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Director, Early Research Project Management


Job Location:

Cambridge - UK

Monthly Salary: Not provided by the employer
Posted: 22 August 2026 (12 days ago)
Application Deadline: 19 November 2026
Vacancies: 1 Vacancy

Job Summary

Position Summary:

Quotient is seeking an experienced Director Early Research Project Management to establish and lead our research project management capability as we scale our somatic genomics drug target discovery platform.

This is a unique opportunity to shape how complex research programs are planned coordinated and delivered within a rapidly growing biotechnology company. This role will partner with scientific leaders and multidisciplinary teams to drive day-to-day program delivery whilst establishing the project management systems governance and ways of working that enable Quotients platform to scale.

Quotients research project teams are highly cross-functional comprising genomic subject matter experts leading study design lab-based teams focusing on technology/assay development high-throughput laboratory operations automation non-lab-based data science teams and other specialist functions.

Reporting to the Head of Research Operations and Strategy the incumbent will operate as a strategic partner to research leadership ensuring programs remain aligned with organisational priorities while driving the governance planning disciplines and operational rigor required to deliver an increasingly complex portfolio. This role will also work closely with drug discovery project management to ensure overall coordination of Quotients end-to-end R&D pipeline.

Responsibilities:

  • Partner with scientific and operational leaders on a day-to-day basis to drive the successful execution of Quotients research portfolio translating research strategy into integrated executable project plans from disease ideation up to target assessment
  • Coordinate multiple cross-functional matrix teams ensuring programs remain aligned to agreed priorities milestones timelines and organisational objectives
  • Become a trusted operational partner to scientific teams by understanding program objectives anticipating delivery challenges proactively identifying risks resource constraints and operational bottlenecks and working collaboratively to implement mitigation plans navigate competing priorities and maintain program momentum
  • Develop maintain and continuously optimise integrated project plans ensuring milestones critical paths dependencies resource requirements and project status accurately reflect program progress
  • Facilitate effective project meetings that drive decisions maintain momentum and ensure actions are clearly documented communicated tracked and delivered
  • Provide portfolio-level visibility through clear reporting dashboards and governance enabling leadership to make informed prioritisation resource and investment decisions
  • Partner with Finance to support program budgeting resource forecasting spend tracking and communication of financial risks
  • Collaborate closely with downstream scientific and operational teams to ensure seamless transition of programs through target assessment target validation drug discovery and later-stage development
  • Continuously assess how projects are planned governed and delivered across Research introducing pragmatic project management tools governance and reporting that improve collaboration and execution without creating unnecessary process
  • Foster a culture of operational excellence cross-functional collaboration and continuous improvement ensuring project management becomes an enabling capability that helps scientists focus on high-value research

Qualifications:

Essential

  • PhD with 5-8 years or BS/MS with 10 years in the biopharma industry preferably in an early therapeutic research or drug discovery setting
  • Demonstrated success in working with or for rapidly growing early-stage biotech companies
  • Experience introducing and/or owning project management governance tools reporting frameworks and portfolio management processes that became embedded within an organization
  • Leadership experience with multi-disciplinary project or program teams in an early drug target identification or drug discovery setting
  • Demonstrated track record guiding cross-functional teams to achieve program goals on aggressive timelines in a matrixed or entrepreneurial biotech environment
  • Exceptional interpersonal facilitation and communication skills with the ability to build consensus across scientific and operational functions
  • Demonstrated ability to operate independently identify organisational needs and implement sustainable improvements without requiring a predefined roadmap
  • Strong business acumen understanding of pre-clinical and clinical drug development strategy and program management best practices
  • Experience managing program budgets and financial reporting in partnership with functional and finance leads

Desirable

  • Experience in genomics-based drug target identification research and/or platform-based drug discovery
  • Prior success taking programs from research through early clinical development; experience with both small molecules and/or biologics

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 Quotient-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).

Quotient Therapeutics and Flagship Pioneering are committed to equal employment opportunity regardless of race color ancestry religion sex national origin sexual orientation age citizenship marital status disability gender identity or Veteran status.

Recruitment & Staffing Agencies:

Quotient Therapeutics (Quotient) and Flagship Pioneering (FSP) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Quotient FSP or their employees is strictly prohibited unless contacted directly by Flagship Pioneerings internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP and FSP will not owe any referral or other fees with respect thereto.

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 their 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


Required Experience:

Director


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