Clinical Logistics Coordinator

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Company:

Adecco
Location:

Ottawa, Ontario, Canada
Salary:

negotiable / month
Job type:

Full-Time
Posted:

2 days ago
Category:

Physicians

Adecco is currently hiring for a Clinical Logistics Coordinator for our Medical Manufacturing client in Ottawa West. This is a 1-year contract opportunity offering full time hours, Monday – Friday. The salary for this position will be determined based on education and experience.

To qualify for this role, you must have a minimum 3 years working in clinical research environment. This position will provide clinical operational support to clinical studies and projects. Interact with other departments and external suppliers and provide logistical support to clinical research teams.

Our client is a diversified health care innovator with a legacy of pioneering work in medical diagnostics and devices. They are dedicated to advancing innovative with-patient diagnostic technology to improve patient care and system efficiency by fundamentally changing the way health care professionals process patients through their system.

Clinical Research Coordinator Responsibilities:

Conducts assigned Clinical operations activities in accordance with applicable regulations, GCP, policies and procedures.

Coordinate procurement of clinical supplies as part of study planning and to provide for ongoing studies.

Plan and manage inventory of clinical supplies and ensure that required supplies and materials are consistently maintained.

Coordinate orders and ship clinical supplies, instruments and specimens to sites for clinical studies: Preparation of shipping documents and liaison with shipping department to coordinate shipments of all clinical materials.

Materials management (safety stocks, inventory management, forecasting), packaging and labelling clinical shipments, SOP revisions and updates.

Follow up to ensure that supplies, instruments, etc. are received on-time and in good condition. Address any problems that arise in a timely manner.

Liaise with other departments (e.g. Facilities, R&D, Quality, Regulatory Affairs, etc.) to support Clinical Operations activities.

Understand and comply with all application EHS policies, procedures and guidelines.

Responsible for implementing and maintaining the effectiveness of the Quality system.

Miscellaneous other duties may be required.

Clinical Logistics Coordinator Requirements:

College Diploma in Science or Business Administration

Bachelor’s Degree preferred

Minimum 3 years in a clinical research environment or a research laboratory with automated IVD assay/instrument experience preferred.

Knowledge of regulations and standards (GCP) affecting IVDs preferred.

Strong organizational and project coordination skills.

Good interpersonal and communication skills.

To be considered for the Clinical Logistics Coordinator contract, please click on Apply Now!

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