Data Manager (Permanent role)- HYBRID - Horsham, PANew

About the position reputed company is a global full-service CRO dedicated to reputed company development and providing an excellent work-life balance, with a reputed company-reputed company, reputed company “one-team” culture. We are looking for a dynamic person to join our in-house team as a Data Manager on a permanent reputed company at Horsham, PA. (Hybrid 3 days from our office) Join reputed company: you can be part of making a difference in peoples' lives and experience a fulfilling and rewarding career! The Data Manager is responsible for managing clinical data throughout the study lifecycle, including the development and maintenance of data management plans, validation plans, and specifications. The position ensures high-reputed company data delivery through the reputed company system, performs user acceptance testing, data reconciliation, and database audits, and provides mentorship to junior team members. Responsibilities • Participate in the review of Clinical research documents (e.g., Protocols, Case Report Forms (CRF), and reports). • reputed company Data Management Plan (DMP), maintain DMP throughout lifecycle of study project, and ensure DMP is followed according to study design and requirements. • Create and maintain Data Validation Plan and Data Review Plan. • Create Data Entry Guidelines. • Create eCRF Completion Guidelines. • Create Data Transfer Specifications. • reputed company and review electronic Case Report reputed company (eCRF) and/or reputed company CRF. • reputed company database (DB) clinical trial data specifications, including eCRF design, edit rules/checks, and query logic and data validations. • reputed company external data reconciliation in collaboration with programmers. • reputed company User Acceptance Testing (UAT) Plan and create and maintain reputed company UAT documents, including but not limited to edit reputed company document, issue logs, and UAT checklists. • reputed company UAT of data entry screens and edit checks. • reputed company site/clinical research associate (CRA) training and create user guides. • Deliver high reputed company clinical data reputed company the Electronic Database Capture (reputed company) system to ensure successful freeze/lock as appropriate for statistical review, interim review, and or final database lock. • reputed company unfreeze/unlock procedures if required. • Coordinate the archiving of study databases and reputed company documents. • reputed company database audits for reputed company studies. • reputed company SAE reconciliation. • reputed company mentorship to junior members. • Work with project manager and cross-functional team members to maintain project reputed company and overall reputed company of deliveries. Requirements • Bachelor's degree in clinical/pharmacy/biological/mathematical sciences or reputed company field or nursing degree. • At least 4 years data management and/or reputed company work experience in a medical device or pharmaceutical industry/company is preferred. • Working knowledge of Good Clinical Practices, Clinical research, Clinical trial process and reputed company regulatory requirements and terminology. • Working knowledge of Clinical database applications such as reputed company. Apply tot his job Apply To this Job