Administration and Staff Positions
To apply for the following positions, send cover letter detailing interest, a current CV and three letters of recommendation to firstname.lastname@example.org. A background check is required for employment.
Manager - Under
administrative review, perform management level work directed toward the
planning, development, implementation, and evaluation of a multi-center,
multi-year grant. This classification requires the use of judgment and
discretion in performing the assigned duties and responsibilities related to
the project. These actions tend to establish precedents and direction for
the project(s). Responsibilities include coordinating the activities of a
multi-center grant; oversee the daily operational activities of the grant and
provide assistance to the grant PI, collaborating with the PI to ensure the
management plan is accurately followed and to coordinate approved changes.
Negotiate contract and/or protocol changes with funding agency/sponsor,
assuming major responsibility for the successful and timely completion of the
tasks that comprise the implementation and analysis phases of a multi-center
grant to include but not limited to planning, development, implementation, and
evaluation, other tasks as assigned.
Writer - Seeking
an experienced medical writer who can be a key member of a multidisciplinary
team that facilitates the transfer of technologies emerging from basic and
clinical research in the field of regenerative medicine. The successful
candidate will be responsible for researching, preparing and coordinating
scientific publications, grant proposals/reports and regulatory documents.
Clinical Manufacturing Center
The Clinical Manufacturing Center is a state-of-the-art GMP- and GTP-compliant, controlled clean room facility that produces novel tissue-engineered/regenerative medicine products. To apply for the following positions, send cover letter detailing interest, a current CV and three letters of recommendation to email@example.com. A background check is required for employment.
QA Supervisor - Responsible for day-to-day quality assurance activities for QC, Facilities and Manufacturing. Provides quality assurance support of project related activities for manufacture of clinical and/or process developmental products through document control, document review and training management. Performs a variety of administrative support functions and operations using manual and electronic systems.
Other Positions: Clinical Manufacturing Center
Various Technicians within the RMCC will perform experiments relating to specific projects using various techniques. A Bachelor’s or Master’s degree and relevant research experience are required.