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Remote Biomarker Operations information

What is remote biomarker operations?

Remote Biomarker Operations involve managing the collection, processing, and analysis of biological markers (biomarkers) from clinical trial participants or patients without requiring them to visit a central location. This work typically leverages digital tools, telemedicine, and at-home sample collection kits to enable decentralized clinical studies. The approach increases patient accessibility and convenience, while still ensuring data quality and regulatory compliance. Professionals in this field coordinate logistics, oversee data management, and collaborate with laboratories to support research and drug development.

What is the difference between Remote Biomarker Operations vs Remote Clinical Data Coordinator?

AspectRemote Biomarker OperationsRemote Clinical Data Coordinator
Required CredentialsBiomarker-related certifications, scientific backgroundClinical data management certifications, healthcare background
Work EnvironmentLaboratory, research settings, or remote data reviewRemote data entry, monitoring, and coordination
Employer & Industry UsagePharmaceutical, biotech, research institutionsClinical research organizations, hospitals, CROs
Search & Comparison IntentFocus on biomarker-specific roles in researchFocus on clinical data management roles

Remote Biomarker Operations involves managing biomarker sample processing and analysis, often requiring scientific expertise. In contrast, Remote Clinical Data Coordinator focuses on managing clinical trial data entry and quality assurance. Both roles are essential in clinical research but differ in their focus and required skills.

How does a remote biomarker operations specialist typically collaborate with clinical research teams?

As a Remote Biomarker Operations specialist, you will work closely with clinical research associates, project managers, laboratory teams, and data managers to ensure smooth collection, handling, and analysis of biomarker samples across multiple study sites. Most collaboration is done virtually, using project management tools, video meetings, and shared documentation platforms, which requires strong communication and organizational skills. You'll often coordinate logistics for sample shipments, troubleshoot data discrepancies, and contribute to protocol development, making teamwork and adaptability essential for success in this role.

What are the key skills and qualifications needed to thrive as a remote biomarker operations professional?

To excel in Remote Biomarker Operations, you need a strong background in life sciences, clinical research, and biomarker assay development, often supported by a relevant degree or equivalent experience. Familiarity with laboratory information management systems (LIMS), data analysis tools, and regulatory compliance (such as GCP or GLP) is typically required. Excellent organizational skills, attention to detail, and effective communication are essential soft skills for coordinating across remote teams and managing complex workflows. These competencies ensure accurate data collection, regulatory adherence, and seamless collaboration in decentralized clinical research environments.
What are popular job titles related to Remote Biomarker Operations jobs in Utah? For Remote Biomarker Operations jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Remote Biomarker Operations jobs in Utah look for? The top searched job categories for Remote Biomarker Operations jobs in Utah are:
Remote Biomarker Operations jobs near you

Director, Clinical Pharmacology

Recursion

Salt Lake City, UT • Remote

$212K - $297K/yr

Other

This job post has expired today. Applications are no longer accepted.

Job description

The Impact You'll Make

You will join an innovative and passionate clinical development team dedicated to improving the lives of patients suffering from devastating diseases.  You will lead the innovative clinical pharmacology and pharmacometrics strategy and execution for a portfolio of rare disease and oncology clinical programs.

In this role, you will:

  • Develop the clinical pharmacology and pharmacometric strategies to accelerate and support the overall product development plan. You'll be the Clinical Pharmacology lead for various programs in clinical development, the representative for regulatory interactions, and propose innovative strategies to get therapies to patients faster.
  • Design clinical studies. You'll provide (clinical) pharmacology input on all clinical study designs, from Phase 1-3 and dedicated Phase 1 clinical pharmacology studies.
  • Author review relevant clinical pharmacology sections for regulatory documents, including Investigator's Brochures (IB), INDs, NDAs, and other regulatory submissions. Act as the clinical pharmacology expert during interactions with health authorities.
  • Interface with cross-functional teams. You'll work closely with clinical study teams, translational teams (DMPK, Translational Modeling and Toxicology), preclinical teams and due diligence teams to ensure clinical pharmacology-related considerations are addressed.
  • Solve drug development questions/problems by overseeing and/or performing modeling and simulation with various tools to expedite decision making.

The Team You'll Join 

You will join the Development Sciences team within Recursion comprising clinical pharmacology, pharmacometrics, translational modeling and clinical biomarkers. The Development Sciences group sits within Recursion's Clinical Development organization. Team members get to sit on both Discovery and Development projects and work in a seamless end-to-end environment at Recursion. The team collaborates closely with clinical development functions (clinical science, clinical operations, regulatory affairs, biostatistics, etc.), as well as discovery functions (DMPK, Biology, Chemistry and Translational Biomarkers). 

The Experience You'll Need

  • Ph.D. in Pharmaceutical Sciences, Pharmacokinetics or related discipline, M.D with a Clinical Pharmacology expertise, or a Pharm D. with a Clinical Pharmacology fellowship, with 5-9+ years of experience in biotech/pharmaceutical drug development.
  • Demonstrated success leading all clinical pharmacology related aspects of drug development. 
  • Ability to work closely with internal and external stakeholders to manage PK, PK-PD, and PK-safety analyses, including non-compartmental analysis, population PK modeling, and PK-PD modeling and simulations to support dose selection, exposure-response and exposure-safety analyses through various phases of drug development.
  • Proficiency with WinNonlin, Monolix, NONMEM, R or other modeling software.
  • Effective skills directed toward driving collaboration, achieving results, influencing, and resolving conflicts across internal and external stakeholders
  • Demonstrated experience responding to regulatory agency questions, preparing clinical pharmacology aspects of regulatory submissions and attending regulatory meetings.
  • Highly motivated, decisive, and results-oriented individual who is proactive, resourceful, and efficient with the flexibility and creativity to excel in and contribute to a rapidly growing drug discovery and development company

Experience in oncology is preferred, but not an absolute requirement. 

Working Location & Compensation:

Making SLC or NYC your home base is ideal; however, we will consider remote work for this position. We ask that remote employees commit to regular on-site visits for routine work and departmental events. 

At Recursion, we believe that every employee should be compensated fairly. Based on the skill and level of experience required for this role, the estimated current annual base range for this role is $212,900 to $297,000. You will also be eligible for an annual bonus and equity compensation, as well as a comprehensive benefits package. 

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