The successful candidate will be responsible for performing assays on samples for pharmaceutical and chemical companies; perform Method development experiments and validate methods according to written procedures.

Roles and Responsibilities:

• Perform assays for the routine batch analysis of... [Full Details]

The successful candidate will assist the Medical Monitor in communications between clinical study site and project staff regarding protocol questions; assist with the review and interpretation of clinical study data; writing, editing, compiling and QC of documents; ensuring the accuracy and quality of applicable... [Full Details]

The successful candidate will have direct patient contact in our Phase I Research Facility. The Research Clinician is responsible for ensuring that clinical trial activities are performed as outlined by the clinical trial protocol. positon is located in Omaha, NE.

The successful candidates will be responsible for the timely completion of paper based or electronic Case Report Forms (CRF) and perform quality control checks of CRFs prior to sponsor review. The Data Coordinator is the primary liaison for the Clinical Research Associate (CRA) during monitoring visits at the Omaha, NE location.

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Role & Responsibility

Responsibilities include, but are not limited to:

• Management of assigned investigational clinical study sites including pre-study, initiation, monitoring and study close-out visits (approximately 65% travel overall can be... [Full Details]

Role & Responsibility

Responsibilities include, but are not limited to:

• Management of assigned investigational clinical study sites including pre-study, initiation, monitoring and study close-out visits (approximately 65% travel overall can be... [Full Details]

Role & Responsibility

Responsibilities include, but are not limited to:

• Management of assigned investigational clinical study sites including pre-study, initiation, monitoring and study close-out visits (approximately 65% travel overall can be... [Full Details]

Role & Responsibility

Responsibilities include, but are not limited to:

• Management of assigned investigational clinical study sites including pre-study, initiation, monitoring and study close-out visits (approximately 65% travel overall can be... [Full Details]

Role & Responsibility

Responsibilities include, but are not limited to:

• Management of assigned investigational clinical study sites including pre-study, initiation, monitoring and study close-out visits (approximately 65% travel overall can be... [Full Details]

Role & Responsibility

Responsibilities include, but are not limited to:

• Management of assigned investigational clinical study sites including pre-study, initiation, monitoring and study close-out visits (approximately 65% travel overall can be... [Full Details]

Role & Responsibility

Responsibilities include, but are not limited to:

• Management of assigned investigational clinical study sites including pre-study, initiation, monitoring and study close-out visits (approximately 65% travel overall can be... [Full Details]

Role & Responsibility

Responsibilities include, but are not limited to:

• Management of assigned investigational clinical study sites including pre-study, initiation, monitoring and study close-out visits (approximately 65% travel overall can be... [Full Details]

Role & Responsibility

Responsibilities include, but are not limited to:

• Management of assigned investigational clinical study sites including pre-study, initiation, monitoring and study close-out visits (approximately 65% travel overall can be... [Full Details]

Role & Responsibility

Responsibilities include, but are not limited to:

• Management of assigned investigational clinical study sites including pre-study, initiation, monitoring and study close-out visits (approximately 65% travel overall can be... [Full Details]

Role & Responsibility

Responsibilities include, but are not limited to:

• Management of assigned investigational clinical study sites including pre-study, initiation, monitoring and study close-out visits (approximately 65% travel overall can be... [Full Details]

The successful candidate will leverage business intelligence resources and business acumen to implement and manage process to pre-qualify leads for pursuit by Business Development . Position can be home based so will consider candidates from any location in the US.

The successful candidate will be responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting of results. May be required to coordinate analysis efforts across multiple research... [Full Details]