Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination

experience

All Essential

Strong verbal and written communication skills along with strong interpersonal skills to

effectively establish rapport, and build collaborate relationships.

All Essential

Strong organizational capabilities to organize multiple projects and competing deadlines for

efficiency and cost-effectiveness.

All Essential

Analytical skills sufficient to work and solve address problems and identify solutions with

reasoned judgment.

All Required

Ability to adapt to changing job demands and priorities; work flexible hours to accommodate

research deadlines.

All Required

Ability to respond to situations in an appropriate and professional manner. All Required

Ability to concentrate and focus in a work environment that contains distracting stimuli and

competing deadlines.

All Required

Ability to be flexible in handling work delegated by more than one individual. All Required

Typing and computer skill/ability including word-processing, use of spreadsheets, email, data

entry. Ability to navigate numerous software programs and applications.

All Required

Ability to handle confidential material information with judgement and discretion. All Required

Working knowledge of the clinical research regulatory framework and institutional requirements. All Essential

Mathematical skills sufficient to prepare clinical research budgets, knowledge of math ability and

knowledge of clinical trials research budgeting process to assist with the preparation of clinical

trial budgets.

All Required

Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice

(GC) for clinical research.

All Required

Be available to work in more than one environment, travel to meetings, off-site visits,

conferences, etc.

All Required