Job Description :
Company Overview:

Creating value by bringing together the right people to achieve results is our motto. Our clients and employees say they choose to work with us because of how we work with them - with service that exceeds their expectations and a personal commitment to their success.

Our client, is the world's largest independent multinational biopharmaceutical company, seeks an accomplished Clinical Supply Chain Specialist.

Manage demand and supply plans for global clinical trials. Execute Process Work Orders and Stock Transfer Orders to ensure patient supply at Client and 3rd Party depots around the world.
Proactively communicate supply issues that may impact ability to dose patients, and work with cross-functional teams to resolve issues as quickly and with as little impact to patients as possible.
Under minimal supervision, manage demand and supply of Phase 1 and Phase 2 Clinical Programs.
The position requires project management skills including time line generation, action tracking, meeting facilitation, effective communication skills and good documentation practices.
Responsibilities will include gathering demand requirements and driving production of Clinical Investigational products, as well as tracking usage and inventory.
Ability to communicate across a wide range of staff levels. Develop effective relationships with partners in the supply chain.
Translate Clinical Development study requirements into an actionable supply plan. Coordinate labeling, packaging, and shipment of packed supplies.
Create and provide multiple planning scenarios based on various combinations of inputs and variables, as required.
Lead forecasting meetings with key stakeholder to ensure the adequacy of supply/re-supply and negotiate resolution of resource conflicts where necessary.
Assess issues with regards to study design, supply availability, and timelines. Promptly identify and escalate risks to study supply to all key stakeholders and internal management.
Strategize with study managers and review study protocols to determine appropriate packaging configurations, blinding techniques, and optimal distribution plans.
Actively participate in planning meetings to ensure that program needs, priorities, and timing are understood.
Serve as the primary interface with Clinical Development, Quality, Biostatistics, Regulatory Affairs, and Clinical Packaging organization to ensure coordination of all activities necessary to fulfill the supply plan.
Provide input to matrix teams on timing, resourcing, and budget projections. Determine distribution strategies for global studies.
Articulate clinical supply chain management processes & strategies to key stakeholders. Review & update existing procedures & SOPs; identify need for & assist in establishment of new procedures & SOPs.

Proficient in MS-Office (Excel, Word, PowerPoint, Outlook
Forecasting or supply planning systems – SAP a plus.
Biotechnology or pharmaceutical industry strongly desired.
Ability to multi-task and prioritize, strong communication skills (verbal/written
Solid demand/supply planning experience, project management, negotiation and facilitation skills.
Sound judgment, analytical, and decision-making skills. Effective influencing and leadership skills. Ability to operate in a team or matrixed environment.
Familiarity with import/export requirements in a global setting is a plus.

I'd love to talk to you if you think this position is right up your alley.

If you're looking for rewarding employment and a company that puts its employees first, we'd like to work with you. We're driven, people driven. We also offer group health Insurance (employee paid on a pre-tax basis

NOTE: “Candidates that are offered a position are required to pass pre-employment drug and background screening”