Sam Mowaswes
Global Director - R&D Business Information Mgmt at Otsuka Pharmaceutical Companies (U.S.)
- Role
- Global Director - R & d Business Information Mgmt at Otsuka Pharmaceutical Companies (U.S.)
- Location
- Edison, NJ, US
- LinkedIn followers
- 500 followers
About Sam Mowaswes
Information Technology leader with expertise in strategy planning, execution, staff development, relationship/vendor management, and competitive positioning of technology to enhance operations in the pharmaceutical, Life Sciences, Consumer Goods, and consulting industries. A business leader who understands the difference between strategic and tactical value while executing with an entrepreneurial approach. Specialties:• Strategic Leadership• R&D Information Mgmt Planning and Execution• Staff Management & Development• Relationship Management• Communication and Negotiation Skills• Governance• Focused Outsourcing• Project Management• Center of Excellence Expertise (CoE)• Regulatory Compliance• Demonstrated leadership in matrix organizations Skilled in managing complex IT initiatives and building trusting business relationships across functions, levels and geographies • Result oriented with adaptability to drive change while managing risk and uncertainty• Responsible for resource planning relative to priority of projects with close coordination with leadership in key business functions • Financial management up to $16 MM annual budget with end-end accountability for staff, consultants, and external vendors• Proficiency in IT strategy, tools, validation, SDCL and change mgmt
Experience
Global Director - R & d Business Information Mgmt
Otsuka Pharmaceutical Companies (U.S.)
Jan 2016 — Present
Education
Monmouth University
Master's degree, Management Information Systems, General
Monmouth University
Master’s Degree, Computer/Information Technology Administration and Management
1981 — 1985
Skills
- Computer System Validation
- Dia Tmf Reference Model
- Biotechnology
- IT Strategy
- Technology Transfer
- Clinical Research
- Sdlc
- Edc
- Ctms
- Drug Discovery
- Data Management
- Management
- Clinical Trials
- Pharmaceutical Industry
- Sop
- Fda
- Clinical Data Management
- 21 Cfr Part 11
- Drug Development
- Gcp
- Life Sciences
- Clinical Development
- Regulatory Affairs
- Lifesciences
- Regulatory Submissions
- Cross-Functional Team Leadership
- Vendor Management
- Competitive Intelligence
- Healthcare
- Knowledge Management
- Leadership
- R&D
- Oncology
- Informatics
- CRO
- Gxp
- Clinical Trial Management
- Pharmaceuticals
- Document Management
- Project Portfolio Management
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