Covance

  • Clinical Research Manager (Oncology) - Sponsor dedicated

    Job Location(s) ES-Madrid
    Job Number
    2018-21850
    Job Category
    Clinical Operations
    Position Type
    Full-Time
  • Job Overview

    The Ass CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and country regulations.

     

    The position has a significant impact on how a country can deliver country-specific trial commitments and objectives especially during the study.

    •  Significant impact on the ability to effectively conduct clinical studies and develop the pipeline, while maintaining local regulatory and compliance requirements in countries. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives. As a customer-facing role, this position will build business relationships and represent Client with investigators, functional outsourcing partners and other external partners and therefore have a significant impact on country-level customer relationships.

     

    • Requires ability to make decisions independently and oversee important activities relevant to clinical research activities in the country according to predetermined global policies and commitments with the support, oversight and supervision of the Country Research Director or Therapeutic Director. Requires strong understanding of local regulatory environment, country regulations, client policies and procedures, quality standards.

     

    • Strong scientific and clinical research knowledge is required for this position. A strong understanding of clinical trial planning, management and metrics is essential as well as the ability to focus on multiple deliverables and protocols simultaneously. Requires skills to effectively build and maintain professional relationships with investigators and other external stakeholders, requiring strong communication, educational/pedagogic, diplomatic and empathic skills. The role will require proven ability to collaborate and lead high performing cross-functional teams also in a virtual environment.

     

    • The position requires strong leadership skills (scientific and business) and ability to coordinate and lead local teams to high performance. Oversee country commitments, compliance and training needs. Additionally, business leadership and alignment with corporate requires that individual has ability to lead across several dimensions simultaneously.

     

    • Works collaboratively with Country and Regional Operations; Pharmacovigilance, Regulatory, Global Medical Affairs and Global Human Health internally; and with external functional outsourcing vendors. Requires coordination and alignment with the regional and broader organization.  Additionally, will work to build and maintain relationships with investigators and other external partners and promote Client’s reputation. In collaboration with CRD, represents Client in Pharma industry issues and in seeking influence in external R&D environment.

    Education / Qualifications

    • University/college degree (life science preferred), or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution.
    • In lieu of the above requirement, candidates with six (6) or more years of relevant clinical research experience in pharmaceutical, CRO industries or experience in a health care setting will be considered.
    • Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries.
    • Thorough understanding of the drug development process.

    Experience

    • Background: Degree in medicine or Health sciences. Background in GCP& ICH, local & Corporate SOPs, and clinical research.
    • Knowledge: GCP & ICH, local & Corporate SOPs
    • Language (language and knowledge level): English - Advanced
    • Professional experience: Need to provide 5 years experience in clinical research project management
    • Strong experinece in Oncology.

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