Clinical Research Coord
Where
- Boston, MA
What you'll be doing
- Maintains research data, patient files, and study database. Acts as liaison between sponsor, and PI. Develops systems for quality assurance/quality control organizes and manages study data. Works with clinicians to screen subjects for suitability of research study participation. Develops and implements recruitment strategies. Acts as study resource for patient and family. Submits all institutional review board (IRB) documentation. Prepares documents and study binders for FDA audits (if needed). Orients and trains junior team members on the study protocols as appropriate. Performs other duties as assigned by management if required.
What your background should be
- Microsoft Excel and Word programs skills. Ability to work independently and as a team member. Analytical skills and ability to resolve technical problems. Ability to multi-task and prioritize responsibilities. Training in CITI and GCP preferred. Minimum 1-2 years of Clinical research experience.
Required Schooling / Training
- BA/BS degree.
Who is the client company
- Concern about hospital & health care services.
- If you are interested in this position, send your resume to apply@kochdavis.com
