The Clinical Laboratory Coordinator is responsible for the management of the laboratory department and activities involving study samples (e.g. blood samples, biopsies, etc.), material and equipment. He is also responsible for laboratory kits, various inventories and maintenance and calibration of clinical and laboratory devices and equipment.

More specifically, the Clinical Laboratory Coordinator must:

• Process the samples received in the laboratory according to the procedures specific to the studies;
• Help with blood draws and other biological samples;
• Creates and modify source documentation to ensure required data is recorded;
• Ensure the shipping and receiving of samples within the time required by the client;
• Ensure optimal storage conditions for samples;
• Participate in the continuous improvement of the laboratory
• Provide quality training to clinical staff performing laboratory tasks;
• Communicates with central and local laboratories for daily correspondences;
• May by required to follow-up on laboratory results;
• Meet quality expectations with regard to the laboratory and sponsor queries;
• Understand the principles and processes for providing excellent customer service internally and externally;
• Understand the clinical research protocols for the studies involved in;
• Respect the established procedures (SOP);
• Plan, organize and prioritize the work in the laboratory order to meet the established deadlines;
• Plan the personnel, space, material and equipment needs of the laboratory;
• Support research coordinators during inspections and audits;
• Participate in the revision of SOPs and laboratory training manuals

REQUIREMENTS

Education

• College degree as medical technologist or laboratory technician
• License to perform blood draws

Experience

• A minimum of 3 years of experience in laboratory

Skills and Knowledge

• Strong interest in science and clinical research;
• Is recognized for his understanding of the scientific process, his ability to analyze and understand research protocols;
• Knowledge of Good Laboratory Practice (GLP) and Transportation of Dangerous Goods (TDG/IATA) regulations;
• Intermediate / advanced knowledge of Microsoft Office Suite (Excel-Word);
• French / English bilingualism (oral and written);
• Demonstrates an ability to learn quickly and an intellectual curiosity;
• Likes teamwork;
• Ability to work on several studies at the same time;
• Integrity, diligence and rigor;
• Autonomy.

OUR COMPANY

The work environment

At Innovaderm, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.

As a Project Coordinator, you will be eligible for the following perks:

• Permanent full-time position
• Complete benefits (medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, social activities)
• Offices near public transportation (Sherbrooke metro station or Saint-Laurent metro station)
• Ongoing learning and development

About Innovaderm

Innovaderm is a contract research organization (CRO) specialized in dermatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Innovaderm continues to grow and expand in North America and Europe.

Innovaderm is committed to providing equitable treatment and equal opportunity to all individuals. As such, Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.

Innovaderm only accepts applicants who can legally work in Canada.