PpThe START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START’s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. /p pSTART represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – the most effective cancer drug in medical history. /p h3Senior Manager, Study Activation (EU) /h3 h3Essential Responsibilities /h3 ul liSupports SSU strategy in close collaboration with the VP, Client Engagement Study Activation /li liCollaborates with central services and site-level study team to ensure SSU timelines and deliverables are met according to internal process, KPIs, and Sponsor goals /li liAccountable for timely start-up activities until Green Light (ready to initiate site milestone) /li liSupports study feasibility and site selection milestones in close collaboration with Pre‑Award Team as well as the site-level study team. /li liSupports and directs all study activation milestones in close collaboration with Study Start‑up Specialist as well as the site-level study team. /li liServes as main contact for issues in SSU phases, escalating as necessary /li liEnsures sites are prepared for "Green Light" and ensures all documentation is in place for initial and subsequent drug release. Responsible for review and sign off of the site "Green Light" /li liOversees EU SSU team activities to achieve start‑up timelines and quality execution, (proposing and implementing corrective actions where appropriate), according to START standards /li liLeads EU SSU team meetings and participates in network study team meetings, as required /li liContribute to the growth and development of departmental staff, processes and systems. /li liAbility to embrace HubSpot, Veeva Vault, FileMaker, and CTMS system and associated functionality and maintain records related to specific area of assignment /li liAssist with in‑service trainings and new hire trainings for staff /li liAssist with special projects as assigned. This includes, but is not limited to, conducting research, preparing presentations and documents as requested /li liServes as a back to the VP and departmental team, when needed /li liPerform additional duties as assigned /li /ul h3Required Education And Experience /h3 ul liBA/BS degree with at least 5 years of experience in pharmaceutical related drug development or direct equivalent experience or advanced degree /li liMust have knowledge of clinical trial conduct, including, multi‑center, global trials. /li liExperience within the EU‑CTR /li liMust have strong knowledge of ICH/GCP guidelines and regulatory requirements. /li liRequires proven project management skills and leadership ability /li liMust have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability. /li liExperience in working cross functionally and with external providers /li liExperience with development implementation of process improvement related initiatives /li liGlobal Experience with site activation activities including submission requirements. /li /ul h3Travel Requirements /h3 ul liTravel: Required to travel up to 20% of the time /li liApproximately 80% of time is spent sitting. /li liVery fast‑paced and ever‑changing healthcare environment. /li liDemanding deadlines and time frames. /li liConstant demand for updating knowledge /li /ul h3Ready to be part of a team changing the future of cancer treatment? /h3 pJoin us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. /p /p #J-18808-Ljbffr