Required:

Bachelor’s Degree or three-to seven years of study coordination or clinical research coordination experience

Ability to work efficiently and complete tasks with a high degree of accuracy. 

Ability to organize multiple projects for efficiency and cost-effectiveness. 

Analytical skills sufficient to work and solve problems. 

Ability to work flexible hours to accommodate research deadlines. 

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

Ability to be flexible in handling work delegated by more than one individual or in the course of delegating work.

Strong interpersonal communication skills to effectively and diplomatically interact with others, including institutional leadership.

Strong written communication skills, ability to compose advanced correspondence and manage large file systems.

Advanced typing and computer skill/ability including word-processing, use of spreadsheets, email and data entry.

Ability to handle confidential material with judgement and discretion. 

Skill in managing diverse, complex tasks and information transfer among multiple constituents. 

Sufficient math ability and knowledge of clinical trials budgeting processes to manage the preparation of clinical trial budgets.

Advance knowledge of the clinical research regulatory framework and institutional requirements. 

Ability to supervise and delegate clerical work as needed. 

Advanced knowledge of Good Clinical Practice (GCP) for clinical research. 

Strong knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research. .

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