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Remote Associate Director Pharmaceutical Jobs (NOW HIRING)

Oscar Health

Associate Director, Tax

Boston, MA · Remote

$162K - $213K/yr

We're hiring an Associate Director, Tax to join our Finance. Oscar is the first health insurance ... This is a remote position, open to candidates who reside in: Boston, MA. You will be fully remote ...

Oscar Health

Associate Director, Tax

Dallas, TX · Remote

$162K - $213K/yr

We're hiring an Associate Director, Tax to join our Finance. Oscar is the first health insurance ... This is a remote position, open to candidates who reside in: Dallas, TX. You will be fully remote ...

Oscar Health

Associate Director, Tax

Atlanta, GA · Remote

$162K - $213K/yr

We're hiring an Associate Director, Tax to join our Finance. Oscar is the first health insurance ... This is a remote position, open to candidates who reside in: Atlanta, GA. You will be fully remote ...

Oscar Health

Associate Director, Tax

Hartford, CT · Remote

$180K - $236K/yr

We're hiring an Associate Director, Tax to join our Finance. Oscar is the first health insurance ... This is a remote position, open to candidates who reside in: Hartford, CT. You will be fully remote ...

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How much do remote associate director pharmaceutical jobs pay per year?

As of Jun 10, 2026, the average yearly pay for remote associate director pharmaceutical in the United States is $164,797.00, according to ZipRecruiter salary data. Most workers in this role earn between $121,500.00 and $200,000.00 per year, depending on experience, location, and employer.

What does a Remote Associate Director in the pharmaceutical industry do?

A Remote Associate Director in the pharmaceutical industry oversees critical projects and teams from a remote location, focusing on areas such as clinical operations, regulatory affairs, or drug development. They are responsible for ensuring projects meet regulatory standards, timelines, and budget while collaborating with internal and external stakeholders. This role also involves strategic planning, people management, and ensuring the successful execution of company goals, all performed remotely using digital communication tools.

How do Remote Associate Directors in the pharmaceutical industry effectively collaborate with cross-functional teams while working off-site?

Remote Associate Directors in the pharmaceutical sector often collaborate with teams across clinical development, regulatory affairs, marketing, and medical affairs. They leverage digital communication platforms such as video conferencing, project management tools, and shared document repositories to maintain consistent communication and alignment. Regular virtual meetings and clear documentation are critical to ensure everyone is updated on project milestones and regulatory requirements. Building strong relationships and establishing clear workflows help overcome the challenges of remote collaboration, making teamwork efficient and projects successful.

What are the key skills and qualifications needed to thrive as a Remote Associate Director in Pharmaceuticals, and why are they important?

To thrive as a Remote Associate Director in Pharmaceuticals, you need deep expertise in pharmaceutical sciences, regulatory affairs, and project management, often backed by an advanced degree and significant industry experience. Familiarity with drug development software, clinical trial management systems, and regulatory submission platforms is typically required. Outstanding leadership, strategic thinking, and cross-functional communication are crucial soft skills for managing remote teams and complex projects. These abilities ensure effective oversight of drug development processes, regulatory compliance, and successful collaboration across geographically dispersed teams.
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Remote Associate Director Pharmaceutical jobs near you
Infographic showing various Remote Associate Director Pharmaceutical job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 89% Full Time, 7% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $164,797 per year, or $79.2 per hour.

