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Clinical Research Proposal Development Jobs in Utah

Isotalent

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Medical Director - Phase 1 Clinical Research

Salt Lake City, UT · On-site

$275 - $400/hr

Contributing medical/scientific insight to business development and proposal review * Helping ... Our client is a clinical research organization dedicated to advancing medical knowledge through ...

Jones & DeMille Engineering

Proposal Writer

UT · On-site

$28 - $35/hr

... development, organization, and production. * Review requests for proposals (RFPs) to identify and interpret requirements and help pursue qualifying projects. * Research and gather the materials and ...

University of Utah

PS Clinical Research Coord

Salt Lake City, UT · On-site

$23.50 - $31.25/hr

Assists the Principal Investigator in the development of study protocols. The incumbent decides how ... Knowledge of Good Clinical Practices, FDA, HIPAA and IRB regulations; an understanding of research ...

IQVIA

Clinical Research Associate

Salt Lake City, UT · On-site

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... We create intelligent connections to accelerate the development and commercialization of innovative ...

New

Layton

Proposal Coordinator

Sandy, UT · On-site

Contributes to content development for proposals and other collateral pieces under the direction/supervision of others. * Supports action planning and progress tracking. * Conducts research to ...

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Clinical Research Proposal Development information

What is clinical research proposal development?

Clinical research proposal development is the process of creating detailed plans for scientific studies involving human participants. This involves defining research objectives, designing study protocols, preparing budgets, and ensuring compliance with ethical and regulatory standards. The proposal often serves as a roadmap for the research team and is submitted to funding agencies or ethical review boards for approval. Properly developed proposals increase the likelihood of funding and successful project implementation.

What are the key skills and qualifications needed to thrive in clinical research proposal development, and why are they important?

To thrive in Clinical Research Proposal Development, you need a strong background in clinical research methodologies, scientific writing, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with grant management systems, budgeting software, and knowledge of IRB processes and funding agency guidelines is typically required. Excellent attention to detail, project management abilities, and strong interpersonal communication make someone stand out in this role. These skills are crucial to ensure proposals are scientifically sound, compliant, and competitive for funding in a highly regulated and collaborative research environment.

What are common challenges faced in clinical research proposal development, and how can I prepare to address them?

A frequent challenge in clinical research proposal development is aligning the research objectives with regulatory requirements and funding agency expectations while ensuring feasibility within timelines and available resources. Effective communication and collaboration with investigators, statisticians, and compliance officers are crucial for addressing these challenges. To prepare, familiarize yourself with funding guidelines, regulatory standards, and project management best practices, and be proactive in seeking feedback from cross-functional teams throughout the proposal drafting process.

What is the difference between Clinical Research Proposal Development vs Clinical Research Coordinator?

AspectClinical Research Proposal DevelopmentClinical Research Coordinator
Primary RoleDevelops and writes research proposals to secure funding and approvalManages and oversees the daily conduct of clinical trials at sites
Required SkillsScientific writing, regulatory knowledge, project planningPatient interaction, study coordination, data collection
Work EnvironmentResearch institutions, pharmaceutical companies, academic settingsClinical sites, hospitals, research centers
CertificationsOften requires knowledge of GCP, regulatory guidelinesOften requires GCP certification, clinical trial training

While Clinical Research Proposal Development focuses on creating detailed research proposals to obtain funding and approval, Clinical Research Coordinators handle the day-to-day management of clinical trials at research sites. Both roles require understanding of GCP and regulatory standards but differ in their primary responsibilities and work environments.

What are popular job titles related to Clinical Research Proposal Development jobs in Utah?

For Clinical Research Proposal Development jobs in Utah, the most frequently searched job titles are:

What job categories do people searching Clinical Research Proposal Development jobs in Utah look for?

The top searched job categories for Clinical Research Proposal Development jobs in Utah are:

What cities in Utah are hiring for Clinical Research Proposal Development jobs?

Cities in Utah with the most Clinical Research Proposal Development job openings:

Clinical Research Proposal Development jobs near you

Medical Director - Phase 1 Clinical Research

Isotalent

Salt Lake City, UT • On-site

$275 - $400/hr

Part-time

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

Job description

Medical Director – Phase 1 Clinical Research

Location: Salt Lake City, Utah | Hybrid, 2–3 days/week

Our client, a respected clinical research organization, is seeking a Medical Director to lead their new Phase 1 program.


Do you have first-in-human clinical trial expertise and a strong reputation across the pharma, biotech, and CRO world? Are you excited by the idea of building a Phase 1 program from the ground up while backed by a well-established research organization? Are you looking for a role where your medical judgment and industry relationships directly shape a growing business? If so, keep reading, this could be exactly the opportunity you've been looking for.


The Comp!

  • Compensation: $275.00 - $400.00/hourly, based on experience
  • + annual bonuses structure
  • Opportunity to become full time in the future


A Day in the Life of the Medical Director
In this role, you'll provide medical and scientific leadership across our client's Phase 1 clinical trials, including first-in-human, dose-escalation, and other early-phase studies. You'll be the go-to physician for participant safety, protocol interpretation, and clinical decision-making, while also representing the organization in front of sponsors, CROs, and industry partners. This is a chance to help lay the medical and scientific foundation for a growing early-phase research program built on a long track record of successful clinical research.


Responsibilities include:

  • Providing medical oversight for Phase 1 and early-phase trials, including first-in-human, single/multiple ascending dose, bioavailability, bioequivalence, and drug-drug interaction studies
  • Serving as the primary medical resource for participant safety, adverse events, and protocol interpretation
  • Reviewing protocols, investigator brochures, informed consent forms, and safety data
  • Evaluating study feasibility and advising on dosing, safety monitoring, and participant populations
  • Participating in safety reviews, dose-escalation decisions, and safety monitoring committees
  • Serving as Principal Investigator for select Phase 1 studies as needed
  • Ensuring trials are conducted per GCP, applicable regulations, and organizational policy
  • Providing clinical guidance to sub-investigators, nurses, coordinators, and research staff
  • Representing the organization in sponsor/CRO meetings, site-selection visits, bid defenses, and audits
  • Building and maintaining relationships with pharma, biotech, CRO, and industry partners
  • Contributing medical/scientific insight to business development and proposal review
  • Helping develop medical policies, SOPs, safety plans, and physician coverage models
  • Advising on staffing, equipment, lab/pharmacy support, and future therapeutic-area expansion
  • Supporting inspection readiness and responding to regulatory/IRB questions on medical oversight


Requirements and Qualifications:

  • MD or DO from an accredited institution
  • Active, unrestricted Utah medical license (or ability to obtain one)
  • Direct first-in-human/early-phase trial experience
  • Experience as PI, Medical Director, medical monitor, sub-investigator, or similar
  • Sponsor/CRO-facing presence and established industry connections
  • FDA/ICH-GCP knowledge, participant safety, AE management, investigator
  • Strong presentation, communication, and relationship-building skills


About the Hiring Company:
Our client is a clinical research organization dedicated to advancing medical knowledge through well-run, participant-focused clinical trials. They value clinical excellence, integrity, and collaboration among their research staff.


Come Join Our Clinical Research Team!
Start by filling out this 3-minute, mobile-friendly application here. We look forward to hearing from you!