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Impd Pay Jobs (NOW HIRING)

AstraZeneca

Associate Director, CMC Lead

Boston, MA · On-site

$136K - $204K/yr

IND/IMPD Readiness: Lead CMC regulatory strategy; guide and contribute to authoring high-quality ... The annual base pay (or hourly rate of compensation) for this position ranges from $136,514 USD to ...

AstraZeneca GmbH

Associate Director, CMC Lead

Boston, MA · On-site

$137 - $205/hr

IND/IMPD Readiness: Lead CMC regulatory strategy; guide and contribute to authoring high-quality ... The annual base pay (or hourly rate of compensation) for this position ranges from $136,514 USD to ...

AstraZeneca

Associate Director, CMC Lead

Boston, MA

$136K - $204K/yr

IND/IMPD Readiness: Lead CMC regulatory strategy; guide and contribute to authoring high-quality ... The annual base pay (or hourly rate of compensation) for this position ranges from $136,514 USD to ...

AstraZeneca

Associate Director, CMC Lead

Boston, MA · On-site

$136K - $204K/yr

IND/IMPD Readiness: Lead CMC regulatory strategy; guide and contribute to authoring high-quality ... The annual base pay (or hourly rate of compensation) for this position ranges from $136,514 USD to ...

GeneFab

Program Manager, CRDMO

Alameda, CA

$140K - $200K/yr

Experience supporting IP, IND, BLA, MAA, or IMPD submissions. * Demonstrated experience leading ... full pay scale for this role across multiple seniority levels; final compensation will be ...

GeneFab

Program Manager, CRDMO

Alameda, CA · On-site

$140K - $200K/yr

Experience supporting IP, IND, BLA, MAA, or IMPD submissions. * Demonstrated experience leading ... The posted salary range reflects the full pay scale for this role across multiple seniority levels ...

GeneFab

Program Manager, CRDMO

Alameda, CA · On-site

$140K - $200K/yr

Experience supporting IP, IND, BLA, MAA, or IMPD submissions. * Demonstrated experience leading ... full pay scale for this role across multiple seniority levels; final compensation will be ...

Dyne Therapeutics

Director, QA GMP Operations

Waltham, MA · On-site

$188K - $230K/yr

... IND/IMPD and BLA/MAAs. * QA support of Tech Transfer and Process Validation activities ... Embrace Dyne's core values and culture #LI-Onsite MA Pay Range $188,000-$230,000 USD The pay range ...

Merck Group

Senior Principal Medical Writer

Billerica, MA · On-site

$126K - $215K/yr

... IND/IMPD, bridging documents, briefing books, etc.). * Solid CTD/CTD-like knowledge; experience ... High attention to quality, accuracy, and compliance Pay Range for this position: $126,900 - 215,400 ...

Otsuka

Senior Manager, Biologics Downstream Development

$150K - $224K/yr

Author and contribute to downstream-related sections of regulatory filings (IND, IMPD, BLA, MAA ... Typically, actual pay will be positioned within the established range, rather than at its minimum ...

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How much do impd pay jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for impd pay in the United States is $20.54, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $22.84 per hour, depending on experience, location, and employer.

What is the difference between Impd Pay vs Payroll Specialist?

AspectImpd PayPayroll Specialist
CredentialsTypically requires knowledge of payroll systems, basic accounting, and relevant certificationsRequires payroll certifications, accounting knowledge, and sometimes HR training
Work EnvironmentOften in finance or HR departments, handling payroll processing and complianceSimilar environment, focusing on payroll processing, data entry, and employee records
Industry UsageUsed across various industries for payroll managementCommonly employed in HR and finance sectors for payroll tasks

Impd Pay and Payroll Specialist roles share similar credentials and work environments, focusing on payroll processing and compliance. While Impd Pay may emphasize specific payroll systems or platforms, both roles are integral to payroll management across industries.

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Impd Pay jobs near you
Infographic showing various Impd Pay job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 65% Full Time, 26% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $42,722 per year, or $20.5 per hour.

