Principal Clinical Data Manager Principal Clinical Data Manager...
Clinical Research Coordinator Responsible for coordinating and performing the collection, distribution and storage/archival of data/study material/study supply generated for assigned studies during clinical research trials. Ensure that the assigned trials stay on track with applicable regulations,
Clinical Study Manager Manages the progress of assigned studies by tracking regulatory/IRB submissions and approvals, recruitment, and enrolment, CRF completion and submission, and data query generation and resolution. Organize delivery of investigational product, laboratory supplies, CRFs
Business Development Manager Generate new business partnerships in staffing industry and help expand on pre-existing relationships. This position will contact prospective clients, secure new business, develop strategic relationships and maintain relationships with clients by positioning Tech Observer in
Cath Lab RN Location: Pompton Plains, NJ 07444 Duration: 6-12 months contract with possible extension Client: Atlantic Health Work Schedule: 10-hour shifts, varying start times. Usual is 07:00 am but could vary between 6 am -
Sr. Director - Clinical Operations This is the main job post content. The job title and description are provided above. If no job description is provided, only the job title is printed....
Job Title 5 to 7 years of experience...
Inspection Technician I Location: Fort Worth, TX 76134 Duration: 12 months contract with possible more extension Summary: The Inspection Technician Associate works in the areas of inspection or quality test of products within the surgical instrumentation
Summary: The main function of a lab technologist is to perform complex laboratory tests. A typical lab technologist usually reports to a biochemist or microbiologist. Job Responsibilities: ? Analyze laboratory findings to check the accuracy of
Document Control Specialist I Location: Lake Forest, CA 92630 Duration: 24 months contract The role is responsible for processing, version controlling, publication and retention of change controls, functional documents and/or GMP records. The role is responsible