Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Evotec

Principal Scientist – ADMET Study and Innovation Manager

Evotec

. Lead and manage partner and client ADMET studies through the full lifecycle, from proposal development and pricing through quality review, data delivery, and final sign-off .

Posted 10/20/2026full-timePrinceton • New Jersey • United StatesLead💰 $134,000 - $155,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in ADMET principles, toxicology, and study management while effectively leading teams and managing client relationships. Proven ability to drive innovation initiatives and improve operational efficiency in scientific environments.

Highest-signal resume keywords
ADMET PrinciplesStudy Management ExperienceClient ManagementInnovation InitiativesRegulatory Compliance

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
BiologyChemistryPharmacologyToxicologyHigh-Throughput ScreeningProposal DevelopmentStudy DesignData InterpretationQuality ReviewProcess Development
Soft Skills
LeadershipProblem-SolvingCustomer-Focused MindsetOrganizational SkillsInterpersonal Skills
Tools & Technologies
CRMLIMSDigital SolutionsIn Vitro Modelling TechnologiesOrgan-On-A-Chip Systems
Industry Keywords
PharmaceuticalBiotechnologyCRODrug DiscoveryStudy Lifecycle

About the role

Key responsibilities & impact
  • Lead and manage partner and client ADMET studies through the full lifecycle, from proposal development and pricing through quality review, data delivery, and final sign-off
  • Serve as primary scientific point of contact for clients, providing expert guidance, data interpretation, and strategic recommendations
  • Review and quality-check routine ADME and toxicology study data
  • Provide technical leadership for customised assays, complex study designs, and challenging scientific enquiries
  • Coordinate internal teams, clients, and external partners throughout the study lifecycle
  • Resolve scientific, operational, and logistical challenges affecting study outcomes or timelines
  • Champion innovation initiatives and support implementation of emerging technologies, NAMs, organ-on-a-chip systems, in vitro modelling technologies, and digital solutions
  • Define and execute innovation roadmaps aligned with business objectives and client needs
  • Support proposals, pricing strategies, study plans, work orders, and technical solutions
  • Represent the organisation in internal and external meetings
  • Contribute to thought leadership, knowledge sharing, process development, and future service opportunities
  • Maintain client and partner relationships and support customer satisfaction and repeat business
  • Monitor study opportunities, revenue trends, and commercial performance metrics
  • Maintain CRM, LIMS, and tracking systems for forecasting, invoicing, and revenue recognition
  • Partner with Finance and Commercial teams on revenue reporting and study reconciliation
  • Improve processes, productivity, operational efficiency, customer experience, quality, throughput, and profitability
  • Coach and mentor Study Management colleagues
  • Foster a collaborative, inclusive, and high-performing team culture
  • Maintain compliance with Health, Safety, Quality, and regulatory requirements
  • Complete mandatory training and maintain training records
  • Complete timesheets and business administration requirements
  • Participate in performance management and development processes

Requirements

What you’ll need
  • Bachelor's, Master's, or PhD degree in Biology, Chemistry, Pharmacology, Toxicology, or a related life science discipline
  • Minimum of five years of relevant industry experience
  • Evidence of leadership in study management, innovation initiatives, or strategic program delivery
  • Relevant experience within the pharmaceutical, biotechnology, CRO, or drug discovery sectors
  • Strong understanding of ADMET principles, assays, toxicology, high-throughput screening, and their application to drug discovery and development programs and processes
  • Demonstrated project, study, or client management experience within a scientific environment
  • Experience supporting client interactions, proposal development, study design, and scientific consultation
  • Excellent written, verbal, presentation, and stakeholder management skills
  • Customer-focused mindset with ability to build trusted relationships internally and externally
  • Strong problem-solving skills, resilience, and ability to navigate complex scientific and operational challenges
  • Proactive, solutions-oriented approach with a track record of delivering results and driving improvements
  • Excellent organisational skills and attention to detail
  • Ability to manage multiple priorities effectively while maintaining quality and responsiveness
  • Strong interpersonal and networking skills for collaboration across multidisciplinary teams
  • Adaptability and positive approach to changing priorities and evolving business needs

Benefits

Comp & perks
  • Discretionary annual bonus
  • Medical, Dental and Vision benefits
  • Short-term and long-term disability
  • Company-paid basic life insurance
  • 401k company match
  • Generous paid time off
  • Paid holidays
  • Wellness benefits
  • Transportation benefits
  • Professional courses, mentorship, and new projects
  • Flexible work options
  • Inclusive culture
  • Innovative projects and cutting-edge technology