Associate Director, CMC Technical Services

Ionis

Boston, MA • On-site, Remote

Full-time

Posted 22 days ago

Job description

Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We're pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.
At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know that our success is a direct result of the exceptional talents and dedication of our employees.
With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money and energy into making our onsite, hybrid and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive.
We're building on our rich history, and we believe our greatest achievements are ahead of us. If you're passionate about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career!
ASSOCIATE DIRECTOR, CMC TECHNICAL SERVICES
SUMMARY:
The candidate for Associate Director, CMC Technical Services will be responsible for managing drug product and packaging supply for Ionis commercial products. This individual will support domestic and global launches and be held accountable for managing relationships and project-related issues with the syringe and vial filling, assembly, and/or packaging suppliers. In addition, the CMC Technical Services SME will be contributing to the development of the long-term commercial supply strategy, including optimization of the existing external vendor portfolio to include manufacture, import/export, testing and release. The role includes review of vendor GMP documents (including but not limited to MBRs, specifications, change controls, validation plans).
RESPONSIBILITIES:
  • Present as "Person-in-Plant" as needed during commercial drug product manufacturing runs
  • Lead the CMO relationships for manufacture of commercial drug product, assembly, and/ or packaging
  • Work closely with the quality team to ensure timely release of commercial drug product
  • Provide CMC support, as needed, for regulatory filings including new marketing authorization applications and questions from health authorities
  • Coordinate vendor submission aspects of annual product updates to regulatory filings
  • Work with Supply Chain and QA to measure CMO performance through implementation and trending of key performance indicators (KPIs). Generate improvement plans as needed
  • Contribute to the review, with Quality, of manufacturing documents, including MBRs, specifications, change controls, and deviations. Ensure that client approval of all CMO documents is provided in a timely and efficient manner
  • Provide CMC input and support for commercially relevant topics to development program teams
  • Determine path forward for optimization of drug supply, including manufacturing, QC testing and QA release strategy for all commercial markets
  • Work with Ionis team to evaluate vendor capabilities of new CMOs or test laboratories
  • Other responsibilities include information contributions to drug product stability programs; tech transfer activities; drug product manufacturing process validation; drug product test method validation; combination product design transfer, resolution of CMC aspects of nonconformance, out-of-specification, and out-of-trend investigations, and development of relevant SOPs

REQUIREMENTS:
  • BS / BA in biology or pharmaceutical sciences, engineering, manufacturing, or science related field plus at least 5 years of relevant cGMP drug product manufacturing experience with at least 12 years of pharmaceutical industry experience overall
    • Preferably M.S. plus at least 5 years of relevant cGMP drug product manufacturing experience with at least 8 years of pharmaceutical industry experience overall
    • Preferably Ph.D. plus at least 5 years of relevant cGMP drug product manufacturing experience with at least 5 years of pharmaceutical industry experience overall
  • Working knowledge of cross-functional drug development processes, FDA/ICH/EMA/ISO guidelines and cGMPs
  • Knowledge of cGMP, contracts, supply agreements, and quality systems as it relates to Contract Manufacturing Organizations
  • Full understanding of complex technical issues in drug product fill/finish manufacturing and packaging.
  • Prior experience with oligonucleotide manufacturing is a plus
  • Prior experience with SAP or other ERP systems are a plus
  • Experience in orphan/rare disease commercialization is a plus
  • Hands on experience with commercial drug product fill / finish manufacturing
  • Hands on experience with commercial drug product global packaging and assembly requirements
  • Understanding of Release testing and experience with drug product stability requirements
  • Experience in interactively working with CMO's and CMO relationship building
  • Strong communication and presentation skills and business partnering ability
  • Strategic, analytical and results-driven thinker with the ability to plan and direct
  • Resourceful and creative problem solver
  • Self-motivated, flexible and creative leader, able to prioritize, multi-task, and work in a fast-paced and demanding environment
  • Problem solving ability related to cGMP manufacturing, technical and regulatory
  • Strong interpersonal skills and ability to work with internal and external stakeholders in a positive, collaborative manner
  • Ability to travel (~15-25%) in the US and internationally

Please visit our website, http://www.ionis.com for more information about Ionis and to apply for this position; reference requisition # IONIS003928
Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits
Full Benefits Link: https://ionis.com/careers#:~:text=Highly%20competitive%20benefits
The pay scale for this position is $178,892 to $224,162
NO PHONE CALLS PLEASE. PRINCIPALS ONLY.
Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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