Clinical Research Coordinator - Surgery

The Department of Surgery is seeking to hire a Limited part time Clinical Research Coordinator to contribute to the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. in this role you will have responsibility for:

• The implementation of research activities for one or more studies.
• Recognizing and performing the necessary tasks to manage projects and prioritizes work to meet necessary deadlines.
• Be responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP).
• Collaborating with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support.

• Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience
• Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
• Strong organizational capabilities to organize multiple projects and competing deadlines forefficiency and cost-effectiveness.
• Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.
• Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines
• Ability to respond to situations in an appropriate and professional manner.
• Ability to concentrate and focus in a workenvironment that contains distracting stimuli and competing deadlines
• Ability to be flexible in handling work delegated by more than one individual.
• Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry.
• Ability to navigate numerous software programs and applications.
• Ability to handle confidential material information with judgement and discretion.
• Working knowledge of the clinical research regulatory framework and institutional requirements.
• Mathematical skills sufficient to prepare clinical research budgets, knowledge of math ability andknowledge of clinical trials research budgeting process to assist with the preparation of clinicaltrial budgets.
• Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) forclinical research.
• Be available to work in more than one environment, travel to meetings, off-site visits,conferences, etc.