Senior Clinical Trial Manager - Job ID: 1955

Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology.

Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and skilled and passionate colleagues.

Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.

Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark. We offer a dynamic workplace for employees to grow and develop their skills.

The Sr. Clinical Trial Manager (Sr CTM) is responsible for effective conduct of Ascendis’ global and regional clinical trials. As a key member of the cross-functional team driving one or more Ascendis’ clinical trials to completion according to agreed timelines and quality, the Sr. CTM contributes directly to Ascendis’ focus on making a meaningful difference in patients’ lives and is part of a global organization with locations in US, Germany and Denmark.

The role will be based in Palo Alto, CA or be remote and reports to the Director, Clinical Operations.

Key Responsibilities

• Foster and maintain favorable clinical site and investigator relationships. Including conducting and/or supporting informational calls for sites and investigators.
• Support in planning and conducting investigator meetings, if applicable.
• Review and/or approve of IP release packages.
• Review monitoring reports for compliance to study protocols, regulations and ICH/GCP.  Track and manage monitoring report metrics. If applicable, serve as a backup monitor to the monitoring team.
• Generate and utilize metric reporting (e.g. CTMS, DM Query Trends, Outstanding Monitoring Reports) to ensure that the study is conducted per plans and communicates issues to Director and CRAs as appropriate.
• Ensure accurate reporting of Protocol Deviations and follows up with monitoring team of any subsequent re-SDV and close out of PDs if applicable. 
• Provides any assistance with findings from Protocol Deviation Review Team meetings and disseminates any applicable information to the CRA team.
• Conducts monitoring meetings, creating agendas and meeting minutes which may include but is not limited to: monitoring team training and tracking, report quality issues, site level issues/trends in data and EDC metrics reporting.  
• Assist in coordinating study specific training or re-training for the internal study team, internal monitoring team and site staff as appropriate.
• Responsible for the ongoing development and maintenance of Trial Master File and Investigator Site Files in Veeva Vault which includes quarterly eTMF reviews. Assists CRAs in ensuring eTMF completeness, eTMF audit findings and resolutions.
• Manages and/or supports vendor management for central laboratory, central IRB, central imaging, patient concierge services, and site payment systems including but not limited to: portal access management for sites and internal teams, report review, sample tracking, metrics review, document reviews and meeting participation
• Facilitate EDC and IRT access requests for site teams.
• Facilitate CRA team access to internal Ascendis systems such as TMF, EDC and vendor systems (e.g. IRT).
• Assist and manage CRA transition meetings which may include creating and/or reviewing transition documentation
• Run Study Team Meetings including providing agendas and meeting minutes.
• Reviews site information/informed consents and completes associated checklists as per Ascendis SOPs.
• Support central and site IRB/IEC and regulatory submissions, as needed.
• Accountable to assist sites, internal staff and CRAs with the preparation for GCP audits
• Maintains CTMS including but not limited to: site and site staff contact information, study level and site level milestones, regulatory submissions and approvals on both study and site level.
• Escalate pertinent CRA performance and site compliance issues when necessary.
• Collaborate with Director of Clinical Operations, data management and CRAs to ensure data quality and compliance with data cleaning timelines.
• Assist CRAs and sites with supply shipment/tracking, sample tracking and IMP shipment tracking and management.
• May review and approve Vendor Data Clarification Forms.
• Prioritize and escalate issues, as needed.
• May develop or assist in developing study related clinical documents (e.g. clinical plans, Informed Consent Form templates, study specific forms and manuals, CRF completion guidelines, study trackers, PSV/SIV slides and other training materials).
• May be responsible for management of clinical vendors (e.g. labs, IP, patient diary, home health care) in conjunction with Associate Director.
• May be responsible for development, review and/or implementation of vendor documentation.
• May perform clinical data review of patient profiles, data listings and summary tables, including query generation
• May meet with Associate Director, Clinical Operations on a regular basis to report deliverables, timelines and employee development.