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Director Project Management Drug Development Jobs

About The Role The Director, Project Management role plays a pivotal role within Creative, shaping ... Professional Development - Exposure to senior leadership, learning and development programs, and ...

Director, Project Management

Chicago, IL ยท On-site

$105K - $125K/yr

Director, Project Management We are a global integrated communications agency seeking a Director of Project Management to partner with client teams, finance, and agency leadership to support ...

Responsibilities The Director, Project Management leads the end-to-end delivery of complex ... development of company-wide standards for scoping, designing, and putting new initiatives into ...

Responsibilities The Director, Project Management leads end-to-end delivery of strategic initiatives and complex transformation programs across W.R. Berkley Corporation. This role drives enterprise ...

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Director Project Management Drug Development information

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$62.5K

$142.1K

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How much do director project management drug development jobs pay per year?

As of Sep 11, 2026, the average yearly pay for director project management drug development in the United States is $142,075.00, according to ZipRecruiter salary data. Most workers in this role earn between $118,000.00 and $150,000.00 per year, depending on experience, location, and employer.

What does a director of project management in drug development do?

A Director of Project Management in Drug Development oversees the planning, execution, and completion of drug development projects within a pharmaceutical or biotechnology company. They coordinate cross-functional teams, manage budgets and timelines, and ensure compliance with regulatory requirements. Their role is critical in bringing new drugs from early research through clinical trials and ultimately to market approval.

What are the key skills and qualifications needed to thrive as a director of project management in drug development?

To thrive as a Director of Project Management in Drug Development, you need extensive experience in pharmaceutical R&D, a deep understanding of clinical trial processes, and often an advanced degree in life sciences or a related field. Familiarity with project management software (such as MS Project), regulatory systems (FDA/EMA guidelines), and certifications like PMP are highly valued. Exceptional leadership, strategic thinking, and cross-functional communication skills set standout professionals apart in this role. These skills ensure complex drug development projects are delivered on time, within budget, and in compliance with regulatory standards, ultimately accelerating the path to successful therapies.

What are some of the biggest challenges faced by a director of project management in drug development, and how can they be addressed?

A Director of Project Management in Drug Development often faces challenges such as managing cross-functional teams, navigating complex regulatory requirements, and ensuring projects stay on time and within budget. Effective communication and leadership skills are essential to align diverse stakeholders, including research, clinical, regulatory, and commercial teams. Proactively identifying potential risks and implementing mitigation strategies, as well as staying current with industry regulations, can help address these challenges and keep projects progressing smoothly.

What are popular job titles related to Director Project Management Drug Development jobs?

For Director Project Management Drug Development jobs, the most frequently searched job titles are:

Infographic showing various Director Project Management Drug Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $142,075 per year, or $68.3 per hour.

Director, Drug Development Project Management & Pipeline Strategy

Cambridge, MA โ€ข On-site

Flagship Pioneering
Biotechnology Research and Developmentย โ€ขย 51 - 200 employees

Other

Posted 22 days ago


Job description

Cambridge, MA USA

Position Summary:

This role will partner closely with Quotientโ€™s drug development project leaders and matrix teams to translate their scientific strategy into robust, integrated drug development project plans, and drive flawless execution of Quotientโ€™s early drug pipeline. This role is accountable for planning, execution, and coordination across functional teams (e.g., drug discovery, translational medicine, biology, drug development strategy, and finance) as well as external CROs and collaborators. The successful candidate will coordinate and run drug development matrix project meetings, maintain governance-ready dashboards and decision logs, oversee budgets, contracts, and resource needs, and readiness for key drug development review milestones. By leveraging subject matter experts across key Research and Development functions to develop end-to-end drug development plans and execution strategies, this role will provide operational and planning leadership to drug development matrix teams, manage risks and interdependencies, consider regulatory and compliance requirements, and support reviews for Quotientโ€™s Executive team and Board of Directors.

This role will also support the development of Quotientโ€™s drug discovery pipeline strategy with scenario-based analyses based on landscape and competitive intelligence data. Given the close integration of Quotientโ€™s proprietary genetics platform into the drug discovery process, this role will interface with research operations and strategy to build a seamless, end-to-end view of Quotientโ€™s R&D pipeline.

This role will report to the Chief Development Officer (CDO). The role could be based at Quotientโ€™s UK or US site.

