Piper Companies is currently seeking a Project Manager, Data Management & Regulatory Use for a remote opportunity to join a non-profit research group dedicated to saving cancer patients by facilitating access and promoting participation in oncology clinical trials..
Responsibilities of the Project Manager, Data Management & Regulatory Use
Manage, mentor, and train data management staff, develop SOPs, and oversee data management projects
Act as a liaison with industry sponsors, Medidata Rave, and study builders for data management deliverables
Review and develop standard library of CRFs, edit checks, and functions while ensuring CDASH/CDISC compliance
Assist in implementing clinical study databases, provide input for process improvement, and manage department SOPs
Participate in meetings, industry collaborations, training assessments, hiring processes, and special projects
Qualifications of the Project Manager, Data Management & Regulatory Use
5+ years of data management experience for oncology clinical trials, preferably in a pharmaceutical company or CRO
Possess a thorough understanding of data collection practices for oncology-specific trials, global data management practices, and regulatory requirements
Medidata Rave experience, with Medidata certification in data management
Bachelor’s degree or equivalent work experience required
Compensation for the Project Manager, Data Management & Regulatory Use
Salary Range: $100,000 - $120,000
Benefits: Comprehensive package includes Medical, Dental, Vision, 401k, Paid Time Off, and Tuition Reimbursement
Keywords: clinical research, clinical, oncology, cancer, oncology clinical trials, clinical trials, clinical project management, project management, PM, CPM, data management, data manager, regulatory use, RU, manager, people management, supervisor, budgets, fiscal, clinical research trials, pharma, pharmaceutical, CRO, clinical research organization, data collection, medidata rave, global trials, SOP, work instructions, mentoring, regulatory, industry liaison, rave, study build, CRF, edit checks, CDASH, CDISC, compliance, SDTM, WI, case report forms, Clinical Data Acquisition Standards Harmonization, Clinical Data Interchange Standards Consortium
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Project Management and Information Technology
Industries
Staffing and Recruiting
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