Associate Director, Nonclinical and Translational Strategy & Operations

Centessa Pharmaceuticals, LLC

$175K — $210K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Advanced degree in life sciences (PhD preferred) such as biology, pharmacology, or biochemistry.
  • 8+ years of experience in program or departmental management for discovery and early-stage development.
  • Strong working knowledge of nonclinical drug development processes.
  • Project management training or PMP certification is advantageous.
  • Ability to synthesize complex scientific and operational data into clear narratives.
  • Proven ability to influence and drive outcomes in a matrixed environment with ambiguity.

Responsibilities

  • Develop and maintain integrated departmental timelines aligned with program objectives.
  • Collaborate with cross-functional program leads to build and monitor nonclinical and translational plans.
  • Maintain tools for project tracking, finance/resource monitoring, and operational metrics.
  • Communicate status, risks, and progress of initiatives with relevant stakeholders.
  • Facilitate collaboration and meetings, providing agendas and taking minutes.
  • Track deliverables from partners and internal teams, and prepare materials for governance submissions.

Benefits

  • 401(k) plan
  • Company-sponsored medical, dental, vision, and life insurance
  • Generous paid time off
  • Health and wellness program
  • Eligible for a discretionary annual bonus
Full Job Description
Description of Role

Nonclinical and Translational Strategy & Operations role will support the planning, execution, and coordination across all programs and operational initiatives. This role partners closely with leaders in toxicology, DMPK, clinical pharmacology, and cross-functional program management to drive alignment, operational rigor and effective communication. The role combines strategic planning, operational coordination, metrics/reporting, and cross-functional communication to help deliver department work product in an fast paced R&D environment.

Key Responsibilities
  • Support development and maintenance of integrated departmental timelines aligned with broader program objectives
  • Partner with cross-functional program leads and PM(s) to build, and monitor integrated nonclinical and translational plans including scope, timing, deliverables and risks
  • Maintain dashboards, project plans, finance/resource tracking tools, and operational metrics to support visibility and decision-making
  • Communicate status, risks, and progress on departmental initiatives and deliverables, in partnership with cross-functional program leads/PMs, ensuring consistent, aligned, high-quality updates and communication to management, partners, and governance teams
  • Facilitate internal collaboration and meetings, including agendas, presentation materials, minutes, decisions, and following up actions
  • Track deliverables from external partners and internal teams, including CROs, with the help of Operations staff, and support preparation high- quality materials for governance and Regulatory submissions

Qualifications
  • Advanced degree in life sciences (PhD preferred), such as biology, pharmacology, biochemistry, or a related field
  • 8+ years of experience in program or departmental management supporting discovery and early-stage development
  • Strong working knowledge of nonclinical drug development (toxicology, pharmacology, DMPK, Translational PKPD, Clinical Pharmacology)
  • Project management training or PMP certification is a plus
  • Exceptional ability to synthesize complex scientific and operational information into clear, executive level narratives
  • Proven capability to operate with ambiguity, influence without authority, and drive outcomes in a matrixed environment
  • Strong communication, collaboration, and interpersonal skills
  • Agile with an ability to respond positively to continuous change and to bring creative solutions to challenges
  • Exceptional computer proficiency - advanced knowledge of and experience with Smartsheet and MS-Office applications (including Word, PowerPoint, and Excel)
  • Excellent analytical and organizational skills (resources, timelines, cost/risk/benefit analysis, and overseeing data management)

Compensation

The annual base salary range for this job level is $175,000 - $210,000. Individual compensation within this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, and job knowledge.

In addition to base pay, this role is eligible for a discretionary annual bonus. Centessa also offers a comprehensive benefits package, which includes a 401(k) plan, company-sponsored medical, dental, vision, and life insurance, generous paid time off, and a health and wellness program.

Work Location

The Associate Director, Nonclinical and Translational Strategy & Operations role is a based in the US, with 25% travel.

POSITION: Full-Time, Exempt

Please note: We will not assign referral rights for any unsolicited resumes from recruitment agencies.

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