Cath Lab RN Location: Morristown, NJ Duration: 6 months contract with possible more extension Work Schedule: 7:00 am to 7:30 pm (3 days/week with one night of call per week which is 7:30 pm to 7:00
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
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
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,
A clinical research organization is looking for a dependable Clinical Trial Associate to provide crucial operational and administrative support to clinical trial teams. The ideal candidate will assist with trial management, documentation, and regulatory compliance. Responsibilities
The Clinical Trial Associate (CTA) provides essential operational and administrative support to clinical trial teams to ensure the effective planning, execution, and close-out of clinical studies. The role supports Clinical Research Associates (CRAs), Clinical Trial Managers
Job Title 5 to 7 years of experience...
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