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Σχέση απασχόλησης - Πλήρης ΑπασχόλησηΕλάχιστη Απαιτούμενη Εκπαίδευση - ΑΕΙΑπαιτούμενη Προϋπηρεσία - Τουλάχιστον 6 έτος/ηΚατηγορίες - Επαγγέλματα Υγείας, Διοίκηση Επιχειρήσεων

Περιγραφή

Clinical Project Manager (CPM)
The mission of the Project Manager is to effectively ensure the successful start, conduct and management of clinical trials (studies), playing a leading role in the planning and controlling of the trial with respect to timelines, milestones, budget and resources.

Responsibilities: 
  • Acting as the main contact point for study planning, budgeting, strategy, oversight and escalation for company’s clients and study teams;
  • Requesting and coordinating all resources required for the proper implementation of study plans and targets;
  • Supervising the project team/s to ensure the conduct of clinical trial/s at selected investigational sites is done according to the approved Protocol, ICH-GCP principles, the applicable SOPs and regulatory requirements;
  • Coordinating feasibility and site selection during the startup phase of a study;
  • Ensuring proper training, support, motivation and oversight of the study teams under their responsibility;
  • Performing regular study progress reviews with the responsible teams to ensure smooth workflow, key milestones achievement and timely resolution of any potential issues or delays;
  • Ensuring the quality of study conduct by performing co-monitoring, CRA evaluation and oversight visits, reviewing monitoring visit reports in accordance with the company plans and requirements, discussing findings and action plans, supporting and overseeing CRAs to ensure implementation, reporting quality risks to QA and Management team/s;
  • Ensuring ongoing risk estimation, mitigation and management of assigned studies and teams, as well as timely reporting to the client and Country Manager/Head of Clinical Operations;
  • Responsible for achieving the overall study recruitment and ensuring all project deliverables meet client expectations as well as company’s standards;
  • Coordination and support on study financial matters, including preparation and negotiation of study budgets, approval of hospital/regulatory fee payments, cost assessment according to the appropriate financial agreements and monthly project billing activities in collaboration with the Project Finance teams;
  • Providing general coaching, training and business experience in the responsible teams and also acts as a motivator and mentor.

Required Skills & Knowledge
  • Minimum 6 years of relevant experience in all aspects of clinical trial set-up, initiation, monitoring and management, with minimum 3 years of project management/line management experience – prior CRO SM/PM experience is a must
  • University Degree in a related field
  • Excellent command of English language (both written and spoken)
  • Self-motivated and able to supervise and motivate study teams of different roles, background and experience
  • Ability to multi-task, prioritize effectively and ensure teams keep deadlines and operate promptly and efficiently
  • Quality and result-oriented
  • Excellent knowledge of MS Windows and MS Office
  • Prior experience and excellent command of internal and/or client CTMS, EDC, eTMF etc.
  • Ability to travel on an as-needed basis
  • Strong interpersonal, communication and organizational skills 
  • Open-minded, team player and passionate about new challenges

The company offers a competitive remuneration package, as well as skills development via continuous training in the Clinical field and rewarding career opportunities in an exciting, international and supporting working environment.