Principal Research Support Specialist, Neurology

Position Summary

The Alzheimer’s Disease and Memory Disorders Center and Translational Genomics Research Laboratory is seeking an enthusiastic, self-motivated Principal Research Support Specialist to coordinate research activities. In this position, you will be responsible for:

• Successful planning, implementation and execution of contracted clinical research activities.
• Management of clinical team members throughout the duration of each clinical trials.
• Assuring clear client and internal team communication, process documentation, and compliance with Good Clinical Practices and procedures set forth by University at Buffalo and its study sponsors.

Outstanding Benefits Package
Working at UB comes with benefits that exceed salary alone. There are personal rewards including comprehensive health and retirement plan options. We also focus on creating and sustaining a healthy mix of work, personal and academic pursuit – all in an effort to support your work-life effectiveness. Visit our benefits website to learn about our benefit packages .

About UB
The University at Buffalo is SUNY’s most comprehensive public research university, and an outstanding place to work. UB amplifies ambition for faculty and staff by offering endless possibilities to achieve more. Here, people from all backgrounds and cultures challenge and inspire each other to discover, learn and succeed. Dedicated staff and engaged faculty collaborate to further knowledge and understanding, and develop tenacious graduates who are valued for their talents and their impact on global society. Visit our website to learn more about the University at Buffalo.

As an Equal Opportunity / Affirmative Action employer, the Research Foundation will not discriminate in its employment practices due to an applicant’s race, color, religion, sex, sexual orientation, gender identity, national origin and veteran or disability status.
Minimum Qualifications

• BS/BA (or equivalent) in one of the life sciences
• at least 5 years experience in managing multiple pharma sponsored clinical trials

Preferred Qualifications

• Thorough knowledge of therapeutic area & clinical research process.
• Strong communication skills (verbal and written) to express complex ideas.
• Excellent organizational and interpersonal skills.
• Positive attitude and ability to interact with all levels of staff to coordinate and execute study activities.
• Ability to manage multiple priorities within various clinical trials.
• Ability to reason independently and recommend specific solutions in clinical settings.
• Understanding of basic data processing functions, including electronic data capture.
• Working knowledge of current ICH GCP guidelines and applicable regulations.
• Ability to work independently, prioritize and work with a matrix team environment is essential.
• Working knowledge of Word and Excel.
• Prior experience in electronic data capture ( EDC ) preferred.
• Able to mentor junior Clinical Trial Assistants and volunteers.
• Willingness and ability to travel, as required.
• CCRC certification is a plus

For more information, click the "How to Apply" button.