experience research, A/B testing, and other strategies to optimize conversion rates without being physically present at the workplace. Remote CROs collaborate with marketing, design, and development teams via digital tools to implement and track changes that drive better results.

What are the key skills and qualifications needed to thrive as a remote CRO?

To thrive as a Remote CRO, you need expertise in data analysis, A/B testing, UX/UI principles, and a background in marketing or a related field. Familiarity with tools like Google Analytics, Optimizely, Hotjar, and certification in CRO or digital marketing are highly valued. Strong communication, problem-solving, and collaboration skills are essential for working effectively with distributed teams and stakeholders. These skills ensure data-driven decision-making and continuous website improvement to maximize conversion rates and business growth.

What are the main challenges faced by a remote CRO when collaborating with cross-functional teams?

As a Remote CRO, one of the main challenges is maintaining clear and consistent communication with cross-functional teams such as marketing, design, and development. Since collaboration happens virtually, it’s essential to use project management tools and regular video meetings to align on goals, share experiment results, and implement changes. Building trust and rapport remotely can require extra effort, but it’s key to ensuring smooth workflows and effective A/B testing cycles. Proactively sharing insights and being responsive to feedback helps foster a collaborative and productive remote environment.

What is the difference between Remote Cro vs Remote Clinical Research Coordinator?

AspectRemote CroRemote Clinical Research Coordinator
Required CredentialsTypically requires advanced degrees in life sciences, clinical research certificationsUsually requires a bachelor's degree in health sciences or related field, with some certifications
Work EnvironmentPrimarily data analysis, protocol oversight, and remote management of clinical trialsCoordination of trial activities, patient interactions, and site communication, often remote
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

The main difference between Remote Cro and Remote Clinical Research Coordinator lies in their focus and responsibilities. Remote Cros typically oversee multiple clinical trials remotely, focusing on data and protocol management, while Remote Clinical Research Coordinators handle trial coordination, patient interactions, and site activities. Both roles require knowledge of clinical research processes, but the Remote Cro often requires more advanced credentials and experience.

What are the most commonly searched types of Cro jobs in Utah?

The most popular types of Cro jobs in Utah are:

What cities in Utah are hiring for Remote Cro jobs?

Cities in Utah with the most Remote Cro job openings:

Pharmacovigilance Expert

micro1 AI

Saint George, UT • Remote

$70 - $80/hr

Part-time

Posted 14 days ago


Job description

Role Title: Pharmacovigilance Expert


Role Type: Contractor


Location: Remote


micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters. This opportunity is ideal for professionals experienced in authoring and reviewing complex safety reports, passionate about data quality, and committed to clear written and verbal communication.


Scope of Work

  1. Author and review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level records.
  2. Apply expert judgment to assess the accuracy and adequacy of interval safety findings, signal evaluations, and benefit-risk conclusions in alignment with best practices.
  3. Assess template and structural conformity to ICH E2F and ICH E2C requirements, including proper section content, presentation of cumulative versus interval data, and completeness of appendices.
  4. Reconcile figures and case counts across report sections and data sources, identifying and documenting discrepancies significant for regulatory review.
  5. Evaluate safety conclusions in light of new data or events, and provide clear, structured written rationales supporting your determinations.
  6. Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis.


Preferred Qualifications

  1. 5+ years of pharmacovigilance or drug safety experience at a sponsor, CRO, or as an independent consultant.
  2. Demonstrated proficiency in authoring or reviewing DSURs and/or PSURs/PBRERs from start to finish.
  3. Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and benefit-risk assessment methodology.
  4. Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness determination, and aggregate safety data analysis.
  5. Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level information.
  6. Advanced degree in life sciences, pharmacy, nursing, or medicine (PharmD, MD, MSc, or equivalent).
  7. Experience in both development-stage and post-marketing safety reporting, QPPV or deputy QPPV roles, safety committee participation, or AI-assisted safety review tools is a plus.