Responsibilities:

  • With drug development matrix teams, support the translation of overarching drug development strategy and vision into integrated, detailed project plans (scope, milestones, critical paths, dependencies, risks) across functions.
  • Monitor progress versus plan; proactively identify issues and interdependencies, elevate to project leads as needed, and coordinate cross-functional mitigation plans
  • Schedule, structure, and run project team meetings (set agendas, pre-reads, minutes, action logs), track and drive closure of decisions and actions.
  • Build and maintain governance-ready views (dashboards, status summaries, decision logs) to enable Quotientโ€™s Executive team and Board of Directors reviews
  • Support SMEs in operational execution with external partners (e.g., CROs), ensuring deliverables, timelines, and obligations are clearly understood and met.
  • Support functional heads in forecasting and tracking resource needs (FTE, external partners) across projects and the pipeline, flag constraints and propose options.
  • Coordinate budgets closely with the VP of Finance and track spend vs. plan and contracted scopes.
  • Establish and maintain a structured risk and issue management process (identification, impact assessment, mitigation/contingency, owners, timelines).
  • Support compliance with regulatory and quality expectations by organizing documentation and tracking contributions to regulatory submissions etc.
  • Maintain shared repositories (SharePoint, dashboards, trackers) for plans, data summaries, and decision histories to improve transparency and continuity.
  • Identify and implement continuous operational improvements to increase DD matrix team efficiency and focus on high-value scientific work.
  • Support the development of Quotientโ€™s drug discovery pipeline strategy and, with members of Research Operations and Strategy, develop a holistic and end-to-end view of Quotientโ€™s Research and Development pipeline.

Qualifications:

  • Bachelorโ€™s degree in biological sciences or related discipline
  • Proven track record of applying project management methodologies in complex, matrixed environments; significant experience (typically 5โ€“10 years) in drug development within pharmaceutical, or biotech industry settings
  • Knowledge and experience in drug discovery and an understanding of the principles of clinical development, drug discovery, regulatory strategy
  • Established expertise and hands-on experience with project management tools (e.g. Microsoft Project, Smartsheet, or equivalent), Microsoft Office applications, and a working understanding of innovative AI and knowledge management technologies (e.g., ChatGPT, Claude, CoPilot, Notion etc)
  • Formal Project Management Qualifications (e.g. PMP or PRINCE2 certification)
  • Advanced scientific degree
  • Demonstrated ability to think strategically and execute multiple projects simultaneously
  • Experience with data, AI, or real-world evidence initiatives
  • Highly effective communication skills (verbal, written, and presentation) for a wide variety of audiences/stakeholders, including technical and business
  • An appreciation of drug target research and/or genetic research workflows and how these interface with drug discovery workflows

Values and Behaviors:

  • Encourage respectful disagreement and cultivate open-minded, ego-free interactions to continuously push each other towards excellence
  • Seek out diverse perspectives; practice active listening and genuine curiosity to ensure all contributions are valued, regardless of source
  • Recognize the impact of your behavior, language and attitudes, and strive for balanced, meaningful exchanges that enhance mutual growth and understanding in all interactions
  • Use a company-first mindset to guide decision-making; prioritize team over individual success
  • Take calculated risks and challenge convention in the quest for exceptional outcomes

About Quotient:

Quotient Therapeutics is a privately-held, early stage company developing breakthrough medicines informed by natural somatic genetic diversity present in patients. Through our work in somatic genomics, we are forging a new status quo for biopharma research and development across a broad pipeline of internal and partnered programs.

The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Sana Biotechnology (SANA), Tessera Therapeutics, Evelo Biosciences (EVLO), Indigo Agriculture, Seres Therapeutics (MCRB), and Syros Pharmaceuticals (SYRS).

Privacy Notice for Applicants:When you apply for a role at Flagship Pioneering or one of its portfolio companies, we collect and use personal information you provide (such as your name, contact details, work history, and application materials) to evaluate your application, communicate with you, and comply with legal obligations. Your application data is processed through Greenhouse, our applicant tracking system, and may also be reviewed using AI-assisted screening tools. We do not sell your personal information. California residents have rights under the CCPA/CPRA including to know, delete, and opt out of the sharing of your personal information. If you are located in the EU or UK, we process your data under GDPR and you have rights to access, rectify, and erase your data. To exercise your rights or for questions, contact privacy@flagshippioneering.com.

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