Campus Pride Jobs

The Clinical Supply Associate Project Manager plans, implements and coordinates the day- to-day clinical supplies activities for early phase and distribution-only clinical research development programs associated with investigational drugs. They have direct responsibility for day-to-day project planning and implementation of tasks necessary to ensure the successful completion of protocols. These tasks include building a comprehensive project plan, production scheduling, procurement coordination with Clinical Supply Commercial team, label design and batch record coordination with the CalCog Operations team, packaging and distribution protocol creations, invoicing and budget tracking, and client communication and expectation management.

The Clinical Supply Associate Project Manager will ensure protocol-specific objectives, timelines and budget guidelines are accomplished. If variances occur, they will immediately report these to the client and process any necessary change orders or amendments to ensure CalCog is being compensated for work performed. They work closely with client representatives and site management staff to identify and propose solutions and corrective actions to complex clinical supply problems.

Additional responsibilities involve ensuring tasks and activities comply with current Good Manufacturing Practices (cGMPs) and under CalCog Standard Operating Procedures (SOPs), plan improvement implementations related to clinical supply routine functions, interact with other departments to implement planned improvements.

Organizational Position The post holder reports directly to a Manager, Project Management or designee, but they will work closely with the Commercial and Operations teams.

Responsibilities Determine scope and operational requirements of the project from the quotation and customer supplied information. Hold a kickoff meeting with the sponsor at project initiation to ensure information is provided so that all parties are fully aware of the scope of the project and their responsibilities within the project. Work with third parties involved in projects, such as IRT providers, CROs or consultants at project initiation to determine and clearly define CalCog responsibilities within the scope of the project. Perform risk assessments at project initiation and continually assess throughout the project. Work together with CalCog internal team and customer to prioritize and mitigate any project risks identified. Responsible for the building, management, and updating of the comprehensive project plan for each project under his/her management; Identify and include on the plan all critical tasks and inter-dependencies impacting project timelines, including tasks being performed by other facilities. Maintain the project plan to always reflect the current status of the tasks associated with the project. Responsible for creation of the packaging summary and/or distribution summary and disseminating them in order that all departments and sponsor are aware of agreed responsibilities and project specific requirements. Lead the activities of the project team at all stages of the project, coordinating tasks and ensuring completion in line with the timelines agreed on the project plan. For any requests for additional services / changes to scope or where a budget has been exhausted, create a change order, and obtain client approval.

Manages flow of return CTM and final CTM accountability and destruction. Record, collate and report customer specific KPIs, agreeing and implementing performance improvement plans, where necessary. Responsible for creating the invoices for the monthly services on time as determined by the invoicing schedule.

Qualifications, Experience and Skills Required Bachelors Degree in Biology/Life Sciences or the equivalent combination of education and 3+ years pharmaceutical research experience required. Ability to organize, plan and prioritize tasks within a high volume, varied workload. Ability to interpret and apply cGMP and GCP knowledge. Strong interpersonal skills and the ability to manage, motivate and influence work behaviors. Proven experience to manage and organize a team. Open-minded, emphatic, and able to adapt to different cultures among our international clients, investigators, study coordinators and projects. Flexible, enthusiastic, and highly motivated to work in a challenging environment. Proficient knowledge of various computer applications- to include Microsoft Office applications (Word, Excel, Outlook). Attention to detail and statistical aptitude.