Senior Clinical Data Manager

eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud – the foundation of digital trials. Together, the elluminate platform and digital data services give clients self-service access to all their data from one centralized location plus advanced analytics that help them make smarter, faster business decisions.  eClinical Solutions is committed to driving innovation in clinical trials through a better approach to data management and data analytics. We use the eClinical Solutions technology platform, elluminate, throughout the data management process to accelerate timelines for our clients and automate manual processes. We believe in a more agile approach to data management using our core technology elluminate - enabling our life sciences clients to proactively manage their clinical programs and make decisions.  You will make an impact:  As a Senior Clinical Data Manager (Sr. CDM) you will independently act as a study lead and are responsible for the oversight, maintenance, and management of clinical trial database(s) for assigned projects through the full data management process life cycle. You are viewed as the CDM expert and will serve as the primary liaison between eClinical personnel and Sponsor personnel. You will create and oversee the database design specifications, validation, maintenance/data cleaning, and closeout activities of project-specific clinical trial databases. As a Senior Clinical Data Manager, you may delegate tasks/responsibilities to multiple team members in multiple projects. You will provide ongoing project oversight to ensure proper planning and timely completion of high-quality Sponsor deliverables.  Accelerate your skills and career within a fast-growing company while impacting the future of healthcare.  Your day to day:  Primary representative for eClinical Solutions and sponsor data management interaction Responsible for monitoring and ensuring adherence to study timelines and deliverables  Accountable for the overall quality of data management activities and deliverables at the study or program level  Ensure efficiency and consistency for data management tasks across programs  Communicate with global study teams  Participate in client study kickoff and closeout/lessons learned meetings  Create materials for and present at Investigator Meetings  Develop content and deliver Sponsor CRA and/or site training  Delegate tasks, support and provide guidance to study data management team  Oversee and/or develop data management documents including DMPs, eCRF Completion Guidelines, CRFs, and Help Text  Oversee and/or Develop Internal System Testing (IST) plan for database/user roles/edit check specifications  Participate in Internal System Testing (IST) on the database/user roles/edit check specifications  Assist with preparation for implementation of a centralized data management platform for strategic data cleaning and reporting  Utilization of centralized data management platform including graphical patient profiles and operational analytics  Compile the sponsor UAT package  Oversee and/or perform data review as documented in the Data Management Plan and Data Validation Specifications  Oversee and/or perform manual review/QC checks as listed in the Data Validation Specifications exception listings and reporting tools  Oversee and/or perform data review for overall consistency and accuracy  Oversee and/or perform vendor data reconciliation (e.g., IVRS, laboratory data) with the clinical database  Oversee and/or perform query processing/resolution  Provide ongoing data management reports and metrics  Oversee and/or develop specifications and collaborate with programming for programming and QC of manual listings, external data reconciliation, metrics and custom reports as needed throughout the study  Define and develop specifications for database, programming and/or edit check changes as needed throughout the study  Track data management issues and ensure follow up to resolution  Identify data issues and/or data trends, communicate to the Clinical Data Management team and Sponsor, assist with development and implementation of action plan  Maintain data management study documentation  Perform steps pertaining to database freeze/lock and coordinate all related activities  Ongoing evaluation of process and participate in process improvement  Assist in the creation and review of SOPs, WIs, and training materials  Mentor junior level staff and peers on all associated tasks within a study  Participate in proposal defenses  Perform other duties as requested by management  Take the first step towards your dream career. Here is what we are looking for in this role.  Qualifications:  Bachelor’s degree in Pharmaceutical/Biotechnology or higher in health-related field preferred  8+ years in Clinical Data Management experience preferred   Knowledge of ICH/GCP guidelines, 21 CFR Part 11, clinical trial methodology  Strong project management experience and project team leadership skills including work planning and work delegation  Experience with EDC and performing data management activities  Excellent verbal and written communication skills  Proficiency in Microsoft Office Applications, specifically MS Project and MS Excel  Experience with EDC and Clinical Data Management Systems   Accelerate your skills and career within a fast-growing company while impacting the future of healthcare. We have shared our story, now we look forward to learning yours! eClinical is a winner of the 2025 Top Workplaces USA Award for Remote Work! We have also received numerous Top Workplaces Culture Excellence Awards celebrating our exceptional company vision, values, and work-life balance. See all the details here: https://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Ftopworkplaces.com%2Fcompany%2Feclinical-solutions%2F&data=05%7C02%7Cjpouch%40eclinicalsol.com%7C5d0e487a96094948042008de133937c8%7Cc55122ac90d94dc2be1508d0cc3c5114%7C0%7C0%7C638969333636899804%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=vaQE5PDYwiNR%2B5Ze%2FGCPEEuVpY5rfvkfuB48SsqGmV0%3D&reserved=0 eClinical Solutions is a people first organization. Our inclusive culture values the contribution that diversity brings to our business. We celebrate individual experiences that connect us and that inspire innovation in our community. Our team seeks out opportunities to learn, grow and continuously improve. Bring your authentic self, you are welcome here! We are proud to be an equal opportunity employer that values diversity. Our management team is committed to the principle that employment decisions are based on qualifications, merit, culture fit and business need.  Pay Range  US Pay Ranges $100,000—$125,000 USD Offices: Mansfield, Massachusetts, United States (US);