Associate Director, Clinical Data Management

Location On Site 4 days per week at our Menlo Park CA or Princeton NJ office About Summit Ivonescimab known as SMT112 is a novel potential first in class investigational bispecific antibody combining the effects of immunotherapy via a blockade of PD 1 with the anti angiogenesis effects associated with blocking VEGF into a single molecule Ivonescimab displays unique cooperative binding to each of its intended targets with multifold higher affinity when in the presence of both PD 1 and VEGF Summit has begun its clinical development of ivonescimab in non small cell lung cancer NSCLC with three active Phase III trials HARMONi is a Phase III clinical trial which intends to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR mutated locally advanced or metastatic non squamous NSCLC who have progressed after treatment with a 3rd generation EGFR TKI eg osimertinibHARMONi 3 is a Phase III clinical trial which is designed to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first line metastatic NSCLCHARMONi 7 is a Phase III clinical trial which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first line metastatic NSCLC whose tumors have high PD L1 expressionIvonescimab is an investigational therapy that is not approved by any regulatory authority in Summits license territories including the United States and Europe Ivonescimab was approved for marketing authorization in China in May 2024 Ivonescimab was granted Fast Track designation by the US Food & Drug Administration FDA for the HARMONi clinical trial setting Overview of Role We are looking for an experienced Associate Director Clinical Data Management that will contribute to and support the companys research and development efforts to create high value therapeutics to address unmet medical needsThe Associate Director Clinical Data Management independently leads the data management components of a clinical trial ranging from small early phase to large global and late phase programs This role will direct the planning implementation and overall direction of executingachieving clinical trial data management activities including CRFeCRF design database development validation programming data review discrepancy management and database lock Additionally the position will manage data management staff Contract Research Organizations CROs and service providers activities in overseeing the data management process life cycle in coordination with internal Biostatistics Clinical and Regulatory teams to ensure the accurate efficient and complete data collection for clinical trials Role and Responsibilities Provide expertise and contribute to the strategy and development of the Clinical Data Management Portfolios to ensure data quality in support of clinical study data milestones and deliverables Lead and support establishment of systems and processes to help ensure clinical data security integrity and long term goals of the business function in alignment with company priorities Leads the data management of overall drug development process with early and late phase clinical trials in large or complex development programs Provides technical expertise to develop and implement clinical data standards data management plans data transfer agreements and data flow processes to ensure timely and quality data delivery for analysis purpose Oversees the process to identify evaluate and select CROs vendors and technology for CDM activities Leads designs andor oversees eCRF design eCRF specifications eCRF completion guidelines annotated CRFs User Acceptance Testing query logic edit checks data query resolution SAE reconciliation between clinical and pharmacovigilance databases vendor data reconciliation & cleaning data migration and database closeout for clinical trials Represents Data Management and promotes productive collaboration with other functions eg Clinical Operations Clinical Development Biostatistics Statistical Programming Translational Science Project Management Regulatory QA and IT to ensure proper alignment around data management activities & deliverables operational excellence compliance with regulations policies procedures and clinical objectives Supports cross functional teams and studies to handle data management questions troubleshoot help resolve issues and mitigate risks Initiates continuous efforts in reviewing and identifying best practices among study teams and enforcing standardization among teams and studies Works with the Director of Clinical Data Science CDS to enhance efficiency optimize costs and drive excellence Works with the Director of Clinical Data Science to establish CDM processes and procedures including SOPs to ensure highest data qualityintegritysecurity and regulatory compliance with FDA regulations GCP ICH guidelines and Good Clinical DM Practices Leads clinical data management activities during regulatory audits ensuring compliance with industry standards and regulations and providing expert input throughout the audit process Works with the Head of Statistical Programming & CDS to manage departmental budget and execute resource planning across multiple projects Works with the Director of Clinical Data Science to provide oversight and guidance as well as establish key performance metrics with CROs to ensure the highest data qualityintegrity and regulatory compliance Accommodate ad hoc data requests between clinical team members scientists and vendors to support data cleaning data entry requirements and exploratory data review if needed Uses scientific and drug development knowledge to anticipate and mitigate data management related challenges during clinical trial execution Reviews and contributes to clinical protocols and amendments study manuals and other study conduct related clinical documents; review clinical data according to these documents All other duties as assigned Experience Education and Specialized Knowledge and Skills Bachelors degree in Life Sciences Computer Science or relevant field of study; or equivalent practical experience A minimum of 10 years of Clinical Data Management experience oncology experience highly desirable in biotechnology or pharmaceutical industry with excellent understanding of late phase clinical drug development processes required Experience with various data collection and Electronic Data Capture EDC systems and understanding of the MedDRA and WHODRUG coding processes Strong track record of line management and supervisory experience of CDM staff shown leadership skills to lead and inspire CDM staff including consultants Excellent interpersonal communication and leadership skills Consistent detail oriented communicative dedicated to do a job well done CRO and vendor oversight experience preferred Strong knowledge of clinical research FDA & ICH GCP GCDMP and related regulatory requirements The pay range for this role is per year Actual compensation packages are based on several factors that are unique to each candidate including but not limited to skill set depth of experience certifications and specific work location This may be different in other locations due to differences in the cost of labor The total compensation package for this position may also include bonus stock benefits andor other applicable variable compensation Summit does not accept referrals from employment businesses andor employment agencies in respect of the vacancies posted on this site All employment businessesagencies are required to contact Summits Talent Acquisition team at recruitingsmmttxcom to obtain prior written authorization before referring any candidates to Summit