Senior Clinical Trial Manager

Senior Clinical Trial ManagerAktis Oncology is seeking a Senior Clinical Trial Manager.This role will report to the Senior Director of Clinical Operations.Responsibilities:Leads and responsible for overall clinical trial management from start-up to database lock for assigned clinical studies.Reviews and authors applicable sections of clinical protocols, CRFs, study reports, IB, informed consent forms and study plans/manuals; implements and monitors progress against project timelinesProactively identifies project risks and develops resolution plansParticipates in the selection of Investigators and vendorsChairs and leads multi-disciplinary internal and external study team meetingsMaintain close communications with internal staff and oversight of CROs and clinical sites to ensure assigned projects meet timeline, budget, and quality goals.Participates in study data review and assists with site management to ensure data quality/timely data entryResponsible for managing approved study budget(s) against trial. Review and approve vendor invoices, including investigator grants and pass-through costs.Assists with the negotiation & establishment of contracts and budgets with external clinical sites and vendorsCollaborate with CMC and clinical supply colleagues to properly project for drug supply needsBroad understanding of operations including those in related development functionsDemonstrates ability to effectively interface with key medical personnel at clinical site(s)Demonstrates ability to flag processes that may not be appropriate for study based on phase, design, and/or use of dataMaintains a flexible, proactive approach to plan for and address issuesPossesses excellent written and oral communication skillsTrain/mentor junior staffQualifications:B.S. degree or equivalent, preferably in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)Minimum of 3-5 years (or 5+ if Senior) of clinical trial management experience in the pharmaceutical, biotech and/or CRO industryOncology therapeutic area experience is required for this position.Radiopharmaceutical experience is a preferredStrong knowledge of ICH Good Clinical Practice guidelinesRequires clinical research operational knowledge, computer literacy, and strong project planning/management including oversight of CROs/vendorsExperience and ability to manage global or regional teams in a virtual environmentProven track record in successfully managing trials from start-up to database lockStrong decision-making and communication/collaboration skills are essential to this position, as are analytic skills and effectiveness in seeking solutions to issuesWillingness to travel up to 10-20% of time (eg site visits, conferences, etc)Strong desire to be part of a patient-centric company.Proven demonstration of transparent communication and fostering open and diverse debate.Ability to work with agility and manage ambiguity.Aktis Oncology is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.