Clinical Manager - Home/office based

Highly Competitive
  1. Clinical Research
  2. Permanent
  3. Italy
Milan
Posting date: 05 Oct 2018
CR.VC.19919_1538743293

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An exciting job vacancy has emerged for a Clinical Manager to join one of the world's largest global CROs. This contract research organisation provides support services to many of the biggest names in pharmaceuticals, biotech, medical devices and health care, and has helped to commercialise many leading therapies. This position will be home based at their site in Milan.

Job Responsibilities:

  • Manage the operational aspects of projects to support right subjects and right data to meet or contractual requirements. Collaborate with project leader and LCA to establish an integrated set of plans with Clinical Manager to be ultimately accountable for results of the clinical team. Represent clinical delivery with customer.
  • Produce and distribute status, tracking and financial reports for the core project team, other functional groups and senior management.
  • Responsible for tracking financial deliverable, reporting and invoicing on projects.
  • Ensure appropriate subject recruitment plans are in place; all outreach or digital offerings are explored and deployed in consultation with the customer. Ensure the Site Recruitment Action Plan (SRAP), patient recruitment target and contingency plans are in place and deployed at trigger points.
  • Deliver the project / program according to the quality management plan. Guide CRAs and advise on critical specific study issues.
  • Manage clinical study set-up, maintenance and follow-up study activities through ongoing tracking and review of study progress. Report progress to appropriate clinical management and project management forums.
  • Accountable for approving final sites lists.
  • Develop the risk management plan from a clinical perspective and coordinate clinical issue escalation and resolution with the Project Leader.
  • Collaborate with other functional groups such as Global Delivery Network (GDN), Labs, Data Management, Pharmacovigilence, and Biostatistics, where necessary, to support milestone achievement and to manage study issues and obstacles.
  • Provide ongoing training and support to the clinical team. Conduct frequent team meetings and ensure regular communication.
  • Drive high performance and efficiency of the clinical team through CRA project objectives, the conduct of monitoring visits. Provide performance feedback to management on clinical team members.
  • Utilize appropriate clinical tools, processes and GDN for the study team to support the execution of clinical deliverable and study timelines.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Valeria Cardo on +44 203 854 0674 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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