KLIFO is looking for talented Senior Project Managers

KLIFO is expanding and wants to engage Senior Project Managers into a dynamic and experienced team within Clinical Operations Solutions. The people we want to engage like to work in a consulting environment with a positive, proactive, flexible and self-driven personality.

We offer a highly flexible, free and trustful working climate with very competent colleagues and exciting clients.

The position as Senior Project Manager:

The Senior Project Manager (SPM) is responsible for the delivery of an agreed trial as defined in the trial outline/protocol, to the agreed quality, budget and timelines.
The SPM may take a main role in larger programs and can also have a mentor role for other employees within the Clinical Operations group:

  • Lead the clinical trial team and coordinate and manage all activities related to clinical trials
  • Planning, delivery and management of clinical trial activities (start-up, operational conduct and closure) according to SOPs and a responsibility split with Sponsor
  • Liaison with clinical trial team members regarding trial design and protocol preparation and ensure the production of the final trial protocol
  • Lead the Risk Based Quality Management (RBQM) process including risk assessment and risk controls
  • Development of project plans for the conduct of the clinical trial
  • Communicate timelines, identify milestones, handle trial budget and report progress for the clinical trials to sponsor and to COS management team
  • Providing advice to clients within the areas of responsibility
  • May participate in global development teams on compound level giving input to clinical development plans and operational strategies across a clinical program

The qualifications of the Senior Project Manager:

  • BSc/MSc in the life sciences field or related discipline and a minimum of 7 years in a similar position in the pharmaceutical industry/CRO
  • Extensive experience within clinical trial management and understanding the principles of clinical drug development
  • Knowledge of GCP guidelines, applicable regulatory requirements, medical terminology and clinical trial processes
  • Experience with multi-country and multi-centre studies
  • Ability to translate client’s needs into a solid project plan
  • Ability to work independently without supervision of a colleague within the group
  • Ability to supervise and coach non-senior personnel within the group
  • Excellent communication skills (written and verbal) in English
  • Microsoft Office skills

We offer:

  • Work within different therapeutic areas and with 
tasks of varying complexity
  • Work with a heterogeneous client pool 
(pharmaceutical companies, established biotech, inexperienced biotech, investigators/academia)
  • Build international client relations
  • Use and elaborate your competences and experience
  • Work in an interactive, flexible and positive working environment with highly competent colleagues


KLIFO has offices in both Denmark, Germany, Sweden and the Netherlands. This position can be located in any of our offices or be home-based.


For more information, please contact Stefan Ingelsson, Team Manager, at 004544226345

Applications should be sent to: moc.ofilk@boj marked Project Manager

KLIFO processes your application and all related personal data exclusively for the specific hiring process. Your data is processed as confidential information, cf. the current data protection law (GDPR).

Deadline: Applications are reviewed on an ongoing basis.

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