Laura Hetman
Senior Director, Clinical Operations
- Role
- Senior Director, Clinical Operations at Tanabe Pharma America
- Location
- Chicago, IL, US
- LinkedIn followers
- 500 followers
About Laura Hetman
A highly motivated clinical operations professional with extensive experience in pharmaceutical clinical research. Renowned as a results-oriented leader with extensive functional and technical expertise. Proven track record in representing global clinical operations as primary point of contact for internal and external stakeholders, strategic partners, and vendors, leading the development of clinical operations processes, and managing clinical study budget planning and forecasting. Skilled in clinical study management, site management leadership, team collaboration, communication, and project management. Dedicated to driving excellence in clinical operations and delivering high-quality results. Areas of Expertise:Study Management (Early Development & Phase 2-4)Site Management LeadershipOrganizational SkillsTeam CollaborationCommunication SkillsTime ManagementLeadership SkillsPeople ManagementBusiness OperationsProject ManagementTherapeutic Area Experience:Oncology (Early and Late Stage)NeuroscienceImmunologyGastrointestinalMetabolic/Cardiovascular
Experience
Senior Director, Clinical Operations
Oct 2024 — Present · Jersey City, NJ, US
Lead a full development team in designing, planning, implementing, and executing clinical trials and programs, Lead the successful delivery of early-stage clinical milestones, drawing on expertise in clinical and regulatory requirements, both local and international, related to the clinical medicine and drug development processes. Lead teams, mentoring and motivating individual team members, to meet overall corporate objectives leading to submission for world-wide marketing applications.Responsible for clinical development strategy, clinical program oversight, and support of clinical interactions with regulatory agencies. Participate in developing the long-range strategic plans and commercial planning and lead the design, implementation, monitoring, analysis, and reporting of clinical studies.
Education
Bradley University
Bachelor's degree, Biology, General
Skills
- Clinical Research
- Pharmaceutical Industry
- Ich-Gcp
- Clinical Development
- Therapeutic Areas
- Gcp
- CRO
- Diabetes
- Clinical Trials
- Clinical Monitoring
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