Administration and Staff Positions
Facilitates the transfer of technologies emerging from basic research in the field of regenerative medicine. Researches, prepares, writes and edits scientific publications for science journals, grant proposals, grant reports and regulatory documents. Only PhDs with a science background and a scientific publication track record will be considered.
1. Partner with Principal Investigators and Authors in writing, editing and preparation of publication manuscripts, grant applications, regulatory documents, etc.
2. Recommend changes/edits to ensure the most persuasive product consistent with the Author’s intended plan.
3. Accurately interpret publication submission requirements.
4. Ensure timely and accurate publication submission.
5. Prepare detailed reports and provide updates to administration on manuscript submissions as requested.
6. Prioritize assigned tasks in a fast paced environment.
Skills and Qualifications:
Strong scientific background and knowledge with history of successful research publication and grant writing experience.
Must demonstrate a clear, high quality, scientific writing style in the English language.
Must possess the ability to manage large writing projects with minimal supervision.
Must demonstrate an ability to train and mentor young researchers with scientific writing.
Ability to work independently and meet deadlines.
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.
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.
To apply for any of the above 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.