Clinical Research Coordinator (Nurse Practitioner) -- Scripps Genomic Medicine (35643BR), Genomics / Translational Medicine, La Jolla, California

Position Profile:

Responsible for conducting clinical trials using good clinical practice under the auspices of a Principal Investigator (including the Deputy Medical Director or the Clinical Lead). CRC often prepares bulk of IRB submission, prepares the informed consent documents, prepares detailed cost analysis, supports subject recruitment, prepares adverse event reporting, prepares and submits case report forms and coordinates delivery of data to the Sponsor as needed.

Basic Qualifications (Required):

Licensed Nurse Practitioner or CA Registered Nurse is highly preferred.

Minimum Qualifications (Required):

Minimum of fifteen years of experience.

Current BLS-American Heart Association required by start date.

Preferred Qualifications:

CCRC preferred.

Contact:

Requisition ID: 35643BR

Web Link:

http://www.scripps.org/about-us__careers__search-jobs

Research Study Coordinator – Division of Hematology/Oncology (19748BR), Children’s Hospital Boston, Boston, Massachusetts

Description:

The Division of Hematology/Oncology is seeking a Research Study Coordinator with at least one year of clinical trials coordination experience.

Under general supervision and in accordance with established protocols, manages and organizes operations of clinical research projects in the Division of Hematology and Stem Cell Transplant.

Disease areas include transplant related diseases e.g. hematologic malignancy, graft-versus-host disease, immunodeficiency, as well as hematologic diseases including bone marrow failure and thalassemia.

Oversees collection, maintenance and retrieval of study data, developing and implementing systems and procedures to ensure accuracy, consistency and conformance with protocol requirements.

Develops and monitors budget and maintains related records.

Assists Principal Investigator in selection, training, supervision and evaluation of support personnel.

Requirements:

BA/BS degree and previous experience in coordinating clinical trials . A demonstrated ability to communicate effectively with patients, vendors, contract research organizations and professional staff. Attention to detail. Outstanding interpersonal skills and the ability to work well as a team member. Proficiency in Spanish a plus.

Contact:

AutoReqId: 19748BR

Web Link:

https://sjobs.brassring.com/1033/ASP/TG/cim_home.asp?partnerid=368&siteid=5205