Clinical Research Manager

Job Overview:


Discover new opportunities to grow your career as a Labcorp Drug Development Clinical Research Manager (CRM).
Labcorp Drug Development is looking to hire a Clinical Research Manager in Turkey. In this position you will be fully dedicated to our sponsor in Istanbul. In this role you will gain exposure to managing projects on a local level.
At Labcorp Drug Development, you can redefine what is possible and discover your extraordinary potential within our Functional Service Provider team (FSP).
As a Labcorp Drug Development employee dedicated to an FSP project you will bring your specialized discipline to a core team working directly with one sponsor. Whether your specialization is in clinical monitoring, clinical project management, data management, biometrics or pharmacovigilance; Labcorp Drug Development has an FSP opportunity to match your area of expertise.


Responsibilities include but are not limted to:

  • Main Point of Contact for assigned protocols and link between Country Operations and clinical trial team
  • Responsible for project management of the assigned studies: actively plans, drive and track execution and performance of deliverables/timelines/results to meet country commitments from feasibility and site selection, recruitment, execution and close out
  • Review Monitoring Visits Reports and raise performance issues and training needs to CRA manager and/or functional vendor and internal management as needed
  • Perform Quality control visits as required
  • Lead local study teams to high performance: train in the protocol other local roles, closely collaborate with and supports CRAs as protocol guide and coordinate activities across the different local country roles ensuring a strong collaboration
  • Responsible for crafting and executing a local risk management plan for assigned studies
  • Ensure compliance with CTMS, eTMF and other key systems
  • Raises as needed different challenges and issues
  • Responsible for collaboration with functional outsourcing vendors, investigators, other external partners
  • Country point of contact for programmatically outsourced trials
  • Serve local business needs as applicable in his/her country (If delegated can sign contracts and run budgets)
  • Collaborate internally with HQ functions and locally with PV, Regulatory and GMA to align on key decisions in his/her studies
  • As a customer-facing role, this position will build business relationships and represent the company with investigators
  • Share protocol-specific information and standard methodologies across countriesclusters


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


Experience:

  • Previous experience in clinical research in pharmaceutical or CRO industries
  • Previous experience in managing trials preferred
  • Deep understanding of local regulatory environment
  • Strong understanding of clinical trial planning, management and metrics is important as well as the ability to focus on multiple deliverables and protocols at a time
  • Ability and skills to lead resource allocation, processes (and controls), productivity, quality and project delivery
  • Strong organizational skills and time management skills
  • Excellent interpersonal skills
  • Proficiency in written and spoken English and local language

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