Senior Clinical Research Coordinator - Hematology/Oncology (Santa Barbara)

Job Description

Description

The\nSenior Clinical Research Coordinator plays a critical role in the overall\noperational management of clinical research/trial/study activities from design,\nset up, conduct, through closeout. The ideal candidate is an experienced professional\nor leader who has direct responsibility for the implementation of research\nactivities for one or more studies which may include multicenter clinical\ntrials (both NIH and industry-sponsored), local investigator-initiated clinical\ntrials, and/or programmatic clinical research activities. Recognize and perform\nnecessary project management tasks and prioritizes work to reach scheduled\ngoals. The Senior Clinical Research Coordinator is a technical leader\nresponsible for ensuring the study protocol and procedures have been completed\naccurately, safely, and in a timely manner. This position may supervise and\ntrain others on projects as necessary. Work with PIs, departments, sponsors,\ninstitutions, and other entities as needed to support and provide guidance on\nthe administration of the compliance, financial, personnel and other related\naspects of studies.

The full annual salary range for this position is: $89,454.77 - $143,904.50

Qualifications

Required:

· Bachelor’s Degree in related area and/or\nequivalent combination of education and experience. Advanced degree preferred

· Minimum of 4+ years of experience in a clinical\nresearch setting

· Analytical skills to assess clinical research\nprotocols and regulatory requirements, define problems, formulate logical\nsolutions, develop alternative solutions, make recommendations, and initiate\ncorrective actions.

· Demonstrated proficiency with Adobe and\nMicrosoft suite software, especially Excel, to perform daily tasks efficiently\nand accurately.

· Knowledge of and experience working with a\nvariety of local and external IRBs, scientific review and other research\ncommittees, national cooperative group sponsors, industry sponsors, federal and\nfoundation funding organizations, etc.

· Ability to adapt to changing job demands and\npriorities, remain flexible including working flexible hours to accommodate\nresearch deadlines.

· High degree of concentration and focus in a work\nenvironment that contains distracting stimuli, competing deadlines, and work\ndelegated by more than one individual.

· Availability to work in more than one\nenvironment, travelling to various clinic sites, meetings, conferences, etc.

· Strong knowledge of and experience working with\na variety of local and external IRBs, scientific review and other research\ncommittees, national cooperative group sponsors, industry sponsors, federal and\nfoundation funding organizations, etc.

· Strong knowledge of clinical research concepts,\npolicies and procedures, and human safety protection regulations and laws.

· Experience with FDA processes and procedures.

· Sufficient experience and knowledge of clinical\ntrials budgeting processes to manage the preparation of clinical trials budgets.