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University of Rochester Sr Clinical Trials Project Mgr in Rochester, New York

GENERAL PURPOSE:

Plans, directs, and coordinates study phases of FDA, NIH and Investigator-Initiated clinical trials for multi-center and single center research with extensive responsibility for staff supervision, oversight of study startup, maintenance and closeout activities, closeout activities, training and regulatory compliance with considerable latitude for the exercise of independent judgement and initiative.

JOB DUTIES AND RESPONSIBILITIES:

  • Plans and implements study management for research projects to ensure objectives outlined in the project will be accomplished in accordance with prescribed priorities, time limitations, and funding conditions through initiation and oversight of team meetings and activities.

  • Supervises and ensures study operations comply with government reporting and funding regulatory requirements including preparation of study activities, protocol, consents, SOP’s IND’s and IDE’s.

  • Coordinates administrative efforts and trains investigators and coordinators at participating centers. Supervises on-site monitoring of participating centers, if applicable.

  • Plans and implements a comprehensive data management and information system in conjunction with the IT/computer programming staff. Develops eCRF’s and assists with data collection, data reports, and analysis.

  • Initiates and participates in meetings, evaluates enrolling centers and confers with sponsor, agencies, IRB’s and University administration.

  • Hires, trains, supervises and evaluates CCRC staff with regard to performance and study responsibilities.

  • Maintains a good working knowledge of the cardiovascular research literature and regulatory compliance issues both in general and as it relates to the specific tasks assigned through attendance at national meetings and interactions with study sponsors.

QUALIFICATIONS:

  • Bachelor's degree required with major course works in appropriate health, social science, or biological science field or equivalent combination of education and experience.

  • Advanced degree in appropriate health, social science, or biological science field or equivalent combination of education and experience preferred.

  • Minimum of 5 years of experience with clinical trials required.

  • Previous personnel/study team management experience preferred.

  • Clinical trials project management experience including extensive knowledge of protocol planning, implementation, coordination, evaluation, and reporting of clinical trials required.

  • Strong verbal and written communication skills, interpersonal skills, attention to detail and organization required.

  • Clinical research professional/project management certification preferred.

The University of Rochester is committed to fostering, cultivating, and preserving a culture of equity, diversity, and inclusion to advance the University’s mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion/creed, sex, sexual orientation, citizenship status, or any other status protected by law. This commitment extends to the administration of our policies, admissions, employment, access, and recruitment of candidates from underrepresented populations, veterans, and persons with disabilities consistent with these values and government contractor Affirmative Action obligations.

How To Apply

All applicants must apply online.

EOE Minorities/Females/Protected Veterans/Disabled

Pay Range

Pay Range: $70,197 - $105,295 Annually

The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job’s compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.

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Location: School of Medicine & Dentistry
Full/Part Time: Full-Time
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