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Our client, a major construction contractor specializing in the implementation of construction work in paving, concrete and civil engineering, is currently seeking an estimator. Nature of...

LIMS Clinical Studies Specialist – (Full-time) – Onsite – Quebec CanadaContract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist with 2+ years’ experience working within Clinical Research within a CRO. A history of working within Clinical studies coordination t

LIMS Clinical Studies Specialist – (Full-time) – Onsite – Quebec CanadaContract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist with 2+ years’ experience working within Clinical Research within a CRO. A history of working within Clinical studies coordination t

A history of working within Clinical studies coordination to include dealing with Study Protocols and Plans from various clinical trials (phases I-IV), and Safety Assessments (Pre-Clinical Toxicology Studies). Contract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist w

A history of working within Clinical studies coordination to include dealing with Study Protocols and Plans from various clinical trials (phases I-IV), and Safety Assessments (Pre-Clinical Toxicology Studies). Contract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist w

A history of working within Clinical studies coordination to include dealing with Study Protocols and Plans from various clinical trials (phases I-IV), and Safety Assessments (Pre-Clinical Toxicology Studies). LIMS Clinical Studies Specialist – (Full-time) – Onsite – Quebec CanadaContract Rese

A history of working within Clinical studies coordination to include dealing with Study Protocols and Plans from various clinical trials (phases I-IV), and Safety Assessments (Pre-Clinical Toxicology Studies). Contract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist w

A history of working within Clinical studies coordination to include dealing with Study Protocols and Plans from various clinical trials (phases I-IV), and Safety Assessments (Pre-Clinical Toxicology Studies). Contract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist w

A history of working within Clinical studies coordination to include dealing with Study Protocols and Plans from various clinical trials (phases I-IV), and Safety Assessments (Pre-Clinical Toxicology Studies). Additionally, this individual should have a thorough understanding of Study Protocols and

LIMS Clinical Studies Specialist – (Full-time) – Onsite – Quebec CanadaContract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist with 2+ years’ experience working within Clinical Research within a CRO. A history of working within Clinical studies coordination t

A history of working within Clinical studies coordination to include dealing with Study Protocols and Plans from various clinical trials (phases I-IV), and Safety Assessments (Pre-Clinical Toxicology Studies). Contract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist w