What are the responsibilities and job description for the Director - Clinical Research Operations position at System One?
Title: Director- Clinical Research Operations
Location: Onsite, Oakland, PA
Schedule: M-F 8 am-5 pm
Type: Direct-Hire/Permanent
Salary: Competitive with excellent benefits !
Start: March 2025
Overview:
A top-ranked research university is currently searching for a DIRECTOR, CLINICAL RESEARCH OPERATIONS . The director will Provides oversight and supervision of all administrative, staffing, and clinical functions for highly
regulated programs, projects, and initiatives within a research program. Facilitates strategic planning, budgetary systems and cost models, and space management. Acts as signatory authority and oversees all reporting functions.
Responsibilities
- Provides oversight and supervision of all administrative and clinical functions for highly regulated
- program/s, projects, and initiatives.
- • Implements and regulates strategic planning concepts, forecasting, budget systems, financial
- accounting, development of cost models, personnel/payroll operations, facilities and space
- management, and research administration for the center.
- • Reviews and authorizes revenues and expenditures; reviews and exercises signatory authority for
- all administrative documents, including personnel, grant applications and contracts, early account
- number authorization, contract modifications, and any other aspects of fiscal operations for the
- center.
- • Supervises staff, including hiring, distributing and reviewing work, performance reviews, and
- documenting disciplinary actions and other human resource administration. Manages work
- schedules and approves timecards. Provides professional development opportunities. Ensures
- that all facility personnel and users are proficient in, and adhere to, standard practices and
- techniques, including proper protocol implementation.
- • Coordinates and oversees all reporting functions, including the annual report and business plan,
- required reports, and progress reports for sponsored research.
- • Oversees the development and enforcement of standard operating practices and development of
- biosafety manual. Ensures compliance with all applicable regulations.
- Bachelor’s degree in addition to a minimum of 7 years of clinical research and/or related experience. At least 5 years in a leadership or supervisory role.
- Process improvement experience.
- MUST have worked and been a manager of a team
- Excellent written and verbal communication skills are essential.
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