Clinical Development Manager
¡Inscríbase sin demora! Se espera un gran volumen de solicitantes para el puesto que se detalla a continuación, no espere para enviar su CV.
Role Overview
This role provides operational and scientific support to the Clinical Development team in the planning, execution, analysis, and oversight of preclinical and clinical studies. The position focuses on studies involving pharmacokinetics, toxicology (including toxicokinetics), and analytical validation, ensuring compliance with regulatory requirements, GLP/GCP principles, and internal quality standards.
Key Responsibilities
Study Planning & Design
Lead the design of preclinical studies and contribute to clinical study design in line with current regulatory requirements for pharmaceuticals and biologics
Support the preparation and review of study protocols, analytical plans, and technical documentation
CRO Management & GLP/GCP Oversight
Identify, evaluate, and manage external Contract Research Organizations (CROs), ensuring scientific quality, regulatory compliance, adherence to timelines, and budget control
Oversee study execution at CROs, ensuring protocol compliance and adherence to GLP/GCP standards
Manage deviations, amendments, and study-related issues
Support or conduct small-scale internal studies when required
Scientific & Analytical Support
Review and assess analytical methods and bioanalytical data supporting pharmacokinetic, toxicokinetic, and pharmacology studies
Calculate and interpret pharmacokinetic parameters
Contribute to the scientific evaluation of study outcomes
Ensure the integrity and consistency of study reports and raw data
Documentation & Regulatory Support
Maintain accurate, complete, and well-organized study documentation (protocols, contracts, reports, raw data, and correspondence) in line with internal procedures
Support regulatory activities by preparing or reviewing technical sections of dossiers (e.g., safety, efficacy, pharmacokinetics)
Contribute to expert reports and regulatory submissions
Prepare or review scientific materials, summaries, and publications to support product development and lifecycle management
Compliance & Continuous Improvement
Stay up to date with relevant regulations, guidelines, and scientific developments
Contribute to process improvements and provide scientific input to cross-functional teams
Support additional activities as required by the Clinical Development team
Location
Remote within Europe, the UK, or the US
Primarily hybrid (home/office-based), with occasional travel for CRO visits, audits, and study-related activities
Candidate Profile
Education
Degree in Veterinary Medicine, Pharmacy, or a related life science discipline
Postgraduate training in pharmacology, toxicology, or a related field xohynlm is highly desirable
Strong understanding of bioanalysis and pharmacokinetics
Experience
Experience within research institutions, universities, CROs, or preferably the pharmaceutical/animal health industry
Prior involvement in preclinical studies, GLP environments, or pharmacokinetic/toxicology projects is preferred
Skills & Competencies
Strong analytical and scientific reasoning skills
Familiarity with statistical principles, data processing workflows, Excel, and pharmacokinetic modelling tools
Excellent communication and interpersonal skills with a collaborative, proactive approach
Ability to manage multiple projects simultaneously while maintaining high-quality documentation
Strong organizational skills and attention to detail
Languages
Fluency in English (spoken and written) is essential