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Parexel

Regional Study Operations Manager

Fuldtid

Tidsbegrænset

Agern Alle 5A, 2970 Hørsholm, Danmark

SE PÅ KORT
ID: 2732915
|
Indrykket for 11 dage siden

When our values align, there's no limit to what we can achieve.
 

Parexel are currently recruiting for an experienced Regional Study Operations Manager to cover clinical trials across Sweden, Norway, Denmark and Finland.

In this role, as Study Operations Manager will be responsible for study, regional or specific country level activities from study startup through conduct and study close. The Study Operations Manager has responsibility for study management aspects of assigned studies, including vendor and budget management.

Some specifics about this advertised role

  • Regional level implementation of Startup and Site Activation Plans
  • Responsible for regional/country/study level Recruitment Strategy
  • Responsible to support the development of study level plans
  • Communication with the local team and internal stakeholders and CRO partner as applicable and as listed above to ensure efficient and timely study delivery of the agreed plans
  • Responsible for study and/or country vendor management and oversight including follow up and coordination of vendor deliverables
  • The Study Operational Manager will be able to work independently and exercise their own judgement.
  • Who are Parexel

    Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

    We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

    You’ll be an influential member of the wider team.

    What we are looking for in the this role

    For every role, we look for professionals who have the determination and courage always to put patient well-being first. That to us is working with heart.

    Here are a few requirements specific to this advertised role.

  • Minimum of 7 years of relevant global/regional clinical trial management experience.
  • Excellent leadership, communication, and organizational skills. Able to multi-task under limited direction and on own initiative.
  • M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential
  • Prior and demonstrable experience working at a senior level within Study start up
  • Husk at skrive i din ansøgning, at du så jobbet hos Ofir

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