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Codify Therapeutics Jobs (NOW HIRING)

Arrowhead Pharmaceuticals

Project Manager

Los Angeles, CA

$110K - $135K/yr

Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is ... Codify tools, templates, and processes used in existing projects into a toolkit for future projects ...

Arrowhead Pharmaceuticals

Project Manager

Pasadena, CA · On-site

$110K - $135K/yr

Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is ... Codify tools, templates, and processes used in existing projects into a toolkit for future projects ...

IQVIA

Consultant

Parsippany, NJ

$71K - $239K/yr

... range of market, therapeutic, prescriber, patient, payer, and competitive related questions ... You will participate in learning communities to codify your data analytics subject-matter expertise ...

IQVIA

Consultant

Wayne, PA

$71K - $239K/yr

... range of market, therapeutic, prescriber, patient, payer, and competitive related questions ... You will participate in learning communities to codify your data analytics subject-matter expertise ...

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Codify Therapeutics information

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How much do codify therapeutics jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for codify therapeutics in the United States is $71.48, according to ZipRecruiter salary data. Most workers in this role earn between $58.41 and $73.08 per hour, depending on experience, location, and employer.

What is the difference between Codify Therapeutics vs Clinical Research Associate?

AspectCodify TherapeuticsClinical Research Associate
Required CredentialsTypically requires a background in life sciences, biology, or pharmacy; degrees such as BS or MS often preferredRequires a degree in life sciences, nursing, or related fields; certifications like CCRA can be advantageous
Work EnvironmentResearch labs, biotech companies, or pharmaceutical firms focused on drug developmentClinical trial sites, hospitals, or research organizations overseeing patient studies
Employer & Industry UsageBiotech and pharmaceutical companies involved in innovative drug researchContract research organizations, pharmaceutical companies, and clinical trial sites

While Codify Therapeutics focuses on drug discovery and development within biotech settings, Clinical Research Associates primarily manage and monitor clinical trials at research sites. Both roles require a background in life sciences but differ in daily responsibilities and work environments.

What are the key skills and qualifications needed to thrive as a Therapeutic Coder, and why are they important?

To thrive as a Therapeutic Coder, you need a strong understanding of medical terminology, anatomy, and coding systems such as ICD-10 and CPT, usually supported by a relevant certification like CPC or CCS. Familiarity with electronic health records (EHR) systems and coding software is essential for efficient and accurate documentation. Attention to detail, analytical thinking, and effective communication are valuable soft skills that help ensure coding accuracy and collaboration with healthcare teams. These skills are crucial for maintaining compliance, optimizing reimbursement, and supporting patient care quality within healthcare organizations.

What typical collaborations can a professional at Codify Therapeutics expect, and how do these impact daily workflows?

At Codify Therapeutics, professionals often work closely with multidisciplinary teams, including researchers, data scientists, clinicians, and regulatory experts. Collaboration is essential for integrating scientific discoveries with data-driven solutions to accelerate drug development. Daily workflows involve regular cross-functional meetings, project updates, and shared problem-solving, which foster innovation and ensure alignment with project goals. This collaborative environment helps employees build a broad skill set and deepen industry knowledge by working alongside experts from various fields.

What is Codify Therapeutics?

Codify Therapeutics is a biotechnology company focused on developing gene therapy solutions for rare and complex diseases. They use advanced gene editing and delivery technologies to create innovative treatments that address unmet medical needs. The company's research often involves collaborations with academic institutions and pharmaceutical partners to accelerate the development of new therapies. Their mission is to improve patient outcomes by translating cutting-edge science into effective medicines.
What cities are hiring for Codify Therapeutics jobs? Cities with the most Codify Therapeutics job openings:
What states have the most Codify Therapeutics jobs? States with the most job openings for Codify Therapeutics jobs include:
What job categories do people searching Codify Therapeutics jobs look for? The top searched job categories for Codify Therapeutics jobs are:
Codify Therapeutics jobs near you
Infographic showing various Codify Therapeutics job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $148,684 per year, or $71.5 per hour.
Project Manager

Project Manager

Arrowhead Pharmaceuticals

Los Angeles, CA

$110K - $135K/yr

Full-time

Posted 9 days ago

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.

Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.

The Position

The Project Manager is an integral part of several Product Teams developing novel RNAi therapeutics for diseases with high unmet need. The Project Manager will work under the Director, Program Management to define and monitor timelines and deliverables. The successful Project Manager will have excellent knowledge in Smartsheet and other program planning and visualization software, good communication skills and enthusiasm for defining and monitoring program plans and milestones at Arrowhead Pharmaceuticals.

This role is based in Pasadena, California, with an expectation to be in office 5 days a week.

Responsibilities

  • Drive cross-functional collaboration to develop and manage integrated late-phase program plans and timelines
  • Facilitate and document meetings, capturing and tracking key decisions, action items, and follow-ups
  • Prepare and deliver presentations, reports, and events to align and engage stakeholders
  • Develop scenario planning models and visualizations to support strategic and operational decisions
  • Coordinate across Product and Work Package Teams with diverse technical and functional backgrounds
  • Standardize and communicate program timelines across teams and the broader portfolio
  • Manage resources and budgets using Smartsheet or equivalent planning and visualization tools
  • Monitor progress, track deliverables, and proactively identify and escalate risks to Program Leadership
  • Maintain dashboards, portfolio updates, and enterprise-level progress reports
  • Support special projects as needed including workshop facilitation to vendor assessments
  • Collaborate within a matrixed organization to integrate program timelines, resolve bottlenecks, and ensure cross-program alignment
  • Codify tools, templates, and processes used in existing projects into a toolkit for future projects as company matures

Requirements

  • Bachelor's degree in a business-related or life sciences field
  • Strong understanding of the life sciences industry
  • 5 years of project planning or coordination experience in high coordination sectors and roles
  • Strong foundation in program and project management principles
  • Proven ability to understand complex interdependencies and maintain attention to detail
  • Demonstrated experience leading or coordinating cross-functional teams
  • Excellent communication, influencing, stakeholder management, and decision-making skills
  • Highly motivated team player with a proactive, collaborative approach
  • Thrives in a dynamic, growing biotech or early commercial-stage environment

Preferred

  • International market entry experience and exposure (e.g., EU, AP)
  • MBA and/or previous consulting, project planning, or coordination experience experience related to biotech, pharmaceuticals, or medical devices sectors
  • Commercial function experience with exposure to other biopharma functions
California pay range
$110,000—$135,000 USD

Arrowhead provides competitive salaries and an excellent benefit package.

Candidates must have current, valid authorization to work in the country where this role is located.

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