Senior Clinical Supply Strategist

2 weeks ago

Johannesburg, South Africa Ultra Personnel Full time

Bachelor of Science Degree (or equivalent) is required.
A min of 4 to 5 years experience in Clinical Supply Management or Clinical research and / or Supply Chain
Must be proficient in Microsoft Office programs including SharePoint.
Ability to demonstrate interest in Patient Quality and Compliance.
Ability to communicate with local authorities and read local documents related to clinical supplies (e.g. Importation, labels, package, etc).

**Work experience to include the following**: drug development, clinical study design including randomization, scientific research, pharmaceutical manufacturing/ packaging/ labeling, sourcing, vendor management, distribution, supply chain management, cGMP requirements, supporting project teams.
Project Management certification is desirable.
Training in project management, supply chain management, scientific or clinical disciplines, clinical sites, comparative agents and/or business administration are desirable.
Demonstrate skills with technical, planning, analytical and financial disciplines.
Experience in managing risk and uncertainty.
Demonstrate good decision-making on sound mix of analysis and judgment.
Demonstrate ability to support complex projects and processes.
Achieve results through influence in a matrix organisation.
Demonstrated experience of coordinating and measuring work, negotiation, conflict management, influencing, process improvement, project management.
Demonstrated ability to coordinate complex projects and processes; MS Office suite advanced proficiency, in particular, Excel.
Inventory management.
Knowledgeable or proficient in data analytics tools such as Business Objects and possess the ability to translate a business need into supporting data with speed and accuracy.
Provide high level and strategic support with regards to clinical
supplies strategy setup/maintenance, forecast, processes optimization, logistics, import/export processes and
global clinical supply requirements.
Serve as the primary point of contact between global teams, strategic partners, vendors brokers, carriers, warehouse and domestic distribution providers to ensure safe and secure movement of clinical supplies to patients. This role will serve as Clinical Supply Operations primary point
of contact for Middle East, Russia and Africa countries.
The position will also support across the region with regards to Expanded Access, Compassionate Use & Post-Trial Access programs and Bioequivalence/Bioavailability (BE/BA) studies support for IP strategy setup/maintenance, whenever needed.
planning, cost effectiveness and timely delivery of high quality clinical supplies.
Proactively ensure quality and compliance through risk identification and mitigation plans, strategic planning and execution, and overall design input on a program and protocol basis.
Ensure compliant and effective IP related activities and projects by interacting with all strategic partners such as Global Chemistry Manufacturing Controls, Worldwide Safety &
Regulatory, Medical Affairs, Corporate Affairs, Pharmacovigilance, Global Product Development,
Global Supply, Finance, Corporate Pricing and Business Units.
Serve as the primary point of contact between the company and strategic partners and vendors to ensure safe and secure movement of clinical supplies to patients in the region.
Lead the development and optimization of import/export processes in MERA.
Ensure compliance with all legal requirements (e.g., EHS, cGMP, ICH/GCP, import/export, Quality Standards) by creating and maintaining a culture committed to quality.

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