I'm partnered with a global CRO who is looking for a Senior Clinical Project Manager based in Poland.The Senior CPM will act as a matrix leader for the global clinical operations team under the supervision of the Clinical Operations Manager and will be accountable for the timely execution of specific tasks within the protocols.**Responsibilities**:Conduct feasibility, pre:study visits, site initiation visits, monitoring visits and/or close out visits as necessaryEnsure that the monitoring team is trained on study specific procedures and aspectsCoordinate and oversee project activitiesUpdate and check the Trial Master File (TMF) of the studies as well as ensuring that the site TMF are checked by the monitoring team according to CRO and Sponsor proceduresCoordinate and oversee project activitiesOrganise project activities and evaluate timeframesManage the vendors involved in the studyReview and approve the Investigator's Folder and Trial Master File prototypeVerify compliance with operating proceduresEnsure that the monitoring activities are conducted as per monitoring plan requirementsReview monitoring, remote monitoring, contact and telephone contact reportsSend regular updates to the SponsorCollaborate in establishing and maintaining SOPs related to Clinical Operations UnitMoreover, the Senior Clinical Project Manager will conduct Feasibility, Pre:study Visit, Site Initiation Visit, Monitoring Visit or Close out visit as necessary (e.g. back:up or directly allocated to the site) if the CPM is compliant with local minimum requirements for monitoring.**Requirements**:Degree in a scientific fieldIn depth knowledge of GCP and techniques for the monitoring of clinical trialsAt least 5 years working as a Clinical Project ManagerFluent in English and PolishAble to coordinate all the activities related to the management of local and international projects including managing interventional clinical trials, monitoring of clinical trials, and guaranteeing the security of information; preferably in CRO environmentWork independently under the supervision of the Head of Clinical Operations Unit and Clinical Operations ManagerAbility to interact with personnel properly and to manage the monitoring activities of CRAs (if required)
