clinical project manager

Lund, Skåne County, Sweden

Description


TFS is growing and we are looking to expand our team in Skåne with a Clinical Project Manager. In this role, you will be working outsourced to one of our clients, a pharmaceutical company in the Helsingborg area.

As project manager you will be managing and coordinating early clinical projects (mainly Phase I/II), you will lead and manage the appointed CRO and follow-up on CRO performance. The position will also be part of the team for clinical study protocol development internally as well as together with appointed CRO.


The main responsibilities of the position include:

  • The overall responsibility for managing projects in accordance with company policies, SOPs, regulatory requirements in addition to financial and contractual obligations.
  • Plan and pro-actively manage multidisciplinary study teams (including Clinical Monitoring, Data Management, Statistics, Medical Writing, Regulatory and Safety) to ensure key milestones are achieved and studies are performed within budget, on schedule and in compliance with the appropriate - quality standards.
  • Pro-actively planning and responsible for identification of critical project task/issues and recommend course of actions to expedite project objectives. Manages the strategic aspects of projects and identify, analyze and minimize/mitigates any risk, including the implications of difference technical and operational choices
  • Communicates effectively with clients to successfully manage the relationship, identify needs and evaluate alternative business solutions and strategies.

  • TFS will provide you with the opportunity to grow in your professional role, to increase your expertise and broaden your experience. You will have the possibility of working either with project in-house or as an outsourced consultant at pharmaceutical, or biotech companies.


    TFS employs 850 clinical research professionals and operates from 25 global locations, conducting clinical trials in over 40 countries. TFS provides clinical research services to large pharmaceutical companies, midsized biopharma, small and virtual biotech, medical device and functional food customers. TFS core therapeutic areas of expertise are Oncology, Immunology, Dermatology, Ophthalmology, CNS, Cardiology and Endocrinology.



    Requirements


  • Bachelor’s Degree, preferably in life science or RN diploma.
  • Minimum 5 year of relevant experience as Project Manager within Clinical Research..
  • In depth knowledge of clinical research regulations governing the conduct of the clinical trials and quality standards
  • Prior CRO experience and experience is an advantage.
  • Experience of managing Neurology trials is a great merit.
  • In depth knowledge of project planning and metrics
  • Demonstrated ability to lead and manage staff
  • Excellent oral and written communication skills in English and Swedish
  • Solid organizational skills and demonstrated ability to prioritize
  • Proven leadership skills and with a pro-active and pragmatic approach to problem solving.
  • Internal and external negotiation skills
  • Willingness to travel as required

  • We are seeking high performing individuals who enjoy a fast-paced environment and have extensive project management experience, managing international studies. You show excellent leadership skills and are able to manage and motivate study team members in a proactive and adaptive way. You have great organizational and communication skills and show high levels of enthusiasm, drive and energy.


    We are looking forward to receiving your application with included CV and a personal letter. We are working with continuous selection so please submit your application as soon as possible


    Welcome to join us and to contribute in placing TFS among the top 7 worldwide CROs. Your job will make a difference!


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