Associate Director, CMC Lead

AstraZeneca

Boston, MA • On-site

$136K - $204K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical

Job description

Job Title: Associate Director, CMC Lead
Introduction to role:
Are you ready to lead early-stage CMC strategy that turns precision radioconjugate science into first-in-human reality? As Associate Director, CMC Lead, you will steer development across a portfolio of alpha-emitting, tumor-targeted medicines, shaping IND-enabling plans and building the foundations for reliable, phase-appropriate clinical supply. Your decisions will determine how fast promising candidates move from discovery to patients.
You will join a team pushing the boundaries of oncology through novel radioconjugates and smart combinations, supported by state-of-the-art radiopharmaceutical manufacturing capabilities and an advancing clinical pipeline. How will you prioritize across multiple candidates, balance scientific rigor with speed, and de-risk the path to first-in-human studies? If you thrive in a dynamic, matrixed environment and enjoy solving complex CMC puzzles, this role puts you at the center of impact.
Accountabilities:
  • Phase 0 CMC Strategy: Define and deliver the pharmaceutical development strategy for the pre-IND/IND-enabling portfolio to drive timely progression to first-in-human readiness.
  • IND/IMPD Readiness: Lead CMC regulatory strategy; guide and contribute to authoring high-quality documentation and data packages for IND/IMPD submissions.
  • API/Drug Product/Analytical Integration: Coordinate API, drug product, and analytical development to establish robust, scalable, phase-appropriate processes and methods.
  • Clinical Supply Strategy: Build and execute supply strategies for Phase 0/Phase I, aligning isotope availability, shelf life, and study timelines to ensure on-time, fit-for-purpose clinical material.
  • Portfolio Leadership: Manage multiple early-stage programs; set priorities, balance resources, and adjust strategies as data emerge to protect the critical path.
  • Cross-Functional Influence: Represent CMC on project teams; shape overall program strategies and inform candidate selection through clear, data-driven risk/benefit assessments.
  • Target and Modality Assessment: Evaluate new molecular targets and modalities for CMC feasibility and developability to guide investment decisions.
  • Transition Enablement: Partner with Program Management, Clinical, Research, Regulatory, Quality, and Supply Chain to enable seamless movement of candidates from research into early development.

Essential Skills/Experience:
  • 7+ years of experience in pharmaceutical/biopharmaceutical product development and manufacturing;
  • Minimum education: Bachelor's degree. Advanced degree in Biochemistry, Pharmaceutical Chemistry, Pharmaceutics, Pharmaceutical Science, Chemical Engineering, or related scientific discipline preferred.
  • Demonstrated experience managing early-phase CMC development, including IND-enabling activities, process development, and analytical method development.
  • Strong project leadership skills with the ability to manage multiple concurrent programs at varying stages of maturity.
  • Demonstrated strong interpersonal and communication skills with the ability to collaborate effectively across functions and influence stakeholders at multiple levels of the organization.
  • Ability to develop and implement phase-appropriate pharmaceutical strategies across CMC areas (API, DP, Analytical) aligned with overall program objectives and timelines.
  • Experience working in a matrix environment and leading cross-functional sub-teams to deliver against defined milestones.
  • Strong problem-solving aptitude with the ability to navigate ambiguity and make sound technical and strategic judgments in a data-limited, early-stage environment.

Desirable Skills/Experience:
  • Experience with radiopharmaceuticals or radioconjugates, including awareness of radiochemistry constraints and alpha-emitting isotopes.
  • Prior authorship or leadership of CMC sections for IND/IMPD filings for biologics, conjugates, or complex modalities.
  • Familiarity with clinical supply strategies for short half-life or just-in-time manufactured products.
  • Hands-on application of Quality by Design, design of experiments, and risk management in early development.
  • Track record of successful tech transfer to GMP facilities and effective collaboration with external partners or CDMOs.
  • Understanding of analytical method lifecycle, including phase-appropriate validation and control strategy development.

The annual base pay (or hourly rate of compensation) for this position ranges from $136,514 USD to $204,771 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.
Why AstraZeneca:
Here you will follow the science with the resources to act on it, working alongside radiochemists, data scientists, clinicians, and CMC leaders who challenge assumptions and unlock new solutions together. We invest deeply in understanding disease biology and harness digital, data science, and AI to better predict clinical success, accelerating promising assets without compromising quality. Expect an environment that values kindness alongside ambition, where bold ideas are welcomed, thoughtful risks are supported, and your expertise directly shapes how innovative medicines reach patients sooner.
Call to Action:
If you are ready to lead pivotal CMC decisions that bring precision radioconjugates to first-in-human studies faster, step forward and shape what science makes possible.
#LI-Hybrid
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.

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