Seuss +

Clinical Project Manager

Seuss +
14 Apr 2021
07 May 2021
Clinical Research
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Clinical Project Manager/Senior Project Manager

Job Summary

Mid-sized, CRO who is expanding globally. We are looking for Clinical Project Manager/Senior Clinical Project Managers to join a global team, we are looking ideally in the following locations, UK, Poland, Czech, Spain or Belgium. The Project Manager/Senior Project Manager (PM) will be responsible for the overall coordination and management of clinical trials from start up through close out activities according to contractual time, quality/ cost parameters. The Clinical Project Manager will lead cross-functional teams and will work with major functional area leads to identify/mitigate/escalate project issues and ensures solutions are implemented

Essential Duties and Responsibilities
  • Primary interface with client representatives as well as staff members in the functional departments to ensure the timely initiation and completion of clinical trials
  • Assigned to manage a range of projects; from the small limited in scope projects (e.g., data management, etc) to larger full service, more-complex Attends and presents at client bid defence meetings.
  • Interacts with clients and company vendors to ensure that all contractual obligations are met.
  • Identifies potential bottlenecks and/or delays; develops and executes contingency plans in order to keep the project on schedule.
  • Ensures adequate resource requirements.
  • Develops Project Management Plan to include timeline and milestones.
  • Coordinates client project team meetings, including development of meeting agendas and minutes.
  • Conducts daily, on-going communication via telephone and email, responding to inquiries and client requests.
  • Interacts with clients and vendors to ensure that all contractual obligations are met.
  • Manages budget throughout the duration of the project and develops out of scope documentation and costs.
  • Manages the project trial master files.
  • Works closely with his/her manager to ensure the timely delivery or completion of project associated tasks.
  • Assists with the development of study specific training and other requirements for internal and external staff, as appropriate.
  • Ensures knowledge of clinical research, clinical therapeutics and regulatory issues, is current through review of journal articles and attendance of relevant professional association meetings
Degree and Experience required!
  • Bachelor / Master’s degree in a related field of study and a minimum of 3 years applicable industry experience or equivalent combination of education and experience.
  • Experience as a PM is a plus.Some experience in conducting clinical trials would be an advantage.
If you would like to apply for this position, please send your CV in WORD and English to

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