AstraZeneca Posted August 4, 2026

Field Clinical Advisor - Cell Therapy - Chicago (IL/WI/IN/MN)

Wilmington, Delaware, United States of America Full time
Clinical Development Associate

AstraZeneca is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Cell Therapy Field Clinical Advisors (FCAs) are part of the Global Cell Therapy Clinical Operations team. They play a critical role in the successful execution of cell therapy clinical trials, driving recruitment, retention, and safety management. Additionally, they allow early insight generation. FCAs focus on clinical study protocol expertise and education, optimizing the patient journey, and cell therapy pipeline engagement. We are looking for close collaboration with other CTCO Functions, Clinical Development, and Medical Affairs across multiple indications and departments to promote AstraZeneca's diverse cell therapy portfolio.

Summary

Cell Therapy Field Clinical Advisors (FCAs) are part of the Global Cell Therapy Clinical Operations team. They play a critical role in the successful execution of cell therapy clinical trials, driving recruitment, retention, and safety management. Additionally, they allow early insight generation. FCAs focus on clinical study protocol expertise and education, optimizing the patient journey, and cell therapy pipeline engagement. We are looking for close collaboration with other CTCO Functions, Clinical Development, and Medical Affairs across multiple indications and departments to promote AstraZeneca's diverse cell therapy portfolio

You Will:

Pipeline mastery at scale: Build knowledge of AstraZeneca's cell therapy pipeline across multiple indications and assets. Convey AstraZeneca's cell therapy strategy, portfolio scope, and product differentiation; ensure compliant messaging across regions.

Systematically assess educational needs across owned sites, deliver advanced protocol training, and escalate patterns to Global Clinical Development with recommendations for enterprise solutions.

Capture applicable field insights (feasibility, operational bottlenecks, patient pathways) and deliver them to global and local partners to lead early risk identification and inform protocol/process adjustments.

Implement targeted protocol education (e.g., inclusion/exclusion criteria application) to lift enrollment rates, reduce screen failures, and minimize attrition.

Be the primary field point for protocol and clinical issues, evaluate and escalate, lead root-cause analysis, and implement corrective/preventive actions to reduce deviations and data queries.

Insight loop and continuous improvement: Systematically capture site-level insights, summarize trends for study teams and partners, and influence protocol/process adjustments and scaling.

Coordinate delivery across CTCO departments, Clinical Development, Medical Affairs, Supply/Logistics, Patient Operations, and Country Ops to ensure rapid, reliable service to partners and study sites.

Maintain current knowledge of local regulations, guidelines, codes of practice, and AstraZeneca policies; translate requirements into practical site actions and support inspection readiness.

Operate within AZ policies/SOPs and local regulations.

Directly improve the speed, quality, and consistency of AstraZeneca's cell therapy trials, reducing cycle times, elevating protocol adherence, and accelerating patient access to innovative treatments.

You Have:

Bachelor's degree in a health-related field required; advanced degree (PharmD, PhD, MSc, NP/PA, MD/RN) is preferred.

A minimum of 5 plus years in clinical research or field-facing roles within oncology/hematology or advanced therapies; direct cell therapy experience.

Concentrated understanding of GCP, clinical trial operations, and cell therapy patient journey

Collaboration and Communication: Excellent partner management ability to translate complex protocols into practical site actions.

Ability to travel at least 50-80% regionally/nationally and internationally to support sites and program needs.

Patient- and site-centric mindset.

Data-informed approach to identify trends, risks, and opportunities for operational improvement.

The annual base pay (or hourly rate of compensation) for this position ranges from  $203,709 to $305,564 USD. Our positions offer eligibility for various incentives, an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing  AZCHumanResources@astrazeneca.com .

AstraZeneca offers an environment where you can be empowered to make bold decisions and move at pace. With a focus on Oncology, we are driven by speed and backed by leadership that empowers every level to prioritize smart risks based on scientific evidence. Our scale, agility, and passion ensure fast delivery every time. Join us in pioneering new frontiers in cancer research, where courage, curiosity, and collaboration drive patient outcomes. Be part of a team committed to improving the lives of millions with cancer.

Ready to take on this exciting challenge? Apply now to join our dynamic team.

#LI-Remote

Date Posted

04-Aug-2026

Closing Date

30-Aug-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

Job details

Seniority
Associate
Function
Clinical Development
Therapeutic area
Not listed
Location
Wilmington, Delaware, United States of America
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 194 comparable Associate Clinical Development roles across 37 biopharma companies.

194Comparable roles tracked
180Currently active
37Companies hiring similar roles
29Countries represented

Salary context

47 of 194 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Clinical Trials Data Associate (P1) · Lilly $79,206/yr – $91,087/yr
Highest disclosed · Statistical Advisor · Gilead Sciences, Inc. $226,185/yr – $292,710/yr
Peer group range $85,146 – $259,448 (median $168,090)

Where these roles are based

Top locations among the 194 comparable roles

United States68
India42
United Kingdom12
China11
Poland8
Germany6

+ 23 more countries

Seniority mix

194 of 194 peers have a known seniority level

Manager146
Associate47
Intern/Fellow/Postdoc1

Therapeutic area mix

16 of 194 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology9
Cardiovascular / CVRM4
Immunology2
Neuroscience1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same seniority Same country
60%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Associate
Same function Same seniority Same country
60%similar
AbbVie Boston, MA Associate
Same function Same seniority Same country
60%similar
AbbVie Irvine, CA Associate
Same function Same seniority Same country
60%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same seniority Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
GRA Regulatory Delivery Excellence, Clinical Regulatory Associate
Lilly · Indianapolis, Indiana, United States of America · Associate
Function Therapeutic area Seniority Country
60%
Clinical Research Associate II
AbbVie · Boston, MA · Associate
Function Therapeutic area Seniority Country
60%
Statistical Advisor
Gilead Sciences, Inc. · Foster City, United States · Associate
Function Therapeutic area Seniority Country
60%
Clinical Research Associate (CRA) - Oncology (Remote)
Merck · Rahway, New Jersey, United States of America · Associate
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.