Project Manager, Clinical Trial Supply

We are looking for a competent, ambitious, passionate individual with attention to detail and ability to manage client projects / orders to completion with excellence.

The role also encompasses a commercial component of either purchasing or selling, so demonstrated experience in procurement or sales in the pharmaceutical sector is a requirement.
Previous knowledge or involvement with clinical trials is a distinct advantage for this role.

Responsibilities to include, but are not limited to:

• Taking full responsibility and accountability for client requests, delivery, and opportunities
• Driving projects towards successful completion while supervising that communication, procurement, logistics, business development, operations, quality and administration abide to regulations and company ́s SOPs
• Ability to read clinical trial protocols and interpret medicine requirements, create and execute an effective clinical trial supply chain solution
• Create an appropriate distribution plan and have oversight of the assigned vendor(s) executing it
• Ability to work independently and proactively to ensure that the supply of all trial materials is delivered to the right place at the right time
• Preparing quotes and follow up on orders for the acquisition of goods
• Provide ongoing budget tracking activities so that projects are run efficiently and in accordance with client approved quotations
• Remain up to date in all GxP and regulatory requirements applicable to the role
• Leads client and vendor related meetings where necessary to discuss clinical supply chain topics or status updates
• Conducts thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigation executed
• Pro-actively communicating the project status to all stakeholders, liaising with all stakeholders to ensure on-time project management
• Develops and sustains customer relationships through direct interaction, responsiveness, and accountability.  Maintain open communication with custoimers using appropriate tools
• Proactively collaborating with other internal departments by maintaining a consistent communication
• Support company's growth by continuously seeking ways to improve quality, range of services and geographic caoverage.

This role is part of the expansion programm at CSI and requires a high degree of profgessionalism where the following skills are essential:

Customer centricity, Result orientation, Market knowledge, Teamwork and Entrepreneurial spirit.

• You have a bachelor's degree and a Master's degree
• Min 5-years experience in CRO/CMO/Pharma (clinical trial supply, project management or pharmaceutical wholesale)(Eseentail)
• Ability to demonstrate good project management skills
• Ability to create effective working relationships with internal and external stakeholders
• Ability to demonstrate effective communication and direction
• You are highly motivated and a reliable team player with proven problem-solving skills
• Experience being an RP highly desired,

In return we offer:

An amazing opportunity to contribute to a fast growing, pharmaceutical company and potentially move along our subsidiaries.

A 'can do' culture where you will be encouraged to get involved in a range of exciting initiatives and to introduce new ideas, work directly with some of the largest Pharmaceuticalcompanies

A warm, welcoming environment based in Central London

The opportunity to learn new skills and ongoing personal development and career opportunities

Competitive salary dependent on experience, annual leave, generous bonus structure and great working environment.

What’s in it for you?

Career Progression: You will be able to develop your career with a wide variety of opportunities and work with highly experience people in the industry.

From continuing your professional development in clinical services, to engaging with Blue Chip Pharmaceutical clients all over the world.

Develop scientific knowledge and expertise in clinical trials and drug development.