Due to our continued growth Precision for Medicine is hiring a Manager, Data Management to line manage a team of Clinical Data Associates.  Candidates can be based in Serbia, Hungary, Poland, Romania or Slovakia.

Position Summary:

The Manager, Data Management manages the day-to-day activities of the Data Management  function in accordance with Standard Operating Procedures (SOPs), regulatory directives, and study specific plans with an emphasis on effective resourcing and development of personnel.

Provides oversight and leading activities for data management projects; coordinates interdepartmental and client communication and helps resolve administrative, personnel, and site issues. In addition, manages all aspects of the clinical trial data management process from study start up to post database lock for Electronic Data Capture (EDC) and paper CRF trials. This position will also oversee and/or perform database development and testing.

Essential functions of the job include but are not limited to:

DM Oversight of sponsor programs, ensuring that there is back-up, continuity, responsiveness, and that tasks are performed in a timely manner for all studies for these clients. May include DM oversight of sponsor programs. 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 develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders. May assist in building clinical databases. May conduct database build UAT and maintain quality controlled database build documentation. Oversee overall quality of the clinical database. May specify requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. Oversee development of the edit check specifications and manual data review specifications. Responsible for creating, revising, appropriate versioning and maintaining data management documentation. Oversee completeness of data management documentation for the Trial Master File. Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed. May review and query clinical trial data according to the Data Management Plan. May perform line listing data review based on the guidance provided by the sponsor and/or Lead DM. May run patient and study level status and metric reporting. Oversee the development requirements and frequency of report delivery. May perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency. May coordinate SAE/AE reconciliation. Liaises with third-party vendors such as external data and EDC vendors in a project[1]manager capacity in support of timelines and data-related deliverables. 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 (SAP) 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 related to data management, database management, applications development and SAS programming activities. Provide technical and operational guidance and direction, checking output of project work, ensuring deliverables are met and performance and professional behaviour management. Attend strategy meetings, bid defense prep meetings, bid defenses, capability presentations, potential client engagement meetings. Reviews Request for Proposals (RFP), proposals, provide project estimates. Provide leadership for cross-functional and organization-wide initiatives, where applicable. Ensures that all 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. Present software demonstrations/trainings, department/company training sessions, present at project meetings. Requires some travel. May perform other duties as assigned

Qualifications:

Minimum Required:

5+ years minimum experience. Bachelors and/or a combination of related experience.

Other Required:

Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook. Able to handle a variety of clinical research tasks. 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 leadership and interpersonal skills 1+ years of leadership experience

Preferred:

Experience in a clinical, scientific or healthcare discipline. Dictionary medical coding (MedDRA and WHODrug) Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.) Oncology and/or Orphan Drug therapeutic experience.

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