Seuss Consulting

Clinical Project Manager

Location
US
Salary
Competitive
Posted
11 Feb 2021
Closes
27 Feb 2021
Ref
135968
Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
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 for candidates located within the USA. 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 v.wilson@consultseuss.com

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