Clinical Research Coordinator - Pediatric Hospital Medicine

Albany Medical Center•Albany, NY

3d•$54,690 - $82,035•Onsite

About The Position

The Research Coordinator serves as an assistant to the Principal Investigator. This includes: communication link between study sponsors, investigators, and institutional officials; serves as a resource for federal and local regulations regarding the conduct of research; coordinates contractual issues related to research projects; establishes and maintains communications throughout the study process with personnel directly associated with the study; coordinates research projects; updates PI/RN on changes to existing as well as new study opportunities.

Requirements

Bachelor’s degree in a scientific discipline.
Minimum of 3 years of research experience is necessary.
Working knowledge of good clinical practices and federal regulations regarding the conduct of research.

Responsibilities

Ensure timely scheduling of potential clinical research patients as alerted by the study team.
Prepare, organize and maintain study binders for patients.
Maintain inventory of study supplies, including study-specific lab kits, source document binders and subject diaries and supplies.
Prepare study-specific, visit-specific lab kits in advance of patient’s scheduled study visit.
Process and prepare laboratory specimens and requisitions as required.
Ship laboratory specimens according to study guidelines.
Filing of study documents in patient source binder and site investigator file binders.
Develop and maintain study-specific spreadsheets for PI for the purpose of tracking specified study details.
Call study patients to confirm upcoming study visit and to remind patient to return required materials.
Unpack/inventory incoming study drugs and insure that study drug is placed and proper store temperature.
Organize and maintain research storage areas, prepare completed study records for off-site storage.
Work closely with Clinical RN and PI.
Respond to laboratory queries
Securing signed/completed consents and paperwork for eligible study patients.
Other duties as assigned as they relate to the patients/study.
Participate in regional hemophilia work groups via virtual and in person meetings.
Attend national hemophilia research/data conferences, both virtually and in person.
Regularly update hemophilia databases per regional/national community of practice standards.