Local Project Manager Clinical Trials - sponsor-dedicated

☞ Labcorp Drug Development

Ver: 158

Día de actualización: 24-10-2024

Ubicación: Munich Bavaria

Categoría: Planificación / Proyectos IT - Software

Industria: Staffing Recruiting Biotechnology Pharmaceuticals

Posición: Entry level

Tipo de empleo: Full-time

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Contenido de trabajo

Job Overview

Local Project Manager Clinical Trials - sponsor-dedicated

Location: Munich, Germany / Home Office, Germany

Labcorp Drug Development has supported the pharmaceutical industry in developing more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers.

If you are looking to take on responsibility, hone your leadership skills and leverage your extensive know-how in clinical trials - ensuring both the success of important clinical studies and meaningful professional development of your team members -, this is the perfect opportunity. You will be working directly with one of our renowned key sponsors, in a role that allows you to have a real impact on people’s health and lives.

What we have to offer: a strong international support network, flexible working solutions that facilitate a genuine work-life balance, a highly competitive compensation package and the opportunity to significantly raise your profile in the industry.

Sounds exciting? Then we cannot wait to hear from you!

As Local Project Manager, You Typically Will
  • Be accountable for the end to end performance for assigned protocols in Germany, in compliance with ICH / GCP and country regulations, internal policies and procedures, quality standards and adverse event reporting requirements
  • Act as the main Point of Contact for assigned protocols and as the link between Country Operations and the clinical trial team
  • Proactively plan, drive and track execution and performance of deliverables, timelines and results to meet country commitments - from feasibility and site selection to recruitment, execution and close out
  • Review reports of monitoring visits, perform quality control visits as needed and escalate performance issues and training needs as needed
  • Lead local study teams to high performance: train and collaborate closely with CRAs as the protocol expert, coordinate activities across local roles and facilitate collaboration amongst (extended) team members
  • Create and execute a local risk management plan and ensure compliance with CTMS, eTMF and other key systems for your assigned studies
  • Coordinate and collaborate with external and internal stakeholders and escalate challenges and issues as needed
  • Develop and nurture trustful, sustainable relationships with our client, investigators and other external partners
Education/Qualifications
  • Degree in a relevant field such as pharmacology, life sciences, clinical trial management, health care (management), nursing, chemistry, biology, oecotrophology etc.,
  • In lieu of the above, an equivalent completed vocational education or equivalent professional experience
Experience
  • Deep expertise in clinical trials within a CRO or a pharmaceutical company across a wide variety of therapeutic areas, - preferably including oncology
  • Professional experience with submissions to the German regulatory authorities - observing all local regulations and guidelines as well as international standards such as ICH and GCP
  • Leadership experience in a comparable position (e.g. Clinical Trial Lead, Clinical Research Manager, Study Start-Up Lead, Clinical Safety / Quality Manager etc.)
  • Experience coaching, mentoring and coordinating teams locally and/or virtually
  • Autonomous team player with excellent time and project management skills
  • Ability to build trustful, sustainable relationships with a wide variety of stakeholders based on your outstanding listening and communication skills
  • Business fluency in German and English – both spoken and written – is a must
    Remote

    2020-49491

    Covance is proud to be an Equal Opportunity Employer:

     As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant’s race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
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Plazo: 08-12-2024

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