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Feasibility Associate Jobs (NOW HIRING)

As a Study Feasibility Associate Director, you will be part of AbbVie's Clinical Development Operations (CDO) function, which is responsible for running clinical trial operations around the world. In ...

New

As a Study Feasibility Associate Director, you will be part of AbbVie's Clinical Development Operations (CDO) function, which is responsible for running clinical trial operations around the world. In ...

New

As a Study Feasibility Associate Director, you will be part of AbbVie's Clinical Development Operations (CDO) function, which is responsible for running clinical trial operations around the world. In ...

New

As a Study Feasibility Associate Director, you will be part of AbbVie's Clinical Development Operations (CDO) function, which is responsible for running clinical trial operations around the world. In ...

New

As a Study Feasibility Associate Director, you will be part of AbbVie's Clinical Development Operations (CDO) function, which is responsible for running clinical trial operations around the world. In ...

New

As a Study Feasibility Associate Director, you will be part of AbbVie's Clinical Development Operations (CDO) function, which is responsible for running clinical trial operations around the world. In ...

New

Collecting data from data assets as well as country associates, site level Investigators, and KOL interviews when required. * Determining site profile. * Developing appropriate feasibility strategies ...

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Feasibility Associate information

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$10

$19

$33

How much do feasibility associate jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for feasibility associate in the United States is $19.87, according to ZipRecruiter salary data. Most workers in this role earn between $14.90 and $20.67 per hour, depending on experience, location, and employer.

What is the difference between Feasibility Associate vs Project Coordinator?

AspectFeasibility AssociateProject Coordinator
Required CredentialsBachelor's degree in related field, analytical skillsBachelor's degree, organizational skills
Work EnvironmentResearch-focused, analytical tasksAdministrative, team coordination
Employer & Industry UsageConsulting, healthcare, engineeringConstruction, IT, corporate projects
Common Search & ComparisonYesNo

The Feasibility Associate primarily conducts research and analysis to assess project viability, focusing on data collection and evaluation. In contrast, the Project Coordinator manages project schedules, resources, and communication. While both roles require organizational skills and collaboration, the Feasibility Associate emphasizes analytical assessment, whereas the Project Coordinator handles project execution and logistics.

What cities are hiring for Feasibility Associate jobs?

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What are the most commonly searched types of Feasibility jobs?

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What states have the most Feasibility Associate jobs?

States with the most job openings for Feasibility Associate jobs include:

What are popular job titles related to Feasibility Associate jobs?

For Feasibility Associate jobs, the most frequently searched job titles are:

Infographic showing various Feasibility Associate job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 67% Full Time, 29% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $41,327 per year, or $19.9 per hour.

Associate Director, Study Feasibility

Irvine, CA

AbbVie
Scientific Research and Development Services • 10K+ employees

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New


AbbVie rating

8.7

Company rating: 8.7 out of 10

Based on 103 frontline employees who took The Breakroom Quiz


Job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

As a Study Feasibility Associate Director, you will be part of AbbVie’s Clinical Development Operations (CDO) function, which is responsible for running clinical trial operations around the world.
In this role you will partner with and advise study teams on design feasibility and certain aspects of design strategy, including country and site selection, protocol review and assessment of patient burden, and related implications for patient recruitment and study timelines. This is a highly collaborative and analytical role, which will rely on your expert facilitation skills, your ability to influence without authority, and your strong experience in clinical study design, operations, and management.

Responsibilities

  • Dynamic leader who designs, prepares, and facilitates cross-functional global strategy discussions that can include 20 or more senior level AbbVie leaders to assess operational feasibility and optimize/develop effective execution strategies.
  • Responsible to support strategic planning for delivery of global phase 2 and phase 3 clinical trials within Abbvie portfolio. Large Scale studies may be conducted in over 35 countries, supported by teams of 250 or more AbbVie study team members with study budgets exceeding 200 million dollars.
  • Responsible for matrix management to help drive analytical insights and study recruitment planning across multiple AbbVie functional teams.
  • Conducts detailed scientific, analytical, and operational analyses to prepare for and support study team engagements.
  • Provides scientific and strategic consultation on country strategy, site selection, protocol and patient burden, recruitment, and timelines.
  • Identifies and analyzes important connections within and across therapeutic areas to optimize study performance at the portfolio level.
  • Leads and manages projects to continuously improve Study Feasibility & Recruitment team capabilities and impacts.
Qualifications
  • Minimum of 8 years of pharmaceutical related experience with at least 5 years in clinical research/project leadership.
  • Bachelor’s or advanced Degree, preferably in pure, applied, or technical sciences
  • Drug development and/or scientific project leadership experience preferred
  • Therapeutic area background in Oncology, Neurology, or Immunology preferred    
  • Strong working knowledge of pharma drug development processes
  • Recognized contributor in complex scientific analyses and decision making 
  • Demonstrated leadership skills with broad scientific, strategic, and business orientations

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​
  • This job is eligible to participate in our long-term incentive programs. 

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.​

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html


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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013