Clinical Research Coordinator - Hematology/Oncology (Santa Barbara)

Description

The

Clinical Research Coordinator supports the operational management of clinical

research activities throughout the study lifecycle, including design, start-up,

conduct, and closeout. This role is responsible for implementing and managing

research activities for one or more studies, prioritizing tasks to meet

required deadlines. The Coordinator plans and organizes study activities to ensure

compliance with study protocols and applicable regulations, including

institutional policies, FDA Code of Federal Regulations (CFR), and ICH Good

Clinical Practice (GCP). The role involves close collaboration with the

Principal Investigator, ancillary departments, central research teams, sponsors,

and external institutions to support compliant study conduct, financial

management, and adequate staffing.

Hourly Salary Range: $36.37 - $58.52

Qualifications Required:

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 for efficiency and

cost-effectiveness. Working knowledge of the clinical research

regulatory framework and institutional requirements. 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 work

environment 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. 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. Working 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. $36.37-58.52 Hourly Monday – Friday, 8:00am - 5:00pm

Salary : $36 - $59