Job Details

Description

TheSenior Clinical Research Coordinator plays a critical role in the overalloperational management of clinical research/trial/study activities from design,set up, conduct, through closeout. The ideal candidate is an experienced professionalor leader who has direct responsibility for the implementation of researchactivities for one or more studies which may include multicenter clinicaltrials (both NIH and industry-sponsored), local investigator-initiated clinicaltrials, and/or programmatic clinical research activities. Recognize and performnecessary project management tasks and prioritizes work to reach scheduledgoals. The Senior Clinical Research Coordinator is a technical leaderresponsible for ensuring the study protocol and procedures have been completedaccurately, safely, and in a timely manner. This position may supervise andtrain others on projects as necessary. Work with PIs, departments, sponsors,institutions, and other entities as needed to support and provide guidance onthe administration of the compliance, financial, personnel and other relatedaspects of studies.

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

Required:

* Bachelor's Degree in related area and/orequivalent combination of education and experience. Advanced degree preferred

* Minimum of 4+ years of experience in a clinicalresearch setting

* Analytical skills to assess clinical researchprotocols and regulatory requirements, define problems, formulate logicalsolutions, develop alternative solutions, make recommendations, and initiatecorrective actions.

* Demonstrated proficiency with Adobe andMicrosoft suite software, especially Excel, to perform daily tasks efficientlyand accurately.

* Knowledge of and experience working with avariety of local and external IRBs, scientific review and other researchcommittees, national cooperative group sponsors, industry sponsors, federal andfoundation funding organizations, etc.

* Ability to adapt to changing job demands andpriorities, remain flexible including working flexible hours to accommodateresearch deadlines.

* High degree of concentration and focus in a workenvironment that contains distracting stimuli, competing deadlines, and workdelegated by more than one individual.

* Availability to work in more than oneenvironment, travelling to various clinic sites, meetings, conferences, etc.

* Strong knowledge of and experience working witha variety of local and external IRBs, scientific review and other researchcommittees, national cooperative group sponsors, industry sponsors, federal andfoundation funding organizations, etc.

* Strong knowledge of clinical research concepts,policies and procedures, and human safety protection regulations and laws.

* Experience with FDA processes and procedures.

* Sufficient experience and knowledge of clinicaltrials budgeting processes to manage the preparation of clinical trials budgets.