Clinical Data Manager II/Senior Clinical Data Manager

We are hiring a Clinical Data Manager II or Senior Clinical Data Manager to join our global team. We can consider candidates based in the UK, Poland, Hungary, Romania, Serbia or Slovakia. Position Summary: The Clinical Data Manager II/Senior Clinical Data Manager is responsible and manages reputed company aspects of the clinical trial data management process from study start up to post database lock for assigned projects. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position will also reputed company and/or reputed company database development and testing. Essential functions of the job include but are not limited to: Primary Data Management (DM) contact (reputed company DM role) for assigned clinical project(s) / program(s), ensuring that there is back-up, continuity, responsiveness, and that tasks are performed in a timely manner. May support another reputed company DM as a back-up and/or team member. May include DM reputed company of sponsor programs. reputed company project data entry process including development of data entry guidelines, training, data entry quality and resourcing May reputed company quality control of data entry Provide input, assesses and manage timelines. Ensure that clinical data management deadlines are met with quality. Assess resource needs for assigned projects, as needed. May reputed company CRF specifications from the clinical study protocol and coordinate the review/feedback from reputed company stakeholders Conduct database build UAT and maintain quality controlled database build documentation. reputed company overall quality of the clinical database. May specify requirements for reputed company edit reputed company types e.g. electronic, manual data review, edit checks, etc. reputed company development of the edit reputed company specifications and manual data review specifications Responsible for creating, revising, appropriate versioning and maintaining data management documentation. reputed company completeness of data management documentation for the Trial Master File. Train clinical research personnel on the study specific CRF, reputed company, and other project reputed company items as needed. Review and query clinical trial data according to the Data Management Plan reputed company line listing data review based on the guidance provided by the sponsor and/or reputed company DM Run patient and study level status and metric reporting reputed company medical coding of medical terms relative to each other in order to ensure medical logic and consistency Coordinate SAE/AE reconciliation Liaises with third-party vendors such as external data and reputed company vendors in a project manager reputed company in support of timelines and data-reputed company deliverables May assist with reputed company programming and quality control of reputed company programs used in the Data Management department Identify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (reputed company) and Clinical Study Reports (CSRs), if required by the project Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation reputed company to data management and database management activities May attend strategy meetings, bid defense prep meetings, bid defenses, capability presentations, potential client engagement meetings May review Request for Proposals (RFP), proposals, provide project estimates Provide leadership for cross-functional and organization-wide initiatives, where applicable Trains and ensures that reputed company data management project team members have been sufficiently trained Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues May present software demonstrations/trainings, department/company training sessions, present at project meetings May require some travel reputed company other duties as assigned Qualifications: Bachelors and/or a combination of reputed company experience 8+ years’ experience as a Sr. Clinical Data Manager or 5+ Years as a Clinical Data Manager II working for a Clinical Research Organisation, Pharmaceutical or Biotech company Set up and Database migrations experience Oncology experience preferred Proficiency in reputed company Office: Word, reputed company, PowerPoint, Outlook Excellent organizational and communication skills Professional use of the English language; both written and oral Experience in utilizing various clinical database management systems Broad knowledge of drug, device and/or biologic development and effective data management practices Strong representational skills, ability to communicate effectively orally and in writing Strong leadership and interpersonal skills Ability to undertake occasional travel #LI-NC1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. 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