Duration - 12 Months+

Location - Remote

• Project management of all promotional and educational materials submitted by Marketing and Training departments for review through the MAP r

Duration: 2 Months

Location: 100% Remote

The internship role in Bioanalytics will introduce the intern to wet lab techniques analyzing nonclinical samples for biodistribution and gene expressio

As a member of the Regulatory Affairs team, the intern will develop and acquire required regulatory skills and knowledge in support of programs.  particularly through their internship project and by participating in routine regulatory activit

Duration: 12 Months+ (High possibility of extension)

The Associate Scientist , Downstream Process Development in MSAT will work in a matrix team management environment with global engineers and scientists to achieve

Duration: 12 Months (Possibilities of Extension)

Receipt and triage of adverse event reports for marketed and investigational products from all sources. Preliminary evaluation of clinical trial, spontaneous (post-marketi

Duration: - 12 Months

• Responsible for clinical flow cytometry biomarker assay development and validation, data generation and analysis, QC, data interpretation and communication to project teams to enable appropri

Duration: 06 Months – 12 Months

The Associate Director/Director – GCP Audits & GLP Quality Assurance will be responsible to lead, manage and coordinate all GCP audits and GLP regulated QA activities. This

• The Senior Clinical Research Director (Sr CRD) is the primary clinical lead for programs and responsible for leading successful clinical trials for novel therapeutics for Ophthalmologic Diseases. The role requires a well-organized, strateg

Detailed Job Description:

Duties:2 years of scrub experience on major OR procedures

Skills:   2 years of scrub experience on major OR procedures