Clinical Study Manager

At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare's hardest challenges and advance what is possible. Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere. We strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. Passionate people who want to make a difference drive our culture. Our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real-world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential. Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let's advance the world of minimally invasive care.About the RoleThis position requires a candidate with extensive experience supporting evidence generation strategy and execution of clinical studies. The Clinical Study Manager role will develop and execute strategies for clinical and outcomes research studies to support regulatory approvals and key strategic evidence initiatives. As a member of the Clinical Affairs team, this role will be responsible for working with key stakeholders to design and develop clinical protocols and execute clinical studies (pre-market or post-market studies), with minimal supervision. The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as with biostatisticians to review and interpret results of clinical studies, develop clinical study reports, or support the development of clinical publications. During trial execution, the CSM will drive the progress of the trial during site selection, site start-up and through enrollment and follow-up. The CSM will clearly provide guidance to the monitors about monitoring needs, and oversee compliance work on the study. The CSM will also take a leadership role in external communication with investigators and study teams. The ideal candidate will have experience previously managing premarket studies in the United States and utilizing resources to research and scope research topics and to provide recommendations on clinical trial strategy. The candidate is also expected to have experience reviewing, interpreting and summarizing clinical literature.ResponsibilitiesResponsible for leading assigned clinical research activitiesCollaborate with internal stakeholders, investigators and KOLs to develop and review study design and concepts, prepare protocol and study outlines and subsequently driving identified initiativesResponsible for the planning and execution of the clinical studies including site selection, analysis of potential patient recruitment and projections, creation of study related documents (protocols, case report forms, Informed consents, Clinical trial agreements, study reports), organizing IRB/EC submissions with follow-through to ensure successful progressResponsible for independently conducting clinical studies on schedule and within budget while ensuring high quality and compliancePerform on-site and remote site qualification visits, site initiation visits, interim monitoring visits and site close out visits.Conduct clinical study monitoring to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring planComplete source data verification of clinical study data entered in an Electronic Data Capture (EDC) system or on a case report form at sites or in data listings to ensure regulatory and protocol compliance and overall accuracyLiaise with sites and support in internal audit/inspection and ensure sponsor audit readinessLiaise with external vendors and sites to negotiate contracts and budgets in collaboration with the legal team and managementTrack study progress and provide regular status reportsWork closely with Biostatisticians on data analysis, interpretation and synthesis, in order to develop clinical study reports and/or support development of scientific publicationsTrack, process and manage site payments and support in study financial tracking by developing tracking tools as necessaryOrganize and lead study meetings and other study activities as assignedMentor junior clinical study manager(s); provide guidance to CRAs and CTAs on monitoring and other study needsFollow corporate (e.g., SOP’s) and regulatory requirements (e.g., GCP and US and OUS guidelines) and proactively manage studies, following such guidelines and requirementsConduct literature searches and familiarize with literature to stay informed and abreast of relevant scientific/clinical knowledge and/or to determine evidence gapsCritically appraise scientific literature and write clinical summaries to assist research and the development of clinical strategies and clinical investigational protocolsReview and revise Clinical Operations Standard Operating Procedures (SOPs) to assist Clinical Affairs leadership with continuous process improvement initiativesFor post-market research, collaborate with commercial groups (i.e., marketing) to understand market trends and utilize information to support of business goals through Clinical Affairs activitiesFor post-market research, provide scientific expertise to the Health Economics and Outcomes Research department for development of outcomes research analysis (including identification of appropriate diagnosis or reimbursement codes, selection of clinical outcomes for procedures of interest)Work with clinical investigators to prepare manuscripts, abstracts, slide presentations, and poster presentations for scientific meetings and publications in collaboration with managementSupport regulatory submission and approval of pre-market clinical studies and 510k(s), responsible for addressing regulatory body questions on clinical study design and results (e.g., protocol, ICF, eCRF, clinical study reports). QualificationsAdvanced degree in a scientific/bioengineering field (M.S., Ph.D. or M.D.) with a minimum of 3-4 years of experience in clinical research, or Bachelor’s degree in a scientific/bioengineering field with a minimum of 5 years of experience in clinical research is preferred Required SkillsPrevious experience implementing, supporting and managing medical device trialsSignificant knowledge of clinical and/or outcomes research study designStrong experience in protocol and ICF development, writing clinical section(s) for regulatory submissionStrong experience in conducting literature searches, reviews and appraisal of the scientific dataExcellent